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Practical use of capecitabine plus oxaliplatin (CAPEOX) with bevacizumab for patients with metastatic colorectal cancer that cannot expect conversion therapy

机译:卡培他滨联合奥沙利铂(CAPEOX)与贝伐单抗在无法期待转化治疗的转移性结直肠癌患者中的实际应用

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Background/Aims: The cytotoxic regimens and bevacizumab (Bev) or anti-EGFR antibody are used for metastatic colorectal cancer (mCRC) that can expect conversion therapy. In this paper, we would present our practical data including the response, survival and toxicity of the capecitabine plus oxaliplatin (CAPEOX) with Bev for mCRC that cannot expect conversion therapy. Methodology: Nineteen patients with mCRC who were treated with CAPEOX with Bev were enrolled. All the patients had the disseminated hepatic, lung, peritoneal metastases or distant lymph node metastasis assessed as no possibility of R0 resection. Results: The median age was 66 (45-85) years old. Target lesion was liver and lung in 9 patients, peritoneum in 5 patients and distant lymph node in 3 patients. CAPEOX with Bev therapy was administered for a median of 8.0 cycles (range, 4-21 cycles). In the 16 evaluable cases, there were no patient with complete response (CR), 9 patients with partial response (PR), 6 with stable disease (SD), and 1 with progressive disease. The objective response rate (CR plus PR) was 56.3%, and disease control rate (CR, PR plus SD) was 93.8%. The median TTP was 9.3 months and the median OS was 21.1 months. No patients treated with surgery even though the good responses were obtained. No severe hematologic adverse toxicities were observed except only one case with grade 3 platelet decrease. Non-hematologic grade 3 events were observed totally 8 patients including 3 for peripheral neuropathy, 2 for bilirubin, and 1 for nausea/vomiting, amylase and stomatitis. Conclusions: We obtained the quite good results of CAPEOX plus Bev as the first-line treatment practically. This regimen might be useful for mCRC that cannot expect conversion therapy.
机译:背景/目的:细胞毒性疗法和贝伐单抗(Bev)或抗EGFR抗体可用于可望接受转化治疗的转移性结直肠癌(mCRC)。在本文中,我们将介绍我们的实际数据,包括卡培他滨联合奥沙利铂(CAPEOX)与Bev联合治疗无法期待转化治疗的mCRC的应答,生存率和毒性。方法:招募了19例接受CAPEOX和Bev治疗的mCRC患者。所有患者均被评估为无R0切除的可能,已扩散为肝,肺,腹膜转移或远处淋巴结转移。结果:中位年龄为66(45-85)岁。目标病灶为肝肺9例,腹膜5例,远处淋巴结3例。 CAPEOX与Bev治疗的中位数为8.0个周期(4-21个周期)。在这16例可评估的病例中,没有患者具有完全缓解(CR),9例具有部分缓解(PR),6例患有稳定疾病(SD)和1例患有进行性疾病。客观缓解率(CR + PR)为56.3%,疾病控制率(CR + PR + SD)为93.8%。 TTP的中位数为9.3个月,OS的中位数为21.1个月。即使获得良好的反应,也没有患者接受手术治疗。除了仅1例3级血小板减少的病例外,未观察到严重的血液学不良反应。共观察到非血液学3级事件8例,其中3例为周围神经病变,2例为胆红素,1例为恶心/呕吐,淀粉酶和口腔炎。结论:我们获得了CAPEOX + Bev作为一线治疗的良好效果。该方案可能对无法进行转化治疗的mCRC有用。

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