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Antitumor Efficacy of Dual Blockade with Encorafenib + Cetuximab in Combination with Chemotherapy in Human BRAFV600E-Mutant Colorectal Cancer.
Napolitano, Stefania; Woods, Melanie; Lee, Hey Min; De Falco, Vincenzo; Martini, Giulia; Della Corte, Carminia Maria; Martinelli, Erika; Famiglietti, Vincenzo; Ciardiello, Davide; Anderson, Amanda; Fowlkes, Natalie Wall; Villareal, Oscar Eduardo; Sorokin, Alexey; Kanikarla, Preeti; Coker, Olu; Morris, Van; Altucci, Lucia; Tabernero, Josep; Troiani, Teresa; Ciardiello, Fortunato; Kopetz, Scott.
Afiliación
  • Napolitano S; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Woods M; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Lee HM; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • De Falco V; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Martini G; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Della Corte CM; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Martinelli E; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Famiglietti V; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Ciardiello D; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Anderson A; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Fowlkes NW; Veterinary Medicine & Surgery Department, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Villareal OE; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Sorokin A; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Kanikarla P; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Coker O; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Morris V; Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Altucci L; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Tabernero J; Medical Oncology Department, Vall d' Hebron Hospital Campus, Barcelona, Spain.
  • Troiani T; Institute of Oncology, University of Vic/Central University of Catalonia, Barcelona, Spain.
  • Ciardiello F; Oncology Institute of Barcelona-Quironsalud, Biomedical Research Center in Cancer, Barcelona, Spain.
  • Kopetz S; Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
Clin Cancer Res ; 29(12): 2299-2309, 2023 06 13.
Article en En | MEDLINE | ID: mdl-37040395
PURPOSE: Encorafenib + cetuximab (E+C) is an effective therapeutic option in chemorefractory BRAFV600E metastatic colorectal cancer (mCRC). However, there is a need to improve the efficacy of this molecular-targeted therapy and evaluate regimens suitable for untreated BRAFV600E in patients with mCRC. EXPERIMENTAL DESIGN: We performed a series of in vivo studies using BRAFV600E mCRC tumor xenografts. Mice were randomized to receive 5-fluoruracil (5-FU), irinotecan, or oxaliplatin regimens (FOLFIRI or FOLFOX), (E+C) or the combination. Patients received long-term treatment until disease progression, with deescalation strategies used to mimic maintenance therapy. Transcriptomic changes after progression on cytotoxic chemotherapy or targeted therapy were assessed. RESULTS: Antitumor activity of either FOLFIRI or E+C was better as first-line treatment as compared with second-line, with partial cross-resistance seen between a cytotoxic regimen and targeted therapy with an average 62% loss of efficacy for FOLFIRI after E+C and a 45% loss of efficacy of E+C after FOLFIRI (P < 0.001 for both). FOLFIRI-treated models had upregulation of epithelial-mesenchymal transition (EMT) and MAPK pathway activation, where E+C treated models had suppressed MAPK signaling. In contrast, with chemotherapy with E+C, EMT and MAPK signaling remained suppressed. FOLFOX or FOLFIRI, each in combination with E+C, were the most active first-line treatments as compared with E+C or to chemotherapy alone. Furthermore, FOLFOX in combination with E+C as first-line induction therapy, followed by E+C ± 5-FU as maintenance therapy, was the most effective strategy for long-term disease control. CONCLUSIONS: These results support the combination of cytotoxic chemotherapy and molecular-targeted therapy as a promising therapeutic approach in the first-line treatment of BRAFV600E mCRC.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Neoplasias del Colon Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Clin Cancer Res Asunto de la revista: NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Neoplasias del Colon Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Clin Cancer Res Asunto de la revista: NEOPLASIAS Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos