Real-world outcomes of FOLFOXIRI plus bevacizumab in patients with metastatic colorectal cancer: the JSCCR-TRIPON study.

IF 2.4 3区 医学 Q3 ONCOLOGY International Journal of Clinical Oncology Pub Date : 2024-12-01 Epub Date: 2024-08-28 DOI:10.1007/s10147-024-02613-0
Yoshiyuki Yamamoto, Hiroki Yukami, Tatsuro Yamaguchi, Hisatsugu Ohori, Sachiko Nagasu, Yoshinori Kagawa, Naotoshi Sugimoto, Hiromichi Sonoda, Kentaro Yamazaki, Atsuo Takashima, Hiroyuki Okuyama, Hiroko Hasegawa, Chihiro Kondo, Eishi Baba, Toshihiko Matsumoto, Yasuyuki Kawamoto, Masato Kataoka, Yoshiaki Shindo, Toshiaki Ishikawa, Taito Esaki, Yosuke Kito, Takeo Sato, Taro Funakoshi, Toshifumi Yamaguchi, Yasuhiro Shimada, Toshikazu Moriwaki
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Abstract

Background: FOLFOXIRI plus bevacizumab is a standard first-line chemotherapy for patients with metastatic colorectal cancer (mCRC). However, due to the severe toxicities, this regimen is not widely used. There is limited data on the real-world efficacy and safety.

Methods: We conducted a retrospective analysis of clinical data from mCRC patients who received FOLFOXIRI plus bevacizumab as first-line chemotherapy at 31 institutions. The initial dose was standardized according to the TRIBE regimen. Induction therapy was defined as a combination of oxaliplatin, irinotecan, and fluorouracil.

Results: Out of 104 patients who met the criteria, the median age was 58 years (range, 16-72). 81% of patients had an eastern cooperative oncology group performance status (PS) of 0. An initial dose reduction was observed in 63% of patients. The median number of preplanned induction therapy cycles was 12 (range, 4-12). The completion of scheduled induction therapy cycles was observed in 45% of patients, with treatment-related toxicities being the main reason for discontinuation (63%). The median progression-free survival and overall survival were 12.8 months (95% CI, 10.6-15.0) and 27.9 months (95% CI 21.6-34.2), respectively. The objective response rate and disease control rate were 63.7% and 98.9%, respectively. The R0 resection rate was 21.2%. The main grade 3 or higher toxicities were neutropenia (51%), febrile neutropenia (10%), and nausea/vomiting (5%). No treatment-related deaths were observed.

Conclusion: In a real-world clinical setting, FOLFOXIRI plus bevacizumab demonstrated efficacy and safety comparable to previous clinical trials.

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FOLFOXIRI 加贝伐单抗治疗转移性结直肠癌患者的实际效果:JSCCR-TRIPON 研究。
背景FOLFOXIRI 加贝伐单抗是转移性结直肠癌(mCRC)患者的标准一线化疗方案。然而,由于毒性严重,该方案并未得到广泛应用。有关其实际疗效和安全性的数据十分有限:我们对 31 家机构接受 FOLFOXIRI 加贝伐单抗一线化疗的 mCRC 患者的临床数据进行了回顾性分析。初始剂量根据 TRIBE 方案进行了标准化。诱导治疗被定义为奥沙利铂、伊立替康和氟尿嘧啶的联合治疗:在104名符合标准的患者中,中位年龄为58岁(16-72岁)。81%的患者在东部肿瘤合作组的表现状态(PS)为0。预计划诱导治疗周期的中位数为12个(范围为4-12个)。45%的患者完成了计划中的诱导治疗周期,治疗相关毒性反应是患者终止治疗的主要原因(63%)。无进展生存期和总生存期的中位数分别为12.8个月(95% CI,10.6-15.0)和27.9个月(95% CI,21.6-34.2)。客观反应率和疾病控制率分别为63.7%和98.9%。R0切除率为21.2%。3级或以上毒性反应主要是中性粒细胞减少(51%)、发热性中性粒细胞减少(10%)和恶心/呕吐(5%)。未发现与治疗相关的死亡病例:结论:在真实世界的临床环境中,FOLFOXIRI联合贝伐珠单抗的疗效和安全性与之前的临床试验相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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