重新定义在难治性转移性结直肠癌中使用瑞非尼和曲氟定/替吡拉西而不使用贝伐单抗:来自ReTrITA研究的发现

IF 4.5 2区 医学 Q1 ONCOLOGY
Cancers Pub Date : 2025-06-18 DOI:10.3390/cancers17122037
Carlo Signorelli, Maria Alessandra Calegari, Annunziato Anghelone, Alessandro Passardi, Chiara Gallio, Alessandro Bittoni, Jessica Lucchetti, Lorenzo Angotti, Emanuela Di Giacomo, Ina Valeria Zurlo, Cristina Morelli, Emanuela Dell'Aquila, Adele Artemi, Donatello Gemma, Alessandra Emiliani, Marta Ribelli, Domenico Cristiano Corsi, Giulia Arrivi, Federica Mazzuca, Federica Zoratto, Mario Giovanni Chilelli, Marta Schirripa, Francesco Schietroma, Maria Grazia Morandi, Fiorenza Santamaria, Manuela Dettori, Antonella Cosimati, Rosa Saltarelli, Alessandro Minelli, Emanuela Lucci-Cordisco, Michele Basso
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引用次数: 0

摘要

背景:瑞非尼(R)和trifluridine/tipiracil (T)被批准用于治疗难治性转移性结直肠癌(mCRC)。然而,这些药物的最佳排序是未知的。ReTrITA研究计划在意大利多中心人群中评估R和T的实际疗效,无论是顺序治疗还是单药治疗。方法:这项回顾性观察性分析包括2012年至2023年间在意大利17个癌症中心接受治疗的1156例mCRC患者。患者分为四组:顺序T/R (n = 261)、顺序R/T (n = 155)、R单药治疗(n = 313)和T单药治疗(n = 427)。主要目标是总生存期(OS)和无进展生存期(PFS),次要目标是疾病控制率、客观缓解率和治疗相关毒性。结果:单药治疗组OS无显著差异(R: 5.0个月;T: 5.9个月;p = 0.8371)或PFS (R: 3.2个月;T: 3.3个月;P = 0.6531)。与T/R相比,顺序R/T组有明显更好的结果:中位OS为16.6个月vs 12.6个月(HR = 0.67;p = 0.0004),中位PFS分别为11.5个月和8.5个月(HR = 0.60;P < 0.0001)。R/T的生存优势在临床亚组中是一致的。毒性谱与已知的安全性数据相当,在R/T序列中报告的中性粒细胞减少率较低。结论:ReTrITA证实了R和T作为单一疗法的有效性,并提供了令人信服的真实证据,表明R/T序列可提高难治性mCRC的生存率。这些发现支持在符合条件的患者中采用regorafenib优先的方法,并且它们强调了未来需要研究联合策略和与fruquininib等新药的比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Redefining the Use of Regorafenib and Trifluridine/Tipiracil Without Bevacizumab in Refractory Metastatic Colorectal Cancer: Findings from the ReTrITA Study.

Background: Regorafenib (R) and trifluridine/tipiracil (T) are approved treatments for metastatic colorectal cancer (mCRC) in refractory cases. However, the optimal sequencing of these agents is unknown. The ReTrITA study planned to assess the real-world efficacy of R and T, administered either sequentially or as monotherapy, in a large Italian multicentre population. Methods: This retrospective observational analysis comprised 1156 mCRC patients treated between 2012 and 2023 at 17 Italian cancer centres. Patients were divided into four groups: sequential T/R (n = 261), sequential R/T (n = 155), R monotherapy (n = 313), and T monotherapy (n = 427). The primary objectives were overall survival (OS) and progression-free survival (PFS), with secondary goals being disease control rate, objective response rate, and treatment-related toxicity. Results: The monotherapy cohorts showed no significant difference in OS (R: 5.0 months; T: 5.9 months; p = 0.8371) or PFS (R: 3.2 months; T: 3.3 months; p = 0.6531). Compared to T/R, the sequential R/T group had significantly better outcomes: median OS was 16.6 vs. 12.6 months (HR = 0.67; p = 0.0004), and median PFS was 11.5 vs. 8.5 months (HR = 0.60; p < 0.0001). The survival advantage of R/T was consistent across clinical subgroups. The toxicity profiles were comparable with known safety data, with a lower prevalence of neutropenia reported in the R/T sequence. Conclusions: ReTrITA confirms the efficacy of R and T as monotherapies and provides compelling real-world evidence that the R/T sequence improves survival in refractory mCRC. These findings support a regorafenib-first approach in patients who are eligible, and they emphasise the need for future research into combination strategies and comparisons with newer drugs such as fruquintinib.

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来源期刊
Cancers
Cancers Medicine-Oncology
CiteScore
8.00
自引率
9.60%
发文量
5371
审稿时长
18.07 days
期刊介绍: Cancers (ISSN 2072-6694) is an international, peer-reviewed open access journal on oncology. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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