Recent progress in mutation-driven therapy, immunotherapy and combination therapy for the treatment of Melanoma

Loading...
Thumbnail Image

Date

Journal Title

Journal ISSN

Volume Title

Publisher

Bentham Science Publishers B.V.

Abstract

With increases in our understanding of the human genome and immune system, the treatment armamentarium for melanoma has benefitted from the development and approval of BRAF inhibitors, MEK inhibitors, immune checkpoint modulators via cytotoxic T-lymphocyte antigen-4 blockade, and PD-1 and PD-L1 inhibitors. These advances, however, have raised questions about combination therapy, the optimal sequential use of these agents, the limited assessment of response using traditional metrics, and the optimal selection of the population to be treated. In this review we summarize recent breakthroughs and then itemize the development of newer agents, potential prognostic and predictive biomarkers, resistance mechanisms, and strategies of combination therapy. We also emphasize the multifaceted attributes of immunotherapy in terms of durable responses and longterm survival that paradoxically necessitate further research into the underlying mechanisms and longer patient follow-up. © 2017 Bentham Science Publishers.

Description

Keywords

Braf inhibitors, Ctla-4 inhibitors, Immunotherapy, Mek inhibitors, Melanoma, Mutationdriven therapy, Pd-1 inhibitors, Pd-l1 inhibitors, Antineoplastic agents, Antineoplastic combined chemotherapy protocols, Combined modality therapy, Ctla-4 antigen, Drug resistance, neoplasm, Humans, Imidazoles, Indoles, Mutation, Oximes, Programmed cell death 1 receptor, Proto-oncogene proteins b-raf, Pyridones, Pyrimidinones, Sulfonamides, Aldesleukin, Atezolizumab, Bevacizumab, Checkpoint kinase inhibitor, Cobimetinib, Cytotoxic t lymphocyte antigen 4, Dabrafenib, Decitabine, Dorgenmeltucel l, Durvalumab, Fotemustine, Ipilimumab, Metformin, Nivolumab, Paclitaxel, Peginterferon, Pembrolizumab, Programmed death 1 receptor, Retinoic acid, Ticilimumab, Trametinib, Trientine, Vemurafenib, Antineoplastic agent, B raf kinase, Braf protein, human, Ctla4 protein, human, Imidazole derivative, Indole derivative, Oxime, Pdcd1 protein, human, Pyridone derivative, Pyrimidinone derivative, Sulfonamide, Cancer combination chemotherapy, Cancer immunotherapy, Cancer staging, Drug efficacy, Drug safety, Drug tolerability, Human, Metastatic melanoma, Multicenter study (topic), Nonhuman, Overall survival, Phase 1 clinical trial (topic), Phase 2 clinical trial (topic), Phase 3 clinical trial (topic), Progression free survival, Randomized controlled trial (topic), Recurrence free survival, Review, Squamous cell carcinoma, Tumor immunity, Drug effects, Drug resistance, Genetics, Immunology, Metabolism, Multimodality cancer therapy, Procedures

Citation

Endorsement

Review

Supplemented By

Referenced By