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乳腺血管肉瘤

Angiosarcoma of the breast.

作者信息

Vorburger Stephan A, Xing Yan, Hunt Kelly K, Lakin Gregory E, Benjamin Robert S, Feig Barry W, Pisters Peter W T, Ballo Matthew T, Chen Lei, Trent Jonathan, Burgess Michael, Patel Shreyaskumar, Pollock Raphael E, Cormier Janice N

机构信息

The Multidisciplinary Sarcoma Center, The University of Texas MD Anderson Cancer Center, Houston, 77230, USA.

出版信息

Cancer. 2005 Dec 15;104(12):2682-8. doi: 10.1002/cncr.21531.

Abstract

BACKGROUND

Angiosarcoma of the breast is a rare entity. The objectives of this study were to evaluate prognostic factors and determine outcomes in a large contemporary series of patients.

METHODS

Clinical and pathologic factors were analyzed in all patients with angiosarcoma of the breast treated between 1990 and 2003. Overall survival (OS) and disease-free survival (DFS) were estimated using the methods of Kaplan and Meier. Multivariate analyses were performed to evaluate prognostic factors.

RESULTS

Fifty-five women with angiosarcoma of the breast were identified. The median age was 49.1 years, and the median follow-up time was 3.7 years. The median OS and DFS were 2.96 years and 2.26 years, respectively. For the 32 patients with primary angiosarcoma of the breast 5-year OS was 59%. Twenty-three (42%) patients had received prior radiation therapy for the treatment of breast cancer. These patients with radiation therapy-associated angiosarcoma were on average 30 years older and less likely to present with distant metastatic disease than patients presenting with radiation-naive angiosarcoma of the breast. Although radiation-naive patients appeared to have had better early DFS and OS, the Kaplan-Meier curves were not statistically different between patients with radiation therapy-associated disease and radiation therapy-naive patients. On multivariate analysis, tumor recurrence (P = 0.006) was the only significant adverse prognostic factor noted for OS.

CONCLUSIONS

In this series of 55 patients with angiosarcoma of the breast, radiation therapy-naive angiosarcomas occurred in younger patients, but they behaved similarly to radiation therapy-associated angiosarcomas.

摘要

背景

乳腺血管肉瘤是一种罕见的疾病。本研究的目的是评估预后因素并确定大量当代患者系列的结局。

方法

分析了1990年至2003年间接受治疗的所有乳腺血管肉瘤患者的临床和病理因素。采用Kaplan-Meier方法估计总生存期(OS)和无病生存期(DFS)。进行多变量分析以评估预后因素。

结果

确定了55例乳腺血管肉瘤女性患者。中位年龄为49.1岁,中位随访时间为3.7年。中位OS和DFS分别为2.96年和2.26年。对于32例原发性乳腺血管肉瘤患者,5年OS为59%。23例(42%)患者曾接受过乳腺癌放疗。与未接受放疗的乳腺血管肉瘤患者相比,这些与放疗相关的血管肉瘤患者平均年龄大30岁,出现远处转移疾病的可能性较小。尽管未接受放疗的患者早期DFS和OS似乎更好,但与放疗相关疾病患者和未接受放疗患者的Kaplan-Meier曲线在统计学上无差异。多变量分析显示,肿瘤复发(P = 0.006)是OS唯一显著的不良预后因素。

结论

在这55例乳腺血管肉瘤患者系列中,未接受放疗的血管肉瘤发生在较年轻患者中,但与放疗相关的血管肉瘤表现相似。

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