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Significance of histologic pattern of carcinoma and sarcoma components on survival outcomes of uterine carcinosarcoma

Authors :
D. Kadogami
Tanja Pejovic
Toru Sugiyama
Masato Nishimura
Takashi Sasaki
Shinya Matsuzaki
Erin A. Blake
Melissa Moffitt
Tadaaki Nishikawa
Lynda D. Roman
A. Wakatsuki
Takuya Moriya
Tsukasa Baba
Frederick R. Ueland
M. Yoshida
Kiyoshi Yoshino
Munetaka Takekuma
Mian M.K. Shahzad
Kazuaki Suda
H. Yoshida
Merieme Klobocista
Miriam D. Post
Kei Kawana
Tetsuro Oishi
T. Yokoyama
Hiroko Machida
Hiroshi Kajiwara
Esther Elishaev
Ken Yamaguchi
Yasuhiko Shiki
M. Andoh
Mikio Mikami
Yutaka Takazawa
Joseph L. Kelley
Tadashi Kimura
Abby M. Richmond
Tomoyuki Fukagawa
Tadayoshi Nagano
Masanori Yasuda
Y. Hazama
I. Podzielinski
Y. Ikeda
D. D. Im
K. Fujiwara
Norichika Ushioda
Koichiro Shimoya
Muneaki Shimada
Marian S. Johnson
Masako Shida
Sosuke Adachi
Koji Matsuo
Y. Ueda
Stephen H. Bush
Shinya Satoh
Ikuo Konishi
Kohei Omatsu
Takayuki Enomoto
Takahito Miyake
K. Iwasaki
Rouzan G. Karabakhtsian
Yoshiaki Yuba
Malcolm S. Ross
Tadao Takano
Terry K. Morgan
Todd B. Sheridan
Satoshi Takeuchi
Kosei Hasegawa
S. W. Li
Paulette Mhawech-Fauceglia
Mayu Yunokawa
Ardeshir Hakam
Source :
Annals of Oncology. 27:1257-1266
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

To examine the effect of the histology of carcinoma and sarcoma components on survival outcome of uterine carcinosarcoma.A multicenter retrospective study was conducted to examine uterine carcinosarcoma cases that underwent primary surgical staging. Archived slides were examined and histologic patterns were grouped based on carcinoma (low-grade versus high-grade) and sarcoma (homologous versus heterologous) components, correlating to clinico-pathological demographics and outcomes.Among 1192 cases identified, 906 cases were evaluated for histologic patterns (carcinoma/sarcoma) with high-grade/homologous (40.8%) being the most common type followed by high-grade/heterologous (30.9%), low-grade/homologous (18.0%), and low-grade/heterologous (10.3%). On multivariate analysis, high-grade/heterologous (5-year rate, 34.0%, P = 0.024) and high-grade/homologous (45.8%, P = 0.017) but not low-grade/heterologous (50.6%, P = 0.089) were independently associated with decreased progression-free survival (PFS) compared with low-grade/homologous (60.3%). In addition, older age, residual disease at surgery, large tumor, sarcoma dominance, deep myometrial invasion, lymphovascular space invasion, and advanced-stage disease were independently associated with decreased PFS (all, P0.01). Both postoperative chemotherapy (5-year rates, 48.6% versus 39.0%, P0.001) and radiotherapy (50.1% versus 44.1%, P = 0.007) were significantly associated with improved PFS in univariate analysis. However, on multivariate analysis, only postoperative chemotherapy remained an independent predictor for improved PFS [hazard ratio (HR) 0.34, 95% confidence interval (CI) 0.27-0.43, P0.001]. On univariate analysis, significant treatment benefits for PFS were seen with ifosfamide for low-grade carcinoma (82.0% versus 49.8%, P = 0.001), platinum for high-grade carcinoma (46.9% versus 32.4%, P = 0.034) and homologous sarcoma (53.1% versus 38.2%, P = 0.017), and anthracycline for heterologous sarcoma (66.2% versus 39.3%, P = 0.005). Conversely, platinum, taxane, and anthracycline for low-grade carcinoma, and anthracycline for homologous sarcoma had no effect on PFS compared with non-chemotherapy group (all, P0.05). On multivariate analysis, ifosfamide for low-grade/homologous (HR 0.21, 95% CI 0.07-0.63, P = 0.005), platinum for high-grade/homologous (HR 0.36, 95% CI 0.22-0.60, P0.001), and anthracycline for high-grade/heterologous (HR 0.30, 95% CI 0.14-0.62, P = 0.001) remained independent predictors for improved PFS. Analyses of 1096 metastatic sites showed that carcinoma components tended to spread lymphatically, while sarcoma components tended to spread loco-regionally (P0.001).Characterization of histologic pattern provides valuable information in the management of uterine carcinosarcoma.

Details

ISSN :
09237534
Volume :
27
Database :
OpenAIRE
Journal :
Annals of Oncology
Accession number :
edsair.doi.dedup.....7afd78783f751406d1d867cf32b900c8
Full Text :
https://doi.org/10.1093/annonc/mdw161