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Home / Education And Resources / Research / ACCC Community Oncology Research Institute / ACORI Research Review / ACORI Research Review September 2020

ACORI RESEARCH REVIEW: SEPTEMBER 2020

Printable Version

A Message from the President's Task Force

By Nadine J. Barrett, PhD, MA, MS

This issue of the ACCC Research Review provides support, perspectives, and resources for follow through on the imperative to make clinical trials more inclusive, diverse, accessible, and representative of our patient populations in communities across the country.

While this task can seem overwhelming, let us consider the fact that as oncology professionals, change drives the work we do. Improving rates of screening and early diagnosis, advancing treatments, eliminating health disparities, and reducing the burden of cancer on society—these overarching goals all demand intentional actions and sustained commitment to achieve change.

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A Focus on the Importance of Collaboration Between Community Groups & Academic Institutions

Each month, we ask an ACCC member to share their expertise in a specific area of research concentration. In this issue, we asked Sanford E. Jeames, DHA, Adjunct Faculty member at Huston Tillotson University in Austin, Texas, and Chair-Elect of the ASCO Health Equity Committee to highlight the importance of community engagement in cancer research. Dr. Jeames is also a member of American Association for Cancer Research (AACR) and the Society of Urologic Nurses and Associates (SUNA). His research interests are in community-based research, cancer prevention, survivorship, and health disparities.

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Featured Clinical Research: Barriers to Clinical Trials Participation

There is no debate: clinical trials are essential to advancement of treatments for cancer and improving patient outcomes. Despite the fact that cancer treatment trials are standard of care and offer patients access to leading-edge therapies, that a clinical trial may be a patient’s only treatment option but also their best option—enrollment in clinical trials is persistently low. Among the consequences of insufficient or slow accrual are trials forced to close due to insufficient enrollment and studies that take so long to complete that their results become less timely.

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AACR Panel on Racism and Racial Inequalities in Cancer Research: Let It Not Be in Vain

At the American Association for Cancer Research (AACR) Virtual Annual Meeting in June a special session hosted by AACR President Antoni Ribas, MD, PhD, FAACR, brought together a distinguished panel of leaders from academia, government, industry, and the patient advocacy community for a frank conversation on racism and racial inequities in cancer research. Persistent disparities exist across the cancer research enterprise. From the health professional standpoint, there continue to be disparities in the numbers of faculty, clinicians, researchers, and allied professionals from racial and ethnic minority populations. Representation at the C-Suite level is rare. From the patient and caregiver perspective, disparities in access to cancer clinical trials, accrual to clinical trials, and in health outcomes are pervasive.

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Guidance for Achieving Diversity, Inclusion, and Equity in Clinical Research

In August, the Multi-Regional Clinical Trials Center of Brigham and Women’s Hospital and Harvard (MRCT Center) released guidance for “Achieving Diversity, Inclusion, and Equity in Clinical Research” along with a companion Toolkit consisting of practical resources to facilitate change.1 The guidance outlines a principled, multi-stakeholder approach to optimize the inclusion of diverse populations in clinical research.

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At-a-Glance Tools from ASCO’s Research Community Forum

Among the many effects of the COVID-19 pandemic has been disruption of cancer clinical research. In response the American Society of Clinical Oncology (ASCO) Research Community Forum is providing tools to help support prioritization of cancer clinical trials as hospitals and health systems move forward. Released in May 2020, Making the Case for Oncology Clinical Research outlines a four-step approach for driving home the benefits and potential impact of research for patients, the oncology program, and the broader community: engagement, awareness and impact, collaborations, and creating a culture of research. Download here.

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