Cancer Cooperative Group Newsletter
Focus: Increasing Minority Accrual
February 2006--Lead Article (posted with permission)
Minority participation in
cancer clinical trials remains
a major challenge and
an ongoing focus for all stakeholders.
Accrual of underserved populations is
often quite low, with far-reaching research
and treatment implications.
For example,
African Americans represent 13% of
the US population, and breast cancer
is the second leading cause of death
among African-American women
(34.1%). However, only 7% of all patients
enrolled in a highly positive breast cancer
study investigating the
addition of Herceptin®
to conventional adjuvant
chemotherapy were African
American. Statistics
for other trials are similar.
In order to increase
minority participation in trials, clinical
researchers require a better understanding
of their patients' eligibility
status as well as their attitudes and
understanding of cancer research.
The Coalition of Cancer Cooperative
Groups is working to narrow this
accrual gap with a new initiative
recently funded by the Breast Cancer
Research Foundation (BCRF).
While the project focus is breast cancer,
the results can provide insights on
minority patient attitudes overall.
The study is designed to help
researchers at point-of-care learn
more about the numbers of minority
women who they screen for possible
participation in clinical trials and the
reasons why these patients are either
ineligible or choose not to participate
in a trial.
TrialCheck®, the Coalition's
searchable database of cancer clinical
trials, will be utilized, along with the
tracking module Enrollment
Tracker®, to follow screening,
eligibility, and enrollment/
nonenrollment patterns
among breast cancer patients
served by participating
sites that serve minority
populations. With these tools, researchers
will be able to pinpoint precise barriers
to minority-based protocol enrollment
among their patients. These findings
will not only inform the sites, but the
collective data will be published in a
full report to assist scientific leaders
nationwide as they consider trial
designs and their inclusivity.
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