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Neoadjuvant paclitaxel/olaparib in comparison to paclitaxel/carboplatinum in patients with HER2-negative breast cancer and homologous recombination deficiency (GeparOLA study)

Authors :
Fasching, P. A.
Link, T.
Hauke, J.
Seither, F.
Jackisch, C.
Klare, P.
Schmatloch, S.
Hanusch, C.
Huober, J.
Stefek, A.
Seiler, S.
Schmitt, W. D.
Uleer, C.
Doering, G.
Rhiem, K.
Schneeweiss, A.
Engels, K.
Denkert, C.
Schmutzler, R. K.
Hahnen, E.
Untch, M.
Burchardi, N.
Blohmer, J-U
Loibl, S.
Fasching, P. A.
Link, T.
Hauke, J.
Seither, F.
Jackisch, C.
Klare, P.
Schmatloch, S.
Hanusch, C.
Huober, J.
Stefek, A.
Seiler, S.
Schmitt, W. D.
Uleer, C.
Doering, G.
Rhiem, K.
Schneeweiss, A.
Engels, K.
Denkert, C.
Schmutzler, R. K.
Hahnen, E.
Untch, M.
Burchardi, N.
Blohmer, J-U
Loibl, S.
Publication Year :
2021

Abstract

Background: The efficacy and toxicity of olaparib as combination therapy in early breast cancer (BC) patients with homologous recombinant deficiency (HRD) [score high and/or germline (g) or tumour (t) BRCA1/2 mutation] is not well described. GeparOLA (ClinicalTriais gov, NCT02789332) investigated olaparib in combination with paclitaxel in HER2-negative early BC with HRD. Patients and methods: Patients with untreated primary HER2-negative cT2-cT4a-d or cT1c with either cN + or pNSIN + or cT1c and triple-negative breast cancer (TNBC) or cT1c and Ki-67>20% BC with HRD were randomised either to paclitaxel (P) 80 mg/m(2) weekly plus olaparib (0) 100 mg twice daily for 12 weeks or P plus carboplatinum (Cb) area under the curve 2 weekly for 12 weeks, both followed by epirubicin/cyclophosphamide (EC). Stratification factors were hormone receptor (HR) status (HR versus HR ) and age (<40 versus >= 40 years). The primary endpoint was pathological complete response (pCR; ypTO/is ypNO). A two-sided one-group chi(2)-test was planned to exclude a pCR rate of <= 55% in the PO-EC arm. Secondary end points were other pCR definitions, breast conservation rate, clinical/ imaging response, tolerability and safety. Results: A total of 107 patients were randomised between September 2016 and July 2018; 106 (PO N = 69; PCb N = 37) started treatment. Median age was 47.0 years (range 25.0-71.0); 36.2% had cT1, 61.0% cT2, 2.9% cT3, and 31.8% cN-positive tumours; grade 3 tumours: 86.8%; Ki-67>20%: 89.6%; TNBC: 72.6%; confirmed gBRCA1/2 mutation: 56.2%. The pCR rate with PO was 55.1% [90% confidence interval (CI) 44.5% to 65.3%] versus PCb 48.6% (90% CI 34.3% to 63.2%). Analysis for the stratified subgroups showed higher pCR rates with PO in the cohorts of patients <40 years and HR patients. Conclusion: GeparOLA could not exclude a pCR rate of <= 55% in the PO arm. PO was significantly better tolerated and the combination merits further evaluation.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1364970676
Document Type :
Electronic Resource