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@ARTICLE{Zheng:157626,
author = {G. Zheng$^*$ and K. Sundquist and J. Sundquist and A.
Försti$^*$ and A. Hemminki and K. Hemminki$^*$},
title = {{I}ncidence {D}ifferences {B}etween {F}irst {P}rimary
{C}ancers and {S}econd {P}rimary {C}ancers {F}ollowing
{S}kin {S}quamous {C}ell {C}arcinoma as {E}tiological
{C}lues.},
journal = {Clinical epidemiology},
volume = {12},
issn = {1179-1349},
address = {Albany, Auckland},
publisher = {Dove Medical Press},
reportid = {DKFZ-2020-01723},
pages = {857 - 864},
year = {2020},
note = {#EA:C050#LA:C050#LA:C020#},
abstract = {Most literature on second primary cancers (SPCs) focuses on
possible factors, which may increase the risk of these
cancers, and little attention has been paid for the overall
incidence differences between first primary cancers (FPCs)
and same SPCs. We wanted to compare the incidence rates for
all common cancers when these were diagnosed as FPCs and
SPCs after invasive and in situ squamous cell carcinoma
(SCC) of the skin, which are usually treated by surgery
only.Cancers were identified from the Swedish Cancer
Registry from the years 1990 through to 2015, and they
included, in addition to skin cancers, 20 male cancers
totaling 484,850 patients and 22 female cancers totaling
452,909 patients. Standardized incidence rates and relative
risks (RRs) were calculated for sex-specific common cancers
as FPC and as SPC after skin SCC. Spearman rank correlations
were used in the analysis of incidence ranking of FPC and
SPC.Of total, 29,061 men and 23,533 women developed invasive
SCC and 27,842 men and 36,383 women in situ SCC. The total
number of 20 other male cancers was 484,850 and of 22 female
cancers it was 452,909. Rank correlations ranged from 0.90
to 0.96 (P~5×10-6), indicating that overall skin SCC did
not interfere with SPC formation. The exceptions were
increased SPC risks for melanoma, sharing risk factors with
skin SCC, and non-Hodgkin and Hodgkin lymphoma, and cancers
of the upper aerodigestive tract, connective tissue, and
male and female genitals suggesting contribution by skin
cancer initiated immune dysfunction.The incidence ranking of
SPCs after skin cancers largely follows the incidence
ranking of FPCs indicating that overall skin SCC does not
greatly interfere with the intrinsic carcinogenic process.
The main deviations in incidence between FPC and SPC
appeared to be due to shared risk factors or immunological
processes promoting immune responsive cancer types.},
cin = {C050 / HD01 / B062 / C020},
ddc = {610},
cid = {I:(DE-He78)C050-20160331 / I:(DE-He78)HD01-20160331 /
I:(DE-He78)B062-20160331 / I:(DE-He78)C020-20160331},
pnm = {313 - Cancer risk factors and prevention (POF3-313)},
pid = {G:(DE-HGF)POF3-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32821171},
pmc = {pmc:PMC7417931},
doi = {10.2147/CLEP.S256662},
url = {https://inrepo02.dkfz.de/record/157626},
}