Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer.

Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer.
复制标题

DOI:
10.1038/sj.bjc.6601970
复制
发表时间:
2004-08-16
影响因子:
8.8
通讯作者:
--
中科院分区:
医学1区
文献类型:
--
作者:

文献摘要

参考文献

被引文献

相似文献

曲妥珠单抗是治疗HER-2过表达的转移性乳腺癌(MBC)患者的有效药物。在接受曲妥珠单抗治疗的患者中观察到脑转移瘤(BM)的发生率较高。对1999年7月至2002年12月在克里斯蒂医院开始曲妥珠单抗治疗转移性乳腺癌的100例患者进行了回顾性图表审查。排除7例患者; 5名患者在开始曲妥珠单抗治疗前发生中枢神经系统转移,2名患者的数据不足。在其余93例患者中,迄今为止有23例(25%)发生BM。总共有46名患者死亡,其中18名(39%)在死亡前被诊断为BM。在23例发生BM的患者中,18例(78%)为激素受体阴性,18例(78%)有内脏疾病。单因素分析显示,脑疾病的发展与激素受体状态和内脏疾病的存在之间存在显着关联。总之,接受曲妥珠单抗治疗的MBC患者中有很高比例发生症状性脑转移。HER-2阳性乳腺癌可能有脑的偏好,或者曲妥珠单抗治疗可能通过延长生存期来改变疾病模式。解决这一问题的新策略需要在这组患者中进行调查。
Trastuzumab is an effective treatment for patients with metastatic breast cancer (MBC) that overexpresses HER-2. A high incidence of brain metastases (BM) has been noted in patients receiving trastuzumab. A retrospective chart review was conducted of 100 patients commencing trastuzumab for metastatic breast cancer from July 1999 to December 2002, at the Christie Hospital. Seven patients were excluded; five patients developed central nervous system metastases prior to starting trastuzumab, and inadequate data were available for two. Out of the remaining 93 patients, 23 (25%) have developed BM to date. In all, 46 patients have died, and of these 18 (39%) have been diagnosed with BM prior to death. Of the 23 patients developing BM, 18 (78%) were hormone receptor negative and 18 (78%) had visceral disease. Univariate analysis showed a significant association between the development of cerebral disease and both hormone receptor status and the presence of visceral disease. In conclusion, a high proportion of patients with MBC treated with trastuzumab develop symptomatic cerebral metastases. HER-2-positive breast cancer may have a predilection for the brain, or trastuzumab therapy may change the disease pattern by prolonging survival. New strategies to address this problem require investigation in this group of patients.
DOI: 10.1200/jco.1999.17.9.2639
发表时间: 1999-09-01
影响因子: 45.3
作者:
Cobleigh, MA;Vogel, CL;Slamon, DJ
通讯作者: Slamon, DJ
DOI: 10.1093/annonc/mdg300
发表时间: 2003-07-01
期刊: ANNALS OF ONCOLOGY
影响因子: 50.5
作者:
Miller, KD;Weathers, T;Sledge, GW
通讯作者: Sledge, GW
DOI: 10.1126/science.3798106
发表时间: 1987-01-09
期刊: SCIENCE
影响因子: 56.9
作者:
SLAMON, DJ;CLARK, GM;MCGUIRE, WL
通讯作者: MCGUIRE, WL
DOI: 10.1200/jco.20.3.719
发表时间: 2002-02-01
影响因子: 45.3
作者:
Vogel, CL;Cobleigh, MA;Press, M
通讯作者: Press, M
DOI: 10.1002/cncr.11436
发表时间: 2003-06-15
期刊: CANCER
影响因子: 6.2
作者:
Bendell, JC;Domchek, SM;Winer, E
通讯作者: Winer, E