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Regorafenib with a fluoropyrimidine for metastatic colorectal cancer after progression on multiple 5-FU-containing combination therapies and regorafenib monotherapy

机译:雷戈非尼联合氟嘧啶用于转移性结直肠癌的多种含5-FU联合疗法和雷戈非尼单药治疗后进展

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摘要

We present 2 patients with metastatic colorectal cancer who had progressed despite treatment with first-line FOLFOX and second-line FOLFIRI combination chemotherapy regimens. After failing these fluoropyrimidine-based regimens, both patients received additional cytotoxic and targeted therapies with eventual disease progression. These therapies included capecitabine plus dabrafenib and trametinib, regorafenib monotherapy, and regorafenib with panitumumab. After exhausting available options, both patients were offered regorafenib with either 5-fluorouracil (5-FU) or capecitabine. These therapies are individually approved for the treatment of colorectal cancer but have not yet been studied in combination. This regimen produced stable disease in both patients with acceptable toxicity. One patient continued therapy for 17 months. Although these patients previously progressed during treatment with regorafenib, capecitabine or 5-FU, the combination had some activity in both cases of refractory metastatic colorectal cancer and may be considered in the palliative setting. In bedside-to-bench cell culture experiments performed after the clinical observations, we observed sensitivity of human colorectal cancer cell lines (N = 4) to single agent regorafenib or 5-FU and evidence of synergy with the combination therapy. Synergistic effects were noted in colorectal cancer cells with KRAS mutation, BRAF mutation, and p53 mutation, as well as mismatch repair deficient cells. Regorafenib suppressed Mcl-1 and Bcl-XL in treated cancer cells that may have contributed to the anticancer efficacy including in combination with 5-FU. The safety and efficacy of regorafenib with 5-FU or capecitabine in combination should be further investigated as a therapy for patients with refractory metastatic colorectal cancer, including individuals who had progressed on regorafenib monotherapy.
机译:我们目前有2例转移性结直肠癌患者,尽管他们采用一线FOLFOX和二线FOLFIRI联合化疗方案进行了治疗。这些基于氟嘧啶的治疗方案失败后,两名患者均接受了额外的细胞毒性和靶向治疗,最终导致疾病进展。这些疗法包括卡培他滨加达拉非尼和曲美替尼,雷戈非尼单药治疗和雷戈非尼联合帕尼单抗。在用尽所有可用药物后,均向两名患者提供了雷戈非尼,5-氟尿嘧啶(5-FU)或卡培他滨。这些疗法已被单独批准用于治疗大肠癌,但尚未进行联合研究。该方案在两名患者中均产生了稳定的疾病,并具有可接受的毒性。一名患者继续治疗17个月。尽管这些患者先前在接受雷戈非尼,卡培他滨或5-FU治疗期间进展,但该联合用药在两种难治性转移性结直肠癌病例中均具有一定的活性,可考虑用于姑息治疗。在临床观察后进行的从床到床的细胞培养实验中,我们观察到人大肠癌细胞系(N = 4)对单药雷戈非尼或5-FU的敏感性以及联合疗法协同作用的证据。在具有KRAS突变,BRAF突变和p53突变的大肠癌细胞以及错配修复缺陷细胞中发现了协同效应。 Regorafenib在治疗的癌细胞中抑制了Mcl-1和Bcl-XL的作用,包括与5-FU联合使用,可能有助于抗癌功效。应将雷戈非尼与5-FU或卡培他滨联合使用的安全性和有效性,作为难治性转移性结直肠癌患者(包括雷戈非尼单一疗法进展的患者)的治疗方法。

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