不可切除胰腺癌诱导治疗后放化疗与化疗的获益:CONKO-007随机试验

IF 41.9 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-10-20 Epub Date: 2025-08-13 DOI:10.1200/JCO-24-01502
Rainer Fietkau, Michael Ghadimi, Robert Grützmann, Uwe A Wittel, Lutz Jacobasch, Waldemar Uhl, Roland S Croner, Wolf Otto Bechstein, Ulf Peter Neumann, Dirk Waldschmidt, Stefan Boeck, Nicolas Moosmann, Anke C Reinacher-Schick, Henriette Golcher, Werner Adler, Sabine Semrau, Dorota Lubgan, Annett Kallies, Markus Hecht, Iris Tischoff, Andrea Tannapfel, Benjamin Frey, Helmut Oettle
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引用次数: 0

摘要

目的:确定诱导化疗加放化疗(CRT)与单独化疗相比,对不可切除的胰腺肿瘤的益处,以肿瘤完全切除,在切除边缘的组织病理学检查中未检测到肿瘤细胞(R0切除率)来衡量。患者和方法:conco -007是一项由研究者发起的开放标签、多中心、III期随机临床试验,纳入了525例不可切除肿瘤患者,495例患者接受了诱导化疗(402例使用氟尿嘧啶、伊立替康和奥沙利铂[FOLFIRINOX], 93例使用吉西他滨)。诱导化疗3个月后无进展的患者(n = 336)被随机分配到继续相同的化疗(n = 167)或CRT (n = 169;50.4Gy(同时使用吉西他滨)。可切除性由一组外科医生集中重新评估。如果可能,建议手术治疗。中期分析后,由于招募缓慢,主要终点从总生存期(OS)改为总R0切除率。中位随访时间为76个月。计划的重要次要终点是手术治疗人群的R0切除率和OS。结果:主要终点(总R0切除率)在治疗组之间无显著差异,CRT组为25%(169例中有43例),化疗组为18%(167例中有30例;P = .113)。次要终点分析显示,手术次数相等(P = .91);CRT后手术患者的R0切除率为69.4%(62例中的43例),高于单纯化疗患者的50.0%(60例中的30例,P = 0.04)。其他切除指标(R0/R1/R2/未切除比)也有利于CRT (P = 0.02)。两组间OS无差异(风险比[HR], 0.937 [95% CI, 0.747 ~ 1.174];P = 0.57;随机分配意向治疗患者)。手术与更长的生存期相关(P < 0.001, HR, 0.525 [95% CI, 0.408 ~ 0.676])。结论:虽然CRT不能提高总R0切除率或生存率,但与单独化疗相比,CRT更能使手术治疗的患者进行R0切除术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benefit of Chemoradiotherapy Versus Chemotherapy After Induction Therapy for Conversion of Unresectable Into Resectable Pancreatic Cancer: The Randomized CONKO-007 Trial.

Purpose: To determine the benefit, measured as complete removal of a tumor so that no tumor cells are detectable during histopathologic examination of the resection margin (R0 resection rate), of induction chemotherapy plus chemoradiotherapy (CRT) compared with chemotherapy alone for unresectable pancreatic tumors.

Patients and methods: CONKO-007, an investigator-initiated open-label, multicentric, phase III randomized clinical trial, enrolled 525 patients with unresectable tumors, and 495 patients received induction chemotherapy (402 with fluorouracil, irinotecan, and oxaliplatin [FOLFIRINOX] and 93 with gemcitabine). Patients without progression after 3 months of induction chemotherapy (n = 336) were randomly assigned for continuation of the same chemotherapy (n = 167) or CRT (n = 169; 50.4Gy concurrently with gemcitabine). Resectability was centrally reassessed by a panel of surgeons. Surgery was recommended if possible. After an interim analysis, the primary end point was changed from overall survival (OS) to overall R0 resection rate because of slow recruitment. The median follow-up was 76 months. Important planned secondary end points were R0 resection rate in the surgically treated population and OS.

Results: The primary end point (overall R0 resection rate) was not significantly different between treatment arms with 25% (43 of 169) in the CRT arm versus 18% in the chemotherapy arm (30 of 167; P = .113). Secondary end point analysis showed that surgery was performed equally often (P = .91); R0 resection rate in patients who underwent surgery was higher after CRT, 69.4% (43 of 62) compared with chemotherapy alone: 50.0% (30 of 60 patients, P = .04). Other parameters of resection (ratio of R0/R1/R2/no resection) also favored CRT (P = .02). No difference in OS was seen between treatment arms (hazard ratio [HR], 0.937 [95% CI, 0.747 to 1.174]; P = .57; randomly assigned intention-to-treat patients). Surgery was associated with longer OS (P < .001, HR, 0.525 [95% CI, 0.408 to 0.676]).

Conclusion: Although not improving overall R0 resection rate or survival, CRT enables a R0 resection in surgically treated patients more often than chemotherapy alone.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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