Barts Cancer Institute, Queen Mary University of London, EC1M 6BQ, UK.
Department of Genitourinary Oncology, St Bartholomew's Hospital, Barts Health NHS Trust, London, EC1A 7BE, UK.
Future Oncol. 2023 Mar;19(7):509-515. doi: 10.2217/fon-2022-0868. Epub 2023 Apr 21.
The standard-of-care for muscle-invasive bladder cancer is radical surgery with neoadjuvant cisplatin-based chemotherapy. Despite curative intent from these interventions, relapse rates post-surgery remain high, with approximately 50% of patients developing local or distant recurrence within 2 years of surgery and a 5-year survival of only 50-60%. Identifying patients who are high risk for relapse post-surgery is a priority. Monitoring patients for circulating tumor DNA (ctDNA) is a minimally invasive approach that appears attractive for selecting patients potentially suitable for adjuvant treatment with checkpoint inhibitors. IMvigor011 (NCT04660344) is a global, double-blind, randomized phase III study assessing the efficacy of atezolizumab (anti-PD-L1) versus placebo in patients with high-risk muscle-invasive bladder cancer who are ctDNA positive post-cystectomy. The primary end point is disease-free survival in participants who are ctDNA positive within 20 weeks of cystectomy.
肌层浸润性膀胱癌的标准治疗方法是根治性手术联合新辅助含顺铂化疗。尽管这些干预措施有治愈的意图,但手术后的复发率仍然很高,大约 50%的患者在手术后 2 年内出现局部或远处复发,5 年生存率仅为 50-60%。确定手术后有高复发风险的患者是当务之急。监测患者的循环肿瘤 DNA(ctDNA)是一种微创方法,对于选择可能适合用检查点抑制剂进行辅助治疗的患者似乎具有吸引力。IMvigor011(NCT04660344)是一项全球性、双盲、随机 III 期研究,评估 atezolizumab(抗 PD-L1)与安慰剂在术后 ctDNA 阳性的高风险肌层浸润性膀胱癌患者中的疗效。主要终点是在术后 20 周内 ctDNA 阳性的参与者的无病生存期。