Evidence map›Paper›PMID 42177446›Full record

ArticleBMC cancer2026

High TROP-2 expression as a predictor of poor neoadjuvant chemotherapy response in luminal B breast cancer: a retrospective clinicopathological study.

Çiğdem Öztürk, Safiye Sümeyye Çubukçu, Bayram Şen, Ahmet Emin Öztürk, Oğuzhan Okcu

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Article in BMC cancer, 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

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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.

Çiğdem ÖztürkDepartment of Pathology, Training and Research Hospital, Recep Tayyip Erdoğan University, Islampaşa, Şehitler Cd. No: 74, Rize Merkez, Rize, 53020, Türkiye.ORCID http://orcid.org/0000-0003-2587-214X
Safiye Sümeyye ÇubukçuDepartment of Pathology, Faculty of Medicine, Recep Tayyip Erdoğan University, Rize, Türkiye.ORCID http://orcid.org/0009-0003-1504-7813
Bayram ŞenDepartment of Biochemistry, Training and Research Hospital, Recep Tayyip Erdoğan University, Rize, Türkiye.ORCID http://orcid.org/0000-0002-4541-881X
Ahmet Emin ÖztürkDepartment of Medical Oncology, Prof Dr Cemil Tascioglu City Hospital, Health Sciences University, Istanbul, Türkiye.ORCID http://orcid.org/0000-0003-3365-5540
Oğuzhan OkcuDepartment of Pathology, Training and Research Hospital, Recep Tayyip Erdoğan University, Islampaşa, Şehitler Cd. No: 74, Rize Merkez, Rize, 53020, Türkiye. oguzhan.okcu@erdogan.edu.tr.ORCID http://orcid.org/0000-0001-7481-4718

Funding

Recep Tayyip Erdoğan University (RTEU) Scientific Research Projects Coordination Unit TSA-2025-2136
6 · The paper itself

Abstract

purposeTrophoblast cell surface antigen 2 (TROP-2) is a type I transmembrane glycoprotein that is expressed on the cell surface. It is overexpressed in various epithelial malignancies. Due to its protumoral biological effects and its role as a target receptor for antibody-drug conjugates, TROP-2 is of particular clinical interest. This study aims to investigate the relationships between TROP-2 expression, clinicopathological parameters, and response to neoadjuvant chemotherapy in invasive breast carcinomas.

methodsTROP-2 expression was evaluated by immunohistochemically from 211 cases of invasive breast carcinoma. The H-score was used in the TROP-2 assessment. Cases with a score of 0-200 were considered low, and cases with a score above 200 were considered high TROP-2 expression.

resultsHigh TROP-2 expression was significantly associated with HER2 negativity (p = 0.019), lymph node metastasis (p = 0.016), and a poor response to neoadjuvant chemotherapy (RCB-II/III) (p = 0.01). Multivariate analysis revealed that molecular subtype, stromal tumor-infiltrating lymphocytes, and high TROP-2 expression were independent predictors of neoadjuvant chemotherapy response.

conclusionHigh TROP-2 expression was found to be associated with adverse clinicopathological parameters and poor response to neoadjuvant chemotherapy, and was identified as an independent predictive biomarker for neoadjuvant response. The lower pathological complete response rates observed in luminal B molecular subtype breast carcinomas with high TROP-2 expression suggest that TROP-2-targeting agents should be investigated more thoroughly in the neoadjuvant therapy setting, particularly in LB subtype cases. Furthermore, assessing TROP-2 expression in each case will aid in optimal patient selection for treatment and contribute to the personalization of oncological therapy.

Indexed as

Antigens, NeoplasmBiomarkers, TumorBreast NeoplasmsCell Adhesion MoleculesAdultAgedErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryLymphatic MetastasisMiddle AgedNeoadjuvant TherapyPrognosisRetrospective StudiesTreatment OutcomeAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesErb-b2 Receptor Tyrosine KinasesTACSTD2 protein, humanBreast carcinomasMolecular subtypeNeoadjuvant chemotherapy responseTROP-2 expression

Identifiers

PMID42177446
PMCPMC13378071

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.