000 02474nam a22003497a 4500
008 210217s20202020 xxu||||| |||| 00| 0 eng d
022 _a1758-8340
024 _a10.1177_1758835920980365 [pii]
024 _a10.1177/1758835920980365 [doi]
024 _aPMC7750570 [pmc]
040 _aOvid MEDLINE(R)
099 _a33414848
245 _aChemo-immunotherapy as first-line treatment for small-cell lung cancer. [Review]
251 _aTherapeutic Advances in Medical Oncology. 12:1758835920980365, 2020.
252 _aTher Adv Med Oncol. 12:1758835920980365, 2020.
253 _aTherapeutic advances in medical oncology
260 _c2020
260 _fFY2021
265 _sepublish
266 _d2021-02-17
520 _aSmall-cell lung cancer (SCLC) is a highly lethal subtype of lung cancer. Despite concerted efforts over the past several decades, there have been limited therapeutic advances. Traditional chemotherapy offers a high response rate and rapid symptomatic improvement, but its benefit is fleeting, and relapse is quick and unforgiving. Immunotherapy has delivered improved outcomes for patients with many cancers and there was compelling rationale for development in SCLC. While initial efforts with cytotoxic T-lymphocyte protein-4 inhibitors failed to improve upon chemotherapy alone, the addition of programmed death ligand-1 (PD-L1) inhibitors to first-line chemotherapy finally provided long-awaited gains in survival. Atezolizumab, when added to carboplatin and etoposide, improved both progression-free survival and overall survival. Durvalumab, when added to platinum plus etoposide, similarly improved OS. Biomarker development has stalled as PD-L1 expression and tumor mutational burden have not been useful predictive biomarkers. However, based on the significant survival improvements, both atezolizumab and durvalumab were approved by the US Food and Drug Administration to be given with first-line chemotherapy, and these regimens represent the new standards of care for SCLC. Copyright (c) The Author(s), 2020.
546 _aEnglish
650 _aIN PROCESS -- NOT YET INDEXED
651 _aMedStar Washington Hospital Center
656 _aMedicine/General Internal Medicine
657 _aJournal Article
657 _aReview
700 _aFarid, Saira
790 _aFarid S, Liu SV
856 _uhttps://dx.doi.org/10.1177/1758835920980365
_zhttps://dx.doi.org/10.1177/1758835920980365
942 _cART
_dArticle
999 _c6118
_d6118