Limiting systemic endocrine overtreatment in postmenopausal breast cancer patients with an ultralow classification of the 70-gene signature.


Journal

Breast cancer research and treatment
ISSN: 1573-7217
Titre abrégé: Breast Cancer Res Treat
Pays: Netherlands
ID NLM: 8111104

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 19 11 2021
accepted: 30 04 2022
pubmed: 20 5 2022
medline: 1 7 2022
entrez: 19 5 2022
Statut: ppublish

Résumé

Guidelines recommend endocrine treatment for estrogen receptor-positive (ER+) breast cancers for up to 10 years. Earlier data suggest that the 70-gene signature (MammaPrint) has potential to select patients that have an excellent survival without chemotherapy and limited or no tamoxifen treatment. The aim was to validate the 70-gene signature ultralow-risk classification for endocrine therapy decision making. In the IKA trial, postmenopausal patients with non-metastatic breast cancer had been randomized between no or limited adjuvant tamoxifen treatment without receiving chemotherapy. For this secondary analysis, FFPE tumor material was obtained of ER+HER2- patients with 0-3 positive lymph nodes and tested for the 70-gene signature. Distant recurrence-free interval (DRFI) long-term follow-up data were collected. Kaplan-Meier curves were used to estimate DRFI, stratified by lymph node status, for the three predefined 70-gene signature risk groups. A reliable 70-gene signature could be obtained for 135 patients. Of the node-negative and node-positive patients, respectively, 20% and 13% had an ultralow-risk classification. No DRFI events were observed for node-negative patients with an ultralow-risk score in the first 10 years. The 10-year DRFI was 90% and 66% in the low-risk (but not ultralow) and high-risk classified node-negative patients, respectively. These survival analyses indicate that the postmenopausal node-negative ER+HER2- patients with an ultralow-risk 70-gene signature score have an excellent 10-year DRFI after surgery with a median of 1 year of endocrine treatment. This is in line with published results of the STO-3-randomized clinical trial and supports the concept that it is possible to reduce the duration of endocrine treatment in selected patients.

Identifiants

pubmed: 35587322
doi: 10.1007/s10549-022-06618-z
pii: 10.1007/s10549-022-06618-z
pmc: PMC9239940
doi:

Substances chimiques

Antineoplastic Agents, Hormonal 0
Tamoxifen 094ZI81Y45

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

265-278

Informations de copyright

© 2022. The Author(s).

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Auteurs

M Opdam (M)

Department of Molecular Pathology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands.

V van der Noort (V)

Biometrics Department, Netherlands Cancer Institute, Amsterdam, Netherlands.

M Kleijn (M)

Medical Affairs, Agendia NV, Amsterdam, Netherlands.

A Glas (A)

Medical Affairs, Agendia NV, Amsterdam, Netherlands.

I Mandjes (I)

Biometrics Department, Netherlands Cancer Institute, Amsterdam, Netherlands.

S Kleiterp (S)

Department of Molecular Pathology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands.

F S Hilbers (FS)

Department of Molecular Pathology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands.

D T Kruger (DT)

Department of Molecular Pathology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands.

A D Bins (AD)

Department of Medical Oncology, Amsterdam UMC, Amsterdam, Netherlands.

P C de Jong (PC)

Department of Medical Oncology, Sint-Antonius Hospital, Nieuwegein, Netherlands.

P P J B M Schiphorst (PPJBM)

Department of Internal Medicine, Streekziekenhuis Koningin. Beatrix, Winterswijk, Netherlands.

T van Dalen (T)

Department of Surgery, Diakonessenhuis, Utrecht, Netherlands.

B Flameling (B)

Department of Medical Oncology, OLVG, Amsterdam, Netherlands.

R C Rietbroek (RC)

Department of Internal Medicine, Red Cross Hospital, Beverwijk, Netherlands.

A Beeker (A)

Department of Medical Oncology, Spaarne Gasthuis, Hoofddorp, Netherlands.

S M van den Heiligenberg (SM)

Department of Medical Oncology, Dijklander Ziekenhuis, Hoorn, Netherlands.

S D Bakker (SD)

Department of Internal Medicine, Zaans Medisch Centrum, Zaandam, Netherlands.

A N M Wymenga (ANM)

Department of Medical Oncology, Medisch Spectrum Twente, Enschede, Netherlands.

I M Oving (IM)

Department of Medical Oncology, Ziekenhuisgroep Twente, Almelo, the Netherlands.

R M Bijlsma (RM)

Department of Medical Oncology, UMCU, Utrecht, Netherlands.

P J van Diest (PJ)

Department of Pathology, UMCU, Utrecht, Netherlands.

J B Vermorken (JB)

Department of Medical Oncology, University Hospital Antwerp (UZA), Edegem, Belgium.
Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

H van Tinteren (H)

Biometrics Department, Netherlands Cancer Institute, Amsterdam, Netherlands.
Trial and Data Center, Princess Maxima Centre for Pediatric Oncology, Heidelberglaan 25, 3584 CS, Utrecht, The Netherlands.
Department of Medical Oncology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands.

S C Linn (SC)

Department of Molecular Pathology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands. s.linn@nki.nl.
Department of Medical Oncology, UMCU, Utrecht, Netherlands. s.linn@nki.nl.
Department of Medical Oncology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands. s.linn@nki.nl.

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