Review
Version 1
Preserved in Portico This version is not peer-reviewed
Therapeutic Opportunities in Cutaneous T-cell Lymphoma
Version 1
: Received: 30 May 2024 / Approved: 3 June 2024 / Online: 3 June 2024 (12:13:18 CEST)
How to cite: Valero-Diaz, S.; Amato, C.; Casar, B. Therapeutic Opportunities in Cutaneous T-cell Lymphoma. Preprints 2024, 2024060069. https://doi.org/10.20944/preprints202406.0069.v1 Valero-Diaz, S.; Amato, C.; Casar, B. Therapeutic Opportunities in Cutaneous T-cell Lymphoma. Preprints 2024, 2024060069. https://doi.org/10.20944/preprints202406.0069.v1
Abstract
Cutaneous T-cell lymphomas (CTCLs) are a heterogeneous group of T-cell lymphomas characterised by high relapse rates and no curative treatments unless the allogeneic stem cell transplantation. The main complication in the management of this kind of malignancy is the variability that characterises the genetic and clinical features among the CTCL subtypes. JAK/STAT, MAPK/ERK, PI3K/Akt, and NF-kB are those signalling pathways that are found altered in CTCL and that are responsible for promoting both T-cell malignancy and the pro-tumorigenic microenvironment. Thus, targeting key players of these pathways can be an advantageous therapeutic option for CTCL. In this review, we aim to summarise the different approaches that precisely inhibit the kinases of each cited signalling. JAK inhibitors seem to be the most promising kinase inhibitors for CTCL. However, adverse events have been reported especially in patients with immunosuppression or an underlying autoimmune disease. More studies are needed, especially clinical trials, to investigate the benefits of these drugs for the treatment of cutaneous T-cell lymphomas.
Keywords
Cutaneous T-Cell Lymphoma; kinase inhibitors; targeted therapy
Subject
Public Health and Healthcare, Public Health and Health Services
Copyright: This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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