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Scheduled prospective tri-weekly modified FOLFOX6 maintenance chemotherapy in the treatment of metastatic colorectal cancer

机译:定期前瞻性三周改良FOLFOX6维持化疗治疗转移性结直肠癌

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Background/Aims: Oxaliplatin, which is effective for colorectal cancer (CRC) in combination with 5-fluorouracil (5-FU) and leucovorin (LV), is widely used for metastatic CRC. With the increasing use of oxaliplatin, however, serious adverse events have been experienced, including hematologic and neurologic toxicities. The aim of this study was to evaluate whether tri-weekly modified FOLFOX6 (mFOLFOX6) maintenance chemotherapy is associated with a low incidence of severe hematologic and neurologic toxicities in the treatment of patients with metastatic CRC. Methodology: We developed a new treatment regimen with mFOLFOX6 biweekly for 8-10 consecutive cycles (induction phase) followed by a 3-week rest period, after which treatment was resumed with cycles of tri-weekly mFOLFOX6 at standard doses (maintenance phase). Validity and complications were investigated retrospectively. Results: Twenty-nine patients were enrolled in this study. The median progression-free survival (PFS) and overall survival (OS) times were 9.4 months and 23 months, respectively. All patients had peripheral neuropathy during treatment, but grade 3 neurotoxicity was observed in only 2 patients (6.9%). Conclusions: mFOLFOX6 maintenance chemotherapy was associated with a very low incidence of grade 3 hematologic and neurologic toxicities. The toxicities associated with PFS and OS were comparable to those reported in the treatment of patients with metastatic CRC. A tri-weekly mFOLFOX maintenance strategy of alternative treatment with a less-toxic regimen may reduce toxicity and maintain efficacy.
机译:背景/目的:奥沙利铂与5-氟尿嘧啶(5-FU)和亚叶酸(LV)联合使用可有效治疗结直肠癌(CRC),广泛用于转移性CRC。然而,随着奥沙利铂使用的增加,已经出现了严重的不良事件,包括血液和神经毒性。这项研究的目的是评估三周改良的FOLFOX6(mFOLFOX6)维持化疗与转移性CRC患者治疗中严重血液学和神经系统毒性的低发生率是否相关。方法:我们开发了一种新的治疗方案,每两周一次使用mFOLFOX6,连续8-10个周期(诱导期),然后休息3周,此后以标准剂量的三周一次mFOLFOX6的周期(维持期)恢复治疗。有效性和并发症进行了回顾性研究。结果:29名患者参加了这项研究。中位无进展生存期(PFS)和总体生存期(OS)时间分别为9.4个月和23个月。所有患者在治疗期间均患有周围神经病,但仅2例(6.9%)观察到3级神经毒性。结论:mFOLFOX6维持化疗与3级血液学和神经系统毒性的发生率极低相关。与PFS和OS相关的毒性与治疗转移性CRC患者的毒性相当。为期三周的mFOLFOX维持策略,采用低毒方案替代治疗,可以降低毒性并维持疗效。

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