## Background: Tamoxifen commonly is used as adjuvant therapy for all stages of breast carcinoma. however, several studies have suggested an association between the use of tamoxifen in breast carcinoma patients and the subsequent development of endometrial carcinoma. the objective of this study was
Outcomes in patients with primary breast cancer and a subsequent diagnosis of endometrial cancer : Comparison of cohorts treated with and without tamoxifen
โ Scribed by Mandana Saadat; Pauline T. Truong; Hosam A. Kader; Caroline H. Speers; Eric Berthelet; Elissa McMurtrie; Ivo A. Olivotto
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 150 KB
- Volume
- 110
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
BACKGROUND.
The study compared tumor characteristics and survival in women with breast cancer who subsequently developed endometrial cancer with or without a history of tamoxifen use.
METHODS.
The British Columbia Cancer Agency registry identified 163 women diagnosed with breast cancer between 1989โ1999 who received a subsequent diagnosis of endometrial cancer. Of these, 55% (n = 90) had a history of tamoxifen use. Outcomes analyzed were breast cancerโspecific survival (BCSS), endometrial cancerโspecific survival (ECSS), and overall survival (OS).
RESULTS.
Median followโup was 9.4 years. Distributions of age, menopausal status, body mass index, and comorbidities were similar in the tamoxifenโtreated and nontamoxifen cohorts. Proportions of aggressive endometrial cancer subtypes including papillary serous, clear cell, and mixed mullerian tumors were higher in the tamoxifen cohort (28% vs14%, P = .03). Distributions of endometrial cancer grade and stage were similar in the 2 groups (P > .05). Hysterectomy and/or oophorectomy were the primary treatments for endometrial cancer in 99% of patients, with comparable pelvic control rates in the tamoxifen and nontamoxifen groups. At 10 years, patients in the tamoxifen group experienced lower BCSS compared with the nontamoxifen group (89% vs 97%, P = .02). No significant differences in ECSS and OS were observed between the 2 groups (ECSS 82% and 82%, P = .85; and OS 69% v. 66%, P = .85).
CONCLUSIONS.
In patients with breast cancer who developed a subsequent endometrial cancer, tamoxifenโtreated patients had higher proportions of aggressive endometrial cancer subtypes, but almost all cases were amenable to surgery, thus resulting in similar endometrial cancer control and survival when compared with nontamoxifen treated patients. Cancer 2007. ยฉ 2007 American Cancer Society.
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