Feasibility, Tolerability and Efficacy of Carfilzomib in Combination with Lenalidomide and Dexamethasone in Relapsed Refractory Myeloma Patients: A Retrospective Real-Life Survey of the Sicilian Myeloma Network

Author:

Conticello Concetta,Romano AlessandraORCID,Del Fabro Vittorio,Martino Enrica Antonia,Calafiore Valeria,Sapienza Giuseppe,Leotta Valerio,Parisi Marina Silvia,Markovic Uros,Garibaldi Bruno,Leotta Salvatore,Cotzia Emilia,Innao Vanessa,Mannina DonatoORCID,Neri Santo,Musso Maurizio,Scalone Renato,Cangialosi Clotilde,Acquaviva Francesco,Cardinale GiovanniORCID,Merenda Anxur,Maugeri Cinzia,Uccello Giuseppina,Poidomani Massimo,Longo Giuseppe,Carlisi Melania,Tibullo Daniele,Di Raimondo Francesco

Abstract

Background: The ASPIRE (NCT01080391) phase 3 trial showed the efficacy of carfilzomib, lenalidomide and dexamethasone (KRd) triplet for relapse and refractory multiple myeloma (RRMM). However, little is known about safety and efficacy of KRd outside a clinical trial context. Methods: Herein we report real life results of KRd given to 130 RRMM patients from 12 Sicilian Centers. Results: Median age was 62 years; patients had received a median of two previous lines of treatment (range 1–10) and 52% were refractory to previous treatment. Median number of KRd cycles was 12 (2–29), with a mean duration of treatment of 12 months; 21 patients had received at least 18 cycles. Overall response rate was 61%, including 18% complete response. Median PFS was 22.9 months, median OS was not reached. Creatinine clearance >30 mL/min, quality of the best achieved response and standard Fluorescence In Situ Hybridization (FISH) risk were independent predictors of favorable outcome. Patients who received the full-dosage of carfilzomib in the first two cycles had a better outcome. Conclusions: KRd was effective and well tolerated and in a considerable proportion of patients, therapy continued beyond the 18th cycle. The finding of a better outcome in patients with the higher cumulative dose of carfilzomib in the first two cycle encourages to maintain the maximum tolerated dose.

Publisher

MDPI AG

Subject

General Medicine

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