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Pembrolizumab plus chemotherapy versus chemotherapy alone for first-line treatment of advanced oesophageal cancer (KEYNOTE-590): a randomised, placebo-controlled, phase 3 study.
Sun, Jong-Mu; Shen, Lin; Shah, Manish A; Enzinger, Peter; Adenis, Antoine; Doi, Toshihiko; Kojima, Takashi; Metges, Jean-Philippe; Li, Zhigang; Kim, Sung-Bae; Cho, Byoung Chul; Mansoor, Wasat; Li, Shau-Hsuan; Sunpaweravong, Patrapim; Maqueda, Maria Alsina; Goekkurt, Eray; Hara, Hiroki; Antunes, Luis; Fountzilas, Christos; Tsuji, Akihito; Oliden, Victor Castro; Liu, Qi; Shah, Sukrut; Bhagia, Pooja; Kato, Ken.
Afiliação
  • Sun JM; Samsung Medical Center, Sungkyunkwan University, Seoul, South Korea. Electronic address: jongmu.sun@skku.edu.
  • Shen L; Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing, China.
  • Shah MA; Weill Cornell Medical College, New York City, NY, USA.
  • Enzinger P; Dana Farber Cancer Institute, Boston, MA, USA.
  • Adenis A; Institut de Recherche en Cancérologie de Montpellier (IRCM), Inserm, Université Montpellier, ICM, Montpellier, France.
  • Doi T; National Cancer Center Hospital East, Kashiwa, Japan.
  • Kojima T; National Cancer Center Hospital East, Kashiwa, Japan.
  • Metges JP; CHU Brest-Institut de Cancerologie et d'Hematologie ARPEGO Network, Brest, France.
  • Li Z; Section of Oesophageal Surgery, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Kim SB; Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
  • Cho BC; Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
  • Mansoor W; Christie Hospital NHS Trust, Manchester, UK.
  • Li SH; Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
  • Sunpaweravong P; Prince of Songkla University Hospital, Songkhla, Thailand.
  • Maqueda MA; Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • Goekkurt E; Hematology Oncology Practice Eppendorf and University Cancer Center Hamburg, Hamburg, Germany.
  • Hara H; Saitama Cancer Center, Saitama, Japan.
  • Antunes L; University Hospital of Santa Maria, Federal University of Santa Maria, and Viver Research Center, Santa Maria, Brazil.
  • Fountzilas C; Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
  • Tsuji A; Kagawa University Hospital, Kagawa, Japan.
  • Oliden VC; Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru.
  • Liu Q; Merck, Kenilworth, NJ, USA.
  • Shah S; Merck, Kenilworth, NJ, USA.
  • Bhagia P; Merck, Kenilworth, NJ, USA.
  • Kato K; National Cancer Center Hospital, Tokyo, Japan.
Lancet ; 398(10302): 759-771, 2021 08 28.
Article em En | MEDLINE | ID: mdl-34454674
ABSTRACT

BACKGROUND:

First-line therapy for advanced oesophageal cancer is currently limited to fluoropyrimidine plus platinum-based chemotherapy. We aimed to evaluate the antitumour activity of pembrolizumab plus chemotherapy versus chemotherapy alone as first-line treatment in advanced oesophageal cancer and Siewert type 1 gastro-oesophageal junction cancer.

METHODS:

We did a randomised, placebo-controlled, double-blind, phase 3 study across 168 medical centres in 26 countries. Patients aged 18 years or older with previously untreated, histologically or cytologically confirmed, locally advanced, unresectable or metastatic oesophageal cancer or Siewert type 1 gastro-oesophageal junction cancer (regardless of PD-L1 status), measurable disease per Response Evaluation Criteria in Solid Tumors version 1.1, and Eastern Cooperative Oncology Group performance status of 0-1, were randomly assigned (11) to intravenous pembrolizumab 200 mg or placebo, plus 5-fluorouracil and cisplatin (chemotherapy), once every 3 weeks for up to 35 cycles. Randomisation was stratified by geographical region, histology, and performance status. Patients, investigators, and site staff were masked to group assignment and PD-L1 biomarker status. Primary endpoints were overall survival in patients with oesophageal squamous cell carcinoma and PD-L1 combined positive score (CPS) of 10 or more, and overall survival and progression-free survival in patients with oesophageal squamous cell carcinoma, PD-L1 CPS of 10 or more, and in all randomised patients. This trial is registered with ClinicalTrials.gov, NCT03189719, and is closed to recruitment.

FINDINGS:

Between July 25, 2017, and June 3, 2019, 1020 patients were screened and 749 were enrolled and randomly assigned to pembrolizumab plus chemotherapy (n=373 [50%]) or placebo plus chemotherapy (n=376 [50%]). At the first interim analysis (median follow-up of 22·6 months), pembrolizumab plus chemotherapy was superior to placebo plus chemotherapy for overall survival in patients with oesophageal squamous cell carcinoma and PD-L1 CPS of 10 or more (median 13·9 months vs 8·8 months; hazard ratio 0·57 [95% CI 0·43-0·75]; p<0·0001), oesophageal squamous cell carcinoma (12·6 months vs 9·8 months; 0·72 [0·60-0·88]; p=0·0006), PD-L1 CPS of 10 or more (13·5 months vs 9·4 months; 0·62 [0·49-0·78]; p<0·0001), and in all randomised patients (12·4 months vs 9·8 months; 0·73 [0·62-0·86]; p<0·0001). Pembrolizumab plus chemotherapy was superior to placebo plus chemotherapy for progression-free survival in patients with oesophageal squamous cell carcinoma (6·3 months vs 5·8 months; 0·65 [0·54-0·78]; p<0·0001), PD-L1 CPS of 10 or more (7·5 months vs 5·5 months; 0·51 [0·41-0·65]; p<0·0001), and in all randomised patients (6·3 months vs 5·8 months; 0·65 [0·55-0·76]; p<0·0001). Treatment-related adverse events of grade 3 or higher occurred in 266 (72%) patients in the pembrolizumab plus chemotherapy group versus 250 (68%) in the placebo plus chemotherapy group.

INTERPRETATION:

Compared with placebo plus chemotherapy, pembrolizumab plus chemotherapy improved overall survival in patients with previously untreated, advanced oesophageal squamous cell carcinoma and PD-L1 CPS of 10 or more, and overall survival and progression-free survival in patients with oesophageal squamous cell carcinoma, PD-L1 CPS of 10 or more, and in all randomised patients regardless of histology, and had a manageable safety profile in the total as-treated population.

FUNDING:

Merck Sharp & Dohme.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Protocolos de Quimioterapia Combinada Antineoplásica / Cisplatino / Anticorpos Monoclonais Humanizados / Fluoruracila / Antineoplásicos Imunológicos / Carcinoma de Células Escamosas de Cabeça e Pescoço Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Protocolos de Quimioterapia Combinada Antineoplásica / Cisplatino / Anticorpos Monoclonais Humanizados / Fluoruracila / Antineoplásicos Imunológicos / Carcinoma de Células Escamosas de Cabeça e Pescoço Tipo de estudo: Clinical_trials Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Lancet Ano de publicação: 2021 Tipo de documento: Article