转移性结直肠癌的动脉内肝化疗:奥沙利铂初始治疗与奥沙利铂预治疗患者的差异

E. El Rawadi , B. Bonnet , L. Pierotti , V. Boige , L. Tselikas , C. Smolenschi , M. Valéry , T. Pudlarz , A. Fuerea , T. De Baere , A. Tarabay , M. Gelli , E. Fernandez-de-Sevilla , D. Malka , A. Hollebecque , M. Ducreux , A. Boilève
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引用次数: 0

摘要

以沙利铂为基础的肝动脉输注(HAI)联合静脉治疗是结直肠癌仅肝转移的一种治疗选择,特别是在姑息性环境中,无论是开始还是在全身化疗失败后。我们的研究旨在评估奥沙利铂初始患者和奥沙利铂预处理患者之间的疗效和耐受性。方法:在2008年至2022年期间,纳入了接受至少一个周期hai -奥沙利铂联合全身治疗的结直肠癌继发肝转移单中心连续患者。结果奥沙利铂初始组包括63例患者(中位年龄58岁),预处理组包括244例患者(中位年龄53岁)。两组患者的特征很好地平衡了。奥沙利铂初始组的所有患者都接受了hai -奥沙利铂治疗,而13%的预处理患者接受了HAI-FOLFIRINOX治疗。中位随访36个月后,奥沙利铂初始组的中位无进展生存期为14个月(11.8-24个月),预处理组的中位无进展生存期为10.1个月(9.4-12.5个月)(P = 0.016)。奥沙利铂初始组的客观缓解率为66.7%,疾病控制率为79.4%,而奥沙利铂初始组为32.4%和77.5% (P <;0.001)。两组间3-4级毒性相当,包括神经病变。未接受奥沙利铂治疗的患者的二次切除/消融率为22.2%,预先治疗的患者为17.6%。结论奥沙利铂在既往全身奥沙利铂治疗后应用肝动脉内输注是可行且有效的;它显示了显著的反应率,而没有增加毒性。它可以提供替代治疗和备用的晚期药物,如瑞非尼和替吡拉西-三氟定,用于进一步的姑息性意图治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intra-arterial hepatic chemotherapy in metastatic colorectal cancer: differences between oxaliplatin-naive versus oxaliplatin-pretreated patients

Background

Oxaliplatin-based hepatic arterial infusions (HAI) combined with intravenous therapy is a therapeutic option for colorectal cancer with liver-only metastasis, notably in the palliative setting, either initially or after failure of systemic chemotherapy. Our study aimed to assess efficacy and tolerance between oxaliplatin-naive patients and oxaliplatin-pretreated patients.

Methods

Between 2008 and 2022, single-center consecutive patients presenting with liver metastasis secondary to colorectal cancer who received at least one cycle of HAI-oxaliplatin combined with systemic therapy were included.

Results

The oxaliplatin-naive arm included 63 patients (median age 58 years) and the pretreated arm included 244 patients (median age 53 years). Patient characteristics were well balanced between the groups. All patients in the oxaliplatin-naive arm received HAI-oxaliplatin while 13% of the pretreated patients received HAI-FOLFIRINOX. After a median follow-up of 36 months, median progression-free survival was 14 months in the oxaliplatin-naive group (range 11.8-24 months) and 10.1 months in the pretreated group (range 9.4-12.5 months) (P = 0.016). The objective response rate was 66.7% and the disease control rate was 79.4% in the oxaliplatin-naive group, versus 32.4% and 77.5% (P < 0.001) in the pretreated group. Grade 3-4 toxicities were comparable between the two groups, including neuropathy. Secondary resection/ablation rate was 22.2% in oxaliplatin-naive patients and 17.6% in pretreated patients.

Conclusion

Oxaliplatin use as an intra-arterial hepatic infusion is feasible and efficient after previous systemic oxaliplatin; it showed significant response rates without increased toxicities. It can provide alternative treatments and spare late-setting drugs such as regorafenib and tipiracil–trifluridine for a further palliative intent treatment.
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