A phase two trial evaluating FOLFIRI plus aflibercept after failure of FOLFOXIRI plus bevacizumab in patients with unresectable metastatic colorectal cancer.

IF 2.4 3区 医学 Q3 ONCOLOGY
Koji Ando, Hironaga Satake, Mototsugu Shimokawa, Hisateru Yasui, Yuji Negoro, Tatsuya Kinjo, Junya Kizaki, Kenji Baba, Hiroyuki Orita, Keiji Hirata, Sanae Sakamoto, Akitaka Makiyama, Hiroshi Saeki, Akihito Tsuji, Hideo Baba, Eiji Oki
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引用次数: 0

Abstract

Background: FOLFOXIRI plus bevacizumab (BEV) is an option for first-line treatment of metastatic colorectal cancer (mCRC). However, there is no consensus on the optimal treatment strategy when disease progresses. The EFFORT open-label, multicenter, single-arm phase II study investigated whether FOLFIRI plus aflibercept retains activity after progression of FOLFOXIRI plus BEV treatment.

Methods: The patients with unresectable mCRC who failed first-line FOLFOXIRI plus BEV received FOLFIRI plus aflibercept. The primary endpoint was progression-free survival (PFS) in the full analysis set (FAS). Angiogenic biomarkers were measured before treatment initiation.

Results: From April 2019 to May 2021, 35 patients were enrolled and 34 were analysed in the FAS population (men, 18; median age, 63 years [range: 32-78]). The primary tumor was left-sided in most cases (23/34), 23 patients were RAS mutant, 3 patients had BRAF V600E mutation and 27 patients had liver metastases. The primary end-point was met with a median PFS of 4.3 months [80% confidence interval [CI] 3.7-5.1]. Median overall survival was 15.2 months [95% CI 8.9-22.7]. Per RECIST, there were 1 complete response, 4 partial responses, 21 stable diseases and 8 disease progressions. Overall response rate was 14.7% [95% CI 5.0-31.1], and disease control rate was 76.5% [95% CI 58.8-89.3]. Responses were more common in patients with high VEGF-C, low VEGF-D and low PlGF levels before treatment.

Conclusion: FOLFIRI plus aflibercept, administered after failure of FOLFOXIRI plus BEV, is effective and has a manageable safety profile. This regimen may be a useful second-line treatment option for these patients.

一项ii期试验评估FOLFIRI +阿非利赛在FOLFOXIRI +贝伐单抗治疗不可切除转移性结直肠癌患者失败后的疗效。
背景:FOLFOXIRI联合贝伐单抗(BEV)是转移性结直肠癌(mCRC)一线治疗的一种选择。然而,对于疾病进展时的最佳治疗策略尚无共识。这项开放标签、多中心、单臂II期研究调查了FOLFIRI + afliberept在FOLFOXIRI + BEV治疗进展后是否保持活性。方法:无法切除的mCRC患者在一线FOLFOXIRI + BEV治疗失败后,接受FOLFOXIRI + afliberept治疗。主要终点是全分析集(FAS)的无进展生存期(PFS)。在治疗开始前测量血管生成生物标志物。结果:2019年4月至2021年5月,纳入35例患者,分析34例FAS人群(男性18例;中位年龄63岁[范围:32-78])。原发肿瘤以左侧肿瘤居多(23/34),RAS突变23例,BRAF V600E突变3例,肝转移27例。主要终点的中位PFS达到了4.3个月[80%置信区间[CI] 3.7-5.1]。中位总生存期为15.2个月[95% CI 8.9-22.7]。根据RECIST, 1例完全缓解,4例部分缓解,21例病情稳定,8例病情进展。总有效率为14.7% [95% CI 5.0-31.1],疾病控制率为76.5% [95% CI 58.8-89.3]。治疗前高VEGF-C、低VEGF-D和低PlGF水平的患者更常见。结论:FOLFIRI + afliberept在FOLFOXIRI + BEV治疗失败后给予,是有效的,并且具有可控的安全性。该方案可能是这些患者的一种有用的二线治疗选择。
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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