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Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy

OBJECTIVE: Uterine serous carcinoma (USC) is an aggressive type 2 endometrial cancer. Data on prognostic factors for patients with early-stage USC without adjuvant therapy are limited. This study aims to assess the baseline recurrence risk of early-stage USC patients without adjuvant treatment and t...

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Autores principales: Tate, Keisei, Yoshida, Hiroshi, Ishikawa, Mitsuya, Uehara, Takashi, Ikeda, Shun-ichi, Hiraoka, Nobuyoshi, Kato, Tomoyasu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920218/
https://www.ncbi.nlm.nih.gov/pubmed/29533019
http://dx.doi.org/10.3802/jgo.2018.29.e34
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author Tate, Keisei
Yoshida, Hiroshi
Ishikawa, Mitsuya
Uehara, Takashi
Ikeda, Shun-ichi
Hiraoka, Nobuyoshi
Kato, Tomoyasu
author_facet Tate, Keisei
Yoshida, Hiroshi
Ishikawa, Mitsuya
Uehara, Takashi
Ikeda, Shun-ichi
Hiraoka, Nobuyoshi
Kato, Tomoyasu
author_sort Tate, Keisei
collection PubMed
description OBJECTIVE: Uterine serous carcinoma (USC) is an aggressive type 2 endometrial cancer. Data on prognostic factors for patients with early-stage USC without adjuvant therapy are limited. This study aims to assess the baseline recurrence risk of early-stage USC patients without adjuvant treatment and to identify prognostic factors and patients who need adjuvant therapy. METHODS: Sixty-eight patients with International Federation of Gynecology and Obstetrics (FIGO) stage I–II USC between 1997 and 2016 were included. All the cases did not undergo adjuvant treatment as institutional practice. Clinicopathological features, recurrence patterns, and survival outcomes were analyzed to determine prognostic factors. RESULTS: FIGO stages IA, IB, and II were observed in 42, 7, and 19 cases, respectively. Median follow-up time was 60 months. Five-year disease-free survival (DFS) and overall survival (OS) rates for all cases were 73.9% and 78.0%, respectively. On multivariate analysis, cervical stromal involvement and positive pelvic cytology were significant predictors of DFS and OS, and ≥1/2 myometrial invasion was also a significant predictor of OS. Of 68 patients, 38 patients had no cervical stromal invasion or positive pelvic cytology and showed 88.8% 5-year DFS and 93.6% 5-year OS. CONCLUSION: Cervical stromal invasion and positive pelvic cytology are prognostic factors for stage I–II USC. Patients with stage IA or IB USC showing negative pelvic cytology may have an extremely favorable prognosis and need not receive any adjuvant therapies.
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spelling pubmed-59202182018-05-01 Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy Tate, Keisei Yoshida, Hiroshi Ishikawa, Mitsuya Uehara, Takashi Ikeda, Shun-ichi Hiraoka, Nobuyoshi Kato, Tomoyasu J Gynecol Oncol Original Article OBJECTIVE: Uterine serous carcinoma (USC) is an aggressive type 2 endometrial cancer. Data on prognostic factors for patients with early-stage USC without adjuvant therapy are limited. This study aims to assess the baseline recurrence risk of early-stage USC patients without adjuvant treatment and to identify prognostic factors and patients who need adjuvant therapy. METHODS: Sixty-eight patients with International Federation of Gynecology and Obstetrics (FIGO) stage I–II USC between 1997 and 2016 were included. All the cases did not undergo adjuvant treatment as institutional practice. Clinicopathological features, recurrence patterns, and survival outcomes were analyzed to determine prognostic factors. RESULTS: FIGO stages IA, IB, and II were observed in 42, 7, and 19 cases, respectively. Median follow-up time was 60 months. Five-year disease-free survival (DFS) and overall survival (OS) rates for all cases were 73.9% and 78.0%, respectively. On multivariate analysis, cervical stromal involvement and positive pelvic cytology were significant predictors of DFS and OS, and ≥1/2 myometrial invasion was also a significant predictor of OS. Of 68 patients, 38 patients had no cervical stromal invasion or positive pelvic cytology and showed 88.8% 5-year DFS and 93.6% 5-year OS. CONCLUSION: Cervical stromal invasion and positive pelvic cytology are prognostic factors for stage I–II USC. Patients with stage IA or IB USC showing negative pelvic cytology may have an extremely favorable prognosis and need not receive any adjuvant therapies. Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology 2018-05 2018-02-19 /pmc/articles/PMC5920218/ /pubmed/29533019 http://dx.doi.org/10.3802/jgo.2018.29.e34 Text en Copyright © 2018. Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tate, Keisei
Yoshida, Hiroshi
Ishikawa, Mitsuya
Uehara, Takashi
Ikeda, Shun-ichi
Hiraoka, Nobuyoshi
Kato, Tomoyasu
Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
title Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
title_full Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
title_fullStr Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
title_full_unstemmed Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
title_short Prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
title_sort prognostic factors for patients with early-stage uterine serous carcinoma without adjuvant therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920218/
https://www.ncbi.nlm.nih.gov/pubmed/29533019
http://dx.doi.org/10.3802/jgo.2018.29.e34
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