First-line Herceptin® monotherapy in metastatic breast cancer
First-line Herceptin® monotherapy in metastatic breast cancer
复制标题
DOI:
10.1159/000055400
复制
发表时间:
2001-01-01
期刊:
影响因子:
3.5
通讯作者:
Stewart, SJ
中科院分区:
文献类型:
--
作者:
Vogel, CL;Cobleigh, MA;Stewart, SJ
The pivotal phase II and III Herceptin (R) trials proved the efficacy and safety of second- or third-line single-agent Herceptin and first-line Herceptin in combination with chemotherapy, respectively. In the current trial, 114 patients were randomized to one of two dose groups of first-line Herceptin monotherapy: standard dose of 4 mg/kg initial dose followed by 2 mg/kg intravenous (i.v.) weekly; or high dose of 8 mg/kg initial dose followed by 4 mg/kg im. weekly. The regimen was generally well tolerated. A similar incidence of adverse events was demonstrated in the two dose groups with the possible exception of acute infusion-related events such as fever and chills as well as rash and dyspnea, which appear to be more prevalent in the higher dose group. The overall response rate was 26% and response rates were similar between the two dose groups (24% for the standard Herceptin dose group and 28% for the high Herceptin dose group). Subgroup analysis determined a higher response rate in IHC 3+ patients (35%) and FISH-positive patients (41%). When women with stable disease for greater than or equal to6 months were included with responders, the clinical benefit rate in IHC 3+ patients was 47%. Median survival was 24.4 months, which is comparable with the survival rate seen in the pivotal phase Ill combination trial (25 months). Therefore, single-agent Herceptin is an important new option for the first-line treatment of HER2-positive metastatic breast cancer patients. Copyright (C) 2001 S. Karger AG, Basel.