肝移植改善癌症结直肠癌肝转移不可治愈患者的预后:一项前瞻性平行试验(COLT试验)

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Carlo Sposito , Filippo Pietrantonio , Marianna Maspero , Fabrizio Di Benedetto , Marco Vivarelli , Giuseppe Tisone , Luciano De Carlis , Renato Romagnoli , Salvatore Gruttadauria , Michele Colledan , Salvatore Agnes , Giuseppe Ettorre , Umberto Baccarani , Guido Torzilli , Stefano Di Sandro , Domenico Pinelli , Lucio Caccamo , Andrea Sartore Bianchi , Carlo Spreafico , Valter Torri , Vincenzo Mazzaferro
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引用次数: 0

摘要

背景接受姑息性化疗的不可切除结直肠癌肝转移患者的5年总生存率(OS)低于30%。肝移植(LT)可以改善OS高达60%-83%(SECA-I和SECA-II试验)。本研究的目的是与纳入三联化疗+抗EGFR III期试验的匹配队列患者相比,评估LT对仅肝脏转移性CRC的疗效。患者和方法COLT试验是一项研究者驱动的、多中心、非随机、开放标签、对照、前瞻性平行试验(ClinicalTrials.gov NCT03803436)。包括患有肝限制性不可切除CLM、RAS和BRAF野生型和治疗性切除原发性结肠癌的过度选择患者。将观察到的移植后结果与TRIPLETE试验(NCT03231722)中匹配队列中获得的结果进行前瞻性的1:5比较。结果主要终点是比较参与COLT试验的患者与参与TRIPLETE试验的符合COLT条件的人群的3年和5年OS。预测COLT人群在5年时OS的预期增加为40%(COLT与TRIPLETE相比,5年时的预期OS为70%对30%)。次要终点是比较5年无病生存率并评估LT的安全性(Dindo-Clavien分类和综合并发症指数)。结论LT在选定的CLM患者中提供了最长的OS。改进选择策略可以使患者获得与其他LT适应症相似的5年OS,并比单独接受化疗的患者获得更好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving Outcome of Selected Patients With Non-Resectable Hepatic Metastases From Colorectal Cancer With Liver Transplantation: A Prospective Parallel Trial (COLT trial)

Background

Patients with unresectable Colorectal Liver Metastases (CLM) receiving palliative chemotherapy have a 5-year overall survival (OS) of less than 30%. Liver transplantation (LT) can improve OS up to 60%-83% (SECA-I and SECA-II trials). The aim of the study is to assess the efficacy of LT in liver-only metastatic CRC compared with a matched cohort of patients included in a phase III trial on triplet chemotherapy + antiEGFR.

Patients and Methods

The COLT trial is an investigator-driven, multicenter, non-randomized, open-label, controlled, prospective, parallel trial (ClinicalTrials.gov NCT03803436). Hyperselected patients with liver-limited unresectable CLM, RAS and BRAF wild-type and curatively removed primary colon cancer are included. The observed post-transplant outcomes will be prospectively compared 1:5 with those obtained in a matched cohort from the TRIPLETE trial (NCT03231722).

Results

Primary endpoint is to compare the 3 and 5-years OS of patients enrolled in the COLT trial with COLT-eligible population enrolled in the TRIPLETE trial. An expected gain in OS of 40% at 5-years is predicted for the COLT population (the expected OS at 5-years in COLT vs. TRIPLETE is 70% vs. 30%). Secondary endpoints are to compare the 5-years disease-free survival and to assess the safety of LT (Dindo-Clavien Classification and the Comprehensive Complication Index).

Conclusion

LT offers the longest OS reported in selected patients with CLM. Improving the selection strategies can give patients a 5-year OS similar to other indications for LT and a better outcome than those undergoing chemotherapy alone.

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CiteScore
7.20
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