Literature DB >> 26684262

New pharmacotherapy options for multiple myeloma.

Roberto Mina1, Chiara Cerrato1, Annalisa Bernardini1, Elena Aghemo1, Antonio Palumbo1.   

Abstract

INTRODUCTION: Novel agents and the availability of autologous stem-cell transplantation have revolutionized the treatment of patients with multiple myeloma. First-generation novel agents namely thalidomide, lenalidomide, and bortezomib have significantly improved response and survival of patients. Second-generation novel agents such as pomalidomide, carfilzomib, and monoclonal antibodies are being tested both in the newly diagnosed and relapse settings, and results are promising. AREAS COVERED: In this review article, the main results derived from Phase III trials with thalidomide, lenalidomide, and bortezomib for the treatment of myeloma patients, both at diagnosis and at relapse, are summarized. Data about second-generation novel agents such as pomalidomide and carfilzomib are also reported. Newer effective drugs currently under investigation and the promising results with monoclonal antibodies are described. EXPERT OPINION: The availability of new effective drugs has considerably increased the treatment options for myeloma patients. A sequential approach including induction, transplantation (when possible), consolidation, and maintenance is an optimal strategy to achieve disease control and prolong survival. Despite these improvements, the best combination, the optimal sequence, and the proper target of newer drugs need to be defined.

Entities:  

Keywords:  Myeloma; first-generation novel agents; second-generation novel agents; therapy

Mesh:

Substances:

Year:  2015        PMID: 26684262     DOI: 10.1517/14656566.2016.1115016

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  7 in total

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Authors:  Qian Zhang; Michael J Lenardo; David Baltimore
Journal:  Cell       Date:  2017-01-12       Impact factor: 41.582

2.  Evaluation of Cardiovascular Toxicity Associated with Treatments Containing Proteasome Inhibitors in Multiple Myeloma Therapy.

Authors:  Andrea Iannaccone; G Bruno; A Ravera; F Gay; M Salvini; S Bringhen; L Sabia; E Avenatti; F Veglio; A Milan
Journal:  High Blood Press Cardiovasc Prev       Date:  2018-03-26

Review 3.  Spotlight on elotuzumab in the treatment of multiple myeloma: the evidence to date.

Authors:  Katja Weisel
Journal:  Onco Targets Ther       Date:  2016-10-05       Impact factor: 4.147

Review 4.  Chemical approaches to targeted protein degradation through modulation of the ubiquitin-proteasome pathway.

Authors:  Ian Collins; Hannah Wang; John J Caldwell; Raj Chopra
Journal:  Biochem J       Date:  2017-03-15       Impact factor: 3.857

5.  Substrate-specific recognition of IKKs mediated by USP16 facilitates autoimmune inflammation.

Authors:  Jian-Shuai Yu; Tao Huang; Yu Zhang; Xin-Tao Mao; Ling-Jie Huang; Yi-Ning Li; Ting-Ting Wu; Jiang-Yan Zhong; Qian Cao; Yi-Yuan Li; Jin Jin
Journal:  Sci Adv       Date:  2021-01-13       Impact factor: 14.136

Review 6.  Kinase inhibitors as potential agents in the treatment of multiple myeloma.

Authors:  Hanley N Abramson
Journal:  Oncotarget       Date:  2016-12-06

7.  Antifibrotic Effects of a Barbituric Acid Derivative on Liver Fibrosis by Blocking the NF-κB Signaling Pathway in Hepatic Stellate Cells.

Authors:  Yuan-Hsi Wang; Fat-Moon Suk; Chao-Lien Liu; Tzu-Lang Chen; Yuh-Ching Twu; Ming-Hua Hsu; Yi-Jen Liao
Journal:  Front Pharmacol       Date:  2020-03-31       Impact factor: 5.810

  7 in total

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