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Tumor Debulking in Combination With Chemotherapy in Multiorgan Metastatic Colorectal Cancer

医学 揭穿 奥沙利铂 结直肠癌 内科学 肿瘤科 临床终点 化疗 肿瘤揭穿 外科 卡培他滨 缓和医疗 无进展生存期 随机对照试验 卵巢癌 中期分析 不利影响 癌症 姑息化疗 化疗方案 进行性疾病 生存分析 存活率 临床试验 前瞻性队列研究
作者
Elske C. Gootjes,Lotte Bakkerus,Anviti A. Adhin,Barbara M. Zonderhuis,Kathelijn S. Versteeg,J. Tuynman,Martijn R. Meijerink,Cornelis J.A. Haasbeek,Johannes H. W. de Wilt,Dirk J. Grünhagen,Ewoud J. Smit,John Primrose,J.A. Bridgewater,Esther van Meerten,Jan-Willem B. de Groot,Mathijs P. Hendriks,Esther Oomen-de Hoop,T. Buffart,Cornelis Verhoef,Henk M. W. Verheul
出处
期刊:JAMA [American Medical Association]
卷期号:335 (15): 1311-1311 被引量:3
标识
DOI:10.1001/jama.2026.1929
摘要

Importance: Local therapy, including surgery, radiation, and ablation, is increasingly used in patients with multiorgan metastatic colorectal cancer (mCRC). However, prospective evidence for a survival benefit of tumor debulking is lacking. Objective: To investigate whether tumor debulking added to palliative chemotherapy improves survival of patients with multiorgan mCRC. Design, Setting, and Participants: This investigator-initiated, open-label, multicenter, randomized clinical trial enrolled patients with multiorgan mCRC between May 2013 and May 2023. The last date of follow-up was April 4, 2024. Patients were enrolled in 27 hospitals in the Netherlands and 1 in the UK. Adult patients with multiorgan mCRC were considered eligible if more than 80% tumor debulking was deemed feasible by resection, radiotherapy, and/or thermal ablation prior to starting first-line palliative chemotherapy. Interventions: After achieving objective tumor response or stable disease after 3 cycles of capecitabine and oxaliplatin or 4 cycles of 5-fluorouracil and oxaliplatin with or without bevacizumab, patients were randomized 1:1 to receive chemotherapy alone (standard care group) or tumor debulking followed by chemotherapy. Main Outcomes and Measures: The primary end point was overall survival. Secondary end points included progression-free survival and serious adverse events. These outcomes were analyzed in the intention-to-treat population, applicable from randomization. A prespecified interim analysis performed after the initial 100 participants were enrolled revealed that the trial was both safe and feasible to proceed. Results: A total of 382 of 454 enrolled patients were randomized: 192 in the chemotherapy alone group (133 [69%] male) and 190 in the chemotherapy plus tumor debulking group (127 [67%] male). The median age was 64 years in both groups. After a median follow-up of 32.3 months, median overall survival in the chemotherapy alone group was 27.5 months vs 30.0 months in the chemotherapy plus tumor debulking group (adjusted hazard ratio, 0.88 [95% CI, 0.70-1.10]; P = .26). Median progression-free survival in the chemotherapy alone group was 10.4 months vs 10.5 months in the chemotherapy plus tumor debulking group (adjusted hazard ratio, 0.83 [95% CI, 0.67-1.02]; P = .08). More patients in the chemotherapy plus tumor debulking vs chemotherapy alone group had any serious adverse events (101 [53%] vs 74 [39%]; P = .006). Conclusions and Relevance: Tumor debulking in addition to first-line palliative systemic treatment failed to improve overall survival compared with systemic treatment alone for patients with multiorgan mCRC and should not be considered standard care. Trial Registration: ClinicalTrials.gov Identifier: NCT01792934.
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