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

dc.contributor.authorAssi, Hazem I.
dc.contributor.authorAssi, Rita E.
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:49:27Z
dc.date.available2025-01-24T11:49:27Z
dc.date.issued2017
dc.description.abstractWith 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.
dc.identifier.doihttps://doi.org/10.2174/1568009616666160719120053
dc.identifier.eid2-s2.0-85011114809
dc.identifier.pmid27628745
dc.identifier.urihttp://hdl.handle.net/10938/30889
dc.language.isoen
dc.publisherBentham Science Publishers B.V.
dc.relation.ispartofCurrent Cancer Drug Targets
dc.sourceScopus
dc.subjectBraf inhibitors
dc.subjectCtla-4 inhibitors
dc.subjectImmunotherapy
dc.subjectMek inhibitors
dc.subjectMelanoma
dc.subjectMutationdriven therapy
dc.subjectPd-1 inhibitors
dc.subjectPd-l1 inhibitors
dc.subjectAntineoplastic agents
dc.subjectAntineoplastic combined chemotherapy protocols
dc.subjectCombined modality therapy
dc.subjectCtla-4 antigen
dc.subjectDrug resistance, neoplasm
dc.subjectHumans
dc.subjectImidazoles
dc.subjectIndoles
dc.subjectMutation
dc.subjectOximes
dc.subjectProgrammed cell death 1 receptor
dc.subjectProto-oncogene proteins b-raf
dc.subjectPyridones
dc.subjectPyrimidinones
dc.subjectSulfonamides
dc.subjectAldesleukin
dc.subjectAtezolizumab
dc.subjectBevacizumab
dc.subjectCheckpoint kinase inhibitor
dc.subjectCobimetinib
dc.subjectCytotoxic t lymphocyte antigen 4
dc.subjectDabrafenib
dc.subjectDecitabine
dc.subjectDorgenmeltucel l
dc.subjectDurvalumab
dc.subjectFotemustine
dc.subjectIpilimumab
dc.subjectMetformin
dc.subjectNivolumab
dc.subjectPaclitaxel
dc.subjectPeginterferon
dc.subjectPembrolizumab
dc.subjectProgrammed death 1 receptor
dc.subjectRetinoic acid
dc.subjectTicilimumab
dc.subjectTrametinib
dc.subjectTrientine
dc.subjectVemurafenib
dc.subjectAntineoplastic agent
dc.subjectB raf kinase
dc.subjectBraf protein, human
dc.subjectCtla4 protein, human
dc.subjectImidazole derivative
dc.subjectIndole derivative
dc.subjectOxime
dc.subjectPdcd1 protein, human
dc.subjectPyridone derivative
dc.subjectPyrimidinone derivative
dc.subjectSulfonamide
dc.subjectCancer combination chemotherapy
dc.subjectCancer immunotherapy
dc.subjectCancer staging
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectDrug tolerability
dc.subjectHuman
dc.subjectMetastatic melanoma
dc.subjectMulticenter study (topic)
dc.subjectNonhuman
dc.subjectOverall survival
dc.subjectPhase 1 clinical trial (topic)
dc.subjectPhase 2 clinical trial (topic)
dc.subjectPhase 3 clinical trial (topic)
dc.subjectProgression free survival
dc.subjectRandomized controlled trial (topic)
dc.subjectRecurrence free survival
dc.subjectReview
dc.subjectSquamous cell carcinoma
dc.subjectTumor immunity
dc.subjectDrug effects
dc.subjectDrug resistance
dc.subjectGenetics
dc.subjectImmunology
dc.subjectMetabolism
dc.subjectMultimodality cancer therapy
dc.subjectProcedures
dc.titleRecent progress in mutation-driven therapy, immunotherapy and combination therapy for the treatment of Melanoma
dc.typeReview

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