Evidence map›Paper›PMID 35462343›Full record

ArticleBreast (Edinburgh, Scotland)2022

Molecular subtyping reveals uniqueness of prognosis in breast ductal carcinoma in situ patients with lumpectomy.

Libo Yang, Mengjia Shen, Yan Qiu, Tingting Tang, Hong Bu

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Article in Breast (Edinburgh, Scotland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Libo YangDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China; Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, China.
Mengjia ShenDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China; Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, China.
Yan QiuDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China; Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, China.
Tingting TangDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China; Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, China.
Hong BuDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, China; Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, China. Electronic address: hongbu@scu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe aimed to analyse the discrepancy in clinical features and prognosis between molecular subtypes in primary ductal carcinoma in situ (DCIS) patients with lumpectomy.

methodsPrimary DCIS patients were identified from the Surveillance, Epidemiology, and End Results registries database from 2010 to 2017. Based on immunohistochemistry markers of hormone receptor (HR) and human epidermal growth factor receptor-2 (HER2), enrolled DCIS cases were divided into four molecular subtypes, HR-HER2-, HR-HER2+, HR + HER2+, and HR + HER2-. Clinical features and prognosis were compared between molecular subtypes. Radiotherapy (RT) effects on prognosis were also analysed in each molecular subtype.

resultsA total of 5,628 DCIS cases were retrospectively enrolled in this study. HR-HER2-, HR-HER2+, HR+HER2+, and HR+HER2- are 299 (5.3%), 498 (8.8%), 1,086 (19.3%), and 3,745 (66.5%), respectively. HR + HER2- cases have smaller tumor size (72.6%, P < 0.001) and lower grade (23.5%, P < 0.001). Comedo necrosis is more frequent in HR-HER2- (24.4%, P < 0.001) and HR-HER2+ DCIS cases (24.3%, P < 0.001). In univariate analyses, HR-HER2+ cases have significantly higher ipsilateral breast event (IBE) recurrence than HR+HER2- cases (P = 0.010). HR-HER2- cases show higher disease-specific mortality than HR+HER2+ cases (P = 0.021). In high-risk DCIS cases, RT reduces the absolute 5-year IBE incidence by 1.3%, 0.7%, 1.9%, and 2.6%, respectively in HR-HER2-, HR-HER2+, HR+HER2+, and HR+HER2- cases, respectively.

conclusionIn this population-based study, DCIS cases have diverse clinical and prognostic features for different molecular subtypes. Adjusting treatment strategies according to DCIS molecular subtypes is worth advancing.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansMastectomy, SegmentalNeoplasm Recurrence, LocalPrognosisRetrospective StudiesBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesDuctal Carcinoma in situLumpectomyMolecular subtypeRecurrence

Identifiers

PMID35462343
PMCPMC9039875

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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.