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Lifesaving cancer treatment without life-threatening side effects

08.18.26 | University of California - Irvine
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Irvine, Calif., Aug. 18, 2026 — CAR T-cell therapy has transformed cancer care, offering new hope to patients with aggressive blood cancers who once had few treatment options. But for some patients, the powerful immunotherapy can trigger a potentially life-threatening complication that causes brain inflammation, confusion, seizures and other serious neurological symptoms.

Researchers at UC Irvine have developed a new framework that could help make CAR T-cell therapy safer by targeting the biological processes believed to drive this complication. Published in Frontiers in Pharmacology , the study stresses that mitochondrial dysfunction is a key contributor to immune effector cell-associated neurotoxicity syndrome and outlines how existing drugs could potentially be repurposed to treat it.

Rather than developing an entirely new medication, the researchers propose evaluating drugs that already have established safety profiles, potentially accelerating the path toward clinical testing and improving outcomes for cancer patients.

“Our work points to mitochondrial dysfunction as a promising therapeutic target for serious neurological complications of CAR T-cell therapy,” says lead author Atena Zahedi, assistant professor of clinical pharmacy practice in UC Irvine’s School of Pharmacy & Pharmaceutical Sciences. “By identifying existing drugs that may be repurposed, we hope to accelerate the development of safer treatment strategies for patients receiving these lifesaving therapies.”

In CAR T-cell therapy, a patient’s immune cells are extracted and enhanced with chimeric antigen receptors, enabling them to recognize and destroy cancer when reintroduced into the body. While the treatment has produced remarkable results for many blood cancers, the intense immune response it generates can sometimes lead to immune effector cell-associated neurotoxicity syndrome (ICANS), a complication that affects the brain and nervous system.

Today, clinicians primarily rely on corticosteroids to control the inflammation. Although effective for many patients, steroids can produce significant side effects and may not address the underlying biological mechanisms driving ICANS.

For co-author, Onwodi Ifejeokwu, this work is personal. She lost a family member in 2021 to B cell lymphoma. Over the course of treatment, she witnessed firsthand how devastating cancer treatment can be on the brain. This loss spurred her passion for neuro-immuno-oncology research. She works alongside her mentors Zahedi, Dean and Griffin to improve the quality of life for cancer patients.

The interdisciplinary UC Irvine team members instead focused on mitochondria, the structures inside cells responsible for producing energy and regulating immune function. Their research suggests that when mitochondria become dysfunctional, they may amplify the inflammatory response that contributes to neurological injury after CAR T-cell therapy.

“One of the greatest opportunities in this work is identifying existing drugs that may be repurposed to better manage the neurological side effects associated with CAR T-cell therapy,” says co-author Shawn Griffin, an oncology pharmacist and associate clinical professor of clinical pharmacy practice at UC Irvine.

“Because many of these [medications] already have established safety profiles, they could potentially move into clinical evaluation more quickly than developing entirely new drugs. Our goal is to accelerate the discovery of safer treatment options that protect patients while preserving the lifesaving benefits of CAR T-cell therapy.”

The study also provides a road map for translating these findings into future clinical research. Senior author Dr. Erin Dean, a medical oncologist at UC Irvine’s Chao Family Comprehensive Cancer Center , is leading related clinical research efforts to evaluate new approaches that could improve patient care.

About the University of California, Irvine: Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation’s top 10 public universities by U.S. News & World Report . The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It’s located in one of the world’s safest and most economically vibrant communities and is Orange County’s second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide. For more on UC Irvine, visit www.uci.edu .

Media access: Radio programs/stations may, for a fee, use an on-campus studio with a Comrex IP audio codec to interview UC Irvine faculty and experts, subject to availability and university approval. For more UC Irvine news, visit news.uci.edu . Additional resources for journalists may be found at https://news.uci.edu/media-resources .

Frontiers in Pharmacology

Repurposing mitochondrial-targeting drugs for management of ICANS in CAR T-cell therapy: a novel steroid-sparing approach

27-Jul-2026

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Carly Murphy
University of California - Irvine
murphyco@uci.edu

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This article is based on a news release from University of California - Irvine. BrightSurf curates and republishes science news from research institutions worldwide; the original release is linked below.

How to Cite This Article

APA:
University of California - Irvine. (2026, August 18). Lifesaving cancer treatment without life-threatening side effects. Brightsurf News. https://www.brightsurf.com/news/LQ4N52K8/lifesaving-cancer-treatment-without-life-threatening-side-effects.html
MLA:
"Lifesaving cancer treatment without life-threatening side effects." Brightsurf News, Aug. 18 2026, https://www.brightsurf.com/news/LQ4N52K8/lifesaving-cancer-treatment-without-life-threatening-side-effects.html.