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Efficacy of Neoadjuvant Carboplatin plus Docetaxel in Triple-Negative Breast Cancer: Combined Analysis of Two Cohorts

Authors :
Ivan Marquez-Rodas
María del Monte-Millán
Carol S. Connor
Marilee McGinness
Sara López-Tarruella
Beatriz Pelaez-Lorenzo
Yolanda Jerez-Gilarranz
Qamar J. Khan
Claire Ward
Ricardo González del Val
Priyanka Sharma
Javier Cortes
Jennifer R. Klemp
María Isabel Palomero
Antoni Picornell
Joshua M.V. Mammen
José A. García-Sáenz
Miguel Martín
Roy A. Jensen
Milagros González-Rivera
Augusti Barnadas
Jaimie Heldstab
Carol J. Fabian
Bruce F. Kimler
Hugo Fuentes Rivera
Henry L. Gomez
Jamie L. Wagner
Aleix Prat
Denisse Bretel Morales
Andrew K. Godwin
Fernando Salvador Moreno
Charles M. Perou
Amanda L. Amin
Tatiana Massarrah
Source :
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid, Consejería de Sanidad de la Comunidad de Madrid, CLINICAL CANCER RESEARCH, r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau, instname
Publication Year :
2016

Abstract

Purpose: Recent studies demonstrate that addition of neoadjuvant (NA) carboplatin to anthracycline/taxane chemotherapy improves pathologic complete response (pCR) in triple-negative breast cancer (TNBC). Effectiveness of anthracycline-free platinum combinations in TNBC is not well known. Here, we report efficacy of NA carboplatin + docetaxel (CbD) in TNBC. Experimental Design: The study population includes 190 patients with stage I–III TNBC treated uniformly on two independent prospective cohorts. All patients were prescribed NA chemotherapy regimen of carboplatin (AUC 6) + docetaxel (75 mg/m2) given every 21 days × 6 cycles. pCR (no evidence of invasive tumor in the breast and axilla) and residual cancer burden (RCB) were evaluated. Results: Among 190 patients, median tumor size was 35 mm, 52% were lymph node positive, and 16% had germline BRCA1/2 mutation. The overall pCR and RCB 0 + 1 rates were 55% and 68%, respectively. pCRs in patients with BRCA-associated and wild-type TNBC were 59% and 56%, respectively (P = 0.83). On multivariable analysis, stage III disease was the only factor associated with a lower likelihood of achieving a pCR. Twenty-one percent and 7% of patients, respectively, experienced at least one grade 3 or 4 adverse event. Conclusions: The CbD regimen was well tolerated and yielded high pCR rates in both BRCA-associated and wild-type TNBC. These results are comparable with pCR achieved with the addition of carboplatin to anthracycline–taxane chemotherapy. Our study adds to the existing data on the efficacy of platinum agents in TNBC and supports further exploration of the CbD regimen in randomized studies. Clin Cancer Res; 23(3); 649–57. ©2016 AACR.

Details

ISSN :
15573265 and 10780432
Volume :
23
Issue :
3
Database :
OpenAIRE
Journal :
Clinical cancer research : an official journal of the American Association for Cancer Research
Accession number :
edsair.doi.dedup.....bd50e2c11440ff5ec0432f3033621cfe