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Efficacy of Neoadjuvant Carboplatin plus Docetaxel in Triple-Negative Breast Cancer: Combined Analysis of Two Cohorts.
Sharma, Priyanka; López-Tarruella, Sara; García-Saenz, Jose Angel; Ward, Claire; Connor, Carol S; Gómez, Henry L; Prat, Aleix; Moreno, Fernando; Jerez-Gilarranz, Yolanda; Barnadas, Augusti; Picornell, Antoni C; Del Monte-Millán, Maria; Gonzalez-Rivera, Milagros; Massarrah, Tatiana; Pelaez-Lorenzo, Beatriz; Palomero, María Isabel; González Del Val, Ricardo; Cortes, Javier; Fuentes Rivera, Hugo; Bretel Morales, Denisse; Márquez-Rodas, Iván; Perou, Charles M; Wagner, Jamie L; Mammen, Joshua M V; McGinness, Marilee K; Klemp, Jennifer R; Amin, Amanda L; Fabian, Carol J; Heldstab, Jaimie; Godwin, Andrew K; Jensen, Roy A; Kimler, Bruce F; Khan, Qamar J; Martin, Miguel.
Afiliação
  • Sharma P; University of Kansas Medical Center, Westwood, Kansas. psharma2@kumc.edu mmartin@geicam.org.
  • López-Tarruella S; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • García-Saenz JA; Medical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.
  • Ward C; University of Kansas Medical Center, Westwood, Kansas.
  • Connor CS; University of Kansas Medical Center, Westwood, Kansas.
  • Gómez HL; Medical Oncology Department, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
  • Prat A; Department of Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain.
  • Moreno F; Translational Genomics Group, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • Jerez-Gilarranz Y; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
  • Barnadas A; Medical Oncology Department, Hospital Clínico San Carlos, Madrid, Spain.
  • Picornell AC; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Del Monte-Millán M; Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Gonzalez-Rivera M; Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Massarrah T; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Pelaez-Lorenzo B; Laboratory of Translational Oncology. Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Palomero MI; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • González Del Val R; Oncology Department, Hospital Clínico, Valladolid, Spain.
  • Cortes J; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Fuentes Rivera H; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Bretel Morales D; Department of Oncology, Ramon y Cajal University Hospital, Madrid, Spain.
  • Márquez-Rodas I; Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • Perou CM; Medical Oncology Department, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
  • Wagner JL; Medical Oncology Department, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
  • Mammen JM; Medical Oncology Service, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • McGinness MK; Department of Genetics, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Klemp JR; Department of Pathology & Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Amin AL; University of Kansas Medical Center, Westwood, Kansas.
  • Fabian CJ; University of Kansas Medical Center, Westwood, Kansas.
  • Heldstab J; University of Kansas Medical Center, Westwood, Kansas.
  • Godwin AK; University of Kansas Medical Center, Westwood, Kansas.
  • Jensen RA; University of Kansas Medical Center, Westwood, Kansas.
  • Kimler BF; University of Kansas Medical Center, Westwood, Kansas.
  • Khan QJ; University of Kansas Medical Center, Westwood, Kansas.
  • Martin M; University of Kansas Medical Center, Westwood, Kansas.
Clin Cancer Res ; 23(3): 649-657, 2017 Feb 01.
Article em En | MEDLINE | ID: mdl-27301700
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadjuvante / Neoplasias de Mama Triplo Negativas Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged País/Região como assunto: America do norte / Europa Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadjuvante / Neoplasias de Mama Triplo Negativas Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged País/Região como assunto: America do norte / Europa Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2017 Tipo de documento: Article