Extended endocrine therapy after 5 years of adjuvant LHRH-agonist in premenopausal patients with node-positive hormone receptor (HR)-positive early breast cancer.
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
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Carmine Valenza
Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA
Yue Zheng
State Key Laboratory of Marine Environmental Science, College of the Environment and Ecology, Xiamen University
Monica Milano
Division of Medical Senology, European Institute of Oncology IRCCS, Milan, Italy
Elisa Giordano
Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy
Lorenzo Guidi
Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy
Pier Paolo Maria Berton Giachetti
European Institute of Oncology IRCCS, Milan, Italy
Laura Boldrini
Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy
Grazia Castellano
Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy
Jalissa Katrini
Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan, Italy
Bianca Malagutti
Division of Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, University of Milan, Milan, Italy
Gabriele Antonarelli
Division of Early Drug Development, European Institute of Oncology IRCCS, University of Milan, Milano, MI, Italy
Fabio Conforti
Division of Medical Oncology, Humanitas Gavazzeni, Bergamo, Italy
Eleonora Pagan
Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy
Vincenzo Bagnardi
Department of Statistics and Quantitative Methods, University of Milano-Bicocca, Milan, Italy
Gregory John Kirkner
Dana-Farber Cancer Institute, Boston, MA
Dario Trapani
Kate Dibble
Dana-Farber Cancer Institute, Boston, MA
Elisabetta Munzone
Giuseppe Curigliano
Ann H. Partridge
Dana–Farber Cancer Institute, Harvard Medical School, Boston