Extended endocrine therapy after 5 years of adjuvant LHRH-agonist in premenopausal patients with node-positive hormone receptor (HR)-positive early breast cancer.

C Carmine Valenza (Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA) Y Yue Zheng (State Key Laboratory of Marine Environmental Science, College of the Environment and Ecology, Xiamen University) M Monica Milano (Division of Medical Senology, European Institute of Oncology IRCCS, Milan, Italy) E Elisa Giordano (Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy) L Lorenzo Guidi (Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy) P Pier Paolo Maria Berton Giachetti (European Institute of Oncology IRCCS, Milan, Italy) L Laura Boldrini (Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy) G Grazia Castellano (Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy) J Jalissa Katrini (Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy) B Bianca Malagutti (Division of Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, University of Milan, Milan, Italy) G Gabriele Antonarelli (Division of Early Drug Development, European Institute of Oncology IRCCS, University of Milan, Milano, MI, Italy) F Fabio Conforti (Division of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy) E Eleonora Pagan (Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy) V Vincenzo Bagnardi (Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy) G Gregory John Kirkner (Dana-Farber Cancer Institute, Boston, MA) D Dario Trapani K Kate Dibble (Dana-Farber Cancer Institute, Boston, MA) E Elisabetta Munzone G Giuseppe Curigliano A Ann H. Partridge (Dana–Farber Cancer Institute, Harvard Medical School, Boston)

Abstract

537 Background: There is no evidence regarding the benefit of extended endocrine therapy (eET) beyond 5 years of adjuvant treatment with LHRH agonists (LHRHa) in premenopausal women with node-positive, HR-positive early breast cancer (eBC). Methods: We conducted a retrospective study on two prospectively maintained datasets (Young Women Study and IEO Breast Cancer Dataset) to evaluate the clinical benefit of eET in women who had completed 5 years of adjuvant LHRHa, remained premenopausal, and had no evidence of distant or locoregional recurrence. This study included <40y women at diagnosis (between 2006 and 2016) with node-positive HR+ eBC, with ductal, lobular, or mixed histological subtypes, receiving or not eET (tamoxifen monotherapy or LHRHa+tamoxifen/aromatase inhibitor [AI]). The primary endpoint was the invasive breast cancer-free survival (IBCFS), calculated from the 5th year of endocrine therapy (ET) and adjusted for dataset, age at diagnosis, histotype, stage, disease subtype, type of adjuvant chemotherapy and ET received. Results: 503 patients were included (see Table): 287 received eET for a median duration of 3.6 years (Interquartile Range: 2.1–5.0). At a median follow-up of 7.05 years (calculated from the 5th year of ET), 50 and 72 IBCFS events occurred in the eET and non-eET groups, respectively. The adjusted Hazard Ratio (HR) for IBCFS comparing the eET to the non-eET group was 0.60 (95% CI,0.41-0.88; p<0.001). For distant recurrence or death, 28 and 46 events occurred, respectively, and the adjusted HR for distant disease free-survival was 0.43 (95% CI, 0.27-0.71). Among patients receiving eET, the adjusted HR for IBCFS comparing tamoxifen monotherapy (n=137) with LHRHa+tamoxifen/AI (n=150) was 0.75 (95% CI, 0.41-1.38). Conclusions: Extending endocrine therapy beyond five years of LHRHa treatment resulted in significantly higher IBCFS and distant metastasis free-survival. Larger prospective studies are required to confirm this finding and determine the most effective eET strategy. Patients' characteristics. Characteristic Extended endocrine therapy(N=287) No extended endocrine therapy(N=216) Age at diagnosis, median (IQR) 37 (35-39) 37 (33-39) Dataset: IEO | YWS, n 273 | 14 212 | 4 Histotype: ductal | lobular | mixed, % 91 | 5 | 4 95 | 3 | 2 pT: pT1 | pT2 | pT3-4, % 37 | 48 | 15 41 | 52 | 7 pN: pN1 | pN2 | pN3, % 64 | 22 | 14 73 | 17 | 10 Luminal A-like | B-like (G3 or HER2+), % 47 | 53 49 | 51 LHRHa combination during years 1-5: tamoxifen | aromatase inhibitor, % 66 | 34 76 | 22 Previous chemotherapy, % 77 70 Previous radiotherapy, % 64 62 G3, grade 3; IEO, European Institute of Oncology; IQR, interquartile range; YWS, Young Women Study.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 537-537
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

C

Carmine Valenza

Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA

Y

Yue Zheng

State Key Laboratory of Marine Environmental Science, College of the Environment and Ecology, Xiamen University

M

Monica Milano

Division of Medical Senology, European Institute of Oncology IRCCS, Milan, Italy

E

Elisa Giordano

Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy

L

Lorenzo Guidi

Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy

P

Pier Paolo Maria Berton Giachetti

European Institute of Oncology IRCCS, Milan, Italy

L

Laura Boldrini

Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy

G

Grazia Castellano

Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy

J

Jalissa Katrini

Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy

B

Bianca Malagutti

Division of Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, University of Milan, Milan, Italy

G

Gabriele Antonarelli

Division of Early Drug Development, European Institute of Oncology IRCCS, University of Milan, Milano, MI, Italy

F

Fabio Conforti

Division of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy

E

Eleonora Pagan

Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy

V

Vincenzo Bagnardi

Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy

G

Gregory John Kirkner

Dana-Farber Cancer Institute, Boston, MA

D

Dario Trapani

K

Kate Dibble

Dana-Farber Cancer Institute, Boston, MA

E

Elisabetta Munzone

G

Giuseppe Curigliano

A

Ann H. Partridge

Dana–Farber Cancer Institute, Harvard Medical School, Boston