| Literature DB >> 28342200 |
Sam Hyatt1, Rhiannon E Jones1, Nicole H Heppel1, Julia W Grimstead1, Chris Fegan1, Graham H Jackson2, Robert Hills1, James M Allan3, Guy Pratt4, Chris Pepper1, Duncan M Baird1.
Abstract
The variable clinical outcomes of Multiple Myeloma (MM) patients are incompletely defined by current prognostication tools. We examined the clinical utility of high-resolution telomere length analysis as a prognostic marker in MM. Cohort stratification, using a previously determined length threshold for telomere dysfunction, revealed that patients with short telomeres had a significantly shorter overall survival (P < 0·0001; HR = 3·4). Multivariate modelling using forward selection identified International Staging System (ISS) stage as the most important prognostic factor, followed by age and telomere length. Importantly, each ISS prognostic subset could be further risk-stratified according to telomere length, supporting the inclusion of this parameter as a refinement of the ISS.Entities:
Keywords: genome instability; multiple myeloma; prognosis; telomere
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Year: 2017 PMID: 28342200 DOI: 10.1111/bjh.14643
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998