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Ten-year follow-up of the observational RASTER study, prospective evaluation of the 70-gene signature in ER-positive, HER2-negative, node-negative, early breast cancer

Authors :
Sonja B. Vliek
Florentine S. Hilbers
Agnes Jager
Valesca P. Retèl
Jolien M. Bueno de Mesquita
Caroline A. Drukker
Sanne C. Veltkamp
Anneke M. Zeillemaker
Emiel J. Rutgers
Harm van Tinteren
Wim H. van Harten
Laura J. van 't Veer
Marc J. van de Vijver
Sabine C. Linn
Pathology
CCA - Imaging and biomarkers
CCA - Cancer Treatment and Quality of Life
Medical Oncology
Health Technology & Services Research
Source :
European Journal of Cancer, 175, 169-179. Elsevier Limited, European Journal of Cancer, 175, 169-179. Elsevier Ltd., European journal of cancer, 175, 169-179. Elsevier
Publication Year :
2022

Abstract

Introduction: Prognostic gene expression signatures can be used in combination with classical clinicopathological factors to guide adjuvant chemotherapy decisions in ER-positive, HER2-negative breast cancer. However, long-term outcome data after introduction of genomic testing in the treatment decision-making process are limited. Methods: In the prospective RASTER study, the tumours of 427 patients with cTanyN0M0 breast cancer were tested to assess the 70-gene signature (MammaPrint). The results were provided to their treating physician to be incorporated in the decision-making on adjuvant systemic therapy. Here, we report the long-term outcome of the 310 patients with ER-positive, HER2-negative tumours by clinical and genomic risk categories at a median follow-up of 10.3 years. Results: Among the clinically high-risk patients, 45 (49%) were classified as genomically low risk. In this subgroup, at 10 years, distant recurrence free interval (DRFI) was similar between patients treated with (95.7% [95% CI 87.7–100]) and without (95.5% [95% CI 87.1–100]) chemotherapy. Within the group of clinically low-risk patients, 56 (26%) were classified as genomically high risk. Within the clinically low-risk group, beyond 5 years, a difference emerged between the genomically high- and low-risk subgroup resulting in a 10-year DRFI of 84.3% (95% CI 74.8–95.0) and 93.4% (95% CI 89.5–97.5), respectively. Interestingly, genomic ultralow-risk patients have a 10-year DRFI of 96.7% (95% CI 90.5–100), largely (79%) without systemic therapy. Conclusions: These data confirm that clinically high-risk, genomically low-risk tumours have an excellent outcome in the real-world setting of shared decision-making. Together with the updated results of the MINDACT trial, these data support the use of the MammaPrint, in ER-positive, HER2-negative, node-negative, clinically high-risk breast cancer patients. Registry: ISRCTN71917916

Details

Language :
English
ISSN :
09598049
Volume :
175
Database :
OpenAIRE
Journal :
European Journal of Cancer
Accession number :
edsair.doi.dedup.....4d7edd507887970d9814de1ccbf3990d