<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sorensen JL</submitter><funding>National Cancer Institute&amp;apos;s (NCI) Surveillance, Epidemiology, and End Results (SEER) Program</funding><funding>National Cancer Institute's (NCI) Surveillance, Epidemiology, and End Results (SEER) Program</funding><funding>Holden Comprehensive Cancer Center, University of Iowa</funding><funding>NCI NIH HHS</funding><pagination>1433-1445</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11636671</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(11)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Sexual and gender minority (SGM) populations experience cancer treatment and survival disparities; however, inconsistent sexual orientation and gender identity (SOGI) data collection within clinical settings and the cancer surveillance system precludes population-based research toward health equity for this population. This qualitative study examined how hospital and central registry abstractors receive and interact with SOGI information and the challenges that they face in doing so.&lt;h4>Methods&lt;/h4>We conducted semi-structured interviews with 18 abstractors at five Surveillance, Epidemiology, and End Results (SEER) registries, as well as seven abstractors from commission on cancer (CoC)-accredited hospital programs in Iowa. Interviews were transcribed, cleaned, and coded us</pubmed_abstract><journal>Cancer causes &amp; control : CCC</journal><pubmed_title>Challenges in collecting information on sexual orientation and gender identity for cancer patients: perspectives of hospital and central cancer registry abstractors.</pubmed_title><pmcid>PMC11636671</pmcid><funding_grant_id>3P30CA086862</funding_grant_id><funding_grant_id>P30 CA086862</funding_grant_id><funding_grant_id>HHSN26100005</funding_grant_id><pubmed_authors>West MM</pubmed_authors><pubmed_authors>Racila AM</pubmed_authors><pubmed_authors>Kahl AR</pubmed_authors><pubmed_authors>Seaman AT</pubmed_authors><pubmed_authors>Amao OA</pubmed_authors><pubmed_authors>Matt BJ</pubmed_authors><pubmed_authors>Charlton ME</pubmed_authors><pubmed_authors>Nash SH</pubmed_authors><pubmed_authors>Sorensen JL</pubmed_authors><pubmed_authors>Bentler S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Challenges in collecting information on sexual orientation and gender identity for cancer patients: perspectives of hospital and central cancer registry abstractors.</name><description>&lt;h4>Purpose&lt;/h4>Sexual and gender minority (SGM) populations experience cancer treatment and survival disparities; however, inconsistent sexual orientation and gender identity (SOGI) data collection within clinical settings and the cancer surveillance system precludes population-based research toward health equity for this population. This qualitative study examined how hospital and central registry abstractors receive and interact with SOGI information and the challenges that they face in doing so.&lt;h4>Methods&lt;/h4>We conducted semi-structured interviews with 18 abstractors at five Surveillance, Epidemiology, and End Results (SEER) registries, as well as seven abstractors from commission on cancer (CoC)-accredited hospital programs in Iowa. Interviews were transcribed, cleaned, and coded us</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-05T07:43:06.737Z</modification><creation>2026-05-14T03:12:20.907Z</creation></dates><accession>S-EPMC11636671</accession><cross_references><pubmed>38954307</pubmed><doi>10.1007/s10552-024-01897-x</doi></cross_references></HashMap>