Literature DB >> 31395603

Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk.

Amit Sud1,2, Subhayan Chattopadhyay2,3, Hauke Thomsen2, Kristina Sundquist4,5,6, Jan Sundquist4,5,6, Richard S Houlston1,7, Kari Hemminki2,4.   

Abstract

Estimating familial cancer risks is clinically important in being able to discriminate between individuals in the population at differing risk for malignancy. To gain insight into the familial risk for the different hematological malignancies and their possible inter-relationship, we analyzed data on more than 16 million individuals from the Swedish Family-Cancer Database. After identifying 153 115 patients diagnosed with a primary hematological malignancy, we quantified familial relative risks (FRRs) by calculating standardized incident ratios (SIRs) in 391 131 of their first-degree relatives. The majority of hematological malignancies showed increased FRRs for the same tumor type, with the highest FRRs being observed for mixed cellularity Hodgkin lymphoma (SIR, 16.7), lymphoplasmacytic lymphoma (SIR, 15.8), and mantle cell lymphoma (SIR, 13.3). There was evidence for pleiotropic relationships; notably, chronic lymphocytic leukemia was associated with an elevated familial risk for other B-cell tumors and myeloproliferative neoplasms. Collectively, these data provide evidence for shared etiological factors for many hematological malignancies and provide information for identifying individuals at increased risk, as well as informing future gene discovery initiatives.
© 2019 by The American Society of Hematology.

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Year:  2019        PMID: 31395603      PMCID: PMC6789511          DOI: 10.1182/blood.2019001362

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


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