Survival Benefit of Palliative Oophorectomy for Patients With Ovarian Metastasis From Baseline Metastatic Gastric Adenocarcinoma

M Matheus Sewastjanow-Silva (The University of Texas MD Anderson Cancer Center, Houston, TX) L Lianchun Xiao A Ahmed Abdelhakeem (2Mayo Clinic, Jacksonville, United States) C Cindy M. Pabon (Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX) K Kohei Yamashita (Department of Gastroenterological Surgery, Graduate School of Medical Sciences, Kumamoto University) K Katsuhiro Yoshimura B Brian D. Badgwell (The University of Texas MD Anderson Cancer Center, Houston, TX) N Naruhiko Ikoma (The University of Texas MD Anderson Cancer Center, Houston, TX) L Larissa Meyer (Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX) T Tara Sagebiel (Department of Abdominal Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX) P Prajnan Das (The University of Texas MD Anderson Cancer Center, Houston, TX) J Jenny J. Li (Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX) J Jaffer A. Ajani M Mariela A. Blum-Murphy (Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX)

Abstract

PURPOSE To compare overall survival (OS) in patients with baseline metastatic gastric adenocarcinoma (GA) with and without ovarian metastasis (OM). Furthermore, within the group that had ovarian metastases, we aimed to assess whether there was a survival benefit (SB) with palliative oophorectomy (PO). PATIENTS AND METHODS This is a single-institution retrospective analysis of the clinicopathological features of women diagnosed with metastatic GA with a comparison of outcomes based on PO status. We identified 240 women with baseline metastatic GAs who were treated at MD Anderson Cancer Center between February 2003 and September 2022. Among these women, we categorized a subgroup of 102 women who had OM from their primary GA. Patients were analyzed whether they underwent PO. RESULTS Patients who developed OM were most often non-Caucasian, had peritoneal involvement, and had tumors that were both human epidermal growth factor receptor 2–negative and PD-L1–negative, with signet ring cell features and diffuse histological type. Among patients with ovarian metastases, those who had PO had an Eastern Cooperative Oncology Group = 0, more comprehensive molecular and immunohistochemical profiling, lower percentage of family history of gastroesophageal malignancies, and lower interval between diagnosis of the GA primary and the OM. PO was associated with significantly improved OS in this subgroup (hazard ratio, 0.5 [95% CI, 0.31 to 0.81]; P = .005). CONCLUSION To our knowledge, this is the largest multiethnic population study assessing SB of PO in patients with GA with OM. Additionally, it is the largest study analyzing survival in this population according to the patient's multiethnic characteristics and metastasis timing and growth patterns. PO presents as a therapeutic option for women with GAs with OM if the patient is clinically suitable for surgical resection.

Article Details

Volume / Issue Vol. 43, Issue 21
Published July 20, 2025
Pages 2361-2371
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

M

Matheus Sewastjanow-Silva

The University of Texas MD Anderson Cancer Center, Houston, TX

L

Lianchun Xiao

A

Ahmed Abdelhakeem

2Mayo Clinic, Jacksonville, United States

C

Cindy M. Pabon

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

K

Kohei Yamashita

Department of Gastroenterological Surgery, Graduate School of Medical Sciences, Kumamoto University

K

Katsuhiro Yoshimura

B

Brian D. Badgwell

The University of Texas MD Anderson Cancer Center, Houston, TX

N

Naruhiko Ikoma

The University of Texas MD Anderson Cancer Center, Houston, TX

L

Larissa Meyer

Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX

T

Tara Sagebiel

Department of Abdominal Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX

P

Prajnan Das

The University of Texas MD Anderson Cancer Center, Houston, TX

J

Jenny J. Li

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

J

Jaffer A. Ajani

M

Mariela A. Blum-Murphy

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX