Evidence map›Paper›PMID 42151664›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Receptor status, molecular subtypes, and survival outcomes of breast cancer following gastric cancer compared with single primary breast cancer.

Ahmet Necati Sanli, Bilal Turan, Deniz Esin Tekcan Sanli, Isa Karaca, Fatih Aydogan

Abstract readComparative Study
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ahmet Necati SanliDepartment of General Surgery, Abdulkadir Yuksel State Hospital, Gaziantep, Türkiye.
Bilal TuranDepartment of General Surgery, Faculty of Medicine, Suleyman Demirel University, Isparta, Türkiye. bturan117@gmail.com.ORCID http://orcid.org/0000-0003-1665-3607
Deniz Esin Tekcan SanliDepartment of Radiology, Faculty of Medicine, Gaziantep University, Gaziantep, Türkiye.
Isa KaracaDepartment of General Surgery, Faculty of Medicine, Suleyman Demirel University, Isparta, Türkiye.
Fatih AydoganAcıbadem Altunizade and Atasehir Hospitals, Istanbul, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBreast cancer is a common second primary malignancy among gastric cancer survivors, yet its biological characteristics and clinical outcomes in this population are not well defined. This study aimed to compare molecular features and survival outcomes between breast cancer developing after gastric cancer and single primary breast cancer, and to clarify whether adverse prognosis is related to tumor biology or patient-related factors. MATERIALS AND

methodsThis retrospective population-based study was conducted using the SEER database. Female patients with breast cancer following gastric cancer were compared with those diagnosed with single primary invasive breast cancer. Molecular subtypes, receptor status, clinicopathologic characteristics, and treatment variables were analyzed. Multivariable logistic regression was used to assess associations with molecular features. Overall survival (OS) and breast cancer-specific survival (CSS) were evaluated using Kaplan-Meier analysis and multivariable Cox regression models.

resultsAmong 593,811 included patients, 266 developed breast cancer after gastric cancer. No significant differences were observed between groups in estrogen receptor, progesterone receptor, HER2 status, or molecular subtype distribution. Prior gastric cancer was not independently associated with breast cancer molecular characteristics. Overall survival was significantly worse in patients with a history of gastric cancer (HR, 1.64), whereas breast cancer-specific survival was comparable between groups. Patients with prior gastric cancer were less likely to receive chemotherapy and radiotherapy.

conclusionBreast cancer developing after gastric cancer shows molecular characteristics similar to primary breast cancer. Inferior overall survival appears to be driven by patient-related factors, such as age, comorbidities, and differences in treatment intensity, rather than tumor biology. Preserved CSS indicates comparable responsiveness to standard treatments and underscores the need to avoid unnecessary undertreatment in this patient population.

Indexed as

Breast NeoplasmsNeoplasms, Second PrimaryStomach NeoplasmsAdultAgedErb-b2 Receptor Tyrosine KinasesFemaleHumansKaplan-Meier EstimateMiddle AgedPrognosisReceptors, EstrogenReceptors, ProgesteroneRetrospective StudiesSEER ProgramSurvival RateERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneBreast cancerGastric cancerMolecular subtypeSecond primary malignancySurvivorship

Identifiers

PMID42151664

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