Geographic Disparities in Access to Cancer Clinical Trials in Canada

Omar Abdel-Rahman1

  • 1Department of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, AB, Canada.

Abstract

Insights

Geographic and cancer type disparities exist in Canadian cancer clinical trials access. The COVID-19 pandemic also negatively impacted trial accessibility, highlighting inequities in clinical trial participation.

Area of Science:

  • Oncology
  • Clinical Trials Research
  • Health Services Research

Background:

  • Equitable access to cancer clinical trials is crucial for advancing cancer care and ensuring all patients can benefit from novel treatments.
  • Geographic and demographic factors can influence patient participation in clinical trials, potentially leading to disparities in access.

Purpose of the Study:

  • To evaluate geographic disparities in access to cancer clinical trials across Canada.
  • To analyze trends in cancer clinical trial registration and funding sources.
  • To compare cancer clinical trial availability between Canada and the United States.

Main Methods:

  • Reviewed cancer clinical trial data from clinicaltrials.gov for trials conducted in Canada between 2005 and 2023.
  • Conducted frequency analyses based on location (national, provincial, urban centers), cancer type, funding source, and time period.
  • Calculated cancer clinical trials per 10,000 persons for Canada and the US.

Main Results:

  • Significant geographic disparities were observed, with cancer clinical trials per 10,000 individuals ranging from 6.79 in New Brunswick to 0 in the territories.
  • Lymphoma trials (32.85 per 1000 cases) were most numerous relative to projected cases, while bladder cancer trials (7.06 per 1000 cases) were least numerous.
  • Industry funding comprised 69% of trials, and the highest trial activity occurred between 2014-2016, with a notable decrease from 2020-2022.

Conclusions:

  • Access to cancer clinical trials in Canada is inequitably distributed, influenced by geographic location and primary tumor site.
  • The COVID-19 pandemic has further exacerbated existing disparities in access to cancer clinical trials.
  • Addressing these disparities is essential for improving cancer care outcomes nationwide.

Related Concept Videos

Clinical Trials: Overview01:11

Clinical Trials: Overview

Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
3.0K
Clinical Trials01:16

Clinical Trials

Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
6.8K
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.3K
Cancer Survival Analysis01:21

Cancer Survival Analysis

Cancer survival analysis focuses on quantifying and interpreting the time from a key starting point, such as diagnosis or the initiation of treatment, to a specific endpoint, such as remission or death. This analysis provides critical insights into treatment effectiveness and factors that influence patient outcomes, helping to shape clinical decisions and guide prognostic evaluations. A cornerstone of oncology research, survival analysis tackles the challenges of skewed, non-normally...
381
Hazard Ratio01:12

Hazard Ratio

The hazard ratio (HR) is a widely used measure in clinical trials to compare the risk of events, such as death or disease recurrence, between two groups over time. It reflects the ratio of hazard rates—the instantaneous risk of the event occurring—between a treatment group and a control group. This measure provides valuable insights into the relative effectiveness of a treatment by assessing how the risk of an event differs between the two groups.
For example, in a clinical trial...
155
Cancer Vaccines01:30

Cancer Vaccines

Cancer treatment vaccines are a rapidly evolving field that offers a promising approach to immunotherapy. Unlike traditional vaccines that prevent diseases, cancer treatment vaccines are designed to treat existing cancers by stimulating the immune system to recognize and attack cancer cells.
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
400