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贝伐珠单抗联合伊立替康为基础的治疗方案在既往奥沙利铂为基础方案治疗后的转移性结直肠癌患者中的应用。

Bevacizumab plus irinotecan-based therapy in metastatic colorectal cancer patients previously treated with oxaliplatin-based regimens.

机构信息

Department of Medical Oncology, Gazi University Faculty of Medicine, Ankara, Turkey.

出版信息

Cancer Invest. 2010 Jan;28(1):33-7. doi: 10.3109/07357900802562996.

Abstract

BACKGROUND

Treatment of patients with metastatic colorectal cancer (MCRC) previously exposed to oxaliplatin-based regimen is challenging. Efficacy and toxicity of bevacizumab plus irinotecan-based regimens were assessed in the second-line treatment of MCRC patients.

PATIENTS AND METHODS

Forty patients with a median age of 53 years (range, 31-75) were retrospectively evaluated. Patients progressing or relapsing after treatment with oxaliplatin-based regimens were given bevacizumab 5 mg/kg every 2 weeks in combination with irinotecan-based regimens. All patients had previously received oxaliplatin either in the adjuvant setting (n = 8) or for metastatic disease (n = 32).

RESULTS

Three patients achieved a complete response (7.5%), 5 partial responses (12.5%) and 14 (35%) stable disease resulting in an overall response rate of 20%. Median progression-free survival was 6 months (95% CI, 4.0-8.0) with a median overall survival of 14 months (95% CI, 10.2-17.8). One-year survival rate was 55.9%. Grade 3-4 toxicities were as follows: neutropenia (n = 15, 37.5%), febrile neutropenia (n = 2, 5%), diarrhea (n = 11, 27.5%), nausea and vomiting (n = 3, 7.5%), gastrointestinal perforation (n = 2, 5%), and thromboembolism (n = 2, 5%).

CONCLUSION

Bevacizumab plus irinotecan-based combination chemotherapy is an active and safe treatment option in patients failing oxaliplatin-based therapy.

摘要

背景

治疗既往接受过奥沙利铂为基础方案治疗的转移性结直肠癌(MCRC)患者具有挑战性。本研究评估了贝伐珠单抗联合伊立替康为基础方案在 MCRC 二线治疗中的疗效和毒性。

方法

回顾性分析 40 例中位年龄为 53 岁(范围 31-75 岁)的患者。接受奥沙利铂为基础方案治疗后进展或复发的患者接受贝伐珠单抗 5mg/kg 每 2 周联合伊立替康为基础方案治疗。所有患者既往均接受过奥沙利铂治疗,辅助治疗 8 例,转移性疾病 32 例。

结果

3 例患者完全缓解(7.5%),5 例部分缓解(12.5%),14 例(35%)疾病稳定,总有效率为 20%。中位无进展生存期为 6 个月(95%CI,4.0-8.0),中位总生存期为 14 个月(95%CI,10.2-17.8)。1 年生存率为 55.9%。3-4 级毒性为:中性粒细胞减少(n=15,37.5%),发热性中性粒细胞减少(n=2,5%),腹泻(n=11,27.5%),恶心和呕吐(n=3,7.5%),胃肠道穿孔(n=2,5%)和血栓栓塞(n=2,5%)。

结论

贝伐珠单抗联合伊立替康为基础方案化疗是奥沙利铂为基础治疗失败患者的有效且安全的治疗选择。

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