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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.
Verreck, Eline E F; Kuijer, Anne; van Steenhoven, Julia E C; Volders, José H; van der Velden, Annette W G; Siesling, Sabine; Timmer-Bonte, Anja N H; Smilde, Tineke J; Imholz, Alex L T; Blanken-Peeters, Charlotte F J M; de Valk, Bart; Vrijaldenhoven, Suzan; Lastdrager, Willem B; Haringhuizen, Annebeth W; Hunting, Jarmo C B; Hovenga, Sjoerd; Nieboer, Peter; Zuetenhorst, Hanneke M; Tetteroo, Geert W M; Smorenburg, Carolien H; van Maaren, Marissa C; van Dalen, Thijs.
Afiliación
  • Verreck EEF; University Utrecht, Utrecht, the Netherlands. e.verreck@erasmusmc.nl.
  • Kuijer A; Department of Surgery, Diakonessenhuis, Bosboomstraat 1, 3582 KE, Utrecht, the Netherlands. e.verreck@erasmusmc.nl.
  • van Steenhoven JEC; Department of Surgery, Erasmus Medical Centre, Dr. Molewaterplein 40, 3015 GD, Rotterdam, the Netherlands. e.verreck@erasmusmc.nl.
  • Volders JH; Department of Surgery, St. Antonius Hospital, Nieuwegein, the Netherlands.
  • van der Velden AWG; Department of Surgery, Diakonessenhuis, Bosboomstraat 1, 3582 KE, Utrecht, the Netherlands.
  • Siesling S; Department of Pathology, University Medical Centre Utrecht, Utrecht, the Netherlands.
  • Timmer-Bonte ANH; Department of Surgery, Diakonessenhuis, Bosboomstraat 1, 3582 KE, Utrecht, the Netherlands.
  • Smilde TJ; Department Internal Medicine, Martini Hospital, Groningen, the Netherlands.
  • Imholz ALT; Department of Health Technology and Services Research, Technical Medical Centre, University of Twente, Enschede, the Netherlands.
  • Blanken-Peeters CFJM; Department of Research and Development, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, the Netherlands.
  • de Valk B; Department Internal Medicine, Alexander Monro Hospital, Bilthoven, the Netherlands.
  • Vrijaldenhoven S; Department Internal Medicine, Jeroen Bosch Hospital, Den Bosch, the Netherlands.
  • Lastdrager WB; Department Internal Medicine, Deventer Hospital, Deventer, the Netherlands.
  • Haringhuizen AW; Department of Surgery, Rijnstate Hospital Arnhem, Arnhem, the Netherlands.
  • Hunting JCB; Deparment Internal Medicine, Spaarne Gasthuis, Hoofddorp, the Netherlands.
  • Hovenga S; Department Internal Medicine, Noordwest Ziekenhuisgroep, Alkmaar, the Netherlands.
  • Nieboer P; Department of Surgery, Gelre Hospital, Apeldoorn, the Netherlands.
  • Zuetenhorst HM; Deparmtent Internal Medicine, Gelderse Vallei Hospital, Ede, the Netherlands.
  • Tetteroo GWM; Department Internal Medicine, St. Antonius Hospital, Nieuwegein, the Netherlands.
  • Smorenburg CH; Department Internal Medicine, Nij Smellinghe Hospital, Drachten, the Netherlands.
  • van Maaren MC; Deparment Internal Medicine, Wilhemina Hospital, Assen, the Netherlands.
  • van Dalen T; Deparment Internal Medicine, Franciscus Gasthuis, Rotterdam, the Netherlands.
Article en En | MEDLINE | ID: mdl-39349887
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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Breast Cancer Res Treat Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Breast Cancer Res Treat Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos