Literature DB >> 28743429

Precision Medicine in Myeloma: Challenges in Defining an Actionable Approach.

Verónica González-Calle1, Niamh Keane1, Esteban Braggio1, Rafael Fonseca2.   

Abstract

Recently, large sequencing studies have provided insights into the mutational landscape of multiple myeloma (MM), identifying actionable mutations and giving a precious opportunity for exploring new targeted therapies. The main goal of precision medicine, matching patients with the right drug, seems to be closer than ever. However, no targeted therapies in MM are approved yet. Several clinical trials testing targeted drugs and enrolling patients with MM are currently ongoing and will provide predictive biomarkers that might support clinical decision making. In this review, we evaluate the evidence supporting the implementation of precision medicine in MM and we discuss the challenges that should be dealt with in this imminent and promising new era.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Actionable mutation; Driver; Immunotherapy; Multiple myeloma; Target therapy

Mesh:

Substances:

Year:  2017        PMID: 28743429     DOI: 10.1016/j.clml.2017.06.021

Source DB:  PubMed          Journal:  Clin Lymphoma Myeloma Leuk        ISSN: 2152-2669


  3 in total

1.  Validation of clinical-grade whole genome sequencing reproduces cytogenetic analysis and identifies mutational landscape in newly-diagnosed multiple myeloma patients: A pilot study from the 100,000 Genomes Project.

Authors:  Oliver C Lomas; Sarah Gooding; Maite Cabes; Helene Dreau; Edward Wilson; Paolo Polzella; Karthik Ramasamy; Angela D Hamblin
Journal:  EJHaem       Date:  2021-08-26

Review 2.  Towards Molecular Profiling in Multiple Myeloma: A Literature Review and Early Indications of Its Efficacy for Informing Treatment Strategies.

Authors:  Wolfgang Willenbacher; Andreas Seeber; Normann Steiner; Ella Willenbacher; Zoran Gatalica; Jeff Swensen; Jeffery Kimbrough; Semir Vranic
Journal:  Int J Mol Sci       Date:  2018-07-18       Impact factor: 5.923

3.  Combination of Histone Deacetylase Inhibitor Panobinostat (LBH589) with β-Catenin Inhibitor Tegavivint (BC2059) Exerts Significant Anti-Myeloma Activity Both In Vitro and In Vivo.

Authors:  Ioanna Savvidou; Tiffany Khong; Sophie Whish; Irena Carmichael; Tara Sepehrizadeh; Sridurga Mithraprabhu; Stephen K Horrigan; Michael de Veer; Andrew Spencer
Journal:  Cancers (Basel)       Date:  2022-02-08       Impact factor: 6.639

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.