Rachyl M. Shanker, MD (she/her/hers)
Research Fellow
National Institutes of Health
Washington, District of Columbia, United States
Nicole Russell, BS
TCU School of Medicine
Fort Worth, Texas, United States
Michael P. O'Leary, MD
Assistant Professor of Surgery
University of California, Irvine
Orange, California, United States
Joal D. Beane, MD
Assistant Professor
Department of Surgery, The Ohio State University Wexner Medical Center
Columbus, Ohio, United States
Alex C. Kim, MD, PhD (he/him/his)
Surgical Oncology
UT Southwestern
Dallas, Texas, United States
Oliver S. Eng, MD (he/him/his)
Associate Professor of Surgery
University of California, Irvine
Orange, California, United States
Tracey Pu, MD
Resident
University of Alabama - Birmingham
Birmingham, Alabama, United States
1195 AA/PC patients were identified. 775 (59.3%) were female, and 67.9% were White. Non-White AA/PC patients were less likely to receive chemotherapy compared to White patients (68.6% vs. 74.1%, p=0.04) and were also less likely to receive CRS/HIPEC (11.0% vs. 17.7%, p=0.002). On subgroup analysis, Non-White patients residing in the most vulnerable SVI Tertile (T3) were less likely to receive any chemotherapy (65.6% vs. 75.0%, p=0.03) or CRS/HIPEC (13.7% vs. 23.1%, p=0.01), while there was no difference in less vulnerable SVI tertiles (all p >0.05).
Conclusions: Non-White patients were less likely to receive CRS/HIPEC in the highest vulnerability tertile compared to White patients. Further investigation is warranted to guide state-level public health policy to increase treatment access for minoritized populations residing in vulnerable areas.