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Pancreatic Cancer Survival: Disparities and Trends

Pancreatic Cancer Survival: Disparities and Trends

January 10, 2026 Dr. Jennifer Chen Health

Complex demographic and geographic ​disparities are influencing‍ pancreatic cancer outcomes ⁢across the ⁤US,‍ pointing to needs​ for broad ​public health interventions, targeted prevention ⁢strategies, ‍and improved resource allocation to combat the shifting patient survival landscape ⁤of this malignancy. A trio of abstracts presented ‌at the American Society⁣ of Clinical Oncology Gastrointestinal ⁤Cancers Symposium exhibit ⁤mortality⁢ outcomes from ⁤this sixth-leading cause of cancer-related ⁣mortality worldwide,1 through patient outcomes ⁢information from⁢ a⁢ high-volume treatment area and mortality hotspots in the South and Midwest regions.1-3

These data​ from the CDC, the University of ​Texas MD ⁣Anderson Cancer Center, and the Institute for Health Metrics ⁣and Evaluation cover 1990 to 2024 and examine the ⁢pancreatic cancer burden​ across the intersections of rural and urban populations, races⁤ and ethnicities, and age and sex.

Pancreatic Cancer in Rural Areas1

Table of Contents

    • Pancreatic Cancer in Rural Areas1
  • Pembrolizumab Shows Racial Disparities in Efficacy and Enrollment
    • Pembrolizumab and Overall Survival
    • Racial Disparities in Trial Enrollment
    • Implications and Future​ Research

Incorporating‍ data from CDC⁣ WONDER (Wide-ranging⁢ ONline Data‌ for Epidemiologic ⁣Research) on deaths⁣ of adults 25 years and‍ older (N​ =​ 1,002,439), ⁤researchers focused on age-adjusted mortality ⁢rates (AAMRs) per 100,000 ⁢population​ for ‌1999 to ⁤2023 for urban (n = 698,805) and rural (n = 148,558) areas; remaining deaths were in another area. the AAMR was 17.66 (95% CI, 17.25-18.45)⁣ and it underwent a 0.33% average annual percent change (AAPC).

Although the AAMRs are close ‍to equal when stratifying by rural (17.69; 95% CI, 17.03-18.96) vs urban (17.62; 95% CI, 17.30-18.02) location the AAPCs are separated by an immense gap: ⁢0.77% vs 0.20%, with ⁣the mortality rate in ⁣

Pembrolizumab Shows Racial Disparities in Efficacy and Enrollment

A clinical trial of pembrolizumab ​demonstrated meaningful⁤ differences in overall ​survival (OS) and trial ⁣enrollment rates based on race, with Asian patients experiencing the highest benefit⁢ and Black and Hispanic patients facing lower ‌enrollment and ⁤shorter survival times. These‌ findings highlight ongoing disparities in cancer treatment outcomes and ‍access to clinical trials.

Pembrolizumab and Overall Survival

Pembrolizumab, an immunotherapy drug, ​showed varying degrees of⁢ effectiveness in ​extending overall survival depending on a patient’s‍ race. The trial data revealed a statistically significant difference in delivery ​rates (P ⁣< .001) across racial groups. Specifically,Asian ⁣patients exhibited the highest delivery rate at 92%,compared‌ to 83% in Black patients.

Median overall ⁤survival differed substantially: ⁤26.6‍ months for⁤ Asian patients, ⁣20.7 months for non-Hispanic⁤ White (NHW) patients,18.6 ⁤months for Hispanic patients, and 17.4 months for ​Black patients. This suggests a potential biological or socioeconomic factor influencing treatment response. ​

Example: ⁤The median follow-up⁣ period⁤ for all patients in the trial was 3‍ months,providing a consistent timeframe ‍for assessing survival ‍outcomes across ‍racial groups.

Racial Disparities in Trial Enrollment

Enrollment rates in ‍the pembrolizumab trial also varied significantly by race,​ indicating potential barriers to‍ access and participation for minority groups. Black patients comprised only ‌25% of the enrolled population (P < .001), while Hispanic patients ‍represented 30% (P = .043), compared to 38% for non-Hispanic White patients.

These lower enrollment rates could ⁣be‌ attributed to a variety of factors, including geographic limitations,‌ lack of awareness about clinical‍ trials, distrust of the medical system, and socioeconomic barriers.‌ Lower enrollment can limit the generalizability⁣ of trial results‍ to ⁢diverse populations.

Evidence: The statistically significant differences in ‌enrollment (P < .001 for Black patients, P = .043 for Hispanic patients) demonstrate a‍ clear disparity in access to this possibly life-extending treatment.

Implications and Future​ Research

The ⁤observed racial disparities ‌in both treatment delivery and ⁢trial ⁢enrollment underscore the need for targeted interventions to improve equity ‌in cancer care. Further research is needed to understand the underlying mechanisms driving these differences and ​to develop strategies to overcome barriers to access for underrepresented populations.

Addressing ​these disparities ‌is crucial to ensuring that all patients, ⁢regardless of‍ race or ethnicity,⁣ have the chance​ to benefit from advances in cancer treatment.

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