Precision medicine for multiple myeloma: The case for translocation (11;14).
Autor: | Bazarbachi AH; Division of Hematology/Oncology, Columbia University Irving Medical Center/New York-Presbyterian Hospital, New York, NY, USA. Electronic address: bazarbachi@gmail.com., Avet-Loiseau H; Cancer Research Center of Toulouse, INSERM, Myeloma Genomics Laboratory, University Cancer Institute Toulouse Oncopole, Université Paul Sabatier, Toulouse, France., Harousseau JL; Institut de Cancerologie de l'Ouest, Centre René Gauducheau, Nantes-St Herblain, France., Bazarbachi A; Department of Internal Medicine, American University of Beirut, Beirut 1107 2020, Lebanon., Mohty M; Sorbonne University, Service d'Hematologie Clinique et Thérapie Cellulaire, Hôpital Saint Antoine, and INSERM UMR 938, Paris, France. Electronic address: mohamad.mohty@inserm.fr. |
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Jazyk: | angličtina |
Zdroj: | Cancer treatment reviews [Cancer Treat Rev] 2024 Nov; Vol. 130, pp. 102823. Date of Electronic Publication: 2024 Sep 03. |
DOI: | 10.1016/j.ctrv.2024.102823 |
Abstrakt: | The t(11;14) translocation is among the most prevalent cytogenetic abnormalities in multiple myeloma (MM), distinguished by its unique features and biology that have been thoroughly explored for decades. What further sets this MM subtype apart is its oscillating prognostic significance, from initially being considered a favorable alteration to intermediate risk and potential future reclassification as favorable risk. Despite not being inherently a high-risk alteration indicative of an aggressive phenotype, it appears that t(11;14)-MM is less responsive to novel agents like proteasome inhibitors and immunomodulatory drugs which have otherwise transformed the disease's treatment landscape, perhaps partially explained by its reduced propensity for immunoglobulin production and oligosecretory nature. However, its distinct reliance on Bcl-2 has heightened its sensitivity to venetoclax. Further subclassification based on morphological and genomic characteristics could enhance our prediction models of treatment responses and enable more tailored therapeutic strategies for patients. This review aims to encapsulate the existing research evidence in this area. Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. (Copyright © 2024 Elsevier Ltd. All rights reserved.) |
Databáze: | MEDLINE |
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