Initial Panitumumab Plus Fluorouracil, Leucovorin, and Oxaliplatin or Plus Fluorouracil and Leucovorin in Elderly Patients With RAS and BRAF Wild-Type Metastatic Colorectal Cancer: The PANDA Trial by the GONO Foundation

Sara Lonardi(Istituto Oncologico Veneto), Cosimo Rasola(Istituto Oncologico Veneto), Riccardo Lobefaro(Fondazione IRCCS Istituto Nazionale dei Tumori), Daniele Rossini(University of Pisa), Vincenzo Formica(Policlinico Tor Vergata), Mario Scartozzi(University of Cagliari), Giovanni Luca Frassineti(Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori), Giorgia Boscolo, Saverio Cinieri(Ospedale A. Perrino), Samantha Di Donato(Hospital of Prato), Nicoletta Pella, Francesca Bergamo(Istituto Oncologico Veneto), Alessandra Raimondi(Fondazione IRCCS Istituto Nazionale dei Tumori), Ermenegildo Arnoldi(Ospedale Papa Giovanni XXIII), Lorenzo Antonuzzo(Azienda Ospedaliero-Universitaria Careggi), Cristina Granetto(Azienda Sanitaria Ospedaliera S.Croce e Carle Cuneo), Fable Zustovich, Monica Ronzoni(IRCCS Ospedale San Raffaele), Silvana Leo(Ospedale Vito Fazzi), Federica Morano(Fondazione IRCCS Istituto Nazionale dei Tumori), Fotios Loupakis(Istituto Oncologico Veneto), Federica Buggin(Istituto Oncologico Veneto), Vittorina Zagonel(Istituto Oncologico Veneto), Matteo Fassan(University of Padua), Chiara Cremolini(University of Pisa), Luca Boni(Ospedale Policlinico San Martino), Filippo Pietrantonio(Fondazione IRCCS Istituto Nazionale dei Tumori), Ermenegildo Arnoldi(Ospedale Papa Giovanni XXIII), Lorenzo Antonuzzo(Azienda Ospedaliero-Universitaria Careggi), Giuseppe Aprile, Antonio Ardizzoia(Istituto Oncologico Veneto), C. Aschele, Editta Baldini, Alberto Ballestrero, Alessandro Bertolini, Roberto Bordonaro, Giorgia Boscolo, Angela Buonadonna, Saverio Cinieri(Ospedale A. Perrino), Matteo Clavarezza(Istituto Oncologico Veneto), Domenico Corsi, Enrico Cortesi, Filippo de Braud(Istituto Oncologico Veneto), Samantha Di Donato(Hospital of Prato), Alfredo Falcone, Adolfo Favaretto, Vincenzo Formica(Policlinico Tor Vergata), Luca Frassineti(Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori), Antonio Frassoldati(Istituto Oncologico Veneto), M. Frisinghelli, Teresa Gamucci, Luca Gianni(Istituto Oncologico Veneto), Filippo Giovanardi(Istituto Oncologico Veneto), Stefania Gori, Roberta Grande, Cristina Granetto(Azienda Sanitaria Ospedaliera S.Croce e Carle Cuneo), Silvana Leo(Ospedale Vito Fazzi), Francesco Leone(Istituto Oncologico Veneto), Sara Lonardi(Istituto Oncologico Veneto), Andrea Luciani, Carlo Milandri, Nicoletta Pella, Andrea Sartore‐Bianchi(University of Cagliari), Mario Scartozzi(University of Cagliari), Nicola Silvestris, Emiliano Tamburini, Gianluca Tomasello, Giuseppe Tonini, Gianpaolo Tortora, Claudio Vergani, Albrto Zaniboni, Fable Zustovich
Journal of Clinical Oncology
August 3, 2023
Cited by 40Open Access
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Abstract

PURPOSE To verify whether both doublet chemotherapy with a modified schedule of fluorouracil, leucovorin, and oxaliplatin (mFOLFOX) and monochemotherapy with fluorouracil plus leucovorin (5-FU + LV) achieve satisfactory efficacy when both regimens are combined with panitumumab (PAN) as initial treatment of elderly patients with RAS/ BRAF wild-type metastatic colorectal cancer (mCRC). PATIENTS AND METHODS PANDA (ClinicalTrials.gov identifier: NCT02904031 ) was an open-label, randomized phase II noncomparative trial in previously untreated patients age 70 years and older with unresectable RAS/ BRAF wild-type mCRC. Patients were randomly assigned 1:1 to mFOLFOX + PAN (arm A) or 5-FU + LV + PAN (arm B) for up to 12 cycles, followed by PAN maintenance. The primary end point was progression-free survival (PFS). In each arm, assuming a null hypothesis of median PFS time ≤6 months and target PFS ≥9.65, 90 patients per arm were needed to achieve 90% power and 5% type I error (one-sided Brookmeyer-Crowley test). RESULTS Between July 2016 and April 2019, 91 patients were randomly assigned to arm A and 92 to arm B. At a median follow-up of 50.0 months (IQR, 45.6-56.4), median PFS was 9.6 and 9.0 months for arm A and B, respectively ( P < .001 in each arm). Overall response rate was 69% and 52%, whereas median overall survival was 23.5 and 22.0 months in arm A and B, respectively. The overall rate of grade >2 chemotherapy-related adverse events was 60% and 37%, respectively. Baseline G8 and Chemotherapy Risk Assessment Scale for High-Age Patients scores were prognostic, but they were not associated with efficacy and safety of the two arms. CONCLUSION Both mFOLFOX and 5-FU + LV + PAN are reasonable options as initial therapy of elderly patients with RAS/ BRAF wild-type mCRC. 5-FU + LV + PAN is associated with a better safety profile.


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