If you or a loved one has been diagnosed with cancer, you may be interested in a clinical trial. Clinical trials test how new medical approaches work in people, focusing on how new treatments may work when other methods have failed. Clinical treatments have resulted in new treatments and prevention options for cancer care.
If you are interested in learning more about a clinical trial, complete the form below or call 864-241-6251. View below all of our active clinical trials.
National Cancer Institute Community Oncology Research Program
The National Cancer Institute proclaimed Prisma Health Cancer Institute among the nation’s best in research with a recent award of $6.7 million to conduct clinical trials and research studies aimed at improving patient outcomes and reducing health disparities. Prisma Health is the only community-based site in S.C. to receive the award. Clinical trials focus on improving cancer prevention, cancer control, screening for early cancers and post-treatment surveillance, while cancer care delivery research focuses on quality of life and understanding the diverse and multi-level factors that affect access to and quality of care.
Clinical trials focus on improving cancer prevention, cancer control, screening for early cancers, and post-treatment surveillance. Cancer care delivery research will focus on quality of life and understanding the diverse and multi-level factors that affect access and quality of care.
With a focus on translational research and personalized medicine, Prisma Health’ Institute for Translational Oncology Research (ITOR) provides some of the most advanced cancer treatments available anywhere in the world, while supporting industry’s crucial need to achieve greater efficiency and expediency in bringing life-saving cancer drugs to patients. The effort to advance these dual goals was what led to the creation of ITOR in 2004.
ITOR is a major pillar of translational cancer research at Prisma Health. The efforts of ITOR include a Phase I Clinical Research Unit, a Biorepository Services platform, and proteomics and enomics capabilities.
ITOR advances cancer care on multiple levels, facilitating pioneering research as well as clinical care delivery. ITOR is committed to translational medicine, which is a branch of medical research that forges a direct link between basic research and patient care. In the case of drug therapies, translational medicine refers to the translation of basic research into beneficial drug treatments for patients.
ITOR focuses on discovering and developing drugs that help people who have cancer.
Prisma Health Human Performance Laboratory (HPL) is the first in the nation to be fully embedded into a cancer research and treatment program.
The HPL, which is working with a limited number of patients on a pilot basis, is a collaborative effort between Greenville Health System and the University of South Carolina School of Medicine Greenville. While its focus is on cancer survivor patients in the Prisma Health Cancer Institute, the lab will ultimately serve all Prisma Health clinical populations.
HPL traditionally have been the province of elite athletes who use the state-of-the-art analysis to improve performance. This the first time that an HPL has been used by a cancer institute to measure the changes in post-treatment cancer survivors — from whole body function all the way down the cellular level — in an effort to improve patient health and outcomes.
At Prisma Health Cancer Institute, we are committed to research in understanding and eliminating barriers to accessing high-quality cancer care. Cancer Care Delivery Research (CCDR) improves clinical outcomes and patient well-being by improving patient, clinician, and organizational factors influencing care delivery. Prisma Health’ CCDR team is comprised of doctors, nurses, and other health professionals committed to merging evidence-based cancer care with patients’ treatment preferences.
Leading the charge at Prisma Health is Matthew F. Hudson, PhD, MPH. Dr. Hudson is the Director of Cancer Care Delivery Research (CCDR). He oversees initiatives examining how social factors, health care infrastructure, provider and patient behavior impact cancer care quality. He co-chaired the National Cancer Institute’s CCDR Coordinating Committee and presently co-chairs NRG Oncology’s CCDR committee. Dr. Hudson is also a research director for Greenville Health System’s Health Sciences Center (HSC)-a regional academic/health care collaborative informing sound clinical practice. Through the HSC, Dr. Hudson contributes to scholarship on patient-centered models of care, healthcare workforce education and development, health care access, and population health. Dr. Hudson holds faculty appointments at Clemson University, the University of South Carolina School of Medicine Greenville, and the Arnold School of Public Health (University of South Carolina). He teaches a course at the Arnold School entitled, “Comparative Effectiveness Research: Interface Opportunity for Public Health and Medicine”.
O’Rourke, M. A., O’Rourke, M. C., & Hudson, M. F. (2017). Reasons to Reject Physician Assisted Suicide/Physician Aid in Dying. Journal of Oncology Practice, 13(10), 683-686.
Jindal, M., Hudson, M. F., Blackhurst, D. W., Coltman, K., & McCoy, G. D. (2016).The Impact of Electronic Cues and Provider Education on Colorectal Cancer Screening. Referral and Patients’ Screening Decision Stage. Journal of the South Carolina Medical Association, 112(1), 169-171.
Russ-Sellers,R., Hudson, M.F., Youkey, J.R., & Horner, R.D. (2014). Achieving Effective Health Service Research Partnerships. Medical Care, 52(4), 289-290.