Panitumumab - In the treatment of metastatic colorectal cancer

被引:28
作者
Hoy, Sheridan M. [1 ]
Wagstaff, Antona J. [1 ]
机构
[1] Wolters Kluwer Hlth, Adis, Auckland 1311, New Zealand
关键词
D O I
10.2165/00003495-200666150-00011
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Panitumumab is a fully human immunoglobulin G2 monoclonal antibody highly selective for the epidermal growth factor receptror (EGFR), which is overexpressed in 25-77% of colorectal cancers. This overexpression is frequently associated with a poor prognosis. In a large, randomised, nonblind, multicentre phase III study in pretreated adult patients with metastatic colorectal cancer and EGFR staining in >= 1% tumour cells, panitumumab 6 mg/kg every 2 weeks plus best supportive care (BSC) was significantly (p < 0.0001) more effective in improving progression-free survival than BSC alone; recipients of panitumumab plus BSC had a 46% lower disease progression rate than those receiving BSC alone after a median follow-up of 19 weeks. A Panitumumab 6 mg/kg every 2 weeks or 2.5 mg/kg/week, administered as monotherapy, produced partial response rates of 8-13%,and stable disease rates of 21-30% in pretreated patients with metastatic colorectal cancer in three noncomparative, multicentre phase II studies. A Preliminary phase II results also suggest a potential role for panitumumab as first-fine therapy in combination with fluorouracil, folinic acid and irinotecan in patients with metastatic colorectal cancer. A Panitumumab was generally well tolerated. Grade 3/4 skin-related toxicities were reported in 14% of patients receiving panitumuinab plus BSC in the phase III study (versus 0% of patients receiving BSC alone). An analysis of pooled data found that high-affinity binding antibodies to panitumumab were detected in < 1 % of patients.
引用
收藏
页码:2005 / 2014
页数:10
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