A Form of Immune Therapy Might be Effective for Multiple Myeloma  

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Posted: 5/11/2014

<span style="font-size:12pt;font-family:Jianhua Yu, PhD
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Jianhua Yu, PhD
 
Craig Hofmeister, MD, MPHCraig Hofmeister, MD, MPH
  • Multiple myeloma is a cancer of the blood that is still incurable, and new therapies are urgently needed.
  • This study describes a type of immune therapy that might effectively treat myeloma.
  • These findings suggest that testing the therapy in clinical trials is warranted.
COLUMBUS, Ohio – A new study by researchers at The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC – James) provides evidence that genetically modifying immune cells might effectively treat multiple myeloma, a disease that remains incurable and will account for an estimated 24,000 new cases and 11,100 deaths in 2014
 
The researchers modified a type of human immune cell – called T lymphocytes, or T cells – to target a molecule called CS1, which is found on more than 95 percent of myeloma cells, and to kill the cells. The researchers grew the modified cells in the lab to increase their numbers and then injected them into an animal model where they again killed human myeloma cells.
 
The findings were published in the journal Clinical Cancer Research.
 
“Despite current drugs and use of bone marrow transplantation, multiple myeloma is still incurable, and almost all patients eventually relapse,” says co-principal investigator and multiple myeloma specialist Craig Hofmeister, MD, MPH, assistant professor of medicine and a member of the OSUCCC – James Translational Therapeutics Program.
 
“This study presents a novel strategy for treating multiple myeloma, and we hope to bring it to patients as part of a phase I clinical trial as soon as possible,” Hofmeister says.
 
“In particular, our study shows that we can modify T lymphocytes to target CS1, and that these cells efficiently destroy human multiple myeloma cells,” says principal investigator Jianhua Yu, PhD, assistant professor of medicine and a member of the OSUCCC – James Leukemia Research Program.
 
“An important possible advantage to this approach is that these therapeutic T cells have the potential to replicate in the body, and therefore they might suppress tumor growth and prevent relapse for a prolonged period," Yu says.
 
For this study, Yu, Hofmeister and their colleagues used cell lines and fresh myeloma cells from patients to produce genetically engineered T cells with a receptor that targets CS1. The researchers then tested the capacity of the modified cells to kill human multiple myeloma cells in laboratory studies and an animal model.
 
The study’s key technical findings include:
  • Compared to control T cells, the modified T cells better recognized multiple myeloma cells that overexpressed CS1, and they became more activated following the recognition;
  • The researchers successfully modified fresh T cells from patients and showed that the cells can be grown (expanded) in the lab, and that they efficiently recognized and eradicated myeloma cells;
  • In animal models, the modified T cells greatly reduced the tumor burden and prolonged overall survival: All mice that received the modified T cells were alive 44 days after treatment versus 29 percent and 17 percent of the study’s two control groups.
Funding from the National Institutes of Health (CA155521, OD018403), Multiple Myeloma Opportunities for Research and Education, the National Blood Foundation, and an OSUCCC – James Pelotonia Idea Grant supported this research.
 
Other Ohio State University researchers involved in this study were Jianhong Chu, Shun He, Youcai Deng, Jianying Zhang, Yong Peng, Tiffany Hughes, Ling Yi, Chang-Hyuk Kwon, Qi-En Wang, Steven M. Devine, Xiaoming He and Xue-Feng Bai.
 
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute strives to create a cancer-free world by integrating scientific research with excellence in education and patient-centered care, a strategy that leads to better methods of prevention, detection and treatment. Ohio State is one of only 41 National Cancer Institute (NCI)-designated Comprehensive Cancer Centers and one of only four centers funded by the NCI to conduct both phase I and phase II clinical trials. The NCI recently rated Ohio State’s cancer program as “exceptional,” the highest rating given by NCI survey teams. As the cancer program’s 228-bed adult patient-care component, The James is a “Top Hospital” as named by the Leapfrog Group and one of the top cancer hospitals in the nation as ranked by U.S.News & World Report.
 
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Note: In early 2014, Ohio State cancer researchers Yu, Hofmeister, Caligiuri, Benson and others published a related study in the journal Leukemia on CS1-targeted natural killer cells.
 
High quality JPEGs are available for Craig Hofmeister, MD, MPH, and for Jianhua Yu, PhD.
 
Contact: Darrell E. Ward, Wexner Medical Center Public Affairs and Media Relations,
614-293-3737, or Darrell.Ward@osumc.edu
 
 


Tags: Multiple Myeloma; Pelotonia; Clinical/Translational Research; Research Findings

The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC – James) 300 W. 10th Ave. Columbus, OH 43210 Phone: 1-800-293-5066 | Email: jamesline@osumc.edu