Panitumumab plus trifluridine/tipiracil as anti-Epidermal Growth Factor Receptor rechallenge therapy in chemo-refractory RAS wild-type metastatic colorectal cancer: the randomized phase 2 VELO trial

Author:

Ciardiello Fortunato1ORCID,Troiani Teresa1,Napolitano Stefania1,De Falco Vincenzo1,Martini Giulia1,Ciardiello Davide1,Martinelli Erika1,Corte Carminia Maria Della2,Esposito Lucia1,Famiglietti Vincenzo1,Liello Alessandra Di2,Avallone Antonio3,Cardone Claudia3,De Stefano Alfonso3,Montesarchio Vincenzo4,Zampino Maria Giulia5,Bordonaro Roberto6,Scartozzi Mario7,Santini Daniele8,Maio Massimo Di9,De Vita Ferdinando10,Altucci Lucia11ORCID,Marrone Francesca10

Affiliation:

1. Department of Precision Medicine, Università degli Studi della Campania Luigi Vanvitelli

2. Department of Precision Medicne, Università degli Studi della Campania Luigi Vanvitelli, Napoli, Italy

3. Oncologia Medica, Istituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione Giovanni Pascale" - IRCCS, Napoli, Italy

4. UOC Oncologia, A.O.R.N. dei Colli (Monaldi-Cotugno-CTO), Napoli, Italy

5. European Institute of Oncology

6. Medical Oncology Unit, ARNAS Garibaldi, Catania, Italy

7. Medical Oncology, University and University Hospital of Cagliari, Cagliari, Italy

8. Oncologia Medica, Campus Biomedico, Roma, Italy

9. Department of Oncology, University of Turin at Ordine Mauriziano Hospital, Turin, Italy

10. Department of Precision Medicine, Università degli Studi della Campania “Luigi Vanvitelli”, Napoli, Italy

11. Department of Precision Medicine, University of Campania

Abstract

Abstract Current therapies for chemo-refractory metastatic colorectal cancer (mCRC) have limited efficacy. Rechallenge with epidermal growth factor receptor (EGFR) inhibitors in RAS wild-type (WT) mCRC could be valuable in this setting. In VELO, a randomized two-arm phase 2 trial, anti-EGFR monoclonal antibody panitumumab plus standard-of-care trifluridine/tipiracil (31 patients, arm B) was compared to trifluridine/tipiracil (31 patients, arm A) as third-line therapy (ClinicalTrials.gov Identifier NCT05468892). Primary endpoint, progression-free survival (PFS), was met. Median PFS was 4.0 months in arm B versus 2.5 months in arm A [hazard ratio (HR): 0.48; 95% CI 0.28–0.82; P = 0.007]. Baseline plasma RAS/BRAF WT circulating tumor DNA identified patients obtaining prolonged clinical benefit with panitumumab plus trifluridine/tipiracil as compared to trifluridine/tipiracil with PFS rates at 6 months of 38.5% versus 13% and at 12 months of 15.4% versus 0%, respectively. These findings warrant further development for liquid biopsy-guided anti-EGFR rechallenge combination strategies in chemo-refractory RAS WT mCRC.

Publisher

Research Square Platform LLC

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