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      Sintilimab versus placebo in combination with chemotherapy as first line treatment for locally advanced or metastatic oesophageal squamous cell carcinoma (ORIENT-15): multicentre, randomised, double blind, phase 3 trial

      research-article
      1 , 2 , 3 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 26 , 28 , ORIENT-15 study group, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
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          Abstract

          Objective

          To evaluate sintilimab versus placebo in combination with chemotherapy (cisplatin plus paclitaxel or cisplatin plus 5-fluorouracil) as first line treatment of unresectable locally advanced, recurrent, or metastatic oesophageal squamous cell carcinoma.

          Design

          Multicentre, randomised, double blind, phase 3 trial.

          Setting

          66 sites in China and 13 sites outside of China between 14 December 2018 and 9 April 2021.

          Participants

          659 adults (aged ≥18 years) with advanced or metastatic oesophageal squamous cell carcinoma who had not received systemic treatment.

          Intervention

          Participants were randomised 1:1 to receive sintilimab or placebo (3 mg/kg in patients weighing <60 kg or 200 mg in patients weighing ≥60 kg) in combination with cisplatin 75 mg/m 2 plus paclitaxel 175 mg/m 2 every three weeks. The trial was amended to allow investigators to choose the chemotherapy regimen: cisplatin plus paclitaxel or cisplatin plus 5-fluorouracil (800 mg/m 2 continuous infusion on days 1-5).

          Main outcome measures

          Overall survival in all patients and in patients with combined positive scores of ≥10 for expression of programmed cell death ligand 1.

          Results

          659 patients were randomly assigned to sintilimab (n=327) or placebo (n=332) with chemotherapy. 616 of 659 patients (93%) received sintilimab or placebo in combination with cisplatin plus paclitaxel and 43 of 659 patients (7%) received sintilimab or placebo in combination with cisplatin plus 5-fluorouracil. At the interim analysis, sintilimab with chemotherapy showed better overall survival compared with placebo and chemotherapy in all patients (median 16.7 v 12.5 months, hazard ratio 0.63, 95% confidence interval 0.51 to 0.78, P<0.001) and in patients with combined positive scores of ≥10 (17.2 v 13.6 months, 0.64, 0.48 to 0.85, P=0.002). Sintilimab and chemotherapy significantly improved progression free survival compared with placebo and chemotherapy in all patients (7.2 v 5.7 months, 0.56, 0.46 to 0.68, P<0.001) and in patients with combined positive scores of ≥10 (8.3 v 6.4 months, 0.58, 0.45 to 0.75, P<0.001). Adverse events related to treatment occurred in 321 of 327 patients (98%) in the sintilimab-chemotherapy group versus 326 of 332 (98%) patients in the placebo-chemotherapy group. Rates of adverse events related to treatment, grade ≥3, were 60% (196/327) and 55% (181/332) in the sintilimab-chemotherapy and placebo-chemotherapy groups, respectively.

          Conclusions

          Compared with placebo, sintilimab in combination with cisplatin plus paclitaxel showed significant benefits in overall survival and progression free survival as first line treatment in patients with advanced or metastatic oesophageal squamous cell carcinoma. Similar benefits of sintilimab with cisplatin plus 5-fluorouracil seem promising.

          Trial registration

          ClinicalTrials.gov NCT03748134.

          Related collections

          Most cited references28

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          Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries

          This article provides a status report on the global burden of cancer worldwide using the GLOBOCAN 2018 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer, with a focus on geographic variability across 20 world regions. There will be an estimated 18.1 million new cancer cases (17.0 million excluding nonmelanoma skin cancer) and 9.6 million cancer deaths (9.5 million excluding nonmelanoma skin cancer) in 2018. In both sexes combined, lung cancer is the most commonly diagnosed cancer (11.6% of the total cases) and the leading cause of cancer death (18.4% of the total cancer deaths), closely followed by female breast cancer (11.6%), prostate cancer (7.1%), and colorectal cancer (6.1%) for incidence and colorectal cancer (9.2%), stomach cancer (8.2%), and liver cancer (8.2%) for mortality. Lung cancer is the most frequent cancer and the leading cause of cancer death among males, followed by prostate and colorectal cancer (for incidence) and liver and stomach cancer (for mortality). Among females, breast cancer is the most commonly diagnosed cancer and the leading cause of cancer death, followed by colorectal and lung cancer (for incidence), and vice versa (for mortality); cervical cancer ranks fourth for both incidence and mortality. The most frequently diagnosed cancer and the leading cause of cancer death, however, substantially vary across countries and within each country depending on the degree of economic development and associated social and life style factors. It is noteworthy that high-quality cancer registry data, the basis for planning and implementing evidence-based cancer control programs, are not available in most low- and middle-income countries. The Global Initiative for Cancer Registry Development is an international partnership that supports better estimation, as well as the collection and use of local data, to prioritize and evaluate national cancer control efforts. CA: A Cancer Journal for Clinicians 2018;0:1-31. © 2018 American Cancer Society.
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            Pembrolizumab plus Chemotherapy in Metastatic Non–Small-Cell Lung Cancer

            First-line therapy for advanced non-small-cell lung cancer (NSCLC) that lacks targetable mutations is platinum-based chemotherapy. Among patients with a tumor proportion score for programmed death ligand 1 (PD-L1) of 50% or greater, pembrolizumab has replaced cytotoxic chemotherapy as the first-line treatment of choice. The addition of pembrolizumab to chemotherapy resulted in significantly higher rates of response and longer progression-free survival than chemotherapy alone in a phase 2 trial.
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              Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy.

              Cancer immunotherapy can induce long lasting responses in patients with metastatic cancers of a wide range of histologies. Broadening the clinical applicability of these treatments requires an improved understanding of the mechanisms limiting cancer immunotherapy. The interactions between the immune system and cancer cells are continuous, dynamic, and evolving from the initial establishment of a cancer cell to the development of metastatic disease, which is dependent on immune evasion. As the molecular mechanisms of resistance to immunotherapy are elucidated, actionable strategies to prevent or treat them may be derived to improve clinical outcomes for patients.
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                Author and article information

                Contributors
                Role: professor
                Role: professor
                Role: professor
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                Role: professor
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                Role: professor
                Role: associate professor
                Role: professor
                Role: associate professor
                Role: professor
                Role: professor
                Role: associate professor
                Role: professor
                Role: associate professor
                Role: professor
                Role: professor
                Role: professor
                Role: professor
                Role: professor
                Role: professor
                Role: chief of department
                Role: professor
                Role: clinical research physician
                Role: statistician
                Role: medical executive director
                Role: professor
                Journal
                BMJ
                BMJ
                BMJ-UK
                bmj
                The BMJ
                BMJ Publishing Group Ltd.
                0959-8138
                1756-1833
                2022
                19 April 2022
                : 377
                : e068714
                Affiliations
                [1 ]Department of Gastrointestinal Oncology, Peking University Cancer Hospital and Institute, Beijing, China
                [2 ]Department of Oncology, The Affiliated Hospital of Jining Medical College, Jining, China
                [3 ]Department of Medical Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China
                [4 ]Special Needs Ward, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China
                [5 ]Department of Medical Oncology, Nantong Tumour Hospital, Nantong, China
                [6 ]Department of Medical Oncology, Northern Jiangsu People's Hospital, Affiliated Hospital to Yangzhou University, Yangzhou, China
                [7 ]Department of Radiotherapy and Chemotherapy, Tangshan People's Hospital, Tangshan, China
                [8 ]Department of Medical Oncology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China
                [9 ]Department of Oncology, Jiangsu Cancer Hospital, Nanjing Medical University, Nanjing, China
                [10 ]Department of Medical Oncology, Anhui Provincial Cancer Hospital, University of Science and Technology of China, Hefei, China
                [11 ]Department of Oncology, Fujian Provincial Hospital, Fuzhou, China
                [12 ]Department of Medical Oncology, Suining Central Hospital, Suining, China
                [13 ]Department of Medical Oncology, The Affiliated Hospital of Qingdao University, Qingdao, China
                [14 ]Department of Thoracic Surgery Ward 2, Yunnan Cancer Hospital, Kunming, China
                [15 ]Department of Medical Oncology, Henan Tumour Hospital, Zhengzhou, China
                [16 ]Department of Thoracic Tumour Radiotherapy Ward 2, Jiangxi Cancer Hospital, Nanchang, China
                [17 ]Department of Medical Oncology, Inner Mongolia People's Hospital, Hohhot, China
                [18 ]Department of Digestive Oncology Ward 2, Harbin Medical University Cancer Hospital, Harbin, China
                [19 ]Department of Medical Oncology, Puyang Oilfield General Hospital, Puyang, China
                [20 ]Department of Medical Oncology Three, Handan Central Hospital, Handan, China
                [21 ]Department of Oncology, Qilu Hospital of Shandong University, Jinan, China
                [22 ]Oncology Department, The First Affiliated Hospital of Henan University of Science and Technology, Luoyang, China
                [23 ]Department of Tumour Chemotherapy, Anhui Provincial Hospital, Hefei, China;
                [24 ]Department of Medical Oncology, Centre François Baclesse, Caen, France;
                [25 ]Department of Gastroenterology and Digestive Oncology, Hôpital Européen Georges Pompidou, Paris, France
                [26 ]Medical Science and Strategy Oncology, Innovent Biologics, China
                [27 ]Department of Statistics, Innovent Biologics, China
                [28 ]Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and Institute, Beijing, China
                Author notes
                Correspondence to: L Shen linshenpku@ 123456163.com
                Author information
                https://orcid.org/0000-0003-1134-2922
                Article
                bmj-2021-068714.R1 luzh068714
                10.1136/bmj-2021-068714
                9016493
                35440464
                70d26b08-6181-419b-9c49-a14fca74d49e
                © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 02 March 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100004312, Eli Lilly and Company;
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                Research

                Medicine
                Medicine

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