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Durvalumab, with or without tremelimumab, plus platinum-etoposide in first-line treatment of extensive-stage small-cell lung cancer: 3-year overall survival update from CASPIAN
L. Paz-Ares, Y. Chen, N. Reinmuth, K. Hotta, D. Trukhin, G. Statsenko, MJ. Hochmair, M. Özgüroğlu, JH. Ji, MC. Garassino, O. Voitko, A. Poltoratskiy, E. Musso, L. Havel, I. Bondarenko, G. Losonczy, N. Conev, H. Mann, TB. Dalvi, H. Jiang, JW. Goldman
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2016
PubMed Central
od 2016
Europe PubMed Central
od 2016
Open Access Digital Library
od 2016-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2016
- MeSH
- etoposid terapeutické užití MeSH
- humanizované monoklonální protilátky MeSH
- lidé MeSH
- malobuněčný karcinom plic * farmakoterapie MeSH
- monoklonální protilátky MeSH
- nádory plic * farmakoterapie MeSH
- platina terapeutické užití MeSH
- protokoly protinádorové kombinované chemoterapie farmakologie terapeutické užití MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
BACKGROUND: In the phase III CASPIAN study, first-line durvalumab in combination with etoposide plus either cisplatin or carboplatin (EP) significantly improved overall survival (OS) versus EP alone in extensive-stage small-cell lung cancer (ES-SCLC). Durvalumab plus tremelimumab plus EP numerically improved OS versus EP, but did not reach statistical significance. Here we report updated OS in censored patients after median follow-up of >3 years. PATIENTS AND METHODS: 805 patients with treatment-naïve ES-SCLC were randomized 1 : 1 : 1 to durvalumab plus EP, durvalumab plus tremelimumab plus EP, or EP. The two primary endpoints were OS for durvalumab plus EP versus EP and for durvalumab plus tremelimumab plus EP versus EP. RESULTS: As of 22 March 2021 (median follow-up 39.4 months, 86% maturity), durvalumab plus EP continued to demonstrate improved OS versus EP: hazard ratio (HR) 0.71 [95% confidence interval (CI) 0.60-0.86; nominal P = 0.0003]; median OS was 12.9 versus 10.5 months, and 36-month OS rate was 17.6% versus 5.8%. Durvalumab plus tremelimumab plus EP continued to numerically improve OS versus EP: HR 0.81 (95% CI: 0.67-0.97; nominal P = 0.0200); median OS was 10.4 months, and 36-month OS rate was 15.3%. Twenty-seven and nineteen patients in the durvalumab plus EP and durvalumab plus tremelimumab plus EP arms, respectively, remained on durvalumab treatment at data cut-off. CONCLUSIONS: Three times more patients were estimated to be alive at 3 years when treated with durvalumab plus EP versus EP, with the majority still receiving durvalumab at data cut-off, further establishing durvalumab plus EP as first-line standard of care for ES-SCLC.
AO Ospedali Riuniti PO Vincenzo Cervello Palermo Italy
Asklepios Lung Clinic Munich Gauting Germany
Cancer and Hematology Centers of Western Michigan Grand Rapids USA
David Geffen School of Medicine at UCLA Los Angeles USA
Dnipropetrovsk Medical Academy Dnipro Ukraine
Fondazione IRCCS Istituto Nazionale dei Tumori Milan Italy
Istanbul University Cerrahpaşa Cerrahpaşa School of Medicine Istanbul Turkey
Karl Landsteiner Institute of Lung Research and Pulmonary Oncology Krankenhaus Nord Vienna Austria
Kyiv City Clinical Oncological Centre Kyiv Ukraine
Medical Oncology UMHAT St Marina Varna Bulgaria
Odessa Regional Oncological Dispensary Odessa Ukraine
Okayama University Hospital Okayama Japan
Omsk Regional Cancer Center Omsk Russian Federation
Petrov Research Institute of Oncology St Petersburg Russian Federation
Samsung Changwon Hospital Sungkyunkwan University School of Medicine Changwon South Korea
Semmelweis University Budapest Hungary
The University of Chicago Department of Medicine Section of Hematology Oncology Chicago USA
Thomayer Hospital 1st Faculty of Medicine Charles University Prague Czech Republic
Citace poskytuje Crossref.org
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