Biweekly cetuximab and irinotecan as third-line therapy in patients with advanced colorectal cancer after failure to irinotecan, oxaliplatin and 5-fluorouracil

被引:76
作者
Pfeiffer, P. [1 ]
Nielsen, D. [3 ]
Bjerregaard, J. [1 ]
Qvortrup, C. [1 ,2 ]
Yilmaz, M. [4 ]
Jensen, B. [3 ]
机构
[1] Odense Univ Hosp, Dept Oncol, DK-5000 Odense C, Denmark
[2] Univ So Denmark, Dept Oncol, Inst Clin Res, Odense, Denmark
[3] Univ Copenhagen, Herlev Hosp, Dept Oncol, DK-2730 Herlev, Denmark
[4] Aalborg Univ, Dept Oncol, Aalborg, Denmark
关键词
advanced colorectal cancer; biweekly; cetuximab; irinotecan; third-line therapy;
D O I
10.1093/annonc/mdn020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Standard weekly cetuximab and irinotecan (CetIri) is an effective regimen in heavily pretreated patients with advanced colorectal cancer (ACRC). Inspired by a pharmacokinetic study demonstrating no differences between weekly and biweekly cetuximab, we present the results of 74 consecutive patients treated with biweekly CetIri. Methods: Biweekly CetIri schedule: cetuximab 500 mg/m(2), first course was given as a 120-min infusion followed 1 h later by irinotecan 180 mg/m(2) as a 30-min infusion. Subsequent courses of cetuximab were given in 60 min, immediately followed by irinotecan-resulting in an overall treatment time of 90 min. Results: All patients had ACRC resistant to 5-fluorouracil and irinotecan and 95% to oxaliplatin. Median age was 63 years, median performance status was 0. Median duration of therapy was 4.3 months. Response rate was 25%. Median progression-free survival and overall survival were 5.4 months and 8.9 months, respectively, comparable to own historical controls receiving weekly CetIri. Grade 3-4 toxicity was rare (skin 7%, nail 3%, diarrhoea 10%, fatigue 3%, neutropenia 9%). One patient experienced severe allergic reaction. Conclusion: Salvage therapy with simplified biweekly CetIri is a convenient, effective and well-tolerated regimen in heavily pretreated patients with ACRC. A confirmatory phase II study is ongoing.
引用
收藏
页码:1141 / 1145
页数:5
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