The BRCA1ness signature is associated significantly with response to PARP inhibitor treatment versus control in the I-SPY 2 randomized neoadjuvant setting
Authors:
- Tesa M. SeversonTesa M. Severson
- Denise M. WolfDenise M. Wolf
- Christina YauChristina Yau
- Justine PeetersJustine Peeters
- Diederik WehkamDiederik Wehkam
- Philip C. SchoutenPhilip C. Schouten
- Suet-Feung ChinSuet-Feung Chin
- Ian J. MajewskiIan J. Majewski
- Magali MichautMagali Michaut
- Astrid BosmaAstrid Bosma
- Bernard PereiraBernard Pereira
- Tycho BismeijerTycho Bismeijer
Open Access
- 25 August 2017
- journal article
- research article
- Published by Springer Nature in Breast Cancer Research
- Vol. 19 (1) , 1-9
Abstract
Patients with BRCA1-like tumors correlate with improved response to DNA double-strand break-inducing therapy. A gene expression-based classifier was developed to distinguish between BRCA1-like and non-BRCA1-like tumors. We hypothesized that these tumors may also be more sensitive to PARP inhibitors than standard treatments. A diagnostic gene expression signature (BRCA1ness) was developed using a centroid model with 128 triple-negative breast cancer samples from the EU FP7 RATHER project. This BRCA1ness signature was then tested in HER2-negative patients (n = 116) from the I-SPY 2 TRIAL who received an oral PARP inhibitor veliparib in combination with carboplatin (V-C), or standard chemotherapy alone. We assessed the association between BRCA1ness and pathologic complete response in the V-C and control arms alone using Fisher’s exact test, and the relative performance between arms (biomarker × treatment interaction, likelihood ratio p < 0.05) using a logistic model and adjusting for hormone receptor status (HR). We developed a gene expression signature to identify BRCA1-like status. In the I-SPY 2 neoadjuvant setting the BRCA1ness signature associated significantly with response to V-C (p = 0.03), but not in the control arm (p = 0.45). We identified a significant interaction between BRCA1ness and V-C (p = 0.023) after correcting for HR. A genomic-based BRCA1-like signature was successfully translated to an expression-based signature (BRC1Aness). In the I-SPY 2 neoadjuvant setting, we determined that the BRCA1ness signature is capable of predicting benefit of V-C added to standard chemotherapy compared to standard chemotherapy alone. I-SPY 2 TRIAL beginning December 31, 2009: Neoadjuvant and Personalized Adaptive Novel Agents to Treat Breast Cancer (I-SPY 2), NCT01042379 .Keywords
Funding Information
- European FP7 RATHER Project (258967)
- I-SPY 2 Trial investigators
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