Rate differences between first and second primary cancers may outline immune dysfunction as a key risk factor

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Zheng , G , Sundquist , K , Sundquist , J , Försti , A , Hemminki , A & Hemminki , K 2020 , ' Rate differences between first and second primary cancers may outline immune dysfunction as a key risk factor ' , Cancer medicine , vol. 9 , no. 21 , pp. 8258-8265 . https://doi.org/10.1002/cam4.3454

Title: Rate differences between first and second primary cancers may outline immune dysfunction as a key risk factor
Author: Zheng, Guoqiao; Sundquist, Kristina; Sundquist, Jan; Försti, Asta; Hemminki, Akseli; Hemminki, Kari
Contributor organization: Department of Oncology
HUS Comprehensive Cancer Center
Research Programs Unit
TRIMM - Translational Immunology Research Program
Helsinki University Hospital Area
Date: 2020-11
Language: eng
Number of pages: 8
Belongs to series: Cancer medicine
ISSN: 2045-7634
DOI: https://doi.org/10.1002/cam4.3454
URI: http://hdl.handle.net/10138/324004
Abstract: Background Many cancers are increased in immunosuppressed patients and evidence is accumulating that immune dysfunction may be a contributing risk factor for second primary cancers (SPCs). The aim of this study was to explore the potential influence of immune mechanisms in SPC. Methods We used the Swedish Cancer Registry (1990-2015) to select 13 male and 14 female first primary cancers (FPCs) that are known to be related to immune suppression. We assessed relative risks (RRs) for any of these as concordant (same first and second cancer) and discordant FPC-SPC pairs. Hierarchical clustering of significant RRs was performed for cancers as FPC and SPC. Results Concordant risks for SPCs were excessive in men and women for nasal (RRs 59.3 for men and 150.6 for women), tongue/mouth (51.7 and 100.8), and lip (32.4 and 61.2) cancers. Heatmaps showed that some cancers, such as skin cancer, tongue/mouth cancers, and non-Hodgkin lymphoma had multiple bidirectional associations as FPC and SPC. Nasal cancer and chronic lymphocytic leukemia had associations mainly as FPC while liver and kidney cancers showed most associations as SPC. Conclusions Immune dysfunction may be a plausible contributing factor for most of the associations, which calls for experimental verification.
Subject: cancer risk
immune suppression
multiple cancers
risk factors
TRANSPLANTATION
INFLAMMATION
LYMPHOMA
3122 Cancers
Peer reviewed: Yes
Rights: cc_by
Usage restriction: openAccess
Self-archived version: publishedVersion


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