首页|期刊导航|结直肠肛门外科|[评论]肿瘤姑息减瘤治疗联合化疗在多器官转移性结直肠癌中应用的随机临床研究:ORCHESTRA研究

[评论]肿瘤姑息减瘤治疗联合化疗在多器官转移性结直肠癌中应用的随机临床研究:ORCHESTRA研究OA

Tumor debulking in combination with chemotherapy in multiorgan metastatic colorectal cancer:the ORCHESTRA randomized clinical trial

中文摘要英文摘要

研究重要性 局部治疗(包括手术、放疗和消融)在多器官转移性结直肠癌患者中的应用日益广泛.然而,目前仍缺乏肿瘤姑息减瘤能够带来生存获益的前瞻性证据.研究目的 探讨在姑息化疗基础上增加肿瘤姑息减瘤治疗是否能够改善多器官转移性结直肠癌患者的生存.研究设计、研究地点及受试者 本研究是一项由研究者发起的开放标签、多中心随机临床试验,于2013年5月至2023年5月期间纳入多器官转移性结直肠癌患者.末次随访日期为2024年4月4日.患者来自荷兰27家医院和英国1家医院.伴有多器官转移的成年结直肠癌患者若在开始一线姑息化疗之前经评估认为能够通过手术切除、放疗和(或)热消融实现80%以上的肿瘤姑息减瘤,则符合入组条件.干预措施 在接受3个周期卡培他滨联合奥沙利铂,或4个周期5-氟尿嘧啶联合奥沙利铂±贝伐珠单抗治疗后,达到客观肿瘤缓解或疾病稳定的患者,按1∶1的比例随机分配至单纯化疗组(标准治疗组)或化疗联合肿瘤姑息减瘤组.主要结局指标与测量 主要终点为总生存期.次要终点包括无进展生存期和严重不良事件.上述结局采用意向治疗人群进行分析,并从随机分组时开始计算.在最初纳入100例受试者后进行了一项预先设定的中期分析,结果显示该试验在安全性和可行性方面均支持继续开展.研究结果 在454例入组患者中,共有382例完成随机分组:单纯化疗组192例(其中男性133例,占69%);化疗联合肿瘤姑息减瘤组190例(其中男性127例,占67%).两组患者的中位年龄均为64岁.经过中位随访32.3个月后,单纯化疗组的中位总生存期为27.5个月,而化疗联合肿瘤姑息减瘤组为30.0个月[校正后风险比(HR)=0.88;95%CI,0.70~1.10;P=0.26].单纯化疗组的中位无进展生存期为10.4个月,而化疗联合肿瘤姑息减瘤组为10.5个月(校正后HR=0.83;95%CI,0.67~1.02;P=0.08).与单纯化疗组相比,化疗联合肿瘤姑息减瘤组出现任意严重不良事件的患者更多[101(53%)vs.74(39%);P=0.006].结论 与临床意义 对于多器官转移性结直肠癌患者,在一线姑息化疗基础上增加肿瘤姑息减瘤治疗,相较于单纯化疗并未改善总生存期,因此不应将其视为标准治疗方案.

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 che-motherapy 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 che-motherapy 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=0.26).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=0.08).More patients in the chemotherapy plus tumor debulking vs chemotherapy alone group had any serious adverse events(101[53%]vs.74[39%];P=0.006).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.

Gootjes E C;Bakkerus L;Adhin A A;张荣欣

中山大学肿瘤防治中心结直肠科 广东 广州 510060

医药卫生

转移性结直肠癌多器官肿瘤姑息减瘤化疗总生存期

metastatic colorectal cancermultiorgantumor debulkingchemotherapyoverall survival

《结直肠肛门外科》 2026 (4)

398-400,3

10.19668/j.cnki.issn1674-0491.2026.04.013

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