Investigating potential disparities in clinical trial eligibility and enrollment at anNCI‐designated comprehensive cancer center

Author:

Patel Monica A.1,Shah Jennifer L.2ORCID,Brinley Floyd John3,Abrahamse Paul H.4,Veenstra Christine M.56ORCID,Schott Anne F.5

Affiliation:

1. Department of Medicine, Division of Hematology, Medical Oncology, and Palliative Care University of Wisconsin Madison Wisconsin USA

2. Department of Radiation Oncology University of Michigan Ann Arbor Michigan USA

3. Bio‐techne: ProteinSimple Inc San Jose California USA

4. Department of Biostatistics University of Michigan Ann Arbor Michigan USA

5. Department of Internal Medicine, Division of Hematology/Oncology University of Michigan Ann Arbor Michigan USA

6. Institute for Healthcare Policy and Innovation University of Michigan Ann Arbor Michigan USA

Abstract

AbstractBackgroundAlthough barriers to trial accrual are well‐reported, few studies have explored trial eligibility and trial offers as potential drivers of disparities in cancer clinical trial enrollment.MethodsWe identified patients with gastrointestinal (GI) or head/neck (HN) malignancies who were seen as new patients at the University of Michigan Health Rogel Cancer Center in 2016. By exhaustive review of the electronic medical record, we assessed the primary outcomes: (1) eligibility for, (2) documented offer of, and (3) enrollment in a clinical trial. All 41 of the clinical trials available to these patients were considered. Independent variables included clinical and non‐clinical patient‐related factors. We assessed associations between these variables and the primary outcomes using multivariable regression.ResultsOf 1446 patients, 43% were female, 15% were over age 75, 6% were Black. 305 (21%) patients were eligible for a clinical trial. Among eligible patients, 154 (50%) had documentation of a trial offer and 90 (30%) enrolled. Among the GI cohort, bivariate analyses demonstrated that older age was associated with decreased trial eligibility. Bivariate analyses also demonstrated that Black race was associated with increased trial offer. After adjustment, patients 75 or older were less likely to be eligible for a clinical trial in the GI cohort; however, we found no significant associations between race and any of the outcomes after adjustment. Among eligible GI patients, we found no significant associations between non‐clinical factors and enrollment. Among the HN cohort, bivariate analyses demonstrated that female sex, older age, Black race, and unpartnered marital status were associated with decreased likelihood of trial offer; however, we found no significant associations between race, age, and marital status and any of the outcomes after adjustment. We found no significant associations between non‐clinical factors and eligibility after adjustment; however, women were less likely to be offered and to enroll in a clinical trial in the HN cohort.ConclusionFactors associated with eligibility, documented offer, and enrollment differed between disease site cohorts at our institution. Future work is needed to ensure the equitable inclusion of women and elderly patients in clinical trials.

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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