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Total neoadjuvant therapy with or without aflibercept in rectal cancer: 3-year results of GEMCAD-1402.
Pesántez, David; Ten Hoorn, Sanne; Machado, Isidro; García-Albéniz, Xabier; Rodríguez-Salas, Nuria; Heredia-Soto, Victoria; Viñal, David; Pericay, Carles; García-Carbonero, Rocio; Losa, Ferran; Alonso, Vicente; Vera, Ruth; Feliu Batlle, Jaime; Gallego, Javier; Salud, Antonieta; Nogué, Miquel; Layos, Laura; Montagut, Clara; Capdevila, Jaume; Vermeulen, Louis; Maurel, Joan; Fernandez-Martos, Carlos.
Afiliación
  • Pesántez D; Department of Medical Oncology, Hospital Clínic of Barcelona, Barcelona, Spain.
  • Ten Hoorn S; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
  • Machado I; Department of Medical Oncology, Center for Experimental and Molecular Medicine (CEMM), Amsterdam University Medical Center, Cancer Center Amsterdam, Amsterdam, the Netherlands.
  • García-Albéniz X; Department of Medical Oncology, Oncode Institute, Amsterdam, the Netherlands.
  • Rodríguez-Salas N; Department of Pathology, Instituto Valenciano de Oncologia and Pathology Department, Hospital Quirón Salud, Valencia, Spain.
  • Heredia-Soto V; RTI Health Solutions, Barcelona, Spain.
  • Viñal D; Department of Medical Oncology, Hospital Universitario La Paz, Madrid, Spain.
  • Pericay C; Translational Oncology Group, IdiPAZ, Madrid, Spain.
  • García-Carbonero R; Faculty of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
  • Losa F; Department of Medical Oncology, Centro de Investigación Biomédica en Red - Cáncer (CIBERONC), Madrid, Spain.
  • Alonso V; Department of Medical Oncology, Hospital Universitario La Paz, Madrid, Spain.
  • Vera R; Translational Oncology Group, IdiPAZ, Madrid, Spain.
  • Feliu Batlle J; Faculty of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
  • Gallego J; Department of Medical Oncology, Centro de Investigación Biomédica en Red - Cáncer (CIBERONC), Madrid, Spain.
  • Salud A; Department of Medical Oncology, Complex Sanitari Parc Tauli, Sabadell, Spain.
  • Nogué M; Department of Medical Oncology, Complex Sanitari Parc Tauli, Sabadell, Spain.
  • Layos L; Medical Oncology Department. Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Montagut C; Medical Oncology Department, Hospital Sant Joan Despí - Moises Broggi, Barcelona, Spain.
  • Capdevila J; Medical Oncology Department, Hospital Universitario Miguel Servet, Zaragoza, Spain.
  • Vermeulen L; Medical Oncology Department, Complejo Hospitalario de Navarra, Pamplona, Spain.
  • Maurel J; Department of Medical Oncology, Hospital Universitario La Paz, Madrid, Spain.
  • Fernandez-Martos C; Translational Oncology Group, IdiPAZ, Madrid, Spain.
J Natl Cancer Inst ; 115(12): 1497-1505, 2023 12 06.
Article en En | MEDLINE | ID: mdl-37405857
ABSTRACT

BACKGROUND:

The results of the Grupo Español Multidisciplinar en Cáncer Digestivo (GEMCAD)-1402 phase II randomized trial suggested that adding aflibercept to modified fluorouracil, oxaliplatin, and leucovorin (mFOLFOX6) induction, followed by chemoradiation and surgery, could increase the pathological complete response (pCR) rate in patients with high-risk, locally advanced rectal cancer. Here we update results up to 3 years of follow-up and evaluate the predictive value of consensus molecular subtypes identified with immunohistochemistry (IHC).

METHODS:

Patients with magnetic resonance imaging-defined T3c-d and/or T4 and/or N2 rectal adenocarcinoma in the middle or distal third were randomly assigned to mFOLFOX6 induction, with aflibercept (mF+A; n = 115) or without aflibercept (mF; n = 65), followed by capecitabine plus radiotherapy and surgery. The risk local relapse, distant metastases, disease-free survival (DFS), and overall survival (OS) were estimated at 3 years. Selected samples were classified via IHC into immune-infiltrate, epithelial, or mesenchymal subtypes.

RESULTS:

mF+A and mF had 3-year DFS of 75.2% (95% confidence interval [CI] = 66.1% to 82.2%) and 81.5% (95% CI = 69.8% to 89.1%), respectively; 3-year OS of 89.3% (95% CI = 82.0% to 93.8%) and 90.7% (95% CI = 80.6% to 95.7%), respectively; 3-year cumulative local relapse incidences of 5.2% (95% CI = 1.9% to 11.0%) and 6.1% (95% CI = 1.7% to 15.0%), respectively; and 3-year cumulative distant metastases rates of 17.3% (95% CI = 10.9% to 25.5%) and 16.9% (95% CI = 8.7% to 28.2%), respectively. pCRs were achieved in 27.5% (n = 22 of 80) and 0% (n = 0 of 10) of patients with epithelial and mesenchymal subtypes, respectively.

CONCLUSION:

Adding aflibercept to mFOLFOX6 induction was not associated with improved DFS or OS. Our findings suggested that consensus molecular subtypes identified with IHC subtypes could be predictive of pCR with this treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias del Recto / Terapia Neoadyuvante Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: J Natl Cancer Inst Año: 2023 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias del Recto / Terapia Neoadyuvante Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: J Natl Cancer Inst Año: 2023 Tipo del documento: Article País de afiliación: España