Regorafenib plus FOLFIRINOX as first-line treatment for patients with RAS-mutant metastatic colorectal cancer (FOLFIRINOX-R trial): a dose-escalation study.

IF 2.7 4区 医学 Q3 ONCOLOGY Cancer Chemotherapy and Pharmacology Pub Date : 2024-09-01 Epub Date: 2024-07-10 DOI:10.1007/s00280-024-04682-4
Antoine Adenis, François Ghiringhelli, Ludovic Gauthier, Thibault Mazard, Ludovic Evesque, Alexandre Evrard, Patrick Chalbos, Aurore Moussion, Sophie Gourgou, Marc Ychou
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Abstract

Purpose: The combination of bevacizumab and FOLFIRINOX is used in patients with RAS-mutant metastatic colorectal cancer (RASm-mCRC). Regorafenib, an oral multi-tyrosine kinase inhibitor, has antiangiogenic properties, cytostatic effects and also true cytotoxic effects, unlike bevacizumab. The aim of this study was to determine the maximum tolerated dose (MTD) and the recommended phase 2 dose (RP2D) of the regorafenib-FOLFIRINOX combination in patients with RASm-mCRC.

Methods: The FOLFIRINOX-R trial was a phase 1/2 study where the dose-escalation part (3 + 3 design with three dose levels, DLs) was completed before its early termination. FOLFIRINOX (14-day cycle) included oxaliplatin (standard dose), folinic acid, fluorouracil and irinotecan (150 or 180 mg/m²). Regorafenib (120 or 160 mg daily) was given from day 4 to day 10 of each cycle. Dose-limiting toxicity (DLT) was studied in the first three cycles. Eligibility criteria included ECOG performance status ≤ 1 and not previously treated RASm-mCRC.

Results: Thirteen patients (median age: 65 years; min-max: 40-76) were enrolled. DLT could not be evaluated in one patient (DL3) due to poor observance. The median treatment duration and median follow-up were 6.2 (min-max: 2.3-10) and 13.4 (min-max: 3.8-18.0) months, respectively. Dose was modified in 12/13 (92%) patients. One grade 3 hypokalemia occurred at DL2. MTD was not reached at DL3. Grade 3 diarrhea was recorded in 7/13 patients (13 events) equally distributed in all DLs.

Conclusion: The RP2D for this regorafenib-FFX combination could not be determined due to a high prevalence of grade 3 diarrhea related to treatment as advised by our Independent Data Monitoring Committee.

Trial registration numbers: ClinicalTrials.gov : NCT03828799.

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瑞戈非尼加 FOLFIRINOX 作为 RAS 突变转移性结直肠癌患者的一线治疗(FOLFIRINOX-R 试验):一项剂量递增研究。
目的:贝伐珠单抗和 FOLFIRINOX 联合疗法适用于 RAS 突变转移性结直肠癌(RASm-mCRC)患者。瑞戈非尼是一种口服多酪氨酸激酶抑制剂,与贝伐珠单抗不同,它具有抗血管生成特性、细胞抑制作用和真正的细胞毒性作用。本研究旨在确定瑞戈非尼-FOLFIRINOX联合疗法在RASm-mCRC患者中的最大耐受剂量(MTD)和二期推荐剂量(RP2D):FOLFIRINOX-R试验是一项1/2期研究,其剂量递增部分(3+3设计,三个剂量水平,DLs)在提前终止前已经完成。FOLFIRINOX(14天周期)包括奥沙利铂(标准剂量)、亚叶酸、氟尿嘧啶和伊立替康(150或180毫克/平方米)。瑞戈非尼(每天120或160毫克)在每个周期的第4天至第10天服用。前三个周期研究剂量限制性毒性(DLT)。入选标准包括ECOG表现状态≤1和既往未接受过RASm-mCRC治疗:13名患者(中位年龄:65岁;最小-最大年龄:40-76岁)入组。一名患者(DL3)的DLT因观察不佳而无法评估。中位治疗时间和中位随访时间分别为 6.2 个月(最短:2.3-10 个月)和 13.4 个月(最短:3.8-18.0 个月)。12/13(92%)名患者的剂量有所调整。DL2时出现了1例3级低钾血症。DL3 时未达到 MTD。7/13例患者出现3级腹泻(13例),平均分布于所有DLs:结论:根据独立数据监控委员会的建议,由于与治疗相关的3级腹泻发生率较高,因此无法确定瑞戈非尼-FFX联合疗法的RP2D:ClinicalTrials.gov : NCT03828799。
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来源期刊
CiteScore
6.10
自引率
3.30%
发文量
116
审稿时长
2.5 months
期刊介绍: Addressing a wide range of pharmacologic and oncologic concerns on both experimental and clinical levels, Cancer Chemotherapy and Pharmacology is an eminent journal in the field. The primary focus in this rapid publication medium is on new anticancer agents, their experimental screening, preclinical toxicology and pharmacology, single and combined drug administration modalities, and clinical phase I, II and III trials. It is essential reading for pharmacologists and oncologists giving results recorded in the following areas: clinical toxicology, pharmacokinetics, pharmacodynamics, drug interactions, and indications for chemotherapy in cancer treatment strategy.
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