Immune checkpoint inhibitors in advanced non–small cell lung cancer

dc.contributor.authorAssi, Hazem I.
dc.contributor.authorKamphorst, Alice O.
dc.contributor.authorMoukalled, Nour M.
dc.contributor.authorRamalingam, Suresh S.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:51:49Z
dc.date.available2025-01-24T11:51:49Z
dc.date.issued2018
dc.description.abstractThe emergence of immune checkpoint inhibitors for the treatment of cancer has led to major changes to the therapeutic landscape of lung cancer. Improvements in overall survival relative to standard chemotherapy have been observed in the first-line and second-line therapy settings for patients with advanced non–small cell lung cancer (NSCLC) who are treated with immune checkpoint inhibitors. Consequently, every patient with advanced-stage NSCLC is now a candidate for immune checkpoint inhibitor therapy. However, it is clear that the benefit from therapy is not universal, and identification of biomarkers to select therapy has assumed importance. In addition to programmed cell death receptor ligand 1 expression, both tissue-based and blood-based markers are under evaluation to select patients. In an era of increasing costs of care and potential for toxicities related to immune checkpoint inhibition, proper patient selection is critical to the optimal use of this new class of agents. In addition, development of novel combination approaches has also emerged as an important way to improve the efficacy of immune checkpoint inhibition. Studies in earlier stages of NSCLC are already underway with the hope of improving the cure rate. In this article, the authors review the current landscape of immune checkpoint inhibitors in the treatment of advanced NSCLC. Cancer 2018;124:248-61. © 2017 American Cancer Society. © 2017 American Cancer Society
dc.identifier.doihttps://doi.org/10.1002/cncr.31105
dc.identifier.eid2-s2.0-85040255379
dc.identifier.pmid29211297
dc.identifier.urihttp://hdl.handle.net/10938/31025
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc.
dc.relation.ispartofCancer
dc.sourceScopus
dc.subjectBiomarkers
dc.subjectCheckpoint inhibitors
dc.subjectImmunotherapy
dc.subjectNon–small cell lung cancer (nsclc)
dc.subjectProgrammed cell death receptor ligand 1 (pd-l1)
dc.subjectB7-h1 antigen
dc.subjectCarcinoma, non-small-cell lung
dc.subjectCtla-4 antigen
dc.subjectHumans
dc.subjectLung neoplasms
dc.subjectProgrammed cell death 1 receptor
dc.subjectSalvage therapy
dc.subjectAtezolizumab
dc.subjectAvelumab
dc.subjectBevacizumab
dc.subjectBiological marker
dc.subjectCarboplatin
dc.subjectCheckpoint kinase inhibitor
dc.subjectCisplatin
dc.subjectCrizotinib
dc.subjectDocetaxel
dc.subjectDurvalumab
dc.subjectErlotinib
dc.subjectGefitinib
dc.subjectGemcitabine
dc.subjectIpilimumab
dc.subjectNivolumab
dc.subjectOsimertinib
dc.subjectPaclitaxel
dc.subjectPembrolizumab
dc.subjectPemetrexed
dc.subjectPlacebo
dc.subjectProgrammed death 1 ligand 1
dc.subjectProgrammed death 1 receptor
dc.subjectTicilimumab
dc.subjectVorinostat
dc.subjectCytotoxic t lymphocyte antigen 4
dc.subjectAdvanced cancer
dc.subjectCancer chemotherapy
dc.subjectCancer combination chemotherapy
dc.subjectCancer staging
dc.subjectChemoradiotherapy
dc.subjectEarly cancer
dc.subjectEnzyme inhibition
dc.subjectHuman
dc.subjectMonotherapy
dc.subjectNon small cell lung cancer
dc.subjectNonhuman
dc.subjectPatient care
dc.subjectPatient selection
dc.subjectPrimary health care
dc.subjectPriority journal
dc.subjectReview
dc.subjectAntagonists and inhibitors
dc.subjectLung tumor
dc.titleImmune checkpoint inhibitors in advanced non–small cell lung cancer
dc.typeReview

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