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Increased prevalence of prior malignancies and autoimmune diseases in patients diagnosed with chronic myeloid leukemia

Authors :
Gunnarsson, Niklas
Höglund, M.
Stenke, L.
Wållberg-Jonsson, Solveig
Sandin, F.
Björkholm, M.
Dreimane, A.
Lambe, M.
Markevärn, Berit
Olsson-Strömberg, U.
Wadenvik, H.
Richter, J.
Själander, Anders
Gunnarsson, Niklas
Höglund, M.
Stenke, L.
Wållberg-Jonsson, Solveig
Sandin, F.
Björkholm, M.
Dreimane, A.
Lambe, M.
Markevärn, Berit
Olsson-Strömberg, U.
Wadenvik, H.
Richter, J.
Själander, Anders
Publication Year :
2016

Abstract

We recently reported an increased incidence of second malignancies in chronic myeloid leukemia (CML) patients treated with tyrosine kinase inhibitors (TKI). To elucidate whether this increase may be linked, not to TKI but rather to a hereditary or acquired susceptibility to develop cancer, we estimated the prevalence of malignancies, autoimmune disease (AD) and chronic inflammatory disease (CID) in CML patients prior to their CML diagnosis. Nationwide population-based registers were used to identify patients diagnosed with CML in Sweden 2002-2012 and to estimate the prevalence of other malignancies, AD and CID prior to their CML diagnosis. For each patient with CML, five matched controls were selected from the general population. Conditional logistic regression was used to calculate odds ratios (OR). Nine hundred and eighty-four CML patients were assessed, representing more than 45 000 person-years of follow-up. Compared with matched controls, the prevalence of prior malignancies and AD was elevated in CML patients: OR 1.47 (95% confidence interval (CI) 1.20-1.82) and 1.55 (95% CI 1.21-1.98), respectively. No associations were detected between CML and previous CID. An increased prevalence of other malignancies and AD prior to the diagnosis of CML suggest that a hereditary or acquired predisposition to cancer and/or autoimmunity is involved in the pathogenesis of CML.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1349003106
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1038.leu.2016.59