<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shiels MS</submitter><funding>Intramural NIH HHS</funding><funding>NCCDPHP CDC HHS</funding><funding>NCHHSTP CDC HHS</funding><funding>NCI NIH HHS</funding><funding>PHS HHS</funding><pagination>2063-71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4470321</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>121(12)</volume><pubmed_abstract>BACKGROUND:It is unknown whether immunosuppression results in more aggressive, advanced stage cancers. Because cancer stage is influenced both by tumor biology and medical surveillance, the authors assessed cancer stage in individuals infected with the human immunodeficiency virus (HIV) and solid organ transplant recipients, 2 immunosuppressed groups with differences in their health care use. METHODS:The authors used data on all cases of 15 cancer types diagnosed during 1996 through 2010 in 2 studies that linked US cancer registries with HIV and transplant registries. Odds ratios (ORs) for advanced (vs local) disease were estimated comparing HIV and transplant populations with immunocompetent individuals in polytomous logistic regression models adjusted for age, sex, race, registry, and year. RESULTS:A total of 8411 of 4.5 million cancer cases occurred in HIV-infected individuals and 7322 of 6.4 million cancer cases occurred in transplant recipients. Compared with immunocompetent patients with cancer, those infected with HIV were more likely to be diagnosed with distant stage lung (OR, 1.13), female breast (OR, 1.99), and prostate (OR, 1.57) cancers, whereas transplant recipients had fewer distant stage lung (OR, 0.54), female breast (OR, 0.75), and prostate (OR, 0.72) cancers. Both immunosuppressed populations had a shift toward advanced stage melanoma (ORs of 1.97 for HIV-infected individuals and 1.82 for transplant recipients) and bladder cancer (ORs of 1.42 for HIV-infected individuals and 1.54 for transplant recipients). CONCLUSIONS:Bladder cancer and melanoma were more likely to be diagnosed at a nonlocal stage in both HIV-infected individuals and transplant recipients, suggesting a role for immunosuppression in their progression. In addition, we observed a shift for some common cancers toward later stages in HIV-infected individuals and toward earlier stages in transplant recipients, which is consistent with differential access to medical care or surveillance.</pubmed_abstract><journal>Cancer</journal><pubmed_title>Cancer stage at diagnosis in patients infected with the human immunodeficiency virus and transplant recipients.</pubmed_title><pmcid>PMC4470321</pmcid><funding_grant_id>U58 DP000832</funding_grant_id><funding_grant_id>5U62PS004011-02</funding_grant_id><funding_grant_id>U62 PS004011</funding_grant_id><funding_grant_id>Z99 CA999999</funding_grant_id><funding_grant_id>N01PC35137</funding_grant_id><funding_grant_id>N01PC35139</funding_grant_id><funding_grant_id>HHSN261201000024C</funding_grant_id><funding_grant_id>HHSN261201000037C</funding_grant_id><funding_grant_id>P30 CA086862</funding_grant_id><funding_grant_id>U62 PS004015</funding_grant_id><funding_grant_id>5U58DP003921-03</funding_grant_id><funding_grant_id>01000024C</funding_grant_id><funding_grant_id>U58 DP003879</funding_grant_id><funding_grant_id>HHSN261201000035I</funding_grant_id><funding_grant_id>U58DP000832</funding_grant_id><funding_grant_id>U58 DP003875</funding_grant_id><funding_grant_id>HHSN261201000035C</funding_grant_id><funding_grant_id>HHSN261201000036C</funding_grant_id><funding_grant_id>HSN261201000032C</funding_grant_id><funding_grant_id>N01-PC-2013-00021</funding_grant_id><funding_grant_id>U58 DP003921</funding_grant_id><funding_grant_id>U58 DP003920</funding_grant_id><funding_grant_id>U58DP003879</funding_grant_id><funding_grant_id>HHSN2612010000</funding_grant_id><funding_grant_id>HHSN261201000034C</funding_grant_id><funding_grant_id>U58 DP003883</funding_grant_id><funding_grant_id>U62 PS001005</funding_grant_id><funding_grant_id>U62PS004001-2</funding_grant_id><funding_grant_id>N01-PC-35142</funding_grant_id><funding_grant_id>U58 DP000848</funding_grant_id><funding_grant_id>U58 DP000807</funding_grant_id><funding_grant_id>HHSN2612</funding_grant_id><funding_grant_id>HHSH234200537009C</funding_grant_id><funding_grant_id>N01-PC-35143</funding_grant_id><funding_grant_id>U58 DP003931</funding_grant_id><funding_grant_id>U58 DP000848-04</funding_grant_id><funding_grant_id>5U62PS004015</funding_grant_id><funding_grant_id>5U58DP003875-01</funding_grant_id><funding_grant_id>5U58DP003883-03</funding_grant_id><funding_grant_id>HHSH250201000018C</funding_grant_id><funding_grant_id>U58 DP000824</funding_grant_id><funding_grant_id>U62 PS004001</funding_grant_id><funding_grant_id>HHSN261201300021C</funding_grant_id><funding_grant_id>5U62PS001005-0</funding_grant_id><funding_grant_id>HHSN261201300021I</funding_grant_id><funding_grant_id>N01-PC-35139</funding_grant_id><funding_grant_id>HHSN261201000026C</funding_grant_id><funding_grant_id>N01PC35143</funding_grant_id><funding_grant_id>5U58/DP003931-02</funding_grant_id><funding_grant_id>N01PC35142</funding_grant_id><funding_grant_id>5U58DP000824-04</funding_grant_id><funding_grant_id>U58DP12-1205 3919-03</funding_grant_id><funding_grant_id>1U58 DP000807-01</funding_grant_id><funding_grant_id>5458DP003920</funding_grant_id><funding_grant_id>N01-PC-35137</funding_grant_id><pubmed_authors>Copeland G</pubmed_authors><pubmed_authors>Pawlish K</pubmed_authors><pubmed_authors>Harrell J</pubmed_authors><pubmed_authors>Shiels MS</pubmed_authors><pubmed_authors>Pfeiffer RM</pubmed_authors><pubmed_authors>Engels EA</pubmed_authors><pubmed_authors>Lynch CF</pubmed_authors><pubmed_authors>Goodman MT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cancer stage at diagnosis in patients infected with the human immunodeficiency virus and transplant recipients.</name><description>BACKGROUND:It is unknown whether immunosuppression results in more aggressive, advanced stage cancers. Because cancer stage is influenced both by tumor biology and medical surveillance, the authors assessed cancer stage in individuals infected with the human immunodeficiency virus (HIV) and solid organ transplant recipients, 2 immunosuppressed groups with differences in their health care use. METHODS:The authors used data on all cases of 15 cancer types diagnosed during 1996 through 2010 in 2 studies that linked US cancer registries with HIV and transplant registries. Odds ratios (ORs) for advanced (vs local) disease were estimated comparing HIV and transplant populations with immunocompetent individuals in polytomous logistic regression models adjusted for age, sex, race, registry, and year. RESULTS:A total of 8411 of 4.5 million cancer cases occurred in HIV-infected individuals and 7322 of 6.4 million cancer cases occurred in transplant recipients. Compared with immunocompetent patients with cancer, those infected with HIV were more likely to be diagnosed with distant stage lung (OR, 1.13), female breast (OR, 1.99), and prostate (OR, 1.57) cancers, whereas transplant recipients had fewer distant stage lung (OR, 0.54), female breast (OR, 0.75), and prostate (OR, 0.72) cancers. Both immunosuppressed populations had a shift toward advanced stage melanoma (ORs of 1.97 for HIV-infected individuals and 1.82 for transplant recipients) and bladder cancer (ORs of 1.42 for HIV-infected individuals and 1.54 for transplant recipients). CONCLUSIONS:Bladder cancer and melanoma were more likely to be diagnosed at a nonlocal stage in both HIV-infected individuals and transplant recipients, suggesting a role for immunosuppression in their progression. In addition, we observed a shift for some common cancers toward later stages in HIV-infected individuals and toward earlier stages in transplant recipients, which is consistent with differential access to medical care or surveillance.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2020-10-29T14:16:28Z</modification><creation>2019-03-27T01:53:34Z</creation></dates><accession>S-EPMC4470321</accession><cross_references><pubmed>25739496</pubmed><doi>10.1002/cncr.29324</doi></cross_references></HashMap>