Do HER-2 positive metastatic breast cancer patients benefit from the use of trastuzumab beyond disease progression? A mono-institutional experience and systematic review of observational studies

被引:47
作者
Fabi, Alessandra [1 ]
Metro, Giulio [1 ]
Ferretti, Gianluigi [1 ]
Giannarelli, Diana [2 ]
Di Cosimo, Serena [1 ]
Papaldo, Paola [1 ]
Mottolese, Marcella [3 ]
Carlini, Paolo [1 ]
Felici, Alessandra [1 ]
Russillo, Michelangelo [1 ]
Cognetti, Francesco [1 ]
机构
[1] Regina Elena Inst Canc Res, Div Med Oncol A, I-00144 Rome, Italy
[2] Regina Elena Inst Canc Res, Dept Stat, Rome, Italy
[3] Regina Elena Inst Canc Res, Dept Pathol, Rome, Italy
关键词
Trastuzumab; HER-2; Metastatic breast cancer; Disease progression;
D O I
10.1016/j.breast.2008.03.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Though preclinical evidence supports the protracted use of trastuzumab to reach sustained anti-tumor activity, the activity of trastuzumab beyond disease progression remains controversial in HER-2 over-expressing (HER-2+) metastatic breast cancer (MBC) patients. We retrospectively evaluated a total of 59 patients with HER-2 + MBC treated at our institution with trastuzumab-based therapies. Our results were added to those obtained in similar observational studies and summary estimates for overall response (OR) and clinical benefit (CB) to first and second trastuzumab-based lines were calculated. In our series of patients we observed an OR of 59.3% and 27% for first and second trastuzumab-based lines, respectively, with a corresponding CB of 83% and 62.2%, respectively. Time to first and second progression were 9.5 months and 6.7 months, respectively. The combined analysis showed an OR of 50% for first trastuzumab-based regimen and 21.2% for second trastuzumab-based line. The corresponding value,.; for CB were 77.6% and 42.6%, respectively. A second trastuzumab-containing regimen beyond progression yields a considerable rate of OR and CB in HER-2 + MBC patients. Randomized trials are warranted. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:499 / 505
页数:7
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