Zhenghang Wang, Xicheng Wang, Xiaoyan Zhang, Jiahua Leng, Ming Cui, Ji Zhang, Quan Wang, Yu Sun, Ting Xu, Mifen Chen, Jian Li, Lin Shen
{"title":"多利帕利单抗、贝伐单抗和伊立替康治疗dMMR/MSI局部晚期结直肠癌:1b/2期临床试验的一期结果","authors":"Zhenghang Wang, Xicheng Wang, Xiaoyan Zhang, Jiahua Leng, Ming Cui, Ji Zhang, Quan Wang, Yu Sun, Ting Xu, Mifen Chen, Jian Li, Lin Shen","doi":"10.1016/j.xcrm.2025.102296","DOIUrl":null,"url":null,"abstract":"<p><p>This is the first stage of the phase 1b/2 trial evaluating the effectiveness and safety of toripalimab, irinotecan, and bevacizumab in patients with rectal cancer refusing up-front surgery or radiation therapy (rectum cohort) and patients with T4NanyM0 colon cancer (colon cohort) with deficiency of mismatch repair (dMMR) or microsatellite instability (MSI). This trial allows a doctor-patient shared decision-making process to determine whether to omit irinotecan or bevacizumab and the optimal surgery timing. The primary endpoint pathological complete response (pCR) rates in the full analysis set (FAS) and per-protocol set (PPS) are 57.1% (95% confidence interval [CI] 28.9-82.3) and 66.7% (34.9-90.1), respectively, in the colon cohort (n = 14) and 75.0% (35.6-95.5) and 100% (51.7-100.0), respectively, in the rectum cohort (n = 8). No disease recurrence occurs in PPS. No grade 4-5 drug-related adverse events are observed. Toripalimab with or without irinotecan and bevacizumab shows promising efficacy and manageable toxicity in dMMR/MSI T4NanyM0 colon cancer and locally advanced rectal cancer (ClinicalTrials.gov: NCT04988191).</p>","PeriodicalId":9822,"journal":{"name":"Cell Reports Medicine","volume":" ","pages":"102296"},"PeriodicalIF":10.6000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12490223/pdf/","citationCount":"0","resultStr":"{\"title\":\"Toripalimab, bevacizumab, and irinotecan in dMMR/MSI locally advanced colorectal cancer: First-stage results from a phase 1b/2 trial.\",\"authors\":\"Zhenghang Wang, Xicheng Wang, Xiaoyan Zhang, Jiahua Leng, Ming Cui, Ji Zhang, Quan Wang, Yu Sun, Ting Xu, Mifen Chen, Jian Li, Lin Shen\",\"doi\":\"10.1016/j.xcrm.2025.102296\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>This is the first stage of the phase 1b/2 trial evaluating the effectiveness and safety of toripalimab, irinotecan, and bevacizumab in patients with rectal cancer refusing up-front surgery or radiation therapy (rectum cohort) and patients with T4NanyM0 colon cancer (colon cohort) with deficiency of mismatch repair (dMMR) or microsatellite instability (MSI). This trial allows a doctor-patient shared decision-making process to determine whether to omit irinotecan or bevacizumab and the optimal surgery timing. The primary endpoint pathological complete response (pCR) rates in the full analysis set (FAS) and per-protocol set (PPS) are 57.1% (95% confidence interval [CI] 28.9-82.3) and 66.7% (34.9-90.1), respectively, in the colon cohort (n = 14) and 75.0% (35.6-95.5) and 100% (51.7-100.0), respectively, in the rectum cohort (n = 8). No disease recurrence occurs in PPS. No grade 4-5 drug-related adverse events are observed. Toripalimab with or without irinotecan and bevacizumab shows promising efficacy and manageable toxicity in dMMR/MSI T4NanyM0 colon cancer and locally advanced rectal cancer (ClinicalTrials.gov: NCT04988191).</p>\",\"PeriodicalId\":9822,\"journal\":{\"name\":\"Cell Reports Medicine\",\"volume\":\" \",\"pages\":\"102296\"},\"PeriodicalIF\":10.6000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12490223/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell Reports Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.xcrm.2025.102296\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Reports Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.xcrm.2025.102296","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/15 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
Toripalimab, bevacizumab, and irinotecan in dMMR/MSI locally advanced colorectal cancer: First-stage results from a phase 1b/2 trial.
This is the first stage of the phase 1b/2 trial evaluating the effectiveness and safety of toripalimab, irinotecan, and bevacizumab in patients with rectal cancer refusing up-front surgery or radiation therapy (rectum cohort) and patients with T4NanyM0 colon cancer (colon cohort) with deficiency of mismatch repair (dMMR) or microsatellite instability (MSI). This trial allows a doctor-patient shared decision-making process to determine whether to omit irinotecan or bevacizumab and the optimal surgery timing. The primary endpoint pathological complete response (pCR) rates in the full analysis set (FAS) and per-protocol set (PPS) are 57.1% (95% confidence interval [CI] 28.9-82.3) and 66.7% (34.9-90.1), respectively, in the colon cohort (n = 14) and 75.0% (35.6-95.5) and 100% (51.7-100.0), respectively, in the rectum cohort (n = 8). No disease recurrence occurs in PPS. No grade 4-5 drug-related adverse events are observed. Toripalimab with or without irinotecan and bevacizumab shows promising efficacy and manageable toxicity in dMMR/MSI T4NanyM0 colon cancer and locally advanced rectal cancer (ClinicalTrials.gov: NCT04988191).
Cell Reports MedicineBiochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
15.00
自引率
1.40%
发文量
231
审稿时长
40 days
期刊介绍:
Cell Reports Medicine is an esteemed open-access journal by Cell Press that publishes groundbreaking research in translational and clinical biomedical sciences, influencing human health and medicine.
Our journal ensures wide visibility and accessibility, reaching scientists and clinicians across various medical disciplines. We publish original research that spans from intriguing human biology concepts to all aspects of clinical work. We encourage submissions that introduce innovative ideas, forging new paths in clinical research and practice. We also welcome studies that provide vital information, enhancing our understanding of current standards of care in diagnosis, treatment, and prognosis. This encompasses translational studies, clinical trials (including long-term follow-ups), genomics, biomarker discovery, and technological advancements that contribute to diagnostics, treatment, and healthcare. Additionally, studies based on vertebrate model organisms are within the scope of the journal, as long as they directly relate to human health and disease.