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Clinical Trial
. 2025 Mar;30(3):514-523.
doi: 10.1007/s10147-025-02701-9. Epub 2025 Feb 1.

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

Affiliations
Clinical Trial

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

Koji Ando et al. Int J Clin Oncol. 2025 Mar.

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.

Keywords: Aflibercept; Colorectal cancer; FOLFIRI; FOLFOXIRI plus bevacizumab; Irinotecan reduced dose; Metastatic.

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Conflict of interest statement

Declarations. Conflict of interest: KA, MS, HY, YN, TK, KT, KB, HO, KH and SS declare no conflicts of interest. HSatake has received research funding from AsahiKASEI Co. Ltd., Ono Pharmaceutical Co. Ltd., Daiichi Sankyo, Taiho Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd. and Sanofi, honoraria from Bayer Co., Ltd., Bristol-Myers Squibb Co., Ltd., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Eli Lilly Japan Co., Ltd., Merck Bio Pharma Co., Ltd., MSD Co., Ltd., Ono Pharmaceutical Co., Ltd., Sanofi Co., Ltd., Taiho Pharmaceutical Co., Ltd., Takeda Co., Ltd. and Yakult Honsha Co., Ltd. AM received honoraria from Eli Lilly, Japan K.K.; Taiho Pharmaceutical Co., Ltd.; Ono Pharmaceutical Co., Ltd.; Bristol-Myers Squibb Co., Ltd.; and Daiichi Sankyo Co., Ltd. HS received research funding from Taiho Pharmaceutical Co. Ltd. and Chugai Pharmaceutical Co. Ltd.. AT received honoraria for lectures from ELI LILLY JAPAN K.K., TAIHO PHARMACEUTICAL CO., LTD., ONO PHARMACEUTICAL Co., Ltd., CHUGAI PHARMACEUTICAL Co., Ltd., Merck Biopharma Co., Ltd., NOVARTIS PHARMA K.K., TAKEDA PHARMACEUTICAL COMPANY LIMITED, DAIICHI SANKYO CO., LTD, MSD K.K., TSUMURA & Co., AstraZeneca K.K., Sun Pharmaceutical Industries Limited, ASAHI KASEI PHARMA CORPORATION. HB received scholarship grants from Eli Lilly Japan and K.K. EO received research funding from Guardant Health and honoraria for lectures from Ono, Takeda, Bayer, Chugai, Taiho, Eli Lilly, and Bristol Myers Squibb. Ethics statement: Approval of the research protocol by an Institutional Reviewer Board: Before the initiating the study, the principal investigator consulted a Certified Review Board (certification no. CRB718005), received approval from the study site manager, and submitted a trial plan to the Ministry of Health, Labour, and Welfare. Informed consent statement: This study was conducted in accordance with the Good Clinical Practice guidelines and guiding principles detailed in the Declaration of Helsinki and in keeping with the applicable local law(s) and regulations (s). Written informed consent for the study procedures was provided by all candidate patients before enrolment. Registry and the registration No. of the study/trial: This study was registered with the Japan Registry of Clinical Trials (registration number: jRCTs071190003). Animal studies: Not applicable.

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