Tumor characteristics and survival outcomes of women with tamoxifen-related uterine carcinosarcoma

被引:17
|
作者
Matsuo, Koji [1 ]
Ross, Malcolm S. [2 ]
Bush, Stephen H. [3 ]
Yunokawa, Mayu [4 ]
Blake, Erin A. [5 ]
Takano, Tadao [6 ]
Ueda, Yutaka [7 ]
Baba, Tsukasa [8 ]
Satoh, Shinya [9 ]
Shida, Masako [10 ]
Ikeda, Yuji [11 ]
Adachi, Sosuke [12 ]
Yokoyama, Takuhei [13 ]
Takekuma, Munetaka [14 ]
Takeuchi, Satoshi [15 ]
Nishimura, Masato [16 ]
Iwasaki, Keita [17 ]
Yanai, Shiori [18 ]
Klobocista, Merieme M. [19 ]
Johnson, Marian S. [20 ]
Machida, Hiroko [1 ]
Hasegawa, Kosei [21 ]
Miyake, Takahito M. [22 ]
Nagano, Tadayoshi [23 ]
Pejovic, Tanja [24 ]
Shahzad, Mian M. K. [3 ]
Im, Dwight D. [25 ]
Omatsu, Kohei [26 ]
Ueland, Frederick R.
Kelley, Joseph L. [2 ]
Roman, Lynda D. [1 ]
机构
[1] Univ Southern Calif, Dept Obstet & Gynecol, Div Gynecol Oncol, 2020 Zonal Ave,IRD520, Los Angeles, CA 90007 USA
[2] Univ Pittsburgh, MaGee Womens Hosp, Dept Obstet & Gynecol, Div Gynecol Oncol, Pittsburgh, PA 15260 USA
[3] Univ S Florida, Moffitt Canc Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Tampa, FL 33620 USA
[4] Natl Canc Ctr, Dept Breast & Med Oncol, Tokyo, Japan
[5] Univ Colorado, Dept Obstet & Gynecol, Div Gynecol Oncol, Boulder, CO 80309 USA
[6] Tohoku Univ, Dept Obstet & Gynecol, Sendai, Miyagi 980, Japan
[7] Osaka Univ, Dept Obstet & Gynecol, Osaka, Japan
[8] Kyoto Univ, Dept Obstet & Gynecol, Kyoto, Japan
[9] Tottori Univ, Dept Obstet & Gynecol, Tottori, Japan
[10] Tokai Univ, Dept Obstet & Gynecol, Hiratsuka, Kanagawa 25912, Japan
[11] Univ Tokyo, Dept Obstet & Gynecol, Tokyo, Japan
[12] Niigata Univ, Dept Obstet & Gynecol, Niigata, Japan
[13] Osaka Rosai Hosp, Dept Obstet & Gynecol, Osaka, Japan
[14] Shizuoka Canc Ctr, Dept Obstet & Gynecol, Shizuoka, Japan
[15] Iwate Med Univ, Dept Obstet & Gynecol, Morioka, Iwate, Japan
[16] Univ Tokushima, Dept Obstet & Gynecol, Tokushima, Japan
[17] Aichi Med Univ, Dept Obstet & Gynecol, Nagakute, Aichi, Japan
[18] Kurashiki Med Ctr, Dept Obstet & Gynecol, Okayama, Japan
[19] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Obstet & Gynecol, Div Gynecol Oncol, Bronx, NY 10467 USA
[20] Univ Kentucky, Dept Obstet & Gynecol, Div Gynecol Oncol, Lexington, KY 40506 USA
[21] Saitama Med Univ, Int Med Ctr, Dept Obstet & Gynecol, Saitama, Japan
[22] Kawasaki Med Sch, Dept Obstet & Gynecol, Okayama, Japan
[23] Kitano Hosp, Dept Obstet & Gynecol, Osaka, Japan
[24] Oregon Hlth & Sci Univ, Dept Obstet & Gynecol, Div Gynecol Oncol, Portland, OR 97201 USA
[25] Mercy Med Ctr, Gynecol Oncol Ctr, Baltimore, MD USA
[26] Canc Inst Hosp, Dept Gynecol, Tokyo, Japan
关键词
Uterine carcinosarcoma; Tamoxifen; Survival outcome; SURGICAL ADJUVANT BREAST; ENDOMETRIAL CANCER; PROGNOSIS; ASSOCIATION; PREVENTION; CARCINOMA; THERAPY; RISK;
D O I
10.1016/j.ygyno.2016.11.042
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. To examine tumor characteristics and survival outcome of women with uterine carcinosarcoma who had a history of tamoxifen use. Methods. This is a multicenter retrospective study examining stage I-IV uterine carcinosarcoma cases based on history of tamoxifen use. Patient demographics, tumor characteristics, treatment pattern, and survival outcomes were compared between tamoxifen users and non-users. Results. Sixty-six cases of tamoxifen-related uterine carcinosarcoma were compared to 1009 cases with no history of tamoxifen use. Tamoxifen users were more likely to be older (mean age, 69 versus 64, P < 0.001) and had a past history of malignancy (100% versus 12.7%, P < 0.001). Tamoxifen-related uterine carcinosarcoma was significantly associated with a higher proportion of stage IA disease (48.4% versus 29.9%) and a lower risk of stage IVB disease (7.8% versus 16.0%) compared to tamoxifen-unrelated carcinosarcoma (P = 0.034). Deep myometrial tumor invasion was less common in uterine carcinosarcoma related to tamoxifen use (28.3% versus 48.8%, P = 0.002). On univariate analysis, tamoxifen use was not associated with progression-free survival (5-year rates 44.5% versus 46.8%, P = 0.48) and disease-specific survival (64.0% versus 59.1%, P = 0.39). After adjusting for age, past history of malignancy, stage, residual disease status at surgery, and postoperative treatment patterns, tamoxifen use was not associated with progression-free survival (adjusted-hazard ratio 0.86, 95% confidence interval 0.50 to 1.50, P = 0.60) and disease-specific survival (adjusted-hazard ratio 0.68, 95% confidence interval 0.36 to 1.29, P = 0.24). Conclusion. Our study suggests that tamoxifen-related uterine carcinosarcoma may have favorable tumor characteristics but have comparable stage-specific survival outcomes compared to tamoxifen-unrelated uterine carcinosarcoma. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:329 / 335
页数:7
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