Evidence map›Paper›PMID 40549385›Full record

ArticleJAMA network open2025

Patient Sexual Orientation and Gender Identity Information Practices in Oncology.

Mandi L Pratt-Chapman, Megan A Mullins, Beck O Gold, Milena E Insalaco, Dana Rosenberg, Edward J Miech, Charles Kamen

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mandi L Pratt-ChapmanDepartment of Medicine, GW Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, DC.
Megan A MullinsDepartment of Health Economics, Systems, and Policy, O'Donnell School of Public Health, UT Southwestern Medical Center, Dallas, Texas.
Beck O GoldDepartment of Medicine, GW Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, DC.
Milena E InsalacoDivision of Supportive Care in Cancer, Department of Surgery, University of Rochester Medical Center, Rochester, New York.
Dana RosenbergDepartment of Medicine, GW Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, DC.
Edward J MiechDepartment of Emergency Medicine, Indiana University School of Medicine, Indianapolis.
Charles KamenDivision of Supportive Care in Cancer, Department of Surgery, University of Rochester Medical Center, Rochester, New York.

Funding

NRG Oncology NCORP Research Base-BIQSFPUG1CA189867 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI Deborah Watkins Bruner, Lisa A. Kachnic · 2014 to 2026
$140.5M
NCI NIH HHS UG1 CA189867
6 · The paper itself

Abstract

Importance: Sexual orientation and gender identity (SOGI) are rarely collected in clinical practice despite national calls to do so. Objective: To explore what facilitators are associated with collection of SOGI data in oncology practice. Design, Setting, and Participants: In this qualitative study with purposive sampling for greatest heterogeneity, semistructured interviews across 23 institutions were conducted in oncology practices in diverse geopolitical regions in the US from September 1, 2022, to August 31, 2023. Main Outcomes and Measures: Interviews were transcribed, double coded using deductive coding based on the Consolidation Framework for Implementation Research, and inductively coded based on emergent themes. Results: Of 23 cancer centers, most were academic cancer centers (14 [61%]) and located in urban settings (17 [74%]); 7 sites (30%) sites systematically collected SOGI data, 11 (48%) partially collected SOGI data, and 5 (22%) did not collect SOGI data. A total of 62 interviews were conducted. Mean (SD) participant age was 46 (11) years; 26 (42%) identified as female. Facilitators associated with collection of SOGI data included external mandates, forced workflows in the electronic medical record, structured data fields, perception that SOGI data were relevant to clinical practice, and leadership support. Among sites that partially collected SOGI data, existence of champions, training for SOGI data collection, and perception of the relevance of SOGI to cancer care were facilitators associated with collection. Sites that systematically collected SOGI data offered more rigorous training on the importance of SOGI data collection for use in practice. Sites that did not collect SOGI data indicated that a mandate or top-down leadership requirement would likely be needed to catalyze SOGI data collection. Conclusions and Relevance: This qualitative study of implementation factors associated with SOGI data collection in outpatient oncology practices found that systematic SOGI data collection occurred in a few centers. Factors associated with SOGI data collection were multifaceted, involving both external mandates and internal factors. Despite the collection of SOGI data, their clinical use varied, suggesting a need for ongoing clinician education and development of strategies to improve the integration of SOGI data into patient care.

Indexed as

Gender IdentityMedical OncologyNeoplasmsSexual BehaviorAdultFemaleHumansMaleMiddle AgedQualitative ResearchUnited States

Identifiers

PMID40549385
PMCPMC12186564

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.