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Endocrine Abstracts (2024) 99 P308 | DOI: 10.1530/endoabs.99.P308

1Alexandra Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece, Endocrine Unit and Diabetes Center, Department of Clinical Therapeutics, Athens, Greece; 2Alexandra Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece., Hematology and Oncology Unit, Department of Clinical Therapeutics, Athens, Greece; 3Aretaieio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece., 2nd Department of Obstetrics and Gynaecology,, Athens, Greece; 4Alexandra Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece., 1st Department of Obstetrics and Gynaecology, Athens, Greece


Introduction: Survival rates for ovarian cancer remain distressingly low. Despite established prognostic factors, the need for identifying modifiable parameters to influence survival outcomes is imperative. Overweight and obesity, prevalent conditions, have been implicated in cancer development and potentially poor survival. However, conflicting data on the association of Body Mass Index (BMI) with Progression-Free Survival (PFS) and Overall Survival (OS) in ovarian cancer patients necessitate further exploration.

Aim: This study aims to investigate the prognostic role of BMI before chemotherapy in women with ovarian cancer, specifically focusing on PFS and OS.

Patients and methods: A retrospective analysis encompassed 1136 patients diagnosed with ovarian carcinomas between 1995 and 2018. Patients were categorized based on BMI at presentation, and a comprehensive examination of clinicopathological, treatment, and survival data was conducted.

Results: In the patient population, normal weight patients (BMI<25 kg/m2) demonstrated a median PFS of 12.8 months (95% CI 11.7–13.9 months), while overweight/obese patients (BMI≥25 kg/m2) exhibited a significantly longer median PFS of 14.9 months (95% CI 13.6–16.4 months, P=0.006). No statistically significant difference was noted in median OS between the two BMI groups. Subgroup analysis for different histological subtypes revealed a statistically significant benefit for overweight and obese patients with serous and endometrioid histology (mPFS 12.9 months, 95% CI 11.7–14.0 vs 15.6 months, 95% CI 13.9–17.3, P=0.012 and 14.6 months 95% CI 13.7–15.5 vs 25.6 months, 95% CI 9.5–41.7, P=0.031, respectively). Additionally, BMI≥25 kg/m2 demonstrated a significant advantage in advanced-stage disease.

Conclusions: The study underscores the intricate association between BMI and ovarian cancer prognosis. While PFS demonstrated a significant difference between BMI groups, OS did not exhibit such disparity.

Volume 99

26th European Congress of Endocrinology

Stockholm, Sweden
11 May 2024 - 14 May 2024

European Society of Endocrinology 

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