Efficacy of NSCLC Rechallenge with Immune Checkpoint Inhibitors Following Disease Progression or Relapse

Immune checkpoint inhibitors (ICI’s) are in the forefront of advanced Non Small Cell Lung Cancer (NSCLC) treatment. Still, only 27- 46% of patients respond to initial therapy with ICI’s and of those, up to 65% develop resistance within four years. After disease progression (PD), treatment options are limited, with 10% Objective Response Rate (ORR) to second or third-line chemotherapy. In this context, ICI rechallenge is an appealing option for NSCLC. Most data on the efficacy of ICI rechallenge are based on retrospective real-world studies of small, heavily pretreated, and heterogeneous patient groups. Despite these limitations, these studies suggest that ICI monotherapy rechallenge in unselected NSCLC patient populations who discontinued initial ICI due to PD is generally ineffective, with a median Progression-Free Survival (PFS) of 1.6-3.1 months and a Disease Control Rate (DCR) of 21.4%-41.6%. However, there is a subpopulation that benefits from this strategy, and further characterization of this subgroup is essential. Furthermore, immunotherapy rechallenge in patients who discontinued initial immunotherapy following treatment protocol completion and progressed after an immunotherapy-free interval showed promising efficacy, with a DCR of 75-81%, according to post-hoc analyses of several clinical trials. Future research of ICI rechallenge for NSCLC should focus on better patient stratification, to reflect the underlying biology of immunotherapy resistance more accurately.

Keywords:

Subject: Biology and Life Sciences - Life Sciences

1. Introduction

From 2015 with the FDA approval of the first Immune checkpoint inhibitor (ICI) for Non-small cell lung cancer (NSCLC) treatment [1,2] to today, immunotherapy (IO) has become the standard of care for patients with metastatic disease [3], and -following recent phase III clinical trial results- it is expected to dominate the treatment field of locally advanced disease as well [4,5]. Despite the undeniable benefit from the introduction of immunotherapy in NSCLC treatment, only 27-46% [6,7,8] of patients with advanced disease respond to therapy with ICI’s. Furthermore, even among responders, resistance to immunotherapy may eventually develop [9]. Based on a pooled-analysis of four clinical trals including patients treated with Nivolumab, 65% of those who respond to treatment initially, will progress within four years [10]. Beyond the point of progression, therapeutic options are limited, and the optimal management strategy is not clear. As we have gained more insight into the dynamic adaptation of cancer cells and the tumour microenvironment, the idea of retreatment with ICI’s following progression after a treatment-free period is considered a reasonable strategy [11]. In this article we perform a comprehensive review of the published literature regarding ICI retreatment of NSCLC patients, following progression to previous line immunotherapy. In the first section, we review the results of retrospective real-world studies. In the second section we discuss the results of rechallenge immunotherapy in subsets of patients from post-hoc analyses of phase III trials, as well as a phase II clinical trial of rechallenge immunotherapy in NSCLC. Finally, we briefly discuss the biological rationale of rechallenge immunotherapy, and the differences in immune response between immunotherapy-naive and immunotherapy pretreated patients, and we propose areas for future research.

1.2. Primary versus Acquired resistance

When the prospect of Immunotherapy Rechallenge is considered, it is pivotal to understand the underlying mechanism of resistance to the first course of immunotherapy. Primary resistance (also called intrinsic or innate) refers to patients who do not respond to immunotherapy, instead they have disease progression quickly. Acquired resistance (also named secondary, adaptive or evasive) on the other hand, refers to patients who responded for a period to immunotherapy, but eventually have disease progression [9,11]. Making this distinction when assessing the efficacy of immunotherapy rechallenge is important, as they indicate different predisposition to immunotherapy response and distinct mechanisms of resistance. A challenge in interpreting studies assessing the efficacy of rechallenge therapy is the lack of consistency in the clinical definition of resistance to immunotherapy. In 2020, the Society for Immunotherapy of Cancer (SITC) Immunotherapy Resistance Taskforce, published their recommendations for defining resistance to PD-1 pathway blockade across solid tumours. They proposed three distinct categories of resistance, based on the Best Overall Response (BOR) and the duration of response to therapy. They defined Primary resistance as: 1. Progressive disease (PD) as the initial response to therapy, or 2. Complete Response (CR), Partial Response (PR) or Stable Disease (SD) for <6 months. Secondary resistance was defined as: 1. CR, PR or SD for >6 months, or 2. Progression within 12 weeks after the last dose of therapy for patients who completed a course of ICI regimen. Finally, patients who either completed an ICI course or stopped due to toxicity, and subsequently progressed >12 weeks after the last dose, were classified separately, and the expert panel proposed ICI retreatment in these patients. Several points regarding these recommendations should be noted. First of all, they are not designed for clinical decision making, rather for the stratification of patients in clinical trials in order to increase the likelihood of positive results. Second, the recommendations are designed to be used across solid tumours, thus they may not reflect the differential biology of each tumour. Third, although the time limit of 6 months has been set by the expert panel, they agree that there is no strong scientific evidence to prove its validity. Finally, patients with SD are pooled with patients who have PR and CR, although research suggests differential tumour and tumour microenvironment biology in these cases [12].

More recently, Schoenfeld et al. proposed modified criteria for clinical acquired resistance, specifically in patients with NSCLC [13]. Their criteria for acquired resistance to ICI therapy were; 1. Prior treatment with Immunotherapy (IO). 2. Objective response to PD(L)-1 blockade (Stable disease (SD) is excluded), and 3. Progression occurring within 6 months of last PD(L)-1 blockade therapy. A potential limitation of this definition is the exclusion of all patients with Best Overall Response (BOR) of SD, classifying this entire population as having primary resistance. Furthermore, it does not entail a minimum duration of response to ICI therapy, as it recognises that the 6 months proposed by SITC has not been validated in the setting of NSCLC. Yet, whether a time limit should be included in the definition in order to optimally select patients needs to be more thoroughly investigated. Like the SITC criteria, they also set a limit after the last immunotherapy dose, however while the SITC puts this limit at 12 weeks (3 months) -based on the half-life of PD-(L)1 inhibitors and subsequently their clearance time-, Schoenfeld et al. set it at 6 months. This is a strength of both recommendations, as it has been proposed that patients who develop resistance during treatment and those who relapse after completion of treatment and a treatment-free interval differ. Relapses may be termed ‘sensitive’ or ‘partially sensitive’ rather than ‘resistant’ if the treatment-free interval from therapy discontinuation to relapse is of long (or intermediate) duration [11]. Yet in this case as well, it is unclear if the time limit of 3 or 6 months is optimal and remains to be validated.

1.2. Oligo- versus Systemic acquired resistance

It has been proposed that the pattern of immune resistance development - reflected on the pattern of radiologic progression - may correspond to different tumour biology and affect the efficacy of immune modulation post disease progression [14]. Thus, a distinction can be made between Oligo-acquired resistance (OligoAR) and Systemic acquired resistance (sAR). OligoAR can be defined as progression in only a few lesions. Assuming that OligoAR may reflect local immune resistance with otherwise sustained anti-tumor immunity, Schoenfeld et al. performed a retrospective analysis of 1,536 patients treated in the Memorial Sloan Kettering Cancer Center with PD-(L)1 blockade (without chemotherapy). They found that patients treated with ICI’s who develop OligoAR in comparison to sAR have increased Overall survival (OS). The authors set the limit for the distinction between oligoAR and sAR at 3 lesions, but whether this is the optimal cut-off for every malignancy and every treatment is not clear. When assessing the efficacy of ICI rechallenge, the pattern of resistance (OligoAR vs sAR) to the initial IO course may be important [14].

2. Methods

A literature search was performed in Pubmed and Scopus using the keywords: “NSCLC”, “Non small cell lung cancer”, “Rechallenge”, “Retreatment”, “Reinitiation”, “Restart”, “Immunotherapy”, “Immune Checkpoint inhibitor”, “ICI”, “PD-1 inhibitor*”, “PD-L1 inhibitor*”, “PD”, “Progression”, “Progressive”. Additional publications were identified from cited articles and through targeted literature search. We defined IO Rechallenge as a subsequent line of therapy with ICI’s in patients who had received ICI in a previous line of treatment, either as monotherapy or as combination therapy, and experienced disease progression either during treatment or after completing the initial ICI course and a treatment-free period. Articles including patients who discontinued the initial course of IO due to adverse events (AE’s) or physician decision were included in this review, provided that they also included populations who had treatment progression prior to IO reintroduction. However, studies focusing only on this population of patients resuming ICI’s after initial discontinuation due to AE’s were not included. As this is a Narrative and not a Systematic review it provides a non-exhaustive view of the topic.

3. Discussion

3.1. Retrospective rw-data

So far, two Systematic Reviews and Meta-analyses by Feng et al. and Cai et al. [15,16] assessing the efficacy and safety of ICI rechallenge in patients with NSCLC have been published. An important limitation of most published retrospective studies on IO rechallenge for NSCLC, is that they do not stratify patients on the basis of acquired resistance versus primary resistance, possibly leading to an underestimation of the potential efficacy of IO rechallenge, had the patients been optimally selected. Furthermore, most of them do not provide explicit information on the patterns of disease progression, and they do not make the distinction between oligoAR and systemic AR. With these limitations in mind, in the following section we present and critically review the results of 13 retrospective studies in the real-world, of IO rechallenge following progression either during, or following completion of initial IO course. They are presented in two separate sections, divided into those where initial IO was discontinued due to disease Progression and those including mixed populations of patients, where IO was discontinued due to PD, toxicity, completion of IO course or physician decision. The respective findings are summarised in Table 1 and Table 2.

3.1.1. Cohorts of patients who discontinued initial IO due to PD.

Fujita et al., 2018 [17]

Fujita et al., conducted a retrospective study of 12 Asian patients, who received first course IO with Nivolumab, and second course with Pembrolizumab. The median PFS at rechallenge (PFS-R) was 3.1 months (range 1.2-12.6 months). The Objective Response Rate at Rechallenge (ORR-R) was 8.3% and the Disease Control Rate at Rechallenge (DCR-R) was 41.6%. All 5 patients with Disease Control (PR or SD) at pembrolizumab rechallenge had PD-L1 TPS ≥ 80%.

Fujita et al., 2020 [18]

This was a retrospective cohort study of 15 Asian patients who received rechallenge IO with anti-PD-1 antibodies after prior anti-PD-L1 treatment. The anti-PD-L1 agents used at At initial IO 14 patients received atezolizumab and 1 patient received durvalumab as consolidation treatment following concurrent chemoradiation. At rechallenge 7 patients nivolumab and 8 patients received pembrolizumab. For Nivolumab, median PFS-R was 1.9 (95% CI 0.4-3.0) months, ORR-R was 0%, and DCR-R was 14.3%. For Pembrolizumab, the respective numbers were 3.1 (95% CI, 1.2-12.6) months, 0% and 37.5%. No patient had Partial or Complete response at rechallenge IO.

In this study, anti-PD-1 treatment following previous anti-PD-L1 therapy showed very poor efficacy. However, patient selection for rechallenge may have been suboptimal, considering that they had overall poor response to prior therapy with Atezolizumab (no patients had PR and only 4 patients had SD), and that 3 patients had already received a PD-1 inhibitor prior to Atezolizumab, meaning that they were subsequently rechallenged with IO for the second time.

Watanabe et al., 2019 [19]

This was a retrospective study of 14 patients (4.4%) conducted at seven centres in Japan. The agent administered at 1st IO course was nivolumab, pembrolizumab and atezolizumab in 11, 1 and 2 patients respectively. At rechallenge, the respective numbers for nivolumab and pembrolizumab were 9 and 5. Eight patients were rechallenged with the same ICI, and 6 switched. Median PFS-R was 1.6 months (95% CI: 0.8–2.6) months. ORR-R and DCR-R were 7.1% and 21.4% respectively. The ORR-R was 12.5% among patients who received the same kind of ICIs in the first and second IO course, and 0% among patients who switched ICIs. Two of three patients, who achieved disease control with rechallenge IO, received radiotherapy between the first and second ICI treatments. These two patients were also the only ones who received intervening radiotherapy. In accordance with the 2020 study by Fujita et al., rechallenge of anti-PD-1 antibody after anti-PD-L1 antibody was ineffective in two of two patients.

Paradoxically, in these cohort studies, all 3 patients with a BOR-R of SD, had PD at first IO course and short duration of therapy. The authors assumed that this phenomenon might be due to pseudoprogression. However, pseudoprogression in IO treated NSCLC, in comparison to Melanoma, is a relatively rare event. Although this unlikely observation cannot be precluded, it highlights a downside of most of these retrospective real-world studies, being that BOR per RECIST 1.1 is not defined by Central Review, and there is potential for interpretation error.

Katayama et al., 2019 [20]

This was a retrospective study of 35 patients conducted across 6 institutions in Japan. The agents used were nivolumab, pembrolizumab and atezolizumab for; 19 (54.3%), 12 (34.3%), and 4 (11.4%) patients at initial IO course and 5 (14.3%), 7 (20.0%) and 23 (65.7%) at rechallenge, respectively. All patients switched ICI agents at rechallenge. Median PFS-R was 2.7 (range, 1.4-3.7). ORR-R and DCR-R were 2.9% and 43%.

In the multivariate analysis, ECOG-PS ≥ 2 at rechallenge was negatively associated with PFS-R (HR 2.38, 95% CI 1.03–5.52, p = 0.043) and BMI >20 was positively associated (HR 0.43, 95% CI 0.19–0.95, p value=0.036).

Xu et al., 2022 [21]

This was a retrospective cohort study of 40 Asian patients. The majority of patients had received the first ICI course (21 (53%)) as a combination treatment with chemotherapy. At rechallenge, 17 (43%) patients received immunotherapy combined with chemotherapy, 20 (50%) immunotherapy with chemotherapy and angiogenesis inhibitor, 10 (25%) IO with angiogenesis inhibitor and only 3 (8%) ICI monotherapy. Median PFS-R was 6.8 months (95% CI 5.8–7.8). ORR-R was 22.5% and DCR-R was 85.0%; BOR was PR for 9 (22.5%), SD for 25 (62.5%) and PD for 6 (15.0%) patients. In the multivariate analysis, no baseline patient or treatment characteristics were associated with PFS-R, although the study may not have been adequately powered to identify such associations.

Compared with the aforementioned studies, the majority of recruited patients in this cohort study received combined chemoimmunotherapy both at first course IO and at the rechallenge setting, which better reflects the current clinical practice. In comparison to most of the studies mentioned so far, of rechallenge IO monotherapy, PFS-R, ORR-R and DCR-R were numerically higher in this study, which may indicate the potential for higher efficacy with rechallenge chemoimmunotherapy.

3.1.2. Cohorts of patients who discontinued initial IO due to PD, toxicity, or physician decision.

Gettinger et al., 2018 [22]

Gettinger et al. assessed the patterns of Acquired resistance in patients from nine clinical trials who developed AR to PD-1 axis inhibitor therapy. They defined Acquired resistance to IO with ICI, as disease progression following PR or CR by RECIST 1.1. criteria or immune-related response criteria. Out of 28 patients included in their analysis, 3 received IO rechallenge. All three received the same ICI in the first and second course, did not receive local therapy or other systemic therapy between the two courses, were off-treatment with durable response for more than 3 months before acquiring resistance to the first IO course, and had oligoAR. These patients more closely mirror the populations of trial post-hoc analyses that will be discussed below. Two of three demonstrated durable response to to 2nd course IO with a PFS of 11 months and 9 months respectively [22].

At this point, it should be noted that the writers defined as AR, all cases of disease progression after a period of response, including patients who successfully completed the initial IO course with durable response. However, as stated in the Introduction, it is debatable whether these patients should be included under the same umbrella of acquired resistance, as these relapses might be ‘partially sensitive’ rather than ‘resistant’ [11]. This possibility is endorsed by the fact that the two patients who responded to rechallenge achieved markedly better response to ICI rechallenge than the average patient discussed in this section. An interesting finding of this study is the pattern of progression to first course IO, as all 28 patients but one experienced OligoAR (< 3 progressive lesions) with Lymph nodes being the predominant site of progression [22].

Niki et al., 2018 [23]

This was a retrospective study of 10 Asian patients who were rechallenged with either nivolumab or pembrolizumab, following progression with prior nivolumab treatment. At rechallenge, 10 patients were retreated with nivolumab and 1 received pembrolizumab. The median PFS-R was 2.7 (0.5–16.1) months. ORR-R was 27% and DCR-R was 45.5%; 3 patients had PR and 2 patients had SD. In this cohort, 4 out of 5 patients who responded to initial IO treatment had disease control in the rechallenge setting as well. The only patient with BOR-1 of PD who achieved PR at rechallenge had received both chemotherapy and radiotherapy between the two IO courses, which led to the assumption that intervening cytotoxic therapy might be associated with increased likelihood of Rechallenge IO response. In patients who achieved disease control, the median duration from the end of initial IO treatment to rechallenge onset (ICI-free interval) was 1.6 months, whereas, for the non-responders it was 4.7 months. Based on this finding, the authors assumed that shorter treatment-free interval between IO courses is related to better rechallenge IO efficacy, which, as we will discuss later, was contradicted in a phase II clinical trial of Nivolumab rechallenge in ICI pretreated patients [24].

Kitagawa et al., 2020 [25]

This was a retrospective study of 17 Asian patients with NSCLC who were rechallenged with a different ICI following initial ICI treatment discontinuation. The reasons for discontinuing treatment were progressive disease (PD) in 10 (58.9%) and irAEs in 7 (41.1%) patients. The median PFS-R was 4.0 (range, 0.4–8.0) months. ORR-R was 5.9% and DCR-R was 58.8%.

Gobinni et al., 2020 [26]

This was a retrospective observational study conducted at 26 institutions in France, of NSCLC patients rechallenged with ICI following progression after treatment discontinuation for at least 12 weeks, due to disease progression (58 (40%)), toxicity (58 (40%)) or clinician decision (28 (20%)). The total number of patients in the study were 144. The agents used at initial IO treatment were anti-PD-1 for 126 (88%) patients and anti-PD-L for 118 (12%), while in the rechallenge setting the corresponding proportions were 136 (94%) and 8 (6%).

Rechallenge efficacy for the entire cohort: PFS-R was 4.4 (3-6.5) months. ORR-R was 16% and DCR-R 47%, with BOR-R being PD for 38% of patients

Rechallenge efficacy per subgroups When excluding patients who discontinued initial IO treatment due to toxicity, ORR-R was 13%, and DCR-R was 44%. All four efficacy measures (PFS-R, OS-R, ORR-R, DCR-R) were numerically shorter in this subgroup.

Although PFS-R in this combined cohort was numerically higher than most of the other studies in this section, the respective PFS-R for the subgroup of 58 patients who discontinued treatment due to PD was similar [2.9 months (95% CI, 2.0-4.4)].

Regarding biomarkers for ICI rechallenge efficacy, only ECOG PS at rechallenge was found independently associated with PFS-R. However in the univariate analyses, PFS-R was additionally positively associated with initial ICI discontinuation due to toxicity (HR =0.54, 95% CI, 0.33-0.86), p=0.02) and negatively associated with patients having received Chemotherapy between the two IO courses (HR =1.81, 95% CI, 1.21-2.72, p=0.004). In this study too, the BOR-R was not associated with BOR-1 (p=1.101). This finding -in line with most of the other studies mentioned so far-, supports that the efficacy of IO retreatment in the setting of NSCLC cannot be predicted based on the initial response per the RECIST 1.1 criteria. This is contradictory to what has been observed in Melanoma patients retreated with ICI’s, and it endorses the idea that radiologic criteria other than RECIST 1.1 should be explored to better predict IO rechallenge response in NSCLC. [13]

Furuya et al., 2021 [27]

This was a retrospective study of 38 Asian patients who received Atezolizumab as IO Rechallenge, after previous anti-PD-1 therapy, across eight institutions. The reasons for first course IO discontinuation were PD, toxicity, or clinician decision, although the frequency of each discontinuation reason is not reported. In contrast to most of the previously mentioned studies, the primary goal of this study was not to assess Rechallenge IO efficacy, thus information for the subpopulation of 38 patients who received Atezolizumab rechallenge is relatively limited. Furthermore, the efficacy measure used was Time to Treatment Failure (TTF), defined as the time interval from ICI onset to treatment discontinuation for any cause, instead of PFS. For Rechallenge IO, TTF-R was 1.9 months while ORR-R and DCR-R were 2.6% and 34.2%, with only 1 patient having PR.

Although it is not reported in the original paper, it is visible from the Swimmers plot that a high percentage of patients (12 out of 38) who received rechallenge therapy with Atezolizumab had PD as BOR at the initial ICI course. These patients most likely have primary resistance and were a priori less likely to respond to rechallenge IO. Furthermore, median time to treatment failure was short and only 10 patients had received first course IO for more than 6 months. These two factors may partly account for the poor efficacy of rechallenge IO reported in this cohort.

Ito et al., 2021 [28]

This was a retrospective multicenter study of NSCLC patients who received PD-1 inhibitors. A subgroup of 37 patients received rechallenge immunotherapy following progression during or after completion of initial ICI treatment. Ten of these patients had initially received PD-1 inhibitor treatment for >1 year without PD. 21 of 37 were rechallenged with the same agent and 16 patients switched to a PD-L1 inhibitor.

The median PFS-R was 2.2 months (95% CI, 1.5–4.3). Interestingly in this study, PFS-R was statistically significantly longer in patients with BOR-1 of CR or PR, (3.8 months, 95% CI, 1.5–NR vs. 1.9 months, 95% CI, 0.8–3.7, p=0.04), who discontinued initial IO for reasons other than PD (6.6 months, 95% CI, 1.5–NR vs. 1.8 months, 95% CI, 1.1–2.8, p=0.01), or who had PFS ≥3 months after initial IO treatment discontinuation (6.6 months, 95% CI, 1.5–NR vs. 1.8 months, 95% CI, 1.4–2.8, p =0.01). The PFS-R was similar for patients treated with PD-1 and PD-L1 inhibitors at rechallenge (2.3 months, 95% CI, 1.4–10.3 vs. 2.1 months, 95% CI, 1.4–4.3, p=0.32).

Takahara et al., 2022 [29]

This was a retrospective cohort study of 24 Asian patients who received rechallenge ICI treatment. Patients had initially received either ICI monotherapy or in combination with chemotherapy and were rechallenged with ICI monotherapy. The reasons for initial IO discontinuation were PD in 17, toxicity in 6 and physician decision in 1 patient. Most patients (17 of 24) switched ICI at rechallenge. No patient rechallenged with the same agent exhibited response at rechallenge.

The ORR-R was 8.3% and the DCR-R was 37.5% with 2 patients having PR and 9 having SD.

Patients with disease control (PR or SD) had significantly longer duration of ICI rechallenge treatment (5.04 vs. 2.54 weeks; p = 0.016). In line with the study by Ito et al. Takahara et al. also found an association between BOR at initial IO and rechallenge efficacy.

Levra et al., 2019 [30]

The final study is discussed separately, as it is the largest of the rw-studies, but it has some important differences and limitations in relation to the ones mentioned previously, which makes its results difficult to compare or draw conclusions from. Levra et al., using data from the French National Hospital discharge database, collected information on all patients receiving Nivolumab treatment between 2015 and 2016. The authors considered Nivolumab to be discontinued if at least 3 infusions were missed. For patients receiving a second course PD-1 inhibitor they defined it as resumption if it was administered after a treatment-free interval, and rechallenge if it was administered after intervening chemotherapy. In total, 1127 patients were included in the resumption group and 390 patients in the rechallenge group. Median OS after nivolumab discontinuation was 15 months (95% CI, 13.9-16.7) in the resumption group and 18.4 months (95% CI, 14.8-21.9) in the rechallenge group. Median OS was significantly longer in patients with initial nivolumab treatment duration of at least 3 months (TTF-1>3 months); The corresponding hazard ratios for the rechallenge group were: 0.35 (95% CI, 0.22 - 0.56; p < 0.0001) for patients treated for 3–6 months and 0.19 (95% CI, 0.10 - 0.33; p < 0.000)] for patients treated for ≥6 months compared to patients treated for < 3 months.

Despite being by far the largest report on rechallenge ICI among NSCLC patients, it has several important limitations. First of all, due to the structure of the database, the information provided on baseline patient characteristics are very limited (only age, sex and specific comorbidities). Second, the only efficacy metric provided is OS, and only for patients who died in hospital. However, OS is not an optimal measure for the retreatment setting, as these kinds of studies inherently introduce attrition bias, considering that patients eligible for rechallenge are likely more fit and predisposed to treatment response than the broader NSCLC population. For instance, the fact that patients with TTF-1>3 months had improved OS, might be related to the mechanism of IO resistance to initial therapy differing in these patients, or it may simply reflect the fact that these patients had a time-limit set for them in which they were alive, meaning that a subset of patients with initially very poor prognosis were all included in the TTF-1<3 months group. Furthermore, the improved OS in patients who received intervening chemotherapy (rechallenge group) compared to patients who resumed Nivolumab after a treatment-free period (resumption group) could be related to intervening chemotherapy having a positive impact on rechallenge IO efficacy, but it may as well be partly or wholly attributed to attrition bias, since the former group had survived per definition for at least one more line of treatment than the latter. Third, importantly for the purposes of our review, there is no account of the reason for the first course IO discontinuation. Thus, patients in the Nivolumab resumption cohort likely represent a mixed population, with some having a treatment-free period due to adverse events, but continuing therapy promptly after, without intervening PD, and some stopping due to achieving maximum benefit, and then relapsing after a long treatment-free interval before retreatment with ICI. With information on the characteristics of the population under review lacking, and no efficacy metrics other than OS reported, it is hard to draw conclusions about the efficacy of rechallenge immunotherapy based on this study.

3.1.3. Overview

Although the cohort size of most of these studies is small, they point to the direction that rechallenge therapy with ICI’s following disease progression during prior ICI treatment, has overall poor efficacy in unselected patient populations. Yet, there seems to be a subpopulation of patients, not yet adequately characterised by the methods used in the published studies, who respond to IO rechallenge. Better stratification of patients in future studies, based on the underlying biology of IO resistance, may lead to better selection and improved rechallenge IO outcomes. Regarding the association between BOR at first course treatment and BOR or PFS at rechallenge, the results are contradictory. The studies by Katayma et al., Gobinni et al., as well as the phase II trial by Akamatsu et al. (mentioned in the following section) revealed no association between BOR-1 and rechallenge IO efficacy. On the contrary Ito et al., and Takahara et al., found a positive association between initial response to IO treatment and PFS-R or longer duration of rechallenge IO respectively. Furthermore, the best powered of these studies by Levra et al., identified an association between TTF-1 and OS-R. In order to more safely assess the association between initial IO response and IO rechallenge efficacy, larger-scale study with central review of response criteria is needed. Regarding the role of intervening systemic therapy between the two courses of IO and the comparative efficacy of IO rechallenge when readministering the same agent compared to administering a different agent, the results of the cohort studies are conflicting, and do not suffice to draw definite conclusions from.

3.2. Post-Hoc analyses of clinical trials

In the following section, we discuss the findings of post-hoc analyses of phase III clinical trials of NSCLC ICI-based treatment, for the subpopulations of patients who were retreated with ICI following disease progression. We only include studies which report efficacy results of subsequent course immunotherapy. The corresponding results are summarised in Table 3. It should be noted that the patient populations assessed in these studies are highly selected; They all completed the first course of immunotherapy with no progression and then, they were rechallenged with the same ICI. As such, they represent the population a priori more likely to respond to immunotherapy retreatment. Furthermore, there is no comparative arm in the post-progression setting, so it is difficult to assess whether rechallenge immunotherapy is preferable to changing the line of treatment. However, a notable number of patients both in clinical trials and in the real-world complete the first course of immunotherapy [31], it is worth summarising the evidence of rechallenge efficacy in those patients.

3.2.1. ΚΕΥΝOΤΕ042

In this phase III randomised trial, previously untreated patients with locally advanced or metastatic NSCLC and PD-L1 TPS > 1% were randomised to receive either Pembrolizumab monotherapy or Platinum-based chemotherapy as first line systemic treatment. Pembrolizumab was discontinued after 35 cycles/2 years of therapy if disease progression had not occurred. Patients in the Pembrolizumab arm who completed 35 cycles or stopped treatment after Complete response (CR) were eligible for second course Pembrolizumab treatment.

From the Pembrolizumab intention-to-treat population, 102 (16.0%) patients completed 35 cycles of treatment. Of those patients, 33 received second-course Pembrolizumab. Median time from random assignment to database cutoff was 63.7 (range, 52.0-75.2) months. ORR-R was 15.2% and DCR-R was 75.8%; 5 patients (15.2%) had PR and 20 (60.6%) had SD. At data cutoff, two of them (6.1%) were alive without disease progression. PFS at subsequent course immunotherapy was not reported, however a Swimmers plot depicting the time-course and response to treatment in this subpopulation can be found in the Supplementary material of the original publication [6]. Frequency of treatment-related adverse events in this subpopulation is also not reported [6].

3.2.2. ΚΕΥΝOΤΕ024

In this phase III open label trial, previously untreated patients with stage IV NSCLC and PD-L1 TPS>50% were randomised to receive either Pembrolizumab monotherapy or platinum-based Chemotherapy as first line treatment. Pembrolizumab was discontinued after 35 cycles/2 years of therapy if disease progression had not occurred. Patients could receive a second course of pembrolizumab (up to 17 cycles) in case of PD following either completion of 35 cycles of pembrolizumab or following confirmed complete response (CR) for patients who had received at least 6 months of treatment, and received 2 more cycles of pembrolizumab after CR.

Thirty-nine of 151 patients (25.8%) in the Pembrolizumab intention-to-treat population, completed 35 cycles/ 2 years of treatment. Median (range) time from completion of 35 cycles to data cutoff was 34.7 months (31.2-44.1). Baseline characteristics of these patients were similar to the overall Pembrolizumab intention-to-treat population, although a higher percentage had ECOG PS 0 (41.0% vs 35.1%) and treated brain metastases (23.1% vs 11.7%).

Twelve patients received a second pembrolizumab course after investigator-assessed PD. ORR-R was 33.3% and DCR-R was 83.3%; All 4 patients (33.3%) who responded had PR, and 6 (50.0%) patients had SD. Treatment response per RECIST 1.1 was assessed by the investigator. At data cutoff, 8 (66.7%) patients were alive and 5 patients (41.7%) had not experienced PD. Five patients (41.7%) experienced treatment-related AEs during the second course, all of them Grade 1 or 2 [8].

3.2.3. ΚΕΥΝOΤΕ010

In KEYNOTE 010, a phase III open label, randomised trial, patients with stage IIIB/IV NSCLC and PD-L1 TPS>1% were randomised to receive either Pembrolizumab monotherapy or Docetaxel as second line treatment, following progression after at least two cycles of platinum-based chemotherapy [7]. Pembrolizumab was discontinued after 35 cycles/2 years of therapy if disease progression had not occurred. In the five-year survival update, Herbst et al., reported the efficacy outcomes for patients who completed treatment with Pembrolizumab, and the subset of these patients who were retreated with Pembrolizumab following post-therapy-completion PD. At data cutoff, 79 patients had completed 35 cycles (2 years) of pembrolizumab. Characteristics of patients who completed IO were similar to the intention-to-treat population, however a higher percentage were < 65 years old (69.6% vs 57.2%), and had PD-L1 TPS >50% (73.4% vs 42.0%), while a smaller percentage had received > 2 prior lines of systemic therapy (19.0% versus 28.7%) or harboured EGFR mutations (1.3% vs 8.8%).

At data cutoff, 21 patients had received second-course pembrolizumab. The ORR-R was 52.3% and DCR-R was 81.0%; 1 patient had CR, 10 patients PR, and 6 patients had SD. Three patients had progressive disease at first restaging and 8 had subsequent disease progression, of which 5 had prior SD and 3 prior PR. Treatment response and disease progression was evaluated per RECIST 1.1 by central review. At data cutoff, 6 (28.6%) patients who received second-course pembrolizumab had died. Regarding treatment-related Adverse events (AE’s), 10 of 21 patients (47.6%) experienced at least one at rechallenge, of which 2 had Grade 3, including one patient with Pneumonitis. All of them had treatment-related AE’s in the first IO course as well [32].

3.2.4. Overview

In summary, all three KEYNOTE trials mentioned in this review (042, 024 and 010), included similar patient populations; NSCLC patients with metastatic disease or metastatic/locally advanced disease, who received rechallenge immunotherapy, were treated with Pembrolizumab both at the initial randomisation, and upon rechallenge, had completed two years of Pembrolizumab prior to retreatment and did not receive any other systematic treatment between the two immunotherapy courses. However, there were some key differences across these three trials; Both KEYNOTE 042 and KEYNOTE 024 assessed Pembrolizumab as first line systemic therapy for previously untreated patients, but KEYNOTE 024 only included patients with PD-L1 TPS> 50%, while KEYNOTE 042 included patients with PD-L1 TPS> 1%. This variation may be enough to account for the difference in ORR at subsequent course IO (15.2 vs 33.3 in KEYNOTE 042 and KEYNOTE 024 accordingly). KEYNOTE 010 on the contrary, included patients treated with Pembrolizumab following progression to previous line platinum-based chemotherapy. ORR to second course ICI in this case was numerically higher (52.3% vs 33.3% and 15.2%) than the other two studies. A likely explanation is that patients who received rechallenge immunotherapy in this study represent a highly selected population, who were intrinsically more responsive to immune modulation. This assumption is enhanced by the fact that the proportion of patients who completed two years of therapy in KEYNOTE 010 was significantly smaller than in the other two studies, particularly KEYNOTE 024, which included a similar population of PD-L1 high patients [6,8,32]. However the possibility that prior chemotherapy affected the likelihood of response to rechallenge immunotherapy (i.e., through increased tumour neoantigen presentation and optimisation of T-cell clonal differentiation during first course immunotherapy) cannot be disregarded.

Interestingly, although ORR-R is numerically quite different in these three trials, DCR-R is relatively similar (75.8 vs 83.3 vs 81.0 for KEYNOTE 042, KEYNOTE 024 and KEYNOTE 010 respectively) [6,8,32]. This is intriguing, as it may indicate that PD-L1 TPS is associated with the probability of response to immunotherapy rechallenge in this population of patients who completed treatment without progression, but not associated with the probability of rapid progression. Another interesting observation is that approximately 20-25% of patients who successfully completed two years of ICI therapy, exhibited rapid progression when rechallenged with the same agent. Better characterisation and tissue analysis of this subpopulation with initially durable response and subsequent resistance tο ΙO could provide valuable insight into the mechanisms of acquired resistance to PD-1 inhibition and help more accurately identify best candidates for ICI rechallenge.

3.3. Phase II trial of Nivolumab retreatment for patients with NSCLC [24]

This open label, multi-institutional, single-arm, phase II trial, was the first study to assess the efficacy of nivolumab rechallenge in patients with NSCLC who responded to ICI and had an ICI-free interval. Although it is a negative study, failing to meet its primary endpoint of ORR-R 20%, several interesting points should be taken into consideration.

In this study, eligible patients needed to have had a clinical benefit at prior ICI-based treatment, defined as CR,PR, or SD for at least 6 months and an ICI-free interval ≥ 60 days. The criterion of clinical benefit is in accordance with the SITC recommendations for defining acquired resistance to IO, although the minimum ICI-free interval was set by the investigators. As already mentioned, the primary endpoint was ORR. The sample size was calculated based on the assumption that it would provide a 10% improvement over the respective efficacy of Chemotherapy in the second and third line (20% vs 10%). Fifty-nine patients were evaluated for Nivolumab rechallenge efficacy. The majority (n = 54, 92%) had initially received IO monotherapy. The cause of discontinuation was irAEs in 20 patients.

ORR-R was 8.5% (95% CI, 2.8%-18.7%), with 5 patients achieving PR. Median PFS-R was 2.6 months (95% CI, 1.6-2.8 months). Notably however, the median PFS-R was 11.1 months for the 5 patients who achieved PR as BOR-R.

Interestingly the multivariate analysis revealed that ICI-free interval was the only significant predictor of longer PFS (≤ 9.2 vs.> 9.2 months; HR, 2.02, 95% CI, 1.10-3.73, p=0.02), which may be associated with the fact that, as stated above, patients with durable response during an adequate treatment-free interval may have partially sensitive, instead of resistant disease.

A very important point to be mentioned is that the patients were heavily pretreated prior to Nivolumab rechallenge, with the median number of chemotherapy lines being 3 (range, 1–6). This translates to the median line of Nivolumab Rechallenge being 4th or 5th (taking into consideration the previous IO line as well). Although the ORR goal “was set on the basis of an assumption that retreatment with nivolumab would improve the ORR from 10% to 20% in the second- or later-line setting”, the ORR of chemotherapy (and similarly rechallenge IO) is not expected to be the same in the 2nd and 4th/5th line of therapy. This fact makes us cautious in the evaluation of the study results.

3.4. Biological rationale - The example of Melanoma

In order to predict response to immunotherapy rechallenge, a better understanding of the biologic adaptations of the tumour and the microenvironment to immune checkpoint inhibition is required. In a study published in 2017 in Cell, Riaz et al., explored tumour cell and T-cell adaptation in 68 patients with Melanoma treated with Nivolumab; 35 previously treated with anti CTLA-4 inhibitor Ipilimumab (Ipi-P) and 33 Ipi-naive (Ipi-N). Although cytolytic activity and response did not differ significantly between the pretreated and non-pretreated populations, T-cell dynamics in response to Nivolumab treatment differed between the two groups. In Ipi-P responders there was an increase in T-cell richness (increased number of CDR3s) without significant change in T-cell evenness, while in Ipi-N patients there was significant decrease in T-cell evenness (increased T-cell diversification) without significant change in T-cell richness. These results, indicate that in Ipi-P patients, Tumour Infiltrating Lymphocytes (TIL’s) are already preselected by the tumour antigenic landscape during prior IO treatment, and resistance may arise from T-cell exhaustion through PD-1/PD-L1 signalling. This upregulation of PD-L1 expression in tumour cells and tumour-infiltrating immune cells happens largely as a response to the secretion of IFNγ, and is part of the adaptive immune resistance. The increased interaction of PD-1 with PD-L1 leads to T cell dysfunction, a phenomenon also called T cell exhaustion [33]. So, in this population of pretreated patients, anti-PD-1 therapy works mainly by alleviating exhaustion among the existing TIL clones, while in Ipi-N patients, anti-PD-1 therapy leads to selective intratumoral expansion of tumour-reactive clonotypes. In this context, we would expect that the mechanism of resistance to the initial CTLA-4 inhibition will determine the probability of response to the subsequent line Immune checkpoint inhibition. If the mechanism of immune evasion is T-cell exhaustion, then IO Retreatment after a time off-treatment is likely to lead to anti-tumor response. However, if acquired resistance is driven by clonal expansion of cancer cells with subclonal mutations, patients are unlikely to respond to IO Rechallenge, since T-cell populations have already been selected to target neoantigens of the initial tumour population, during the prior IO course. In the clinical setting, this indicates that in patients who immediately progressed during anti-CTLA-4 treatment, rechallenge is likely to be a futile strategy. Accordingly, in patients with initial Partial or Complete response, IO rechallenge is likely a reasonable strategy, although more research is needed to identify biomarkers predictive of response. Finally, Stable disease remains a grey zone, probably reflecting mixed cancer cell populations with differential immune responses. This diverse patient population is most in need of predictive biomarkers for IO retreatment response, and might benefit more from a multimodality treatment strategy following progression, such as immunotherapy combined with chemotherapy. In the setting of Melanoma, this assumption has been confirmed clinically, as response to prior IO is related to the probability of response to rechallenge IO. However, in NSCLC both Akamatsu et al. and Gobbini et al. found that response to rechallenge IO was independent of response to first course IO. At this point it is important to note that the research cited above focused on patients with melanoma receiving PD-1 inhibitors who were previously treated with a CTLA-4 inhibitor, while in NSCLC, patients are rechallenged with PD-(L)1 based regimens after previous PD axis inhibition. In this respect, the mechanism of resistance to initial IO treatment and T-cell dynamics differ in these patients and similar research is needed in the setting of NSCLC to know if these results are applicable in this setting as well.

4. Conclusions

Based on current evidence the authors would consider IO rechallenge in patients who successfully completed first course IO and subsequently progressed after an adequate treatment free interval, taking into account their PS and AE’s at prior IO. The data mined during this review is not sufficient to similarly educate retreatment decisions in the setting of durable response following discontinuation due to AE’s. Regarding patients who progressed during first IO treatment, the limited existing evidence does not show superior ORR with rechallenge ICI’s compared to subsequent line chemotherapy in unselected NSCLC patient populations. Yet, as there are no properly designed prospective comparative studies of the two treatment strategies, no definite conclusions can be currently drawn in this respect. Finally, based on the current evidence, it seems that BOR per RESIST 1.1 at initial course IO is not an adequate measure of Rechallenge IO efficacy and predictive markers are needed to guide decisions in this setting.

5. Future directions

In order to determine if the underlying biology of resistance can be expressed clinically, future research of immunotherapy retreatment should include a more explicit description of radiologic progression, taking into consideration the dynamic change of each lesion rather than a gross definition of Disease progression based on RECIST 1.1. criteria. For instance, oligoprogression is likely to indicate a different biological mechanism of IO resistance than systemic progression. Another interesting field of research is the role of radiotherapy in IO pretreated patients. There are indications from small retrospective cohort studies, that patients subjected to local radiotherapy respond better to IO retreatment. Comparing T-cell dynamics between patients treated with IO rechallenge who either did or did not receive prior radiotherapy would provide valuable insight into the way that radiotherapy can affect neoantigen presentation34 and subsequent T-cell differentiation and clonal expansion. Finally, more research is needed to validate and optimise the proposed criteria for clinical definition of acquired immunotherapy resistance in the setting of NSCLC. Some important questions to be answered in this respect are; 1. How do we better classify resistance in patients with SD as the best overall response to first course IO? 2. Should there be a minimum duration of response to distinguish between primary and acquired resistance, and if yes, what should the cut-off be? 3. Are RECIST criteria enough, or had we better account for tumour kinetics and individual lesion response patterns to tailor more personalised treatments in the post-IO progression setting?

Author Contributions

MEL: Conceptualization, Investigation, Writing - Original draft; VN: Conceptualization, Writing - review & editing; VS: Writing - review & editing; OF: Writing - review & editing; EK: Supervision, Writing - review & editing. All authors provided a critical review of the manuscript and approved the final version to be published.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

Kazandjian D, Suzman DL, Blumenthal G, et al. FDA Approval Summary: Nivolumab for the Treatment of Metastatic Non-Small Cell Lung Cancer With Progression On or After Platinum-Based Chemotherapy. The Oncologist. 2016;21(5):634-642. [CrossRef]
Paz-Ares L, Horn L, Borghaei H, et al. Phase III, randomized trial (CheckMate 057) of nivolumab (NIVO) versus docetaxel (DOC) in advanced non-squamous cell (non-SQ) non-small cell lung cancer (NSCLC). J Clin Oncol. 2015;33(18_suppl):LBA109-LBA109. [CrossRef]
Ettinger DS, Wood DE, Aisner DL, et al. NCCN Guidelines Insights: Non-Small Cell Lung Cancer, Version 2.2021. J Natl Compr Cancer Netw JNCCN. 2021;19(3):254-266. [CrossRef]
O’Reilly D, Botticella A, Barry S, et al. Treatment Decisions for Resectable Non-Small-Cell Lung Cancer: Balancing Less With More? Am Soc Clin Oncol Educ Book Am Soc Clin Oncol Annu Meet. 2023;43:e389950. [CrossRef]
Ettinger DS, Wood DE, Aisner DL, et al. NCCN Guidelines^® Insights: Non–Small Cell Lung Cancer, Version 2.2023: Featured Updates to the NCCN Guidelines. J Natl Compr Canc Netw. 2023;21(4):340-350. [CrossRef]
de Castro G, Kudaba I, Wu YL, et al. Five-Year Outcomes With Pembrolizumab Versus Chemotherapy as First-Line Therapy in Patients With Non–Small-Cell Lung Cancer and Programmed Death Ligand-1 Tumor Proportion Score ≥ 1% in the KEYNOTE-042 Study. J Clin Oncol. 2023;41(11):1986-1991. [CrossRef]
Herbst RS, Baas P, Kim DW, et al. Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial. Lancet Lond Engl. 2016;387(10027):1540-1550. [CrossRef]
Reck M, Rodríguez-Abreu D, Robinson AG, et al. Five-Year Outcomes With Pembrolizumab Versus Chemotherapy for Metastatic Non–Small-Cell Lung Cancer With PD-L1 Tumor Proportion Score ≥ 50%. J Clin Oncol. 2021;39(21):2339-2349. [CrossRef]
Schoenfeld AJ, Hellmann MD. Acquired Resistance to Immune Checkpoint Inhibitors. Cancer Cell. 2020;37(4):443-455. doi:10.1016/j.ccell.2020.03.017. [CrossRef]
Antonia SJ, Borghaei H, Ramalingam SS, et al. Four-year survival with nivolumab in patients with previously treated advanced non-small-cell lung cancer: a pooled analysis. Lancet Oncol. 2019;20(10):1395-1408. [CrossRef]
Kuczynski EA, Sargent DJ, Grothey A, Kerbel RS. Drug rechallenge and treatment beyond progression--implications for drug resistance. Nat Rev Clin Oncol. 2013;10(10):571-587. [CrossRef]
Riaz N, Havel JJ, Makarov V, et al. Tumor and Microenvironment Evolution during Immunotherapy with Nivolumab. Cell. 2017;171(4):934-949.e16. [CrossRef]
Schoenfeld AJ, Antonia SJ, Awad MM, et al. Clinical definition of acquired resistance to immunotherapy in patients with metastatic non-small-cell lung cancer. Ann Oncol Off J Eur Soc Med Oncol. 2021;32(12):1597-1607. [CrossRef]
Schoenfeld AJ, Rizvi HA, Memon D, et al. Systemic and Oligo-Acquired Resistance to PD-(L)1 Blockade in Lung Cancer. Clin Cancer Res Off J Am Assoc Cancer Res. 2022;28(17):3797-3803. [CrossRef]
Cai Z, Zhan P, Song Y, Liu H, Lv T. Safety and efficacy of retreatment with immune checkpoint inhibitors in non-small cell lung cancer: a systematic review and meta-analysis. Transl Lung Cancer Res. 2022;11(8):1555-1566. [CrossRef]
Feng Y, Tao Y, Chen H, et al. Efficacy and safety of immune checkpoint inhibitor rechallenge in non-small cell lung cancer: A systematic review and meta-analysis. Thorac Cancer. 2023;14(25):2536-2547. [CrossRef]
Fujita K, Uchida N, Kanai O, Okamura M, Nakatani K, Mio T. Retreatment with pembrolizumab in advanced non-small cell lung cancer patients previously treated with nivolumab: emerging reports of 12 cases. Cancer Chemother Pharmacol. 2018;81(6):1105-1109. [CrossRef]
Fujita K, Yamamoto Y, Kanai O, et al. Retreatment with anti-PD-1 antibody in non-small cell lung cancer patients previously treated with anti-PD-L1 antibody. Thorac Cancer. 2020;11(1):15-18. doi:10.1111/1759-7714.13241. [CrossRef]
Watanabe H, Kubo T, Ninomiya K, et al. The effect and safety of immune checkpoint inhibitor rechallenge in non-small cell lung cancer. Jpn J Clin Oncol. 2019;49(8):762-765. [CrossRef]
Katayama Y, Shimamoto T, Yamada T, et al. Retrospective Efficacy Analysis of Immune Checkpoint Inhibitor Rechallenge in Patients with Non-Small Cell Lung Cancer. J Clin Med. 2019;9(1):102. [CrossRef]
Xu Z, Hao X, Yang K, et al. Immune checkpoint inhibitor rechallenge in advanced or metastatic non-small cell lung cancer: a retrospective cohort study. J Cancer Res Clin Oncol. 2022;148(11):3081-3089. [CrossRef]
Gettinger SN, Wurtz A, Goldberg SB, et al. Clinical Features and Management of Acquired Resistance to PD-1 Axis Inhibitors in 26 Patients With Advanced Non–Small Cell Lung Cancer. J Thorac Oncol. 2018;13(6):831-839. [CrossRef]
Niki M, Nakaya A, Kurata T, et al. Immune checkpoint inhibitor re-challenge in patients with advanced non-small cell lung cancer. Oncotarget. 2018;9(64):32298-32304. [CrossRef]
Akamatsu H, Teraoka S, Takamori S, et al. Nivolumab Retreatment in Non-Small Cell Lung Cancer Patients Who Responded to Prior Immune Checkpoint Inhibitors and Had ICI-Free Intervals (WJOG9616L). Clin Cancer Res Off J Am Assoc Cancer Res. 2022;28(15):OF1-OF7. [CrossRef]
Kitagawa S, Hakozaki T, Kitadai R, Hosomi Y. Switching administration of anti-PD-1 and anti-PD-L1 antibodies as immune checkpoint inhibitor rechallenge in individuals with advanced non-small cell lung cancer: Case series and literature review. Thorac Cancer. 2020;11(7):1927-1933. [CrossRef]
Gobbini E, Toffart AC, Pérol M, et al. Immune Checkpoint Inhibitors Rechallenge Efficacy in Non-Small-Cell Lung Cancer Patients. Clin Lung Cancer. 2020;21(5):e497-e510. [CrossRef]
Furuya N, Nishino M, Wakuda K, et al. Real-world efficacy of atezolizumab in non-small cell lung cancer: A multicenter cohort study focused on performance status and retreatment after failure of anti-PD-1 antibody. Thorac Cancer. 2021;12(5):613-618. [CrossRef]
Ito S, Asahina H, Honjo O, et al. Prognostic factors in patients with advanced non-small cell lung cancer after long-term Anti-PD-1 therapy (HOT1902). Lung Cancer Amst Neth. 2021;156:12-19. [CrossRef]
Takahara Y, Tanaka T, Ishige Y, et al. Efficacy and predictors of rechallenge with immune checkpoint inhibitors in non-small cell lung cancer. Thorac Cancer. 2022;13(4):624-630. [CrossRef]
Giaj Levra M, Cotté FE, Corre R, et al. Immunotherapy rechallenge after nivolumab treatment in advanced non-small cell lung cancer in the real-world setting: A national data base analysis. Lung Cancer Amst Neth. 2020;140:99-106. [CrossRef]
Kim H, Kim D, Kim M, et al. Long-term outcomes in patients with advanced and/or metastatic non–small cell lung cancer who completed 2 years of immune checkpoint inhibitors or achieved a durable response after discontinuation without disease progression: Multicenter, real-world data (KCSG LU20-11). Cancer. 2022;128(4):778-787. [CrossRef]
Herbst RS, Garon EB, Kim DW, et al. Five Year Survival Update From KEYNOTE-010: Pembrolizumab Versus Docetaxel for Previously Treated, Programmed Death-Ligand 1-Positive Advanced NSCLC. J Thorac Oncol Off Publ Int Assoc Study Lung Cancer. 2021;16(10):1718-1732. [CrossRef]
O’Donnell JS, Teng MWL, Smyth MJ. Cancer immunoediting and resistance to T cell-based immunotherapy. Nat Rev Clin Oncol. 2019;16(3):151-167. [CrossRef]
Rodríguez-Ruiz ME, Vanpouille-Box C, Melero I, Formenti SC, Demaria S. Immunological Mechanisms Responsible for Radiation-Induced Abscopal Effect. Trends Immunol. 2018;39(8):644-655. [CrossRef]

Table 1. Summary of ICI Rechallenge efficacy from retrospective real-world studies of patients who discontinued initial course IO due to disease progression.

Study		Fujita et al., 2018 [17]		Watanabe et al., 2019 [19]		Katayama et al., 2019 [20]		Fujita et al., 2020 [18]		Xu et al., 2022 [28]
No of patients		12		14		35		15		40
Discontinuation reason*		PD		PD		PD		PD		PD
IO course		1st course	Rechallenge	1st course	Rechallenge	1st course	Rechallenge	1st course	Rechallenge	1st course	Rechallenge
Agent used		Anti-PD-1	Anti-PD-1	Anti-PD (L)-1	Anti-PD-1	Anti-PD (L)-1	Anti-PD (L)-1	Anti-PD-L1	Anti-PD-1	Anti-PD-1 + Chemo + anti-angio	Anti-PD (L)-1 + Chemo + anti-angio
Nivolumab, N (%)		12 (100)	12 (100)	11 (78.6)	9 (64.3)	19 (54.3)	7 (20.0)	0 (0)	8 (53.3)	NR	NR
Pembrolizumab, N (%)		0 (0)	0 (0)	1 (7.1)	5 (35.7)	12 (34.3)	5 (14.3)	0 (0)	7 (46.7)	NR	NR
Atezolizumab, N (%)		0 (0)	0 (0)	2 (14.3)	0 (0)	4 (11.4)	23 (65.7)	14 (93.3)	0 (0)	NR	NR
Durvalumab, N (%)		0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	1 (6.7)	0 (0)	NR	NR
Immunotherapy-free interval		NR		NR		5.2 (3.5-7.9)		NR		NR
Line of treatment, Median (Range)		3 (2-5)	NR	NR	NR	3 (1–15)	4 (2–19)	NR	NR	1 (1-NR)	2 (2-NR)
No of cycles, Median (Range)		12.5 (2–32)	3.5 (1–17)	NR	NR	NR	NR	5 (1-15)	Nivolumab: 4 (1-7)Pembrolizumab: (1-14)	NR	NR
PFS [Median (95% CI)], months		6.2 (2.8-13.7)	3.1 (1.2-12.6)	3.7 (1.3-7.1)	1.6 (0.8–2.6)	4 (3–4.6)	2.7 (1.4-3.7)	Atezolizumab: 2.8 Durvalumab: 6.0	Nivolumab: 1.9 (0.4-3.0)Pembrolizumab: 2.8 (0.47–13.4)	5.7 (4.1-7.2)	6.8 (5.8–7.8)
ORR (N, %)		7 (58.3)	1 (8.3)	3 (21.4)	1 (7.1)	12 (34.3)	1 (2.9)	0 (0)	0 (0)	14 (35)	9 (22.5)
DCR (N, %)		9 (75)	5 (41.6)	8 (57.1)	3 (21.4)	24 (68.6)	15 (43.0)	4 (28.6)	Nivolumab:1/7 (14.3)Pembrolizumab: 3/8 (37.5)	33 (83)	34 (85.0)
BOR
	CR	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)	0 (0)
	PR	7 (58.3)	1 (8.3)	3 (21.4)	1 (7.1)	12 (34.3)	1 (2.9)	0 (0)	0 (0)	14 (35)	9 (22.5)
	SD	2 (16.7)	4 (33.3)	5 (35.7)	2 (14.3)	12 (34.3)	14 (40.0)	4 (28.6)	Nivolumab:1/ 7 (14.3)Pembrolizumab: 3/8 (37.5)	19 (48)	25 (62.5)
	PD	3 (25)	6 (50.0)	6 (42.9)	11 (78.6)	10 (28.6)	18 (51.4)	9 (64.3)	Nivolumab: 5/7 (71.4)Pembrolizumab: 4/8 (50.0)	7 (18)	6 (15.0)

*Discontinuation reason of the initial ICI course.

Table 2. Summary of ICI Rechallenge efficacy from retrospective real-world studies of patients who discontinued initial course IO due to disease progression, adverse events or physician decision.

Study		Niki et al., 2018 [19]		Kitagawa et al., 2020 [24] *1		Gobinni et al., 2020 [25]		Furuya et al., 2021 [26]		Ito et al., 2021 [27]
No of patients		11		17		144		38		37
Discontinuation reason		NR		PD, Toxicity		PD, Toxicity, Physician decision		PD, Toxicity, Physician decision		Mixed
IO course		1st course	Rechallenge	1st course	Rechallenge	1st course	Rechallenge	1st course	Rechallenge	1st course	Rechallenge
Agent used		Anti-PD-1	Anti-PD-1	Anti-PD-1	Anti-PD-L1	Anti-PD (L)-1	Anti-PD (L)-1	Anti-PD-1	Anti-PD-L1	Anti-PD-1	Anti-PD (L)-1
Nivolumab, N (%)		11 (100)	1 (9.1)	11 (64.7)	2 (11.8)	NR	NR	29 (76.3)	0 (0)	NR	10
Pembrolizumab, N (%)		0 (0)	10 (90.9)	4 (23.5)	0 (0)	NR	NR	8 (21.1)	0 (0)	NR	11
Atezolizumab, N (%)		0 (0)	0 (0)	2 (11.8)	15 (88.2)	NR	NR	0 (0)	38 (100)	0 (0)	16
Durvalumab, N (%)		0 (0)	0 (0)	0 (0)	0 (0)	NR	NR	0 (0)	0 (0)	0 (0)	0 (0)
Immunotherapy-free interval		4.2 (1.0-12.7) months.		NR		NR		NR		NR
Line of treatment, Median (Range)		5 (3-8)	NR	2 (1-4)	3 (2-9)	2 (1-(>3))	3 (1-(>3))	NR	NR	NR	NR
PFS [Median (95% CI)], months		4.9 (0.7-18.2)	2.7 (0.5–16.1)	9.7 (0.7–34.9)	4.0 (0.4–8.0)	13 (10-16.5)	4.4 (3-6.5)	NR	NR	NR	2.2 (1.5–4.3)
ORR (N, %)		5 (45)	3 (27.2)	6 (35.3)	1 (5.9)	50	16	8 (21.1)	1 (2.6)	22 (59.5)	NR
DCR (N, %)		7 (63)	5 (45.5)	9 (52.9)	10 (58.8)	76	47	24 (63.2)	13 (34.2)	31 (83.8)	NR
BOR
	CR	0 (0)	0 (0)	0 (0)	0 (0)	10 (7)	5 (3)	0 (0)	0 (0)	1 (0.03)	NR
	PR	5 (45)	3 (27.2)	6 (35.3)	1 (5.9)	61 (43)	18 (13)	8 (21.1)	1 (2.6)	21 (56.8)	NR
	SD	2 (18.2)	2 (18.2)	9 (52.9)	9 (52.9)	38 (26)	45 (31)	16 (42.1)	12 (31.6)	9 (24.3)	NR
	PD	4 (36.4)	6 (54.5)	2 (11.8)	7 (41.2)	26 (18)	54 (38)	11 (29.9)	19 (50)	6 (16.2)	NR

Table 3. Summary of post-hoc analyses of phase III clinical trials for ICI NSCLC treatment in which a subpopulation of patients was rechallenged with the same ICI following completion of treatment and subsequent disease progression.

Trial name (line)		KEYNOTE 042 (first)	KEYNOTE 024 (first)	KEYNOTE 010 (second)
Population *¹(selection)		1,274 (PD-L1≥1%)	305 (PD-L1≥50%)	1,033 (PD-L1≥1%)
Arms		1) Pem200mg Q3w 2) Chemo	1)Pem200mg Q3w, 2)Chemo	1)Pem2mg/kg Q2w 2) Pem10mg/kg Q2w 3) Doce 75mg/m2 Q3w
ORR-1 (N, %)
	Total population	174 (27.3) (95% CI, 23.9 to 31.0)	71 (46.1) (95% CI, 38.1 to 54.3)	Pem2 mg/kg: 62 (18) Pem10 mg/kg: 64 (18)
	PD-L1 TPS>50%	117 (39.1) (95% CI, 33.6 to 44.9)	71 (46.1) (95% CI, 38.1 to 54.3)	Pem2 mg/kg: 42 (30) Pem10 mg/kg: 44 (29)
DCR-1 (N, %)		420 (65.9) for PD-L1 TPS>1% 206 (68.9) for PD-L1 TPS>50%.	106 (68.8)	NR
Second course ICI
N out of intention-to-treat ICI patients		33 of 637	12 of 154	21 of 690
N out of patients who completed ICI treatment		33 of 102	12 of 39	21 of 79
Data cut-off [Median (Range)], months		63.7 (52.0-75.2) from randomisation	34.7 months (31.2-44.1) from completion of first ICI course*	68.1 (60.5‒74.5) from randomisation
ORR-R (N, %)		5 (15.2)	4 (33.3)	11 (52.3)
DCR-R (N%)		25 (75.8)	10 (83.3)	17 (81.0)
BOR-R
	CR (N, %)	0 (0.0)	0 (0.0)	1 (4.8)
	PR (N, %)	5 (15.2)	4 (33.3)	10 (47.6)
	SD (N, %)	20 (60.6)	6 (50)	6 (28.6)
	PD (N, %)	3 (9.1)	1 (8.3)	3 (14.3)
PD by data cutoff (N, %)		15 (45.	3 (25)	11 (52.3)
Death by data cutoff (N, %)		11 (33.3)	4 (33.3)	6 (28.6)
AE’s (No of patients, %)		NR	5 (41.7)	10 (47.6)

NR: Not reported. AE’s: Adverse Events.; *¹ Intention-to-treat population.; *² Time from randomisation to IO completion was approximately 24 months.

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.

MDPI Initiatives

Important Links

Choose an area of interest and we will send you notifications of new preprints at your preferred frequency.

Disclaimer