Relapsed and refractory multiple myeloma: A systematic review and network meta‐analysis of the efficacy of novel therapies

Author:

Minakata Daisuke1ORCID,Fujiwara Shin‐ichiro12ORCID,Yokoyama Daizo1,Noguchi Atsuto1,Aoe Shuka1,Oyama Takashi1,Koyama Shunsuke1,Murahashi Rui1,Nakashima Hirotomo1,Hyodo Kazuki1,Ikeda Takashi1,Kawaguchi Shin‐ichiro1,Toda Yumiko1,Ito Shoko1,Nagayama Takashi1,Mashima Kiyomi1ORCID,Umino Kento1,Morita Kaoru1,Ashizawa Masahiro1,Yamamoto Chihiro1ORCID,Hatano Kaoru1,Sato Kazuya1ORCID,Ohmine Ken1,Kanda Yoshinobu13ORCID

Affiliation:

1. Division of Hematology, Department of Medicine Jichi Medical University Tochigi Japan

2. Division of Cell Transplantation and Transfusion Jichi Medical University Tochigi Japan

3. Division of Hematology Jichi Medical University Saitama Medical Center Saitama Japan

Abstract

SummaryThe prognosis of multiple myeloma (MM) has dramatically improved with the development of new drugs, and it has become important to determine the appropriate combinations of these novel agents. This study was a systematic review and network meta‐analysis (NMA) of randomized trials in patients with relapsed and/or refractory (RR) MM. The PubMed, Cochrane, and Embase databases were searched for randomized trials from 1 January 2002 to 28 February 2022 of patients treated for MM. The primary end‐point was progression‐free survival (PFS), evaluated as a hazard ratio (HR) with a 95% confidence interval (95% CI) compared to dexamethasone (DEX). The p‐score was used to rank treatments. Of a total of 1136 abstracts screened, 37 studies were selected, including 34 treatment options for RRMM. Daratumumab, lenalidomide and DEX was found to be the best treatment for RRMM, with the best HR compared to DEX (HR, 0.13; 95% CI, 0.08–0.20; p‐score 0.9796). There was no evidence of significant heterogeneity (I2, 41.3%; p = 0.146). The current NMA confirmed the excellent efficacy of three‐drug regimens including anti‐CD38 antibodies to treat RRMM and provides background data to evaluate the efficacy of chimeric antigen receptor T‐cell treatments and bispecific T‐cell engager therapies.

Publisher

Wiley

Subject

Hematology

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