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一线抗表皮生长因子受体(EGFR)双药方案治疗左侧及野生型转移性结直肠癌患者的诱导后管理:一项多中心研究

Post-Induction Management in Patients With Left-Sided and Wild-Type Metastatic Colorectal Cancer Treated With First-Line Anti-EGFR-Based Doublet Regimens: A Multicentre Study.

作者信息

Parisi Alessandro, Cortellini Alessio, Venditti Olga, Filippi Roberto, Salvatore Lisa, Tortora Giampaolo, Ghidini Michele, Nigro Olga, Gelsomino Fabio, Zurlo Ina Valeria, Fulgenzi Claudia, Lombardi Pasquale, Roselló Keränen Susana, Depetris Ilaria, Giampieri Riccardo, Morelli Cristina, Di Marino Pietro, Di Pietro Francesca Romana, Zanaletti Nicoletta, Vitale Pasquale, Garajova Ingrid, Spinelli Gian Paolo, Zoratto Federica, Roberto Michela, Petrillo Angelica, Aimar Giacomo, Patruno Leonardo, D'Orazio Carla, Ficorella Corrado, Ferri Claudio, Porzio Giampiero

机构信息

Medical Oncology, St. Salvatore Hospital, L'Aquila, Italy.

Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.

出版信息

Front Oncol. 2021 Oct 27;11:712053. doi: 10.3389/fonc.2021.712053. eCollection 2021.

Abstract

BACKGROUND

Few data regarding post-induction management following first-line anti-epidermal growth factor receptor (EGFR)-based doublet regimens in patients with left-sided wild-type metastatic colorectal cancer (mCRC) are available.

METHODS

This multicenter, retrospective study aimed at evaluating clinicians' attitude, and the safety and effectiveness of post-induction strategies in consecutive patients affected by left-sided wild-type mCRC treated with doublet chemotherapy plus anti-EGFR as first-line regimen, who did not experience disease progression within 6 months from induction initiation, at 21 Italian and 1 Spanish Institutions. The measured clinical outcomes were: progression-free survival (PFS), overall survival (OS), adverse events, and objective response rate (ORR).

RESULTS

At the data cutoff, among 686 consecutive patients with left-sided wild-type mCRC treated with doublet plus anti-EGFR as first-line regimen from March 2012 to October 2020, 355 eligible patients have been included in the present analysis. Among these, 118 (33.2%), 66 (18.6%), and 11 (3.1%) received a maintenance with 5-fluorouracil/leucovorin (5FU/LV)+anti-EGFR, anti-EGFR, and 5FU/LV, respectively, while 160 (45.1%) patients continued induction treatment (non-maintenance) until disease progression, unacceptable toxicity, patient decision, or completion of planned treatment. The median period of follow-up for the overall population was 33.7 months (95%CI = 28.9-35.6). The median PFS values of the 5FU/LV+anti-EGFR, anti-EGFR, 5FU/LV, and non-maintenance cohorts were 16.0 (95%CI = 14.3-17.7, 86 events), 13.0 (95%CI = 11.4-14.5, 56 events), 14.0 (95%CI = 8.1-20.0, 8 events), and 10.1 months (95%CI = 9.0-11.2, 136 events), respectively ( < 0.001). The median OS values were 39.6 (95%CI = 31.5-47.7, 43 events), 36.1 (95%CI = 31.6-40.7, 36 events), 39.5 (95%CI = 28.2-50.8, 4 events), and 25.1 months (95%CI = 22.6-27.6, 99 events), respectively ( < 0.001). After adjusting for key covariates, a statistically significant improvement in PFS in favor of 5FU/LV+anti-EGFR (HR = 0.59, 95%CI = 0.44-0.77, < 0.001) and anti-EGFR (HR = 0.71, 95%CI = 0.51-0.98, = 0.039) compared to the non-maintenance cohort was found. Compared to the non-maintenance cohort, OS was improved by 5FU/LV+anti-EGFR (HR = 0.55, 95%CI = 0.38-0.81, = 0.002) and, with marginal significance, by anti-EGFR (HR = 0.67, 95%CI = 0.51-0.98, = 0.051). No difference was found in ORR. Any grade non-hematological and hematological events were generally higher in the non-maintenance compared to the maintenance cohorts.

CONCLUSION

Among the treatment strategies following an anti-EGFR-based doublet first-line induction regimen in patients affected by left-sided wild-type mCRC treated in a "real-life" setting, 5FU/LV+anti-EGFR resulted the most adopted, effective, and relatively safe regimen.

摘要

背景

关于左侧野生型转移性结直肠癌(mCRC)患者一线基于抗表皮生长因子受体(EGFR)的双联方案诱导治疗后的管理数据较少。

方法

这项多中心回顾性研究旨在评估21家意大利机构和1家西班牙机构中,接受双联化疗加抗EGFR作为一线方案治疗且诱导开始后6个月内未出现疾病进展的左侧野生型mCRC连续患者中,临床医生的态度以及诱导后策略的安全性和有效性。测量的临床结局包括:无进展生存期(PFS)、总生存期(OS)、不良事件和客观缓解率(ORR)。

结果

在数据截止时,在2012年3月至2020年10月期间接受双联加抗EGFR作为一线方案治疗的686例连续左侧野生型mCRC患者中,355例符合条件的患者纳入本分析。其中,分别有118例(33.2%)、66例(18.6%)和11例(3.1%)接受了5-氟尿嘧啶/亚叶酸钙(5FU/LV)+抗EGFR、抗EGFR和5FU/LV维持治疗,而160例(45.1%)患者继续诱导治疗(非维持治疗)直至疾病进展、出现不可接受的毒性、患者决定或完成计划治疗。总体人群的中位随访期为33.7个月(95%CI = 28.9 - 35.6)。5FU/LV+抗EGFR、抗EGFR、5FU/LV和非维持治疗组的中位PFS值分别为16.0个月(95%CI = 14.3 - 17.7,86例事件)、13.0个月(95%CI = 11.4 - 14.5,56例事件)、14.0个月(95%CI = 8.1 - 20.0,8例事件)和10.1个月(95%CI = 9.0 - 11.2,136例事件)(P < < 0.001)。中位OS值分别为39.6个月(95%CI = 31.5 - 47.7,43例事件)、36.1个月(95%CI = 31.6 - 40.7,36例事件)、39.5个月(95%CI = 28.2 - 50.8,4例事件)和25.1个月(95%CI = 22.6 - 27.6,99例事件)(P < < 0.001)。在调整关键协变量后,发现与非维持治疗组相比,5FU/LV+抗EGFR(HR = 0.59,95%CI = 0.44 - 0.77,P < < 0.001)和抗EGFR(HR = 0.71,95%CI = 0.51 - 0.98,P = 0.039)的PFS有统计学显著改善。与非维持治疗组相比,5FU/LV+抗EGFR使OS得到改善(HR = 0.55,95%CI = 0.38 - 0.81,P = 0.002),抗EGFR使OS有边缘显著性改善(HR = 0.67,95%CI = 0.51 - 0.98,P = 0.051)。ORR未发现差异。与维持治疗组相比,非维持治疗组的任何级别非血液学和血液学事件总体上更高。

结论

在“现实生活”环境中接受基于抗EGFR的双联一线诱导方案治疗的左侧野生型mCRC患者的治疗策略中,5FU/LV+抗EGFR是采用最多、最有效且相对安全的方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a65e/8579084/af01d42992e5/fonc-11-712053-g001.jpg

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