According to a new study published in Gastroenterology by researchers at Virginia Commonwealth University (VCU) Massey Cancer Center and University of Florida Health, Black, Hispanic, Indigenous, and Asian Americans remain conspicuously absent from pancreatic cancer clinical trials aimed at testing the most recent treatment advances for this deadly disease.
Not only does this lack of diversity hurt patients belonging to these minority groups—who already shoulder a disproportionate pancreatic cancer burden—but it hurts science, too.
“If we don’t have good diversity in clinical trials, how will we ever know whether we have certain drugs that work better in some populations than others?” said study senior author Jose Trevino, MD, a surgical oncologist who holds a Distinguished Professorship of Oncology at VCU. “We could be throwing away a really good treatment option for racial and ethnic minority patients.”
For this study, Trevino and colleagues searched the ClinicalTrials.gov database for pancreatic cancer treatment trials conducted in the U.S. between 2005 and 2020. Since demographics aren’t typically reported during recruitment, the researchers focused on trials with results—a total of 207 trials, with 8,429 participants altogether.
These data revealed that over the last 15 years, there has been a steady increase in the proportion of pancreatic cancer trials reporting participants’ race and ethnicity, with a sizeable bump after reporting became federally mandated in 2017. In 2020, all the trials included in this study reported the race and ethnicity of participants. However, the actual inclusion of racial and ethnic minorities has stayed flat over time, stuck at the same disproportionately low rates for more than a decade.
During the study period, only 8% of pancreatic cancer clinical trial participants were Black, even though 12% of pancreatic cancer cases occur among the Black community. Likewise, Hispanic patients make up 6% of trial participants but 9% of cases, Asians account for 2% of trial participants but 3% of cases, and Indigenous Americans make up 0.3% of trial participants but 0.4% of cases.
The researchers attribute this lack of diversity to several factors, including mistrust of the medical establishment, implicit bias among clinicians, strict clinical trial inclusion criteria, and lack of diversity among the clinicians who are recruiting patients to trials. The paper lays out concrete steps to address these issues.
Edited by Gary Cramer