PIK3CA alterations and benefit with neratinib: analysis from the randomized, double-blind, placebo-controlled, phase III ExteNET trial

被引:17
作者
Chia, Stephen K. L. [1 ]
Martin, Miguel [2 ]
Holmes, Frankie A. [3 ]
Ejlertsen, Bent [4 ]
Delaloge, Suzette [5 ]
Moy, Beverly [6 ]
Iwata, Hiroji [7 ]
von Minckwitz, Gunter [8 ]
Mansi, Janine [9 ]
Barrios, Carlos H. [10 ]
Gnant, Michael [11 ,12 ]
Tomasevic, Zorica [13 ]
Denduluri, Neelima [14 ]
Separovic, Robert [15 ]
Kim, Sung-Bae [16 ]
Jakobsen, Erik Hugger [17 ]
Harvey, Vernon [18 ]
Robert, Nicholas [19 ,20 ]
Smith, John, II [21 ]
Harker, Graydon [22 ]
Zhang, Bo [23 ]
Eli, Lisa D. [23 ]
Ye, Yining [23 ]
Lalani, Alshad S. [23 ]
Buyse, Marc [24 ]
Chan, Arlene [25 ,26 ]
机构
[1] Univ British Columbia, British Columbia Canc Agcy, 600 West 10th Ave, Vancouver, BC V5Z 4E6, Canada
[2] Univ Complutense Madrid, Inst Invest Sanitaria Gregorio Maranon, Madrid, Spain
[3] Texas Oncol PA, Houston, TX USA
[4] Rigshosp, Copenhagen, Denmark
[5] Inst Gustave Roussy, Villejuif, France
[6] Massachusetts Gen Hosp, Canc Ctr, Boston, MA 02114 USA
[7] Aichi Canc Ctr, Chikusa Ku, Nagoya, Aichi, Japan
[8] German Breast Grp Forsch GmbH, Luisenkrankenhaus, Dusseldorf, Neu Isenburg, Germany
[9] Kings Coll London, Guys Hosp, Biomed Res Ctr, London, England
[10] Pontificia Univ Catolica Rio Grande do Sul, Sch Med, Porto Alegre, RS, Brazil
[11] Med Univ Vienna, Dept Surg, Vienna, Austria
[12] Med Univ Vienna, Comprehens Canc Ctr, Vienna, Austria
[13] Daily Chemotherapy Hosp, Inst Oncol & Radiol Serbia, Belgrade, Serbia
[14] Virginia Canc Specialists, Arlington, VA USA
[15] Sestre Milosrdnice Univ Hosp Ctr, Univ Hosp Tumors, Zagreb, Croatia
[16] Univ Ulsan, Asan Med Ctr, Seoul, South Korea
[17] Lillebaelt Hosp, Vejle, Denmark
[18] Auckland City Hosp, Auckland, New Zealand
[19] McKesson Specialty Hlth, The Woodlands, TX USA
[20] US Oncol Network, The Woodlands, TX USA
[21] Compass Oncol, Portland, OR USA
[22] Utah Canc Specialists, Salt Lake City, UT USA
[23] Puma Biotechnol Inc, Los Angeles, CA USA
[24] IDDI, Louvain, Belgium
[25] Breast Canc Res Ctr WA, Perth, WA, Australia
[26] Curtin Univ, Nedlands, WA, Australia
来源
BREAST CANCER RESEARCH | 2019年 / 21卷
关键词
Breast cancer; Drug targets; Neratinib; PIK3CA; Prognostic; Predictive; PATHOLOGICAL COMPLETE RESPONSE; PLUS ADJUVANT CHEMOTHERAPY; BREAST-CANCER EXTENET; BIOMARKER ANALYSIS; SOMATIC MUTATION; COPY NUMBER; NSABP B-31; TRASTUZUMAB; RECEPTOR; THERAPY;
D O I
10.1186/s13058-019-1115-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundNeratinib is an irreversible pan-HER tyrosine kinase inhibitor that inhibits PI3K/Akt and MAPK signaling pathways after HER2 receptor activation. The ExteNET study showed that neratinib significantly improved 5-year invasive disease-free survival (iDFS) in women who completed trastuzumab-based adjuvant therapy for early breast cancer (EBC). We assessed the prognostic and predictive significance of PIK3CA alterations in patients in ExteNET.MethodsParticipants were women aged 18years (20years in Japan) with stage 1-3c (modified to stage 2-3c in February 2010) operable breast cancer, who had completed (neo)adjuvant chemotherapy plus trastuzumab 2years before randomization, with no evidence of disease recurrence or metastatic disease at study entry. Patients were randomized to oral neratinib 240mg/day or placebo for 1year. Formalin-fixed, paraffin-embedded primary tumor specimens underwent polymerase chain reaction (PCR) PIK3CA testing for two hotspot mutations in exon 9, one hot-spot mutation in exon 20, and fluorescence in situ hybridization (FISH) analysis for PIK3CA amplification. The primary endpoint (iDFS) was tested with log-rank test and hazard ratios (HRs) estimated using Cox proportional-hazards models.ResultsAmong the intent-to-treat population (n=2840), tumor specimens were available for PCR testing (991 patients) and PIK3CA FISH (702 patients). Overall, 262 samples were PIK3CA altered: 201 were mutated (77%), 52 (20%) were amplified, and 9 (3%) were mutated and amplified. iDFS was non-significantly worse in placebo-treated patients with altered vs wild-type PIK3CA (HR 1.34; 95% CI 0.72-2.50; P=0.357). Neratinib's effect over placebo was significant in patients with PIK3CA-altered tumors (HR 0.41; 95% CI 0.17-0.90, P=0.028) but not PIK3CA wild-type tumors (HR 0.72; 95% CI 0.36-1.41; P=0.34). The interaction test was non-significant (P=0.309).ConclusionsAlthough there was a greater absolute risk reduction associated with neratinib treatment of patients with PIK3CA-altered tumors in ExteNET, current data do not support PIK3CA alteration as a predictive biomarker of response to neratinib in HER2-positive EBC.Trial registrationClinicalTrials.gov, NCT00878709. Trial registered April 9, 2009.
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