<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cook M</submitter><funding>NCI NIH HHS</funding><pagination>82-88</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8666386</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>42(1)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Merkel cell carcinoma (MCC) is a rare, aggressive neuroendocrine skin cancer with higher incidence among whites, elderly, and immunosuppressed patients. Although immunosuppressed MCC patients are at higher risk of recurrence and MCC-related death, it is unknown whether immunosuppression type is associated with differential outcomes.&lt;h4>Materials and methods&lt;/h4>We retrospectively evaluated 89 nonmetastatic MCC patients with a diagnosis of chronic immunosuppression. Immunosuppression was categorized as chronic lymphocytic leukemia (31% of cohort), other hematologic malignancies (18%), solid organ transplant (21%), autoimmune disease (21%), and human immunodeficiency virus acquired deficiency syndrome (8%). Progression-free survival (PFS) and MCC-specific survival (MSS) were estimated with the cumulative incidence function. Overall survival (OS) was estimated by the Kaplan-Meier method.&lt;h4>Results&lt;/h4>With a median follow-up of 52 months, 53 deaths occurred (42 from MCC, 7 unknown, and 4 non-MCC). Two-year PFS, MSS, and OS were 30%, 55%, and 52%, respectively. Human immunodeficiency virus/acquired deficiency syndrome and solid organ transplant patients were diagnosed with MCC at a younger age (median 55 and 59 y, respectively) and with more advanced stage disease compared with other immunosuppressed subgroups. PFS did not significantly differ among the 5 immunosuppression subgroups (P=0.30), but significant differences were observed in MSS and OS (both P=0.01). Controlling for potential confounders for OS, including age and stage, immunosuppression type was still significantly associated with risk of death (P=0.01).&lt;h4>Conclusions&lt;/h4>Among immunosuppressed MCC patients, recurrent MCC is the major cause of mortality. The risk of death from MCC differs among immunosuppression types, suggesting important biological differences in host-tumor immune interactions.</pubmed_abstract><journal>American journal of clinical oncology</journal><pubmed_title>Differential Outcomes Among Immunosuppressed Patients With Merkel Cell Carcinoma: Impact of Immunosuppression Type on Cancer-specific and Overall Survival.</pubmed_title><pmcid>PMC8666386</pmcid><funding_grant_id>P01 CA225517</funding_grant_id><funding_grant_id>P30 CA015704</funding_grant_id><pubmed_authors>Baker K</pubmed_authors><pubmed_authors>Cook M</pubmed_authors><pubmed_authors>Parvathaneni U</pubmed_authors><pubmed_authors>Tseng YD</pubmed_authors><pubmed_authors>Bhatia S</pubmed_authors><pubmed_authors>Nguyen MH</pubmed_authors><pubmed_authors>Redman M</pubmed_authors><pubmed_authors>Lachance K</pubmed_authors><pubmed_authors>Nghiem P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential Outcomes Among Immunosuppressed Patients With Merkel Cell Carcinoma: Impact of Immunosuppression Type on Cancer-specific and Overall Survival.</name><description>&lt;h4>Objectives&lt;/h4>Merkel cell carcinoma (MCC) is a rare, aggressive neuroendocrine skin cancer with higher incidence among whites, elderly, and immunosuppressed patients. Although immunosuppressed MCC patients are at higher risk of recurrence and MCC-related death, it is unknown whether immunosuppression type is associated with differential outcomes.&lt;h4>Materials and methods&lt;/h4>We retrospectively evaluated 89 nonmetastatic MCC patients with a diagnosis of chronic immunosuppression. Immunosuppression was categorized as chronic lymphocytic leukemia (31% of cohort), other hematologic malignancies (18%), solid organ transplant (21%), autoimmune disease (21%), and human immunodeficiency virus acquired deficiency syndrome (8%). Progression-free survival (PFS) and MCC-specific survival (MSS) were estimated with the cumulative incidence function. Overall survival (OS) was estimated by the Kaplan-Meier method.&lt;h4>Results&lt;/h4>With a median follow-up of 52 months, 53 deaths occurred (42 from MCC, 7 unknown, and 4 non-MCC). Two-year PFS, MSS, and OS were 30%, 55%, and 52%, respectively. Human immunodeficiency virus/acquired deficiency syndrome and solid organ transplant patients were diagnosed with MCC at a younger age (median 55 and 59 y, respectively) and with more advanced stage disease compared with other immunosuppressed subgroups. PFS did not significantly differ among the 5 immunosuppression subgroups (P=0.30), but significant differences were observed in MSS and OS (both P=0.01). Controlling for potential confounders for OS, including age and stage, immunosuppression type was still significantly associated with risk of death (P=0.01).&lt;h4>Conclusions&lt;/h4>Among immunosuppressed MCC patients, recurrent MCC is the major cause of mortality. The risk of death from MCC differs among immunosuppression types, suggesting important biological differences in host-tumor immune interactions.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2024-11-13T22:49:53.114Z</modification><creation>2024-11-13T22:49:53.114Z</creation></dates><accession>S-EPMC8666386</accession><cross_references><pubmed>30211723</pubmed><doi>10.1097/COC.0000000000000482</doi><doi>10.1097/coc.0000000000000482</doi></cross_references></HashMap>