Population-based Study of Prosigna-PAM50 and Outcome Among Postmenopausal Women With Estrogen Receptor-positive and HER2-negative Operable Invasive Lobular or Ductal Breast Cancer.


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 2020
Historique:
received: 23 07 2019
revised: 18 01 2020
accepted: 26 01 2020
pubmed: 8 4 2020
medline: 9 10 2021
entrez: 8 4 2020
Statut: ppublish

Résumé

The Prosigna-PAM50 risk of recurrence (ROR) score has documented clinical utility for the prediction of 10-year distant recurrence (DR). The present study investigated the value of Prosigna-PAM50 for predicting 10-year DR and overall survival after 5 years of endocrine treatment for postmenopausal patients with invasive lobular carcinoma. Using the Danish Breast Cancer Group database, we identified patients with a diagnosis from 2000 to 2003 of estrogen receptor-positive, human epidermal growth factor receptor 2-negative invasive ductal (n = 1570) or lobular (n = 341) cancer > 20 mm or 1 to 3 positive lymph nodes and applied multivariate Cox models. The median follow-up for DR was 9.3 years and for overall survival 15.2 years. Of the 341 lobular and 1570 ductal cases, 140 (41%) and 349 (22%) were classified as low ROR, with a 10-year DR rate of 7.7% (95% confidence interval [CI], 3.7%-13.6%) and 3.5% (95% CI, 1.8%-6.2%), respectively. The 10-year DR rate for the intermediate ROR group for those with lobular cancer was 18% (95% CI, 10.1%-27.9%) compared with 9.7% (95% CI, 6.7%-13.4%) for those with ductal cancer. Luminal B tumors had a significantly worse outcome than luminal A tumors in both lobular (hazard ratio, 1.89; 95% CI, 1.03%-3.45%; P = .04) and ductal (hazard ratio, 3.18; 95% CI, 2.29%-4.43%; P < .0001) cancer. Prosigna PAM-50 provides significant prognostic information beyond the clinicopathologic factors in patients with invasive lobular breast cancer. Those with lobular cancer had worse 10-year DR rates compared with those with ductal cancer in the same ROR category. Our results could have an effect on the treatment decisions regarding the addition of chemotherapy for those in the intermediate ROR group.

Identifiants

pubmed: 32253134
pii: S1526-8209(20)30029-X
doi: 10.1016/j.clbc.2020.01.013
pii:
doi:

Substances chimiques

Antineoplastic Agents, Hormonal 0
Aromatase Inhibitors 0
Biomarkers, Tumor 0
Receptors, Estrogen 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e423-e432

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Anne-Vibeke Lænkholm (AV)

Department of Surgical Pathology, Zealand University Hospital, Slagelse, Denmark. Electronic address: anlae@regionsjaelland.dk.

Maj-Britt Jensen (MB)

Danish Breast Cancer Cooperative Group, Rigshospitalet, Copenhagen, Denmark.

Jens Ole Eriksen (JO)

Department of Surgical Pathology, Zealand University Hospital, Slagelse, Denmark.

Anne Roslind (A)

Department of Pathology, Herlev and Gentofte Hospital, Herlev, Denmark.

Wesley Buckingham (W)

NanoString Technologies Inc, Seattle, WA.

Sean Ferree (S)

NanoString Technologies Inc, Seattle, WA.

Torsten Nielsen (T)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.

Bent Ejlertsen (B)

Danish Breast Cancer Cooperative Group, Rigshospitalet, Copenhagen, Denmark; Department of Oncology, Danish Breast Cancer Cooperative Group, Rigshospitalet, Copenhagen, Denmark.

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Classifications MeSH