Evidence map›Paper›PMID 40583394›Full record

ArticleFuture oncology (London, England)2025

Optimizing neoadjuvant treatment in HER2-positive breast cancer: the role of HER2, HR, PD-L1 expression and regimen selection.

Mei Dai, Danhua Zhang, Chen Wu, Lun Li

Abstract read
In one paragraph

Article in Future oncology (London, England), 2025. 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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

4 authors.

Mei DaiDepartment of General Surgery, Second Xiangya Hospital, Central South University, Changsha, China.
Danhua ZhangDepartment of General Surgery, Second Xiangya Hospital, Central South University, Changsha, China.
Chen WuDepartment of Medical Cosmetology and Aesthetic Plastic Surgery, The First People Hospital of Changde City, Central South University, Changde, China.
Lun LiDepartment of General Surgery, Second Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-5651-1067

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough neoadjuvant therapy (NAT) significantly improves the pathological complete response (pCR) rate in HER2-positive breast cancer patients, approximately 30-40% of patients remain non-responsive. Identifying predictive factors is critical for treatment optimization.

methodsWe retrospectively analyzed 179 HER2-positive breast cancer patients treated with NAT (without immunotherapy) followed by surgery at our center between August 2022 and October 2024. Clinicopathological data, treatment regimens, and pCR status were assessed. Logistic regression and ROC analysis determined independent predictors and PD-L1 cutoff.

resultsHormone receptor (HR)-negative status (OR = 2.36, 1.12-5.01), HER2 3+ (OR = 7.84, 2.34-26.31), and high PD-L1 (CPS >27.5, OR = 3.42, 1.18-9.87) independently predicted pCR. The pCR rates for the TCbHP and THP regimens were 67.4% and 60.0%, respectively, with no statistically significant difference (

conclusionHER2 3+, PD-L1 CPS > 27.5 and HR-negative are independent predictors of pCR. The TCbHP and THP regimens have comparable efficacy, and both are superior to the AC-THP regimen.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesNeoadjuvant TherapyAdultAgedBiomarkers, TumorFemaleHumansMiddle AgedReceptors, EstrogenReceptors, ProgesteroneRetrospective StudiesTrastuzumabTreatment OutcomeB7-H1 AntigenBiomarkers, TumorCD274 protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneTrastuzumabbreast cancerERBB2HER2neoadjuvant therapypCRPD-L1

Identifiers

PMID40583394
PMCPMC12330251

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