Future oncology (London, England) · 2019
Targeted agents or immuno-oncology therapies as first-line therapy for BRAF-mutated metastatic melanoma: a real-world study.
СтатьяРандомизированное исследованиеНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Luke Jason J, Ghate Sameer R, Kish Jonathan, Lee Choo Hyung, McAllister Lindsay, Mehta Sonam, Ndife Briana, Feinberg Bruce A
Аннотация
Aim: Targeted therapy (TT) and immuno-oncology (IO) drugs are approved for patients with BRAF mutant metastatic melanoma (MM). We compared real-world outcomes for first-line (1L) TT versus 1L IO to evaluate optimal sequencing. Materials & methods: Physicians-identified BRAF mutant MM patients initiating 1L TT or IO therapies and extracted treatment, disease and clinical outcomes including disease response which were compared between TT and IO and individual regimens. Results: 440 MM patients (TT = 283, IO = 157) were identified. A higher proportion of TT patients had liver metastases (46.3 vs 35.0%) and abnormal lactate dehydrogenase (61.1 vs 42.7%). IO-treated had a RECIST-determined response rate of 45.9 versus 60.1% for TT and time on treatment of 7.2 versus 11.4 months, respectively. There was no survival difference between cohorts. Conclusion: Despite higher risk patients, 1L TT resulted in higher response rate and longer treatment duration suggesting a preferred 1L sequence.
Предметные рубрики MeSH
AgedAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsAzetidinesCTLA-4 AntigenDisease-Free SurvivalFemaleHumansImidazolesImmunotherapyIpilimumabMaleMelanomaMiddle AgedMolecular Targeted TherapyMutationNeoplasm MetastasisNivolumabOximesPiperidinesProgrammed Cell Death 1 ReceptorProto-Oncogene Proteins B-rafPyridonesPyrimidinonesTreatment OutcomeVemurafenib