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贝伐珠单抗、伊立替康、亚叶酸和氟尿嘧啶静脉推注(BIFF 方案)每两周 1 次治疗转移性结直肠癌的疗效和耐受性:意大利南部肿瘤协作组的经验。

Efficacy and tolerability of biweekly bevacizumab, irinotecan, folinic acid and fluorouracil intravenous bolus (BIFF Regimen) in patients with metastatic colorectal cancer: the southern Italy cooperative oncology group experience.

机构信息

National Cancer Institute, Naples, Italy.

出版信息

Clin Colorectal Cancer. 2011 Mar 1;10(1):42-7. doi: 10.3816/CCC.2011.n.006.

Abstract

BACKGROUND

We have extensively assessed a biweekly regimen of irinotecan plus folinic acid and fluorouracil bolus (IRIFAFU) in metastatic colorectal cancer (MCRC). Here, we report on the safety and activity of BIFF (bevacizumab plus IRIFAFU) regimen in 94 mCRC patients.

PATIENTS AND METHODS

Bevacizumab 5 mg/kg (1 hour), and irinotecan 180 mg/m(2) (1 hour) were given intravenously on day 1, 6S-folinic acid 250 mg/m(2) (2 hours), and fluorouracil 850 mg/m(2) (bolus) were given intravenously on day 2 every 2 weeks for a median of 9 cycles per patient (range, 1-12), and maintenance bevacizumab alone was delivered in 16 cases.

RESULTS

Grade ≥ 3 hematologic toxicities were neutropenia (50%) and febrile neutropenia (5%). Most common grade 3 nonhematologic side effects were diarrhea (20%), vomiting (7%), nausea (4%), and stomatitis (4%). Severe hypertension (1%) and epistaxis (1%) rarely occurred. Six complete responses and 44 partial responses were registered, giving a response rate of 53% (95% CI, 43%-64%). Median progression-free survival was 11.5 months (95% CI, 9.0-14.0 months). Forty-three (46%) patients eventually died, and the median overall survival was 24.0 months (95% CI, 20.2-27.8 months).

CONCLUSION

Bevacizumab appeared to increase the activity of the IRIFAFU regimen without worsening its tolerability. Efficacy of BIFF was comparable with that reported with other bevacizumab plus irinotecan-based combinations.

摘要

背景

我们已广泛评估了转移性结直肠癌(MCRC)中两周一次的伊立替康加亚叶酸和氟尿嘧啶推注(IRIFAFU)方案。在此,我们报告了 94 例 MCRC 患者中 BIFF(贝伐单抗加 IRIFAFU)方案的安全性和疗效。

患者和方法

贝伐单抗 5mg/kg(1 小时),伊立替康 180mg/m²(1 小时)于第 1 天静脉给药,6S-亚叶酸 250mg/m²(2 小时),氟尿嘧啶 850mg/m²(推注)于第 2 天静脉给药,每 2 周为 1 个周期,每位患者的中位数为 9 个周期(范围为 1-12 个周期),16 例患者接受贝伐单抗维持治疗。

结果

≥3 级血液学毒性为中性粒细胞减少症(50%)和发热性中性粒细胞减少症(5%)。最常见的 3 级非血液学不良反应为腹泻(20%)、呕吐(7%)、恶心(4%)和口腔炎(4%)。严重高血压(1%)和鼻出血(1%)很少发生。共登记了 6 例完全缓解和 44 例部分缓解,缓解率为 53%(95%CI,43%-64%)。中位无进展生存期为 11.5 个月(95%CI,9.0-14.0 个月)。43 例(46%)患者最终死亡,中位总生存期为 24.0 个月(95%CI,20.2-27.8 个月)。

结论

贝伐单抗似乎增加了 IRIFAFU 方案的活性,而不增加其耐受性。BIFF 的疗效与其他贝伐单抗联合伊立替康的方案相当。

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