Format

Send to

Choose Destination
Cancer. 2019 Apr 15;125(8):1313-1318. doi: 10.1002/cncr.31925. Epub 2018 Dec 18.

Acquisition of sexual orientation and gender identity data among NCI Community Oncology Research Program practice groups.

Author information

1
Department of Oncology, Mayo Clinic, Rochester, Minnesota.
2
Division of Biostatistics, Mayo Clinic, Rochester, Minnesota.
3
Department of Social Sciences and Health Policy, Wake Forest School of Medicine, Winston-Salem, North Carolina.
4
Department of Surgery, University of Wisconsin, Madison, Wisconsin.
5
Nemours Center for Healthcare Delivery Science, Nemours Children's Health System, Wilmington, Delaware.
6
Department of Radiology, University of Michigan, Ann Arbor, Michigan.
7
Spartanburg Medical Center, Spartanburg, South Carolina.
8
SWOG Statistical Center, Fred Hutchinson Cancer Research Center, Seattle, Washington.
9
Department of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
10
Cancer Control Unit, University of Rochester, Rochester, New York.

Abstract

BACKGROUND:

Sexual and gender minority individuals face numerous cancer-related inequities, many of which appear to be underreported. However, to the best of the authors' knowledge, no one has assessed rates of acquisition of sexual orientation and gender identity (SOGI) data within community oncology settings.

METHODS:

Community oncology practices that were part of the NCI Community Oncology Research Program (NCORP) network were asked whether they routinely collected SOGI information and coded this information in their electronic medical records. The proportion of practice groups reporting routine collection of sexual and/or gender minority information was calculated. Potential associations between the collection of SOGI information and practice group-level and state-level characteristics (from Gallup poll data) were also provided.

RESULTS:

Twenty-four percent of the responding NCORP practice groups reported routine collection of sexual orientation information, and 10% reported collection of gender identity information. Practices located in western regions of the United States, practices in states with higher proportions of sexual and gender minority-identifying individuals, and practices with lower proportions of non-Hispanic patients were more likely to ask patients about sexual orientation and/or gender identity.

CONCLUSIONS:

US oncology practices that participate in research do not frequently collect SOGI information from patients with cancer. Educational initiatives should inform oncology staff and providers about the importance of collecting gender identity and sexual orientation information to improve existent disparities faced by sexual and gender minority patients.

KEYWORDS:

disclosure; gender identity; sexual and gender minorities; sexual orientation

PMID:
30561776
PMCID:
PMC6443419
[Available on 2020-04-15]
DOI:
10.1002/cncr.31925

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center