Durvalumab plus platinum–etoposide versus platinum–etoposide in first-line treatment of extensive-stage small-cell lung cancer (CASPIAN): a randomised, controlled, open-label, phase 3 trial. Issue 10212 (23rd November 2019)
- Record Type:
- Journal Article
- Title:
- Durvalumab plus platinum–etoposide versus platinum–etoposide in first-line treatment of extensive-stage small-cell lung cancer (CASPIAN): a randomised, controlled, open-label, phase 3 trial. Issue 10212 (23rd November 2019)
- Main Title:
- Durvalumab plus platinum–etoposide versus platinum–etoposide in first-line treatment of extensive-stage small-cell lung cancer (CASPIAN): a randomised, controlled, open-label, phase 3 trial
- Authors:
- Paz-Ares, Luis
Dvorkin, Mikhail
Chen, Yuanbin
Reinmuth, Niels
Hotta, Katsuyuki
Trukhin, Dmytro
Statsenko, Galina
Hochmair, Maximilian J
Özgüroğlu, Mustafa
Ji, Jun Ho
Voitko, Oleksandr
Poltoratskiy, Artem
Ponce, Santiago
Verderame, Francesco
Havel, Libor
Bondarenko, Igor
Kazarnowicz, Andrzej
Losonczy, György
Conev, Nikolay V
Armstrong, Jon
Byrne, Natalie
Shire, Norah
Jiang, Haiyi
Goldman, Jonathan W
Batagelj, Emilio
Casarini, Ignacio
Pastor, Anea Viviana
Sena, Susana Noemi
Zarba, Juan Jose
Burghuber, Otto
Hartl, Sylvia
Hochmair, Maximilian J
Lamprecht, Bernd
Studnicka, Michael
Alberto Schlittler, Luis
Augusto Martinelli de Oliveira, Fabricio
Calabrich, Aknar
Colagiovanni Girotto, Gustavo
Dos Reis, Peo
Fausto Nino Gorini, Carlos
Rafael Martins De Marchi, Peo
Serodio da Rocha Baldotto, Clarissa
Sette, Claudia
Zukin, Mauro
Conev, Nikolay V
Dudov, Assen
Ilieva, Rumyana
Koynov, Krassimir
Krasteva, Rositsa
Tonev, Ivan
Valev, Spartak
Venkova, Violetka
Bi, Minghong
Chen, Chengshui
Chen, Yuan
Chen, Zhendong
Fang, Jian
Feng, Jifeng
Han, Zhigang
Hu, Jie
Hu, Yi
Li, Wei
Liang, Zongan
Lin, Zhong
Ma, Rui
Ma, Shenglin
Nan, Kejun
Shu, Yongqian
Wang, Kai
Wang, Mengzhao
Wu, Gang
Yang, Nong
Yang, Zhixiong
Zhang, Helong
Zhang, Wei
Zhao, Jun
Zhao, Yanqiu
Zhou, Caicun
Zhou, Jianying
Zhou, Xiangdong
Havel, Libor
Kolek, Vitezslav
Koubkova, Leona
Roubec, Jaromir
Skrickova, Jana
Zemanova, Milada
Chouaid, Christos
Hilgers, Werner
Lena, Hervé
Moro-Sibilot, Denis
Robinet, Gilles
Souquet, Pierre-Jean
Alt, Jürgen
Bischoff, Helge
Grohe, Christian
Laack, Eckart
Lang, Susanne
Panse, Jens
Reinmuth, Niels
Schulz, Christian
Bogos, Krisztina
Csánky, Eszter
Fülöp, Anea
Horváth, Zsolt
Kósa, Judit
Laczó, Ibolya
Losonczy, György
Pajkos, Gábor
Pápai, Zsuzsanna
Pápai Székely, Zsolt
Sárosi, Veronika
Somfay, Attila
Somogyiné Ezer, Éva
Telekes, Anás
Bar, Jair
Gottfried, Maya
Heching, Norman Isaac
Zer Kuch, Alona
Bartolucci, Roberta
Bettini, Anna Cecilia
Delmonte, Angelo
Garassino, Marina Chiara
Minelli, Mauro
Roila, Fausto
Verderame, Francesco
Atagi, Shinji
Azuma, Koichi
Goto, Hisatsugu
Goto, Koichi
Hara, Yu
Hayashi, Hidetoshi
Hida, Toyoaki
Hotta, Katsuyuki
Kanazawa, Kenya
Kanda, Shintaro
Kim, Young Hak
Kuyama, Shoichi
Maeda, Tadashi
Morise, Masahiro
Nakahara, Yasuharu
Nishio, Makoto
Nogami, Naoyuki
Okamoto, Isamu
Saito, Haruhiro
Shinoda, Masahiro
Umemura, Shigeki
Yoshida, Tatsuya
Claessens, Niels
Cornelissen, Robin
Heniks, Lizza
Hiltermann, Jeroen
Smit, Egbert
Staal van den Brekel, Agnes
Kazarnowicz, Andrzej
Kowalski, Dariusz
Mańdziuk, Slawomir
Mróz, Robert
Wojtukiewicz, Marek
Ciuleanu, Tudor
Ganea, Doina
Ungureanu, Anei
Dvorkin, Mikhail
Luft, Alexander
Moiseenko, Vladimir
Poltoratskiy, Artem
Sakaeva, Dina
Smolin, Alexey
Statsenko, Galina
Vasilyev, Alexander
Vladimirova, Lyubov
Anasina, Igor
Chovanec, Jozef
Demo, Pavol
Godal, Robert
Kasan, Peter
Stresko, Marian
Urda, Michal
Cho, Eun Kyung
Ji, Jun Ho
Kim, Joo-Hang
Kim, Sang-We
Lee, Gyeong-Won
Lee, Jong-Seok
Lee, Ki Hyeong
Lee, Kyung Hee
Lee, Yun Gyoo
Amelia Insa Molla, Maria
Domine Gomez, Manuel
Ignacio Delgado Mingorance, Juan
Isla Casado, Dolores
Lopez Brea, Marta
Majem Tarruella, Margarita
Morán Bueno, Teresa
Navarro Mendivil, Alejano
Paz-Ares Rodríguez, Luis
Ponce Aix, Santiago
Rosario Garcia Campelo, Maria
Chang, Gee-Chen
Chen, Yen-Hsun
Chiu, Chao-Hua
Hsia, Te-Chun
Lee, Kang-Yun
Li, Chien-Te
Wang, Chin-Chou
Wei, Yu-Feng
Wu, Shang-Yin
Alacacıoğlu, Ahmet
Çiçin, Irfan
Demirkazik, Ahmet
Erman, Mustafa
Göksel, Tuncay
Özgüroğlu, Mustafa
Adamchuk, Hryhoriy
Bondarenko, Igor
Kolesnik, Oleksii
Kryzhanivska, Anna
Ostapenko, Yuriv
Shevnia, Serhii
Shparyk, Yaroslav
Trukhin, Dmytro
Ursol, Grygorii
Voitko, Nataliia
Voitko, Oleksandr
Vynnychenko, Ihor
Babu, Sunil
Chen, Yuanbin
Chiang, Anne
Chua, Winston
Dakhil, Shaker
Dowlati, Afshin
Goldman, Jonathan W
Haque, Basir
Jamil, Rodney
Knoble, Jeanna
Lakhanpal, Shailena
Mi, Kailhong
Nikolinakos, Petros
Powell, Steven
Ross, Helen
Schaefer, Eric
Schneider, Jeffrey
Spahr, Joseph
Spigel, David
Stilwill, Joseph
Sumey, Christopher
Williamson, Michael
… (more) - Abstract:
- Summary: Background: Most patients with small-cell lung cancer (SCLC) have extensive-stage disease at presentation, and prognosis remains poor. Recently, immunotherapy has demonstrated clinical activity in extensive-stage SCLC (ES-SCLC). The CASPIAN trial assessed durvalumab, with or without tremelimumab, in combination with etoposide plus either cisplatin or carboplatin (platinum–etoposide) in treatment-naive patients with ES-SCLC. Methods: This randomised, open-label, phase 3 trial was done at 209 sites across 23 countries. Eligible patients were adults with untreated ES-SCLC, with WHO performance status 0 or 1 and measurable disease as per Response Evaluation Criteria in Solid Tumors, version 1.1. Patients were randomly assigned (in a 1:1:1 ratio) to durvalumab plus platinum–etoposide; durvalumab plus tremelimumab plus platinum–etoposide; or platinum–etoposide alone. All drugs were administered intravenously. Platinum–etoposide consisted of etoposide 80–100 mg/m 2 on days 1–3 of each cycle with investigator's choice of either carboplatin area under the curve 5–6 mg/mL per min or cisplatin 75–80 mg/m 2 (administered on day 1 of each cycle). Patients received up to four cycles of platinum–etoposide plus durvalumab 1500 mg with or without tremelimumab 75 mg every 3 weeks followed by maintenance durvalumab 1500 mg every 4 weeks in the immunotherapy groups and up to six cycles of platinum–etoposide every 3 weeks plus prophylactic cranial irradiation (investigator's discretion)Summary: Background: Most patients with small-cell lung cancer (SCLC) have extensive-stage disease at presentation, and prognosis remains poor. Recently, immunotherapy has demonstrated clinical activity in extensive-stage SCLC (ES-SCLC). The CASPIAN trial assessed durvalumab, with or without tremelimumab, in combination with etoposide plus either cisplatin or carboplatin (platinum–etoposide) in treatment-naive patients with ES-SCLC. Methods: This randomised, open-label, phase 3 trial was done at 209 sites across 23 countries. Eligible patients were adults with untreated ES-SCLC, with WHO performance status 0 or 1 and measurable disease as per Response Evaluation Criteria in Solid Tumors, version 1.1. Patients were randomly assigned (in a 1:1:1 ratio) to durvalumab plus platinum–etoposide; durvalumab plus tremelimumab plus platinum–etoposide; or platinum–etoposide alone. All drugs were administered intravenously. Platinum–etoposide consisted of etoposide 80–100 mg/m 2 on days 1–3 of each cycle with investigator's choice of either carboplatin area under the curve 5–6 mg/mL per min or cisplatin 75–80 mg/m 2 (administered on day 1 of each cycle). Patients received up to four cycles of platinum–etoposide plus durvalumab 1500 mg with or without tremelimumab 75 mg every 3 weeks followed by maintenance durvalumab 1500 mg every 4 weeks in the immunotherapy groups and up to six cycles of platinum–etoposide every 3 weeks plus prophylactic cranial irradiation (investigator's discretion) in the platinum–etoposide group. The primary endpoint was overall survival in the intention-to-treat population. We report results for the durvalumab plus platinum–etoposide group versus the platinum–etoposide group from a planned interim analysis. Safety was assessed in all patients who received at least one dose of their assigned study treatment. This study is registered at ClinicalTrials.gov, NCT03043872, and is ongoing. Findings: Patients were enrolled between March 27, 2017, and May 29, 2018. 268 patients were allocated to the durvalumab plus platinum–etoposide group and 269 to the platinum–etoposide group. Durvalumab plus platinum–etoposide was associated with a significant improvement in overall survival, with a hazard ratio of 0·73 (95% CI 0·59–0·91; p=0·0047]); median overall survival was 13·0 months (95% CI 11·5–14·8) in the durvalumab plus platinum–etoposide group versus 10·3 months (9·3–11·2) in the platinum–etoposide group, with 34% (26·9–41·0) versus 25% (18·4–31·6) of patients alive at 18 months. Any-cause adverse events of grade 3 or 4 occurred in 163 (62%) of 265 treated patients in the durvalumab plus platinum–etoposide group and 166 (62%) of 266 in the platinum–etoposide group; adverse events leading to death occurred in 13 (5%) and 15 (6%) patients. Interpretation: First-line durvalumab plus platinum–etoposide significantly improved overall survival in patients with ES-SCLC versus a clinically relevant control group. Safety findings were consistent with the known safety profiles of all drugs received. Funding: AstraZeneca. … (more)
- Is Part Of:
- Lancet. Volume 394:Issue 10212(2019)
- Journal:
- Lancet
- Issue:
- Volume 394:Issue 10212(2019)
- Issue Display:
- Volume 394, Issue 10212 (2019)
- Year:
- 2019
- Volume:
- 394
- Issue:
- 10212
- Issue Sort Value:
- 2019-0394-10212-0000
- Page Start:
- 1929
- Page End:
- 1939
- Publication Date:
- 2019-11-23
- Subjects:
- Medicine -- Periodicals
Medicine -- Periodicals
Medicine
Medicine
Electronic journals
Periodicals
610.5 - Journal URLs:
- http://www.thelancet.com/ ↗
http://www.sciencedirect.com/science/journal/01406736 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/S0140-6736(19)32222-6 ↗
- Languages:
- English
- ISSNs:
- 0140-6736
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- Legaldeposit
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