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Efficacy of neoadjuvant carboplatin plus docetaxel in triple-negative breast cancer: Combined analysis of two cohorts

  • Priyanka Sharma
  • , Sara López-Tarruella
  • , Jose Angel García-Saenz
  • , Claire Ward
  • , Carol S. Connor
  • , Henry L. Gómez
  • , Aleix Prat
  • , Fernando Moreno
  • , Yolanda Jerez-Gilarranz
  • , Augusti Barnadas
  • , Antoni C. Picornell
  • , Maria Del Monte-Millán
  • , Milagros Gonzalez-Rivera
  • , Tatiana Massarrah
  • , Beatriz Pelaez-Lorenzo
  • , María Isabel Palomero
  • , Ricardo González Del Val
  • , Javier Cortes
  • , Hugo Fuentes Rivera
  • , Denisse Bretel Morales
  • Iván Márquez-Rodas, Charles M. Perou, Jamie L. Wagner, Joshua M.V. Mammen, Marilee K. McGinness, Jennifer R. Klemp, Amanda L. Amin, Carol J. Fabian, Jaimie Heldstab, Andrew K. Godwin, Roy A. Jensen, Bruce F. Kimler, Qamar J. Khan, Miguel Martin
  • University of Kansas Medical Center
  • Instituto de Investigación Sanitaria Gregorio Marañón
  • San Carlos University Hospital
  • Instituto Nacional de Enfermedades Neoplásicas Eduardo Cáceres Graziani
  • Hospital Clinic
  • Vall d'Hebron University Hospital
  • Institut d'Investigacions Biomèdiques August Pi Sunyer (IDIBAPS)
  • Universitat Autònoma de Barcelona
  • Hospital Universitario de Valladolid
  • Hospital Ramón y Cajal
  • UNC Lineberger Comprehensive Cancer Center
  • The University of North Carolina at Chapel Hill

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

122 Citas (Scopus)

Resumen

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 x 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.

Idioma originalInglés
Páginas (desde-hasta)649-657
Número de páginas9
PublicaciónClinical Cancer Research
Volumen23
N.º3
DOI
EstadoPublicada - 1 feb. 2017
Publicado de forma externa

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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