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在伊立替康、奥沙利铂和5-氟尿嘧啶治疗失败后,西妥昔单抗和伊立替康作为晚期结直肠癌患者的三线治疗方案。

Cetuximab and irinotecan as third line therapy in patients with advanced colorectal cancer after failure of irinotecan, oxaliplatin and 5-fluorouracil.

作者信息

Pfeiffer Per, Nielsen Dorte, Yilmaz Mette, Iversen Anja, Vejlø Christian, Jensen Benny Vittrup

机构信息

Department of Oncology, Odense University Hospital, Odense, Denmark.

出版信息

Acta Oncol. 2007;46(5):697-701. doi: 10.1080/02841860601009455.

Abstract

Cetuximab (Erbitux) in combination with irinotecan is the most promising combination in heavily pretreated patients with advanced colorectal cancer. Efficacy of this combination was confirmed in the pivotal BOND I study. The aim of the present study was to evaluate efficacy and toxicity of a combination regimen of cetuximab and irinotecan but in contrast to the BOND I study all patients had previously received 5-FU, oxaliplatin and irinotecan and all had progressed during or shortly after completion of treatment. Before January 2005 salvage therapy with cetuximab and irinotecan was not used in Denmark. The Danish government had initiated a national programme for patients with advanced cancer and according to this programme the National Board of Health may approve and finance experimental treatment. From January 2005 to September 2005, 65 consecutive patients were treated with cetuximab (weekly) and irinotecan (each 2 or 3 weeks) at three university hospitals. Median age was 57 years (23-78), and median performance status was 1 (0-3). Response rate was 20%, median TTP was 5.5 months and median OS was 10.4 months. Response and survival was significantly correlated with severity of skin toxicity. Toxicity grade 3 was rare (skin toxicity 8%, diarrhoea 10%, nausea 3%, vomiting 3%, fatigue 8%). Salvage therapy with cetuximab and irinotecan is effective in patients pretreated with irinotecan, and oxaliplatin and in a general population the results from the BOND I study was confirmed.

摘要

西妥昔单抗(爱必妥)联合伊立替康是晚期结直肠癌经大量前期治疗患者中最有前景的联合方案。该联合方案的疗效在关键的BOND I研究中得到了证实。本研究的目的是评估西妥昔单抗和伊立替康联合方案的疗效和毒性,但与BOND I研究不同的是,所有患者此前均接受过氟尿嘧啶、奥沙利铂和伊立替康治疗,且均在治疗期间或治疗结束后不久病情进展。在2005年1月之前,丹麦未使用西妥昔单抗和伊立替康进行挽救治疗。丹麦政府启动了一项针对晚期癌症患者的国家项目,根据该项目,国家卫生委员会可批准并资助实验性治疗。从2005年1月至2005年9月,连续65例患者在三家大学医院接受了西妥昔单抗(每周一次)和伊立替康(每2或3周一次)治疗。中位年龄为57岁(23 - 78岁),中位体能状态为1(0 - 3)。缓解率为20%,中位疾病进展时间为5.5个月,中位总生存期为10.4个月。缓解和生存与皮肤毒性的严重程度显著相关。3级毒性罕见(皮肤毒性8%,腹泻10%,恶心3%,呕吐3%,疲劳8%)。西妥昔单抗和伊立替康的挽救治疗对接受过伊立替康和奥沙利铂前期治疗的患者有效,并且在一般人群中证实了BOND I研究的结果。

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