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Post-Induction Management in Patients With Left-Sided RAS and BRAF Wild-Type Metastatic Colorectal Cancer Treated With First-Line Anti-EGFR-Based Doublet Regimens: A Multicentre Study.
Parisi, Alessandro; Cortellini, Alessio; Venditti, Olga; Filippi, Roberto; Salvatore, Lisa; Tortora, Giampaolo; Ghidini, Michele; Nigro, Olga; Gelsomino, Fabio; Zurlo, Ina Valeria; Fulgenzi, Claudia; Lombardi, Pasquale; Roselló Keränen, Susana; Depetris, Ilaria; Giampieri, Riccardo; Morelli, Cristina; Di Marino, Pietro; Di Pietro, Francesca Romana; Zanaletti, Nicoletta; Vitale, Pasquale; Garajova, Ingrid; Spinelli, Gian Paolo; Zoratto, Federica; Roberto, Michela; Petrillo, Angelica; Aimar, Giacomo; Patruno, Leonardo; D'Orazio, Carla; Ficorella, Corrado; Ferri, Claudio; Porzio, Giampiero.
Affiliation
  • Parisi A; Medical Oncology, St. Salvatore Hospital, L'Aquila, Italy.
  • Cortellini A; Department of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
  • Venditti O; Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
  • Filippi R; Department of Surgery and Cancer, Imperial College London, London, United Kingdom.
  • Salvatore L; Medical Oncology, St. Salvatore Hospital, L'Aquila, Italy.
  • Tortora G; Department of Oncology, University of Turin, Turin, Italy.
  • Ghidini M; Division of Medical Oncology, Candiolo Cancer Institute, Fondazione Del Piemonte Per L'oncologia-Istiruto di Ricerca e Cura a Carattere Scientifico (FPO-IRCCS), Candiolo, Italy.
  • Nigro O; Centro Oncologico Ematologico Subalpino, Azienda Universitaria Ospedaliera Città della Salute e della Scienza di Torino, Turin, Italy.
  • Gelsomino F; Università Cattolica del Sacro Cuore, Rome, Italy.
  • Zurlo IV; Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
  • Fulgenzi C; Università Cattolica del Sacro Cuore, Rome, Italy.
  • Lombardi P; Medical Oncology, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
  • Roselló Keränen S; Medical Oncology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Depetris I; Medical Oncology, ASST Sette Laghi, Ospedale di Circolo e Fondazione Macchi, Varese, Italy.
  • Giampieri R; Department of Oncology and Hematology, Division of Oncology, University Hospital of Modena, Modena, Italy.
  • Morelli C; Medical Oncology, "Vito Fazzi" Hospital, Lecce, Italy.
  • Di Marino P; Medical Oncology, Campus Bio-Medico, University of Rome, Rome, Italy.
  • Di Pietro FR; Division of Medical Oncology, Candiolo Cancer Institute, Fondazione Del Piemonte Per L'oncologia-Istiruto di Ricerca e Cura a Carattere Scientifico (FPO-IRCCS), Candiolo, Italy.
  • Zanaletti N; Department of Medical Oncology, Hospital Clínico Universitario de Valencia, INCLIVA Biomedical Research Institute, University of Valencia, Valencia, Spain.
  • Vitale P; CIBERONC, Instituto de Salud Carlos III, Madrid, Spain.
  • Garajova I; Medical Oncology, ASL TO4, Ospedale Civile di Ivrea, Turin, Italy.
  • Spinelli GP; Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, AOU Ospedali Riuniti-Ancona, Ancona, Italy.
  • Zoratto F; Medical Oncology Unit and PhD Program in Systems and Experimental Medicine (XXXV cycle), Tor Vergata University Hospital, Rome, Italy.
  • Roberto M; Department of Medical, Oral and Biotechnological Sciences and Center for Advance Studies and Technology (CAST), G. D'Annunzio University, Chieti, Italy.
  • Petrillo A; Clinical Oncology Unit, S.S. Annunziata Hospital, Chieti, Italy.
  • Aimar G; IRCCS Istituto Dermopatico dell'Immacolata (IDI), Rome, Italy.
  • Patruno L; Experimental Clinical Abdominal Oncology Unit, Istituto Nazionale Tumori-IRCCS-Fondazione G.Pascale, Naples, Italy.
  • D'Orazio C; Department of Precision Medicine, Università della Campania "Luigi Vanvitelli", Naples, Italy.
  • Ficorella C; Medical Oncology Unit, University Hospital of Parma, Parma, Italy.
  • Ferri C; UOC Territorial Oncology-AUSL Latina-CdS Aprilia-University of Rome "Sapienza", Rome, Italy.
  • Porzio G; Medical Oncology, Santa Maria Goretti Hospital, Latina, Italy.
Front Oncol ; 11: 712053, 2021.
Article in En | MEDLINE | ID: mdl-34778029
BACKGROUND: Few data regarding post-induction management following first-line anti-epidermal growth factor receptor (EGFR)-based doublet regimens in patients with left-sided RAS/BRAF wild-type metastatic colorectal cancer (mCRC) are available. METHODS: This multicenter, retrospective study aimed at evaluating clinicians' attitude, and the safety and effectiveness of post-induction strategies in consecutive patients affected by left-sided RAS/BRAF wild-type mCRC treated with doublet chemotherapy plus anti-EGFR as first-line regimen, who did not experience disease progression within 6 months from induction initiation, at 21 Italian and 1 Spanish Institutions. The measured clinical outcomes were: progression-free survival (PFS), overall survival (OS), adverse events, and objective response rate (ORR). RESULTS: At the data cutoff, among 686 consecutive patients with left-sided RAS/BRAF wild-type mCRC treated with doublet plus anti-EGFR as first-line regimen from March 2012 to October 2020, 355 eligible patients have been included in the present analysis. Among these, 118 (33.2%), 66 (18.6%), and 11 (3.1%) received a maintenance with 5-fluorouracil/leucovorin (5FU/LV)+anti-EGFR, anti-EGFR, and 5FU/LV, respectively, while 160 (45.1%) patients continued induction treatment (non-maintenance) until disease progression, unacceptable toxicity, patient decision, or completion of planned treatment. The median period of follow-up for the overall population was 33.7 months (95%CI = 28.9-35.6). The median PFS values of the 5FU/LV+anti-EGFR, anti-EGFR, 5FU/LV, and non-maintenance cohorts were 16.0 (95%CI = 14.3-17.7, 86 events), 13.0 (95%CI = 11.4-14.5, 56 events), 14.0 (95%CI = 8.1-20.0, 8 events), and 10.1 months (95%CI = 9.0-11.2, 136 events), respectively (p < 0.001). The median OS values were 39.6 (95%CI = 31.5-47.7, 43 events), 36.1 (95%CI = 31.6-40.7, 36 events), 39.5 (95%CI = 28.2-50.8, 4 events), and 25.1 months (95%CI = 22.6-27.6, 99 events), respectively (p < 0.001). After adjusting for key covariates, a statistically significant improvement in PFS in favor of 5FU/LV+anti-EGFR (HR = 0.59, 95%CI = 0.44-0.77, p < 0.001) and anti-EGFR (HR = 0.71, 95%CI = 0.51-0.98, p = 0.039) compared to the non-maintenance cohort was found. Compared to the non-maintenance cohort, OS was improved by 5FU/LV+anti-EGFR (HR = 0.55, 95%CI = 0.38-0.81, p = 0.002) and, with marginal significance, by anti-EGFR (HR = 0.67, 95%CI = 0.51-0.98, p = 0.051). No difference was found in ORR. Any grade non-hematological and hematological events were generally higher in the non-maintenance compared to the maintenance cohorts. CONCLUSION: Among the treatment strategies following an anti-EGFR-based doublet first-line induction regimen in patients affected by left-sided RAS/BRAF wild-type mCRC treated in a "real-life" setting, 5FU/LV+anti-EGFR resulted the most adopted, effective, and relatively safe regimen.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Observational_studies / Prognostic_studies Language: En Journal: Front Oncol Year: 2021 Document type: Article Affiliation country: Italia Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Observational_studies / Prognostic_studies Language: En Journal: Front Oncol Year: 2021 Document type: Article Affiliation country: Italia Country of publication: Suiza