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Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience

Objectives: Ovarian granulosa cell tumour is rare. This study aims to report the clinical characteristics and long-term outcomes of adult-type ovarian granulosa cell tumour (AOGCT) at King Faisal Specialist Hospital and Research Centre (KFSH&RC) and to determine the prognostic factors affecting...

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Autores principales: Alhusaini, Hamed, Elshenawy, Mahmoud A, Badran, Ahmed, Elshentenawy, Ayman, Mohieldin, Ahmed, Mostafa Gad, Ahmed, Omar, Ayman, Shaheen, Amgad, Elhassan, Tusneem, Soudy, Hussein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719055/
https://www.ncbi.nlm.nih.gov/pubmed/36475202
http://dx.doi.org/10.7759/cureus.31045
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author Alhusaini, Hamed
Elshenawy, Mahmoud A
Badran, Ahmed
Elshentenawy, Ayman
Mohieldin, Ahmed
Mostafa Gad, Ahmed
Omar, Ayman
Shaheen, Amgad
Elhassan, Tusneem
Soudy, Hussein
author_facet Alhusaini, Hamed
Elshenawy, Mahmoud A
Badran, Ahmed
Elshentenawy, Ayman
Mohieldin, Ahmed
Mostafa Gad, Ahmed
Omar, Ayman
Shaheen, Amgad
Elhassan, Tusneem
Soudy, Hussein
author_sort Alhusaini, Hamed
collection PubMed
description Objectives: Ovarian granulosa cell tumour is rare. This study aims to report the clinical characteristics and long-term outcomes of adult-type ovarian granulosa cell tumour (AOGCT) at King Faisal Specialist Hospital and Research Centre (KFSH&RC) and to determine the prognostic factors affecting relapse and survival. Methods: We retrospectively reviewed patients with AOGCT, from 1988 to 2014, who were treated at our institution. Baseline characteristics, pathological findings, and outcomes were analysed and reported. Results: Sixty-one patients with AOGCT were identified with a median age of 49 years. Median follow-up was 5.0 years (range 2.1-8.2 years). 74% of patients were FIGO (International Federation of Gynecology and Obstetrics) stage I, whereas 7% were stage II, 5% were stage III, and unknown in 14% of the cases. The most common presenting symptoms included abdominal pain (43%) and vaginal bleeding (43%). The majority of patients (38 patients, 62%) were treated with total abdominal hysterectomy and bilateral salpingo-oophorectomy. Five (8%) patients received adjuvant chemotherapy. Sixteen patients (26%) relapsed with a median time to relapse of 5.5 years (0.7-8.1 years). Half of the recurrences (eight patients, 50%) occurred after five years of diagnosis. Five-year overall survival and disease-free survival (DFS) were 93% and 84%, respectively. Factors associated with a high risk of recurrence were the presence of ascites (p=0.000) and elevated preoperative CA 125 level (p=0.048). The overall survival was significantly influenced by the menopausal status (premenopausal 100% vs. postmenopausal 84%; p=0.02), preoperative CA 125 (normal 100% vs. elevated 64%; p=0.005), ascites (present 33% vs. absent 100%; p=0.000), and age (<55 years 100% vs. ≥ 55 years 77%; p= 0.002). Conclusion: This study confirms a good outcome for patients with AOGCT. They require long-term follow-up as late recurrences can occur many years post definitive therapy. The presence of ascites and elevated preoperative CA 125 levels were associated with a higher risk of recurrence and poor prognosis. Outcomes appear unaffected by fertility-sparing surgery or adjuvant chemotherapy.
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spelling pubmed-97190552022-12-05 Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience Alhusaini, Hamed Elshenawy, Mahmoud A Badran, Ahmed Elshentenawy, Ayman Mohieldin, Ahmed Mostafa Gad, Ahmed Omar, Ayman Shaheen, Amgad Elhassan, Tusneem Soudy, Hussein Cureus Oncology Objectives: Ovarian granulosa cell tumour is rare. This study aims to report the clinical characteristics and long-term outcomes of adult-type ovarian granulosa cell tumour (AOGCT) at King Faisal Specialist Hospital and Research Centre (KFSH&RC) and to determine the prognostic factors affecting relapse and survival. Methods: We retrospectively reviewed patients with AOGCT, from 1988 to 2014, who were treated at our institution. Baseline characteristics, pathological findings, and outcomes were analysed and reported. Results: Sixty-one patients with AOGCT were identified with a median age of 49 years. Median follow-up was 5.0 years (range 2.1-8.2 years). 74% of patients were FIGO (International Federation of Gynecology and Obstetrics) stage I, whereas 7% were stage II, 5% were stage III, and unknown in 14% of the cases. The most common presenting symptoms included abdominal pain (43%) and vaginal bleeding (43%). The majority of patients (38 patients, 62%) were treated with total abdominal hysterectomy and bilateral salpingo-oophorectomy. Five (8%) patients received adjuvant chemotherapy. Sixteen patients (26%) relapsed with a median time to relapse of 5.5 years (0.7-8.1 years). Half of the recurrences (eight patients, 50%) occurred after five years of diagnosis. Five-year overall survival and disease-free survival (DFS) were 93% and 84%, respectively. Factors associated with a high risk of recurrence were the presence of ascites (p=0.000) and elevated preoperative CA 125 level (p=0.048). The overall survival was significantly influenced by the menopausal status (premenopausal 100% vs. postmenopausal 84%; p=0.02), preoperative CA 125 (normal 100% vs. elevated 64%; p=0.005), ascites (present 33% vs. absent 100%; p=0.000), and age (<55 years 100% vs. ≥ 55 years 77%; p= 0.002). Conclusion: This study confirms a good outcome for patients with AOGCT. They require long-term follow-up as late recurrences can occur many years post definitive therapy. The presence of ascites and elevated preoperative CA 125 levels were associated with a higher risk of recurrence and poor prognosis. Outcomes appear unaffected by fertility-sparing surgery or adjuvant chemotherapy. Cureus 2022-11-03 /pmc/articles/PMC9719055/ /pubmed/36475202 http://dx.doi.org/10.7759/cureus.31045 Text en Copyright © 2022, Alhusaini et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Oncology
Alhusaini, Hamed
Elshenawy, Mahmoud A
Badran, Ahmed
Elshentenawy, Ayman
Mohieldin, Ahmed
Mostafa Gad, Ahmed
Omar, Ayman
Shaheen, Amgad
Elhassan, Tusneem
Soudy, Hussein
Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience
title Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience
title_full Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience
title_fullStr Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience
title_full_unstemmed Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience
title_short Adult-Type Ovarian Granulosa Cell Tumour: Treatment Outcomes From a Single-Institution Experience
title_sort adult-type ovarian granulosa cell tumour: treatment outcomes from a single-institution experience
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719055/
https://www.ncbi.nlm.nih.gov/pubmed/36475202
http://dx.doi.org/10.7759/cureus.31045
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