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Clinicians' Attitude to Doublet Plus Anti-EGFR Versus Triplet Plus Bevacizumab as First-line Treatment in Left-Sided RAS and BRAF Wild-Type Metastatic Colorectal Cancer Patients: A Multicenter, "Real-Life", Case-Control Study.
Parisi, Alessandro; Porzio, Giampiero; Cannita, Katia; Venditti, Olga; Avallone, Antonio; Filippi, Roberto; Salvatore, Lisa; Tortora, Giampaolo; Ribelli, Marta; Nigro, Olga; Gelsomino, Fabio; Spallanzani, Andrea; Zurlo, Valeria; Leo, Silvana; Dell'Aquila, Emanuela; Claudia, Fulgenzi; Lombardi, Pasquale; Keränen, Susana Roselló; Aimar, Giacomo; Depetris, Ilaria; Giampieri, Riccardo; Morelli, Cristina; De Tursi, Michele; Tinari, Nicola; Di Pietro, Francesca Romana; De Galitiis, Federica; Zanaletti, Nicoletta; Troiani, Teresa; Vitale, Pasquale; Garajova, Ingrid; Ghidini, Michele; Spinelli, Gian Paolo; Zoratto, Federica; Roberto, Michela; Ierino, Debora; Petrillo, Angelica; D'Orazio, Carla; Ficorella, Corrado; Cortellini, Alessio.
Afiliação
  • Parisi A; Medical Oncology, St. Salvatore Hospital, University of L'Aquila, L'Aquila, Italy; Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy. Electronic address: alexparis@hotmail.it.
  • Porzio G; Medical Oncology, St. Salvatore Hospital, University of L'Aquila, L'Aquila, Italy; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Cannita K; Medical Oncology, St. Salvatore Hospital, University of L'Aquila, L'Aquila, Italy.
  • Venditti O; Medical Oncology, St. Salvatore Hospital, University of L'Aquila, L'Aquila, Italy.
  • Avallone A; Experimental Clinical Abdominal Oncology Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G.Pascale, Napoli, Italy.
  • Filippi R; Department of Oncology, University of Turin, Italy; Medical Oncology 1, Città della Salute e della Scienza di Torino, Italy.
  • Salvatore L; Università Cattolica del Sacro Cuore, Rome, Italy; Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
  • Tortora G; Università Cattolica del Sacro Cuore, Rome, Italy; Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
  • Ribelli M; Università Cattolica del Sacro Cuore, Rome, Italy; Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
  • Nigro O; Medical Oncology, ASST Sette Laghi, Ospedale di Circolo e Fondazione Macchi, Varese, Italy.
  • Gelsomino F; Department of Oncology and Hematology, Division of Oncology, University Hospital of Modena, Modena, Italy.
  • Spallanzani A; Department of Oncology and Hematology, Division of Oncology, University Hospital of Modena, Modena, Italy.
  • Zurlo V; Medical Oncology, "Vito Fazzi" Hospital, Lecce, Italy.
  • Leo S; Medical Oncology, "Vito Fazzi" Hospital, Lecce, Italy.
  • Dell'Aquila E; Medical Oncology, Campus Bio-Medico, University of Rome, Rome, Italy.
  • Claudia F; Medical Oncology, Campus Bio-Medico, University of Rome, Rome, Italy.
  • Lombardi P; Department of Oncology, University of Turin, Italy.
  • Keränen SR; Department of Medical Oncology. Hospital Clínico Universitario de Valencia, INCLIVA Biomedical Research Institute, University of Valencia, Valencia, Spain.; CIBERONC, Instituto de Salud Carlos III, Madrid, Spain.
  • Aimar G; Department of Oncology, University of Turin, Italy; Division of Medical Oncology, Candiolo Cancer Institute, FPO - IRCCS, Candiolo (TO), Italy.
  • Depetris I; Medical Oncology, ASL TO4, Ospedale Civile di Ivrea, Ivrea, Turin, Italy.
  • Giampieri R; Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, AOU Ospedali Riuniti-Ancona, Italy.
  • Morelli C; Medical Oncology Unit and PhD program in Systems and Experimental Medicine (XXXV cycle), Tor Vergata University Hospital, Rome, Italy.
  • De Tursi M; Department of Medical, Oral and Biotechnological Sciences, Center for Advance Studies and Technology (CAST), G. D'Annunzio University, Chieti, Italy; Clinical Oncology Unit, S.S. Annunziata Hospital, Chieti, Italy.
  • Tinari N; Department of Medical, Oral and Biotechnological Sciences, Center for Advance Studies and Technology (CAST), G. D'Annunzio University, Chieti, Italy; Clinical Oncology Unit, S.S. Annunziata Hospital, Chieti, Italy.
  • Di Pietro FR; IRCCS Istituto Dermopatico dell'Immacolata (IDI), Rome, Italy.
  • De Galitiis F; IRCCS Istituto Dermopatico dell'Immacolata (IDI), Rome, Italy.
  • Zanaletti N; Experimental Clinical Abdominal Oncology Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G.Pascale, Napoli, Italy.
  • Troiani T; Department of Precision Medicine, Università della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Vitale P; Department of Precision Medicine, Università della Campania "Luigi Vanvitelli", Napoli, Italy.
  • Garajova I; Medical Oncology Unit, University Hospital of Parma, Parma, Italy.
  • Ghidini M; Medical Oncology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano.
  • Spinelli GP; UOC Territorial Oncology - AUSL Latina-CdS Aprilia, University of Rome "Sapienza", Italy.
  • Zoratto F; Medical Oncology, Santa Maria Goretti Hospital, Latina, Italy.
  • Roberto M; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Oncology Unit, Sant'Andrea Hospital, Rome, Italy.
  • Ierino D; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Oncology Unit, Sant'Andrea Hospital, Rome, Italy.
  • Petrillo A; Medical Oncology Unit, Ospedale del Mare, Naples, Italy.
  • D'Orazio C; Medical Oncology, St. Salvatore Hospital, University of L'Aquila, L'Aquila, Italy; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Ficorella C; Medical Oncology, St. Salvatore Hospital, University of L'Aquila, L'Aquila, Italy; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Cortellini A; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy; Department of Surgery and Cancer, Imperial College London, London, United Kingdom.
Clin Colorectal Cancer ; 20(4): 318-325, 2021 12.
Article em En | MEDLINE | ID: mdl-34380594
BACKGROUND: Doublets plus antiepidermal growth factor receptors monoclonal antibodies (EGFRi) are widely considered the preferable first-line regimen in patients with left-sided RAS/BRAF wild-type metastatic colorectal cancer (mCRC), resulting superior in terms of activity and efficacy compared to doublets plus bevacizumab. However, data comparing doublet plus EGFRi and triplet plus bevacizumab are lacking, and the relative benefit of an intensive regimen plus an antiangiogenic backbone in this population is debated. METHODS: This multicenter, retrospective study aimed at evaluating clinicians' attitude to triplet-bevacizumab and doublet-EGFRi as first-line regimen in patients with left-sided RAS/BRAF wild-type mCRC treated in clinical practice at 22 Oncology Units from March 2012 to October 2020. A random case-control matching was performed to compare activity (ORR), and effectiveness (PFS, OS, secondary resection rate of metastases with curative intent) between triplet-bevacizumab and doublet-EGFRi, on the basis of ECOG-PS, age, gender, and burden of disease. RESULTS: A total of 718 patients were consecutively treated with doublet-EGFRi (686, 95.5%) or triplet-bevacizumab (32, 4.5%). After case-control matching, median PFS was 13.6 (95% CI, 8.9-31.7) and 16.1 (95% CI, 12.1-36.8) months (P= .621), while median OS was 30.2 (95% CI, 14.4-69.5) and 38.1 (95% CI, 33.1-101.1) months (P= .0283) in the doublet-EGFRi and the triplet-bevacizumab cohort, respectively. The ORR was 65.6% and 90.6% (P= .016), while the secondary resection rate was 18.8% and 46.9% (P= .016), in the doublet-EGFRi and the triplet-bevacizumab cohort, respectively. Triplet-bevacizumab was associated with a higher incidence of G3/G4 neutropenia (25.0% vs. 12.5%, P= .041). CONCLUSION: Although a doublet-EGFRi remains the recommended upfront regimen in patients with left-sided RAS and BRAF wild-type mCRC, our real life data suggest a triplet-bevacizumab might be at least equally active and effective in properly selected cases.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Proteínas Proto-Oncogênicas B-raf Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Colorectal Cancer Assunto da revista: GASTROENTEROLOGIA / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Proteínas Proto-Oncogênicas B-raf Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Colorectal Cancer Assunto da revista: GASTROENTEROLOGIA / NEOPLASIAS Ano de publicação: 2021 Tipo de documento: Article