A review on the treatment of multiple myeloma with small molecular agents in the past five years

Eur J Med Chem. 2022 Feb 5:229:114053. doi: 10.1016/j.ejmech.2021.114053. Epub 2021 Dec 17.

Abstract

Multiple myeloma is currently incurable, and the incidence rate is increasing year by year worldwide. Although in recent years the combined treatment plan based on proteasome inhibitors and immunomodulatory drugs has greatly improved the treatment effect of multiple myeloma, most patients still relapse and become resistant to current treatments. To solve this problem, scientists are committed to developing drugs with higher specificity, such as iberdomide, which is highly specific to ikaros and aiolos. This review aims to focus on the small molecular agents that are being researched/clinically used for the treatment of multiple myeloma, including the target mechanism, structure-activity relationship and application prospects of small molecular agents.

Keywords: Multiple myeloma; Research overview; Small molecular agents.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Biomarkers, Tumor / chemistry
  • Combined Modality Therapy
  • Deubiquitinating Enzymes / chemistry
  • Drug Development
  • Drug Resistance
  • Histone Deacetylases / chemistry
  • Humans
  • Ikaros Transcription Factor / chemistry
  • Immunomodulating Agents / chemistry*
  • Immunomodulating Agents / pharmacology
  • Models, Molecular
  • Morpholines / chemistry
  • Morpholines / pharmacology
  • Multiple Myeloma / drug therapy*
  • Phthalimides / chemistry
  • Phthalimides / pharmacology
  • Piperidones / chemistry
  • Piperidones / pharmacology
  • Proteasome Inhibitors / chemistry*
  • Proteasome Inhibitors / pharmacology
  • Treatment Outcome
  • Ubiquitin-Protein Ligases / chemistry

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Immunomodulating Agents
  • Morpholines
  • Phthalimides
  • Piperidones
  • Proteasome Inhibitors
  • Ikaros Transcription Factor
  • iberdomide
  • Ubiquitin-Protein Ligases
  • Deubiquitinating Enzymes
  • Histone Deacetylases