Neoadjuvant buparlisib plus trastuzumab and paclitaxel for women with HER2+ primary breast cancer: A randomised, double-blind, placebo-controlled phase II trial (NeoPHOEBE)

Loibl S, De La Pena L, Nekljudova V, Zardavas D, Michiels S, Denkert C, Rezai M, Bermejo B, Untch M, Lee SC, Turri S, Urban P, Kuemmel S, Steger G, Gombos A, Lux MP, Piccart MJ, Von Minckwitz G, Baselga J, Loi S (2017)

Publication Type: Journal article

Publication year: 2017

Journal

Book Volume: 85

Pages Range: 133-145

DOI: 10.1016/j.ejca.2017.08.020

Abstract

AIM: The Neoadjuvant PI3K inhibition in HER2 OverExpressing Breast cancEr (NeoPHOEBE) trial evaluated the efficacy and safety of buparlisib, a pan-phosphatidylinositol 3-kinase (PI3K) inhibitor, plus trastuzumab and paclitaxel as neoadjuvant treatment for human epidermal growth factor receptor-2 positive (HER2+) breast cancer. METHODS: NeoPHOEBE was a neoadjuvant, phase II, randomised, double-blind study. Women with HER2+ breast cancer were randomised within two independent cohorts by PIK3CA mutation status and, in each cohort stratified by oestrogen receptor (ER) status to receive buparlisib or placebo plus trastuzumab (first 6 weeks) followed by buparlisib or placebo with trastuzumab and paclitaxel. Primary end-point was pathological complete response (pCR) rate; key secondary end-point was objective response rate (ORR) at 6 weeks. Exploratory end-points were evaluation of Ki67 levels and change in tumour infiltrating lymphocytes (TILs) in intermediate biopsies at day 15. RESULTS: Recruitment was suspended mainly due to liver toxicity after enrolment of 50 of the planned 256 patients. In each arm (buparlisib n = 25; placebo n = 25) 21 patients (84%) had wild type PIK3CA and 4 patients (16%) had mutant PIK3CA. Overall, pCR rate was similar between buparlisib and placebo arms (32.0% versus 40%; one-sided P = 0.811). A trend towards higher ORR (68.8% versus 33.3%; P = 0.053) and a significant decrease in Ki67 (75% versus 26.7%; P = 0.021) was observed in buparlisib versus placebo arm in the ER+ subgroup (Pinteraction = 0.03). CONCLUSIONS: Addition of the pan-PI3K inhibitor buparlisib to taxane-trastuzumab-based therapy in HER2+ early breast cancer was not feasible. However, the higher ORR and Ki67 reduction in the ER+, HER2+ subgroup indicates a potential role for PI3K-targeted therapy in this setting and may warrant further investigation with better-tolerated second-generation PI3K inhibitors. TRIAL REGISTRATION IDENTIFIER: NCT01816594.

Involved external institutions

GBG Forschungs GmbH (German Breast Group) Germany (DE) Solti Innovative Breast Cancer Research Spain (ES) Institut Jules Bordet Belgium (BE) Institut Gustave-Roussy France (FR) Charité - Universitätsmedizin Berlin Germany (DE) Luisenkrankenhaus Düsseldorf Germany (DE) Hospital Clínico Universitario de Valencia Spain (ES) HELIOS Kliniken Germany (DE) National University of Singapore (NUS) Singapore (SG) Novartis Pharma S.A.S. France (FR) Novartis AG Switzerland (CH) Kliniken Essen-Mitte Germany (DE) Medizinische Universität Wien Austria (AT) Université libre de Bruxelles (ULB) / Free University of Brussels Belgium (BE) Peter MacCallum Cancer Centre Australia (AU)

How to cite

APA:

Loibl, S., De La Pena, L., Nekljudova, V., Zardavas, D., Michiels, S., Denkert, C.,... Loi, S. (2017). Neoadjuvant buparlisib plus trastuzumab and paclitaxel for women with HER2+ primary breast cancer: A randomised, double-blind, placebo-controlled phase II trial (NeoPHOEBE). European Journal of Cancer, 85, 133-145. https://dx.doi.org/10.1016/j.ejca.2017.08.020

MLA:

Loibl, Sibylle, et al. "Neoadjuvant buparlisib plus trastuzumab and paclitaxel for women with HER2+ primary breast cancer: A randomised, double-blind, placebo-controlled phase II trial (NeoPHOEBE)." European Journal of Cancer 85 (2017): 133-145.

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