Effectiveness of adjuvant systemic therapy following complete cytoreductive surgery in patients with recurrent granulosa cell tumours of the ovary.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 Jan 2024
Historique:
received: 09 09 2023
accepted: 09 01 2024
medline: 11 1 2024
pubmed: 11 1 2024
entrez: 10 1 2024
Statut: epublish

Résumé

Aim of the present analysis is to compare the impact of antihormonal therapy versus cytotoxic chemotherapy versus a watch a wait approach on disease-free survival (DFS) in the adjuvant setting of patients who underwent complete cytoreductive surgery(CRS) for recurrent adult type granulosa cell tumours of the ovary (GCT). Moreover, we wished to identify prognostic risk factors for recurrence. We included recurrent GCT-patients who underwent CRS resulting in total macroscopic tumour clearance, treated in two gynaecological cancer centres over a 20-year period (2000-2020). CRS was performed for 51 recurrences in 26 GCT-patients. Adjuvant systemic treatments were as follows: chemotherapy in 21 cases, hormonotherapy in 10 cases, no systemic treatment in 20 cases. There were no statistically significant differences in DFS between chemotherapy, hormonotherapy and no systemic treatment: median DFS was 57, 36 and 57 months, respectively (p = 0.616). Extra-pelvic and/or multifocal tumour dissemination were found to be independent predictive factors for subsequent recurrences. In the cases with both lower and upper abdominal involvement (n = 18), patients who received chemotherapy (n = 9) had longer DFS than those who had hormonotherapy (n = 2) or no adjuvant therapy (n = 7) at all: median DFS was 36, 13 and 15 months, respectively (p = 0.9). Our findings do not encourage the administration of adjuvant therapy following complete CRS for GCT-relapse. Selected high-risk patients with disseminated disease may derive clinical benefit from additional chemotherapy, larger-scale multicentre studies are warranted to define treatment algorithms for this rare disease.

Identifiants

pubmed: 38200105
doi: 10.1038/s41598-024-51752-x
pii: 10.1038/s41598-024-51752-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

993

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Harika Yumru Celiksoy (H)

Department of Gynaecologic Oncology, Istanbul University Faculty of Medicine, Istanbul, Turkey. harika.yumru@istanbul.edu.tr.

Catriona Dickie (C)

Department of Gynaecologic Oncology, Imperial College London Faculty of Medicine, London, UK.

Michael J Seckl (MJ)

Department of Medical Oncology, Imperial College London Faculty of Medicine, London, UK.

Esra Aydın (E)

Department of Medical Oncology, Istanbul University Faculty of Medicine, Istanbul, Turkey.

Hamdullah Sozen (H)

Department of Gynaecologic Oncology, Istanbul University Faculty of Medicine, Istanbul, Turkey.

Samet Topuz (S)

Department of Gynaecologic Oncology, Istanbul University Faculty of Medicine, Istanbul, Turkey.

Christina Fotopoulou (C)

Department of Gynaecologic Oncology, Imperial College London Faculty of Medicine, London, UK.

Classifications MeSH