Elevated CA 15.3 in Newly Diagnosed Breast Cancer: A Retrospective Study.


Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
08 2022
Historique:
received: 05 01 2022
revised: 28 03 2022
accepted: 20 04 2022
pubmed: 7 6 2022
medline: 2 8 2022
entrez: 6 6 2022
Statut: ppublish

Résumé

To examine the relationship between baseline elevated CA 15.3 (>30 kU/L) and the prevalence of primary or secondary metastatic disease in breast cancer. We performed a retrospective, single-center cohort study on patients with newly diagnosed breast cancer and baseline CA 15.3> 30 kU/L, diagnosed between 2000-2015. Information on tumor characteristics, pre-treatment CA 15.3, staging results, treatment approach, disease recurrence and death were collected from individual medical files. For every tumor subtype, the optimal cut-off value of CA 15.3 for determining primary metastatic disease is determined. Eight hundred ninety-four patients with baseline CA15.3 > 30 kU/L were included of which 38% were diagnosed with primary metastatic disease while 15% subsequently developed secondary metastatic disease, with a median follow-up of 74 months. LuminalHER2 tumors had the highest proportion of primary metastatic disease (48%), Triple Negative tumors had the highest proportion of secondary metastatic disease (24%) (p=0.008). A higher CA 15.3 value corresponds to higher risk of both primary and secondary metastatic disease (p<0.001). For the determination of primary metastatic disease, optimal cut-off values for CA 15.3 range between 44 kU/L (Triple Negative) and 59 kU/L (Luminal B). In patients with newly diagnosed breast cancer and baseline elevated CA 15.3>30 kU/L, 38% presents with primary metastatic disease and 15% develops secondary metastatic disease, with a median follow-up of 74 months. Our results can help clinicians to identify patients at risk of primary or secondary metastatic disease via information on tumor subtype and baseline CA 15.3.

Identifiants

pubmed: 35668001
pii: S1526-8209(22)00076-3
doi: 10.1016/j.clbc.2022.04.007
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

579-587

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

Jannes Heylen (J)

Department of Internal Medicine, University Hospitals Leuven, Leuven, Belgium. Electronic address: jannes.heylen@student.kuleuven.be.

Kevin Punie (K)

Department of General Medical Oncology/Multidisciplinary Breast Center, University Hospitals Leuven - Campus Gasthuisberg, Leuven, Belgium.

Ann Smeets (A)

Surgical Oncology/Multidisciplinary Breast Center, University Hospitals Leuven - Campus Gasthuisberg, Leuven, Belgium.

Patrick Neven (P)

Department of Gynaecological Oncology/Multidisciplinary Breast Center, University Hospitals Leuven - Campus Gasthuisberg, Leuven, Belgium.

Caroline Weltens (C)

Department of Radiotherapy/Multidisciplinary Breast Center, University Hospitals Leuven - Campus Gasthuisberg, Leuven, Belgium.

Annouschka Laenen (A)

Department of Public Health and Primary Care, Interuniversity Institute for Biostatistics and Statistical Bioinformatics, Catholic University Leuven, Leuven, Belgium.

Hans Wildiers (H)

Department of General Medical Oncology/Multidisciplinary Breast Center, University Hospitals Leuven - Campus Gasthuisberg, Leuven, Belgium.

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Classifications MeSH