Abstract

Treatment of Lenalidomide Exposed or Refractory Multiple Myeloma: Network Meta-Analysis of Lenalidomide-Sparing Regimens.

Highlights

  • Over the past 10 years, the treatment of multiple myeloma (MM) dramatically changed due to the introduction of a number of new agents and combination regimens both in the frontline and in the relapsed/refractory setting

  • At least 11 classes of therapeutic agents, including steroids, alkylators, proteasome inhibitors (PI: bortezomib, carfilzomib, ixazomib), immunomodulatory agents, monoclonal antibodies, HDAC-inhibitors, BCL2 inhibitors, selective inhibitors of nuclear export, drug-conjugated mAbs, bispecific agents and CAR-T, are approved alone or in different combinations for the treatment of this disease, while few or no data are available to guide the therapeutic strategy to adopt at diagnosis or relapse [1]

  • We used the NMA approach, demonstrating that, whenever possible, the combination of an anti-CD38 agent with a PI should represent the first choice in order to achieve the best result in term of PFS in both the lena-exposed and lena-refractory RRMM population

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Summary

INTRODUCTION

Over the past 10 years, the treatment of multiple myeloma (MM) dramatically changed due to the introduction of a number of new agents and combination regimens both in the frontline and in the relapsed/refractory setting. At least 11 classes of therapeutic agents, including steroids, alkylators (melphalan and cyclophosphamide), proteasome inhibitors (PI: bortezomib, carfilzomib, ixazomib), immunomodulatory agents (thalidomide, lenalidomide, pomalidomide), monoclonal antibodies (mAbs: elotuzumab, daratumumab), HDAC-inhibitors (panobinostat), BCL2 inhibitors (venetoclax), selective inhibitors of nuclear export (selinexor), drug-conjugated mAbs (belantamab mafodotin), bispecific agents and CAR-T, are approved (or are going to be approved) alone or in different combinations for the treatment of this disease, while few or no data are available to guide the therapeutic strategy to adopt at diagnosis or relapse [1]. Network Meta-Analysis of Lenalidomide-Sparing Regimens evidence on the efficacy of seven different lenalidomide-sparing regimens (bortezomib-dexamethasone, VD; daratumumab-VD, DVD; carfilzomib-D, KD; daratumumab-KD, KdD; pomalidomide-VD, PVD; isatuximab-KD, IKD; selinexor-VD, SVD) in lenalidomide-exposed and lenalidomide-refractory patients, to provide statistical evidence to support clinical decision making (Supplementary Figure 1)

EVIDENCE FROM CLINICAL TRIALS
BORT previously exposed
DISCUSSION
Findings
AUTHOR CONTRIBUTIONS
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