Oral melphalan, prednisone, and thalidomide in elderly patients with multiple myeloma: updated results of a randomized controlled trial

Antonio Palumbo(Azienda Ospedaliero Universitaria San Giovanni Battista), Sara Bringhen(Azienda Ospedaliero Universitaria San Giovanni Battista), Anna Marina Liberati, Tommaso Caravita(St. Eugenio Hospital), Antonietta Falcone(Casa Sollievo della Sofferenza), Vincenzo Callea(Ospedali Riuniti di Foggia), Marco Montanaro(Ospedale Sant'Anna), Roberto Ria, Antonio Capaldi(Candiolo Cancer Institute), Renato Zambello(University of Padua), Giulia Benevolo(Azienda Ospedaliero Universitaria San Giovanni Battista), Daniele Derudas, Fausto Dore(University of Sassari), Federica Cavallo(Azienda Ospedaliero Universitaria San Giovanni Battista), Francesca Gay(Azienda Ospedaliero Universitaria San Giovanni Battista), Patrizia Falco(Azienda Ospedaliero Universitaria San Giovanni Battista), Giovannino Ciccone(Azienda Ospedaliero Universitaria San Giovanni Battista), Pellegrino Musto(Centro di Riferimento Oncologico della Basilicata), Michèle Cavo, Mario Boccadoro(Azienda Ospedaliero Universitaria San Giovanni Battista)
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Abstract

The initial analysis of the oral combination melphalan, prednisone, and thalidomide (MPT) in newly diagnosed patients with myeloma showed significantly higher response rate and longer progression-free survival (PFS) than did the standard melphalan and prednisone (MP) combination and suggested a survival advantage. In this updated analysis, efficacy and safety end points were updated. Patients were randomly assigned to receive oral MPT or MP alone. Updated analysis was by intention to treat and included PFS, overall survival (OS), and survival after progression. After a median follow-up of 38.1 months, the median PFS was 21.8 months for MPT and 14.5 months for MP (P = .004). The median OS was 45.0 months for MPT and 47.6 months for MP (P = .79). In different patient subgroups, MPT improved PFS irrespective of age, serum concentrations of beta(2)-microglobulin, or high International Staging System. Thalidomide or bortezomib administration as salvage regimens significantly improved survival after progression in the MP group (P = .002) but not in the MPT group (P = .34). These data confirm activity of MPT for PFS but failed to show any survival advantage. New agents in the management of relapsed disease could explain this finding. The study is registered at www.clinicaltrials.gov as #NCT00232934.


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