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Pathological Response and Survival in Triple-Negative Breast Cancer Following Neoadjuvant Carboplatin plus Docetaxel.
Sharma, Priyanka; López-Tarruella, Sara; García-Saenz, José Angel; Khan, Qamar J; Gómez, Henry L; Prat, Aleix; Moreno, Fernando; Jerez-Gilarranz, Yolanda; Barnadas, Agustí; Picornell, Antoni C; Monte-Millán, María Del; González-Rivera, Milagros; Massarrah, Tatiana; Pelaez-Lorenzo, Beatriz; Palomero, María Isabel; González Del Val, Ricardo; Cortés, Javier; Fuentes-Rivera, Hugo; Morales, Denisse Bretel; Márquez-Rodas, Iván; Perou, Charles M; Lehn, Carolyn; Wang, Yen Y; Klemp, Jennifer R; Mammen, Joshua V; Wagner, Jamie L; Amin, Amanda L; O'Dea, Anne P; Heldstab, Jaimie; Jensen, Roy A; Kimler, Bruce F; Godwin, Andrew K; Martín, Miguel.
Affiliation
  • Sharma P; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas. psharma2@kumc.edu mmartin@geicam.org.
  • López-Tarruella S; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • García-Saenz JA; Department of Medical Oncology, Hospital Clínico San Carlos, Madrid, Spain.
  • Khan QJ; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Gómez HL; Department of Medical Oncology, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
  • Prat A; Department of Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain.
  • Moreno F; Translational Genomics and Targeted Therapeutics in Solid Tumors, Institut d'Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
  • Jerez-Gilarranz Y; Department of Medical Oncology, Hospital Clínico San Carlos, Madrid, Spain.
  • Barnadas A; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • Picornell AC; Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Monte-Millán MD; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • González-Rivera M; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • Massarrah T; Laboratory of Translational Oncology, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
  • Pelaez-Lorenzo B; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • Palomero MI; Department of Oncology, Hospital Clínico, Valladolid, Spain.
  • González Del Val R; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • Cortés J; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • Fuentes-Rivera H; Department of Oncology, Ramón y Cajal University Hospital, Madrid, Spain. Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
  • Morales DB; Department of Medical Oncology, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
  • Márquez-Rodas I; Department of Medical Oncology, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
  • Perou CM; Department of Medical Oncology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, CIBERONC, GEICAM, Madrid, Spain.
  • Lehn C; Departments of Genetics and Pathology & Laboratory Medicine, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Wang YY; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Klemp JR; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Mammen JV; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Wagner JL; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Amin AL; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • O'Dea AP; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Heldstab J; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Jensen RA; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Kimler BF; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Godwin AK; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
  • Martín M; Division of Medical Oncology, University of Kansas Medical Center, Westwood, Kansas.
Clin Cancer Res ; 24(23): 5820-5829, 2018 12 01.
Article in En | MEDLINE | ID: mdl-30061361
ABSTRACT

PURPOSE:

Prognostic value of pathologic complete response (pCR) and extent of pathologic response attained with anthracycline-free platinum plus taxane neoadjuvant chemotherapy (NAC) in triple-negative breast cancer (TNBC) is unknown. We report recurrence-free survival (RFS) and overall survival (OS) according to degree of pathologic response in patients treated with carboplatin plus docetaxel NAC. PATIENTS AND

METHODS:

One-hundred and ninety patients with stage I-III TNBC were treated with neoadjuvant carboplatin (AUC6) plus docetaxel (75 mg/m2) every 21 days × 6 cycles. pCR (no evidence of invasive tumor in breast and axilla) and Residual cancer burden (RCB) were evaluated. Patients were followed for recurrence and survival. Extent of pathologic response was associated with RFS and OS using the Kaplan-Meier method.

RESULTS:

Median age was 51 years, and 52% were node-positive. pCR and RCB I rates were 55% and 13%, respectively. Five percent of pCR patients, 0% of RCB I patients, and 58% of RCB II/III patients received adjuvant anthracyclines. Three-year RFS and OS were 79% and 87%, respectively. Three-year RFS was 90% in patients with pCR and 66% in those without pCR [HR = 0.30; 95% confidence interval (CI), 0.14-0.62; P = 0.0001]. Three-year OS was 94% in patients with pCR and 79% in those without pCR (HR = 0.25; 95% CI, 0.10-0.63; P = 0.001). Patients with RCB I demonstrated 3-year RFS (93%) and OS (100%) similar to those with pCR. On multivariable analysis, higher tumor stage, node positivity, and RCB II/III were associated with worse RFS.

CONCLUSIONS:

Neoadjuvant carboplatin plus docetaxel yields encouraging efficacy in TNBC. Patients achieving pCR or RCB I with this regimen demonstrate excellent 3-year RFS and OS without adjuvant anthracycline.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Triple Negative Breast Neoplasms Type of study: Prognostic_studies Limits: Adult / Aged / Aged80 / Female / Humans / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Combined Chemotherapy Protocols / Triple Negative Breast Neoplasms Type of study: Prognostic_studies Limits: Adult / Aged / Aged80 / Female / Humans / Middle aged Language: En Journal: Clin Cancer Res Journal subject: NEOPLASIAS Year: 2018 Document type: Article