{"title":"一线durvalumab联合铂依托泊苷治疗日本广泛期小细胞肺癌患者","authors":"Eisuke Mochizuki , Shun Matsuura , Naoki Koshimizu , Suguru Kojima , Shogo Sakurai , Satoshi Kishimoto , Mitsuru Niwa , Masayuki Watanuki , Ryunosuke Inaba , Sho Takuma , Yusuke Inoue , Masato Karayama , Naoki Inui , Takafumi Suda","doi":"10.1016/j.ctarc.2025.100972","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Platinum-based chemotherapy combined with immune checkpoint inhibitor therapy has recently been introduced for treating extensive-stage small-cell lung cancer (ES-SCLC). In the Phase III CASPIAN study, first-line etoposide (Etoposide) with cisplatin / carboplatin (EP) plus durvalumab significantly improved survival in patients with ES-SCLC. However, it included few Japanese patients, underscoring the need for evaluating the efficacy and safety of this treatment specifically in the Japanese population.</div></div><div><h3>Methods</h3><div>Patients with treatment-naïve ES-SCLC were retrospectively investigated at eight hospitals in Japan, between August 1, 2020 and December 31, 2023. They received EP plus durvalumab (four cycles) every 3 weeks, followed by maintenance durvalumab every 4 weeks until disease progression. The primary endpoint was safety, while the secondary endpoints were overall survival, progression-free survival, objective response rate, and disease control rate.</div></div><div><h3>Results</h3><div>Sixty-nine patients aged 48–91 years (median: 72 years) were included. Most had an Eastern Cooperative Oncology Group performance status of 0 or 1. Grade ≥3 adverse events occurred in 72.5 % of patients and immune-related adverse events in 21.7 %. The median overall survival was 15.0 months (95 % confidence interval: 11.6–20.0), while the median progression-free survival was 5.0 months (95 % confidence interval: 4.3–5.8). Objective response and disease control rates were 75.4 % and 92.8 %, respectively.</div></div><div><h3>Conclusion</h3><div>First-line EP plus durvalumab was effective and well tolerated in Japanese patients with ES-SCLC in a real-world setting aligning with findings of global studies. This regimen should be considered the standard of care for Japanese patients with ES-SCLC.</div></div>","PeriodicalId":9507,"journal":{"name":"Cancer treatment and research communications","volume":"44 ","pages":"Article 100972"},"PeriodicalIF":2.4000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"First-line durvalumab plus platinum–etoposide in Japanese patients with extensive-stage small-cell lung cancer\",\"authors\":\"Eisuke Mochizuki , Shun Matsuura , Naoki Koshimizu , Suguru Kojima , Shogo Sakurai , Satoshi Kishimoto , Mitsuru Niwa , Masayuki Watanuki , Ryunosuke Inaba , Sho Takuma , Yusuke Inoue , Masato Karayama , Naoki Inui , Takafumi Suda\",\"doi\":\"10.1016/j.ctarc.2025.100972\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Platinum-based chemotherapy combined with immune checkpoint inhibitor therapy has recently been introduced for treating extensive-stage small-cell lung cancer (ES-SCLC). In the Phase III CASPIAN study, first-line etoposide (Etoposide) with cisplatin / carboplatin (EP) plus durvalumab significantly improved survival in patients with ES-SCLC. However, it included few Japanese patients, underscoring the need for evaluating the efficacy and safety of this treatment specifically in the Japanese population.</div></div><div><h3>Methods</h3><div>Patients with treatment-naïve ES-SCLC were retrospectively investigated at eight hospitals in Japan, between August 1, 2020 and December 31, 2023. They received EP plus durvalumab (four cycles) every 3 weeks, followed by maintenance durvalumab every 4 weeks until disease progression. The primary endpoint was safety, while the secondary endpoints were overall survival, progression-free survival, objective response rate, and disease control rate.</div></div><div><h3>Results</h3><div>Sixty-nine patients aged 48–91 years (median: 72 years) were included. Most had an Eastern Cooperative Oncology Group performance status of 0 or 1. Grade ≥3 adverse events occurred in 72.5 % of patients and immune-related adverse events in 21.7 %. The median overall survival was 15.0 months (95 % confidence interval: 11.6–20.0), while the median progression-free survival was 5.0 months (95 % confidence interval: 4.3–5.8). Objective response and disease control rates were 75.4 % and 92.8 %, respectively.</div></div><div><h3>Conclusion</h3><div>First-line EP plus durvalumab was effective and well tolerated in Japanese patients with ES-SCLC in a real-world setting aligning with findings of global studies. This regimen should be considered the standard of care for Japanese patients with ES-SCLC.</div></div>\",\"PeriodicalId\":9507,\"journal\":{\"name\":\"Cancer treatment and research communications\",\"volume\":\"44 \",\"pages\":\"Article 100972\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cancer treatment and research communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S246829422500108X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer treatment and research communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S246829422500108X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
First-line durvalumab plus platinum–etoposide in Japanese patients with extensive-stage small-cell lung cancer
Background
Platinum-based chemotherapy combined with immune checkpoint inhibitor therapy has recently been introduced for treating extensive-stage small-cell lung cancer (ES-SCLC). In the Phase III CASPIAN study, first-line etoposide (Etoposide) with cisplatin / carboplatin (EP) plus durvalumab significantly improved survival in patients with ES-SCLC. However, it included few Japanese patients, underscoring the need for evaluating the efficacy and safety of this treatment specifically in the Japanese population.
Methods
Patients with treatment-naïve ES-SCLC were retrospectively investigated at eight hospitals in Japan, between August 1, 2020 and December 31, 2023. They received EP plus durvalumab (four cycles) every 3 weeks, followed by maintenance durvalumab every 4 weeks until disease progression. The primary endpoint was safety, while the secondary endpoints were overall survival, progression-free survival, objective response rate, and disease control rate.
Results
Sixty-nine patients aged 48–91 years (median: 72 years) were included. Most had an Eastern Cooperative Oncology Group performance status of 0 or 1. Grade ≥3 adverse events occurred in 72.5 % of patients and immune-related adverse events in 21.7 %. The median overall survival was 15.0 months (95 % confidence interval: 11.6–20.0), while the median progression-free survival was 5.0 months (95 % confidence interval: 4.3–5.8). Objective response and disease control rates were 75.4 % and 92.8 %, respectively.
Conclusion
First-line EP plus durvalumab was effective and well tolerated in Japanese patients with ES-SCLC in a real-world setting aligning with findings of global studies. This regimen should be considered the standard of care for Japanese patients with ES-SCLC.
期刊介绍:
Cancer Treatment and Research Communications is an international peer-reviewed publication dedicated to providing comprehensive basic, translational, and clinical oncology research. The journal is devoted to articles on detection, diagnosis, prevention, policy, and treatment of cancer and provides a global forum for the nurturing and development of future generations of oncology scientists. Cancer Treatment and Research Communications publishes comprehensive reviews and original studies describing various aspects of basic through clinical research of all tumor types. The journal also accepts clinical studies in oncology, with an emphasis on prospective early phase clinical trials. Specific areas of interest include basic, translational, and clinical research and mechanistic approaches; cancer biology; molecular carcinogenesis; genetics and genomics; stem cell and developmental biology; immunology; molecular and cellular oncology; systems biology; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; cancer policy; and integration of various approaches. Our mission is to be the premier source of relevant information through promoting excellence in research and facilitating the timely translation of that science to health care and clinical practice.