Anti-angiogenesis therapy with bevacizumab for patients with ovarian granulosa cell tumors

被引:67
作者
Tao, Xia [1 ]
Sood, Anil K. [1 ,2 ]
Deavers, Michael T. [3 ]
Schmeler, Kathleen M. [1 ]
Nick, Alpa M. [1 ]
Coleman, Robert L. [1 ]
Milojevic, Ljiljana [1 ]
Gershenson, David M. [1 ]
Brown, Jubilee [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
Bevacizumab; Angiogenesis; Targeted therapy; Granulosa cell tumor; Stromal ovarian tumor; Ovarian cancer; ENDOTHELIAL GROWTH-FACTOR; VASCULAR-PERMEABILITY FACTOR; CANCER; COMBINATION; BLEOMYCIN; CISPLATIN; PROGNOSIS; ETOPOSIDE; TAXANES; MITOGEN;
D O I
10.1016/j.ygyno.2009.04.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objective. Ovarian granulosa cell tumors tend to respond poorly to chemotherapy. We examined the clinical efficacy of bevacizumab with or without concurrent chemotherapy and evaluated the angiogenic characteristics of these patients' tumors. Methods. We conducted a retrospective review of all patients seen at our institution from February 2004 to October 2008 who received bevacizumab for ovarian sex cord-stromal tumors. We performed immunohistochemical staining for vascular endothelial growth factor (VEGF) and CD31 when tissue was available: microvessel density was measured based on CD31 staining. Clinical data were abstracted from a chart review. We identified 8 patients who were treated with bevacizumab; 7 had adult granulosa cell tumors Results. and one had a juvenile granulosa cell tumor. All patients had recurrent disease and had been previously treated with cytotoxic chemotherapy (median 3.5 regimens: range, 1-6). One patient had a complete clinical response to bevacizumab therapy, 2 patients had a partial response, 2 patients had stable disease, and 3 patients' disease progressed, yielding a response rate of 38% and a clinical benefit rate of 63%. The median progression-free survival was 7.2 months and overall survival was not reached at a median follow-up of 23.6 months after initiating bevacizumab. VEGF overexpression and microvessel density were associated with poor outcome but sample size was too small to calculate statistical significance. Conclusions. Anti-VEGF therapy is highly effective in patients with granulosa cell tumors. Based on our observations, a prospective trial has been initiated using single-agent bevacizumab in patients with recurrent ovarian sex cord-stromal tumors. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:431 / 436
页数:6
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