BluePrint molecular subtypes predict response to neoadjuvant pertuzumab in HER2-positive breast cancer.


Journal

Breast cancer research : BCR
ISSN: 1465-542X
Titre abrégé: Breast Cancer Res
Pays: England
ID NLM: 100927353

Informations de publication

Date de publication:
19 06 2023
Historique:
received: 15 11 2022
accepted: 25 05 2023
medline: 21 6 2023
pubmed: 20 6 2023
entrez: 19 6 2023
Statut: epublish

Résumé

The introduction of pertuzumab has greatly improved pathological complete response (pCR) rates in HER2-positive breast cancer, yet effects on long-term survival have been limited and it is uncertain which patients derive most benefit. In this study, we determine the prognostic value of BluePrint subtyping in HER2-positive breast cancer. Additionally, we evaluate its use as a biomarker for predicting response to trastuzumab-containing neoadjuvant chemotherapy with or without pertuzumab. From a cohort of patients with stage II-III HER2-positive breast cancer who were treated with neoadjuvant chemotherapy and trastuzumab with or without pertuzumab, 836 patients were selected for microarray gene expression analysis, followed by readout of BluePrint standard (HER2, Basal and Luminal) and dual subtypes (HER2-single, Basal-single, Luminal-single, HER2-Basal, Luminal-HER2, Luminal-HER2-Basal). The associations between subtypes and pathological complete response (pCR), overall survival (OS) and breast cancer-specific survival (BCSS) were assessed, and pertuzumab benefit was evaluated within the BluePrint subgroups. BluePrint results were available for 719 patients. In patients with HER2-type tumors, the pCR rate was 71.9% in patients who received pertuzumab versus 43.5% in patients who did not (adjusted Odds Ratio 3.43, 95% CI 2.36-4.96). Additionally, a significantly decreased hazard was observed for both OS (adjusted hazard ratio [aHR] 0.45, 95% CI 0.25-0.80) and BCSS (aHR 0.46, 95% CI 0.24-0.86) with pertuzumab treatment. Findings were similar in the HER2-single subgroup. No significant benefit of pertuzumab was seen in other subtypes. In patients with HER2-type or HER2-single-type tumors, pertuzumab significantly improved the pCR rate and decreased the risk of breast cancer mortality, which was not observed in other subtypes. BluePrint subtyping may be valuable in future studies to identify patients that are likely to be highly sensitive to HER2-targeting agents.

Sections du résumé

BACKGROUND
The introduction of pertuzumab has greatly improved pathological complete response (pCR) rates in HER2-positive breast cancer, yet effects on long-term survival have been limited and it is uncertain which patients derive most benefit. In this study, we determine the prognostic value of BluePrint subtyping in HER2-positive breast cancer. Additionally, we evaluate its use as a biomarker for predicting response to trastuzumab-containing neoadjuvant chemotherapy with or without pertuzumab.
METHODS
From a cohort of patients with stage II-III HER2-positive breast cancer who were treated with neoadjuvant chemotherapy and trastuzumab with or without pertuzumab, 836 patients were selected for microarray gene expression analysis, followed by readout of BluePrint standard (HER2, Basal and Luminal) and dual subtypes (HER2-single, Basal-single, Luminal-single, HER2-Basal, Luminal-HER2, Luminal-HER2-Basal). The associations between subtypes and pathological complete response (pCR), overall survival (OS) and breast cancer-specific survival (BCSS) were assessed, and pertuzumab benefit was evaluated within the BluePrint subgroups.
RESULTS
BluePrint results were available for 719 patients. In patients with HER2-type tumors, the pCR rate was 71.9% in patients who received pertuzumab versus 43.5% in patients who did not (adjusted Odds Ratio 3.43, 95% CI 2.36-4.96). Additionally, a significantly decreased hazard was observed for both OS (adjusted hazard ratio [aHR] 0.45, 95% CI 0.25-0.80) and BCSS (aHR 0.46, 95% CI 0.24-0.86) with pertuzumab treatment. Findings were similar in the HER2-single subgroup. No significant benefit of pertuzumab was seen in other subtypes.
CONCLUSIONS
In patients with HER2-type or HER2-single-type tumors, pertuzumab significantly improved the pCR rate and decreased the risk of breast cancer mortality, which was not observed in other subtypes. BluePrint subtyping may be valuable in future studies to identify patients that are likely to be highly sensitive to HER2-targeting agents.

Identifiants

pubmed: 37337299
doi: 10.1186/s13058-023-01664-x
pii: 10.1186/s13058-023-01664-x
pmc: PMC10280902
doi:

Substances chimiques

pertuzumab K16AIQ8CTM
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

71

Informations de copyright

© 2023. The Author(s).

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Auteurs

M C Liefaard (MC)

Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

A van der Voort (A)

Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

M S van Ramshorst (MS)

Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

J Sanders (J)

Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

S Vonk (S)

Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Core Facility Molecular Pathology and Biobanking, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

H M Horlings (HM)

Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

S Siesling (S)

Department of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.
Department of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, The Netherlands.

L de Munck (L)

Department of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.

A E van Leeuwen (AE)

Dutch Breast Cancer Research Group, BOOG Study Center, Amsterdam, The Netherlands.

M Kleijn (M)

Department of Research and Development, Agendia NV, Amsterdam, The Netherlands.

L Mittempergher (L)

Department of Research and Development, Agendia NV, Amsterdam, The Netherlands.

M M Kuilman (MM)

Department of Research and Development, Agendia NV, Amsterdam, The Netherlands.

A M Glas (AM)

Department of Research and Development, Agendia NV, Amsterdam, The Netherlands.

J Wesseling (J)

Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.

E H Lips (EH)

Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

G S Sonke (GS)

Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands. g.sonke@nki.nl.

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Classifications MeSH