Back to Search Start Over

Endocrine Therapy Response and 21-Gene Expression Assay for Therapy Guidance in HR+/HP2-Early Breast Cancer

Authors :
Nitz, Ulrike A.
Gluz, Oleg
Kuemmel, Sherko
Christgen, Matthias
Braun, Michael
Aktas, Bahriye
Luedtke-Heckenkamp, Kerstin
Forstbauer, Helmut
Grischke, Eva-Maria
Schumacher, Claudia
Darsow, Maren
Krauss, Katja
Nuding, Benno
Thill, Marc
Potenberg, Jochem
Uleer, Christoph
Warm, Mathias
Fischer, Hans Holger
Malter, Wolfram
Hauptmann, Michael
Kates, Ronald E.
Graeser, Monika
Wuerstlein, Rachel
Shak, Steven
Baehner, Frederick
Kreipe, Hans H.
Harbeck, Nadia
Nitz, Ulrike A.
Gluz, Oleg
Kuemmel, Sherko
Christgen, Matthias
Braun, Michael
Aktas, Bahriye
Luedtke-Heckenkamp, Kerstin
Forstbauer, Helmut
Grischke, Eva-Maria
Schumacher, Claudia
Darsow, Maren
Krauss, Katja
Nuding, Benno
Thill, Marc
Potenberg, Jochem
Uleer, Christoph
Warm, Mathias
Fischer, Hans Holger
Malter, Wolfram
Hauptmann, Michael
Kates, Ronald E.
Graeser, Monika
Wuerstlein, Rachel
Shak, Steven
Baehner, Frederick
Kreipe, Hans H.
Harbeck, Nadia
Publication Year :
2022

Abstract

PURPOSE To our knowledge, WSG-ADAPT-HR+/HER2- (ClinicalTrials.gov identifier: NCT01779206; n = 5,625 registered) is the first trial combining the 21-gene expression assay (recurrence score [RS]) and response to 3-week preoperative endocrine therapy (ET) to guide systemic therapy in early breast cancer. MATERIALS AND METHODS Baseline and postendocrine Ki67 (Ki67(post)) were evaluated centrally. In the en docrine trial, all patients received exclusively ET: patients with pathologic regional lymph node status (pN) 0-1 (ie, 0-3 involved lymph nodes) entered control arm if RS <= 11 and experimental arm if RS12-25 with ET response (Ki67(post) <= 10%). All other patients (including N0-1 RS12-25 without ET response) received dose-dense chemotherapy (CT) followed by ET in the CT trial. Primary end point of the endocrine trial was non-inferiority of 5-year invasive disease-free survival (5y-iDFS) in experimental (v control) arm; secondary end points included distant DFS, overall survival, and translational research. RESULTS Intention-to-treat population comprised 2,290 patients (n = 1,422 experimental v n = 868 control): 26.3% versus 34.6% premenopausal and 27.4% versus 24.0% pN1. One-sided 95% lower confidence limit of the 5y-iDFS difference was -3.3%, establishing prespecified noninferiority (P = .05). 5y-iDFS was 92.6% (95% CI, 90.8 to 94.0) in experimental versus 93.9% (95% CI, 91.8 to 95.4) in control arm; 5-year distant DFS was 95.6% versus 96.3%, and 5-year overall survival 97.3% versus 98.0%, respectively. Differences were similar in age and nodal subgroups. In N0-1 RS12-25, outcome of ET responders (ET alone) was comparable with that of ET nonresponders (CT) for age > 50 years and superior for age <= 50 years. ET response was more likely with aromatase inhibitors (mostly postmenopausal) than with tamoxifen (mostly premenopausal): 78.1% versus 41.1% (P< .001). ET response was 78.8% in RS0-11, 62.2% in RS12-25, and 32.7% in RS > 25 (n = 4,203, P < .001). CONCLUSION WSG

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1383745338
Document Type :
Electronic Resource