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70-Gene signature-guided adjuvant systemic treatment adjustments in early-stage ER+ breast cancer patients: 7-year follow-up of a prospective multicenter cohort study

  • Eline E.F. Verreck*
  • , Anne Kuijer
  • , Julia E.C. van Steenhoven
  • , José H. Volders
  • , Annette W.G. van der Velden
  • , Sabine Siesling
  • , Anja N.H. Timmer-Bonte
  • , Tineke J. Smilde
  • , Alex L.T. Imholz
  • , Charlotte F.J.M. Blanken-Peeters
  • , Bart de Valk
  • , Suzan Vrijaldenhoven
  • , Willem B. Lastdrager
  • , Annebeth W. Haringhuizen
  • , Jarmo C.B. Hunting
  • , Sjoerd Hovenga
  • , Peter Nieboer
  • , Hanneke M. Zuetenhorst
  • , Geert W.M. Tetteroo
  • , Carolien H. Smorenburg
  • Marissa C. van Maaren, Thijs van Dalen
*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: A previous prospective multicenter study revealed the change of the oncologists’ chemotherapy advice due to the 70-Gene signature (GS) test result in half of the estrogen receptor-positive (ER+) invasive early-stage breast cancer patients with disputable chemotherapy indication. This resulted in less patients receiving chemotherapy. This study aims to complement these results by the 7-year oncological outcomes according to the 70-GS test result and the oncologists’ pre-test advice. Methods: Patients operated for early-stage ER+ breast cancer with disputable chemotherapy indication, had been prospectively included between 2013 and 2015. Oncologists were asked whether they intended to administer adjuvant chemotherapy before deployment of the 70-GS test. Information on adjuvant systemic treatment and oncological outcome was obtained through active follow-up by data managers of the Netherlands Cancer Registry. The primary endpoint of this study was distant metastasis-free survival (DMFS) according to the genomic risk. Exploratory analyses were done to evaluate DMFS in relation to the oncologists’ pre-test advice. Results: After a median follow-up of 7 years, distant metastases were diagnosed in 23 of the 606 patients (3.8%) and 36 (5.9%) patients had died. The DMFS rate for the 357 70-GS genomic low-risk patients was 94.2% (95% CI 91.2–96.2) and 89.1% for the 249 genomic high-risk patients (95% CI 84.3–92.4). Of the low-risk patients 3% had received chemotherapy compared to 80% of the high-risk patients. For the subgroups based on the pre-test oncologists’ advice (no chemotherapy/chemotherapy/unsure) there were no clinically relevant differences in DMFS (89.8, 93.2 and 92.0%, respectively), while comparable proportions of patients had received chemotherapy. Conclusions: In patients with early-stage ER+ breast cancer with a disputable chemotherapy indication it is sensible to deploy the 70-GS to better select patients for adjuvant chemotherapy.

Original languageEnglish
Pages (from-to)331-340
Number of pages10
JournalBreast Cancer Research and Treatment
Volume209
Issue number2
Early online date30 Sept 2024
DOIs
Publication statusPublished - Jan 2025

Keywords

  • 70-Gene Signature
  • Chemotherapy decision
  • Luminal breast cancer

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