| Literature DB >> 27605156 |
Ramón García-Sanz1, Luis Antonio Corchete1, Miguel Alcoceba1, María Carmen Chillon1, Cristina Jiménez1, Isabel Prieto1, María García-Álvarez1, Noemi Puig1, Immaculada Rapado2, Santiago Barrio2, Albert Oriol3, María Jesús Blanchard4, Javier de la Rubia5, Rafael Martínez6, Juan José Lahuerta2, Marcos González Díaz1, María Victoria Mateos1, Jesús Fernando San Miguel7, Joaquín Martínez-López2, María Eugenia Sarasquete1.
Abstract
Bortezomib- and thalidomide-based therapies have significantly contributed to improved survival of multiple myeloma (MM) patients. However, treatment-induced peripheral neuropathy (TiPN) is a common adverse event associated with them. Risk factors for TiPN in MM patients include advanced age, prior neuropathy, and other drugs, but there are conflicting results about the role of genetics in predicting the risk of TiPN. Thus, we carried out a genome-wide association study based on more than 300 000 exome single nucleotide polymorphisms in 172 MM patients receiving therapy involving bortezomib and thalidomide. We compared patients developing and not developing TiPN under similar treatment conditions (GEM05MAS65, NCT00443235). The highest-ranking single nucleotide polymorphism was rs45443101, located in the PLCG2 gene, but no significant differences were found after multiple comparison correction (adjusted P = .1708). Prediction analyses, cytoband enrichment, and pathway analyses were also performed, but none yielded any significant findings. A copy number approach was also explored, but this gave no significant results either. In summary, our study did not find a consistent genetic component associated with TiPN under bortezomib and thalidomide therapies that could be used for prediction, which makes clinical judgment essential in the practical management of MM treatment.Entities:
Keywords: bortezomib-induced peripheral neuropathy; genome-wide association studies; multiple myeloma; thalidomide-induced peripheral neuropathy
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Year: 2016 PMID: 27605156 DOI: 10.1002/hon.2337
Source DB: PubMed Journal: Hematol Oncol ISSN: 0278-0232 Impact factor: 5.271