The therapies are still in the early stages of development, but researchers are optimistic about the results.
It’s not often that a treatment makes high ranking members of the American Cancer Society say “whoa.”
That’s what happened when Dr. Otis Brawley discussed the results of three recent CAR-T therapies, however. According to a report from CNN,1 the former chief medical officer of the American Cancer Society was highly impressed not just by the results of the studies, but at the speed at which the treatments seemed to work.
The studies revolved around treatments for gliobastoma, an incredibly hard to treat and often deadly form of brain cancer. The vast majority of patients don’t survive three years after diagnosis, with the average only making it 14 months.
The new studies referenced in the report involve treatments that are designed to reprogram the body’s immune response in a way that allows it to attack the tumors. The brain tumors that develop as a result of gliobastoma deceive the body by tricking the body into releasing a naturally occurring T-cell that can suppress the immune response, allowing the tumors to continue to grow.
At least one of the therapies reprogramed the body’s response so that the suppressor T-cells will instead attack the tumors. The results of the studies showed, in some cases, the tumors shrinking, and even disappearing, very quickly. In some cases, results were noticeable within just a few hours.
Another one of the studies referenced in the report used CAR-T therapies to target a specific protein created by the brain tumors (interleukin-13 receptor alpha 2).
However, it’s important to note that these studies are still in the early stages. Also, why the therapy was successful at shrinking and, in some cases, destroying the tumors, the many patients saw their cancer come back within a fairly short time period (within a month or two in some cases). While the CAR-T therapies showed promise at reducing the tumors, in most cases they were not a cure for cancer and the tumors did return.
Some patients involved in the studies did see their tumors disappear and not return, although these cases are described as outliers.
Researchers believe that with some adjustments, they can improve the treatment’s response. Despite the temporary impact of the treatment, the results are still considered to be highly impressive. Brawley told CNN that the impact of the treatment on the tumors was “shocking” to him.
Dr. Donald O’Rourke is the lead researcher on the of a trial at the University of Penn that combined the methods of the two other studies.
He discussed some of the side effects of the studies with CNN, saying, “When you treat someone with this powerful treatment in the brain who has a lot of tumor in there, the brain gets very inflamed, and they basically have a long, low-grade kind of chronic weakness syndrome. That is the result, sort of like a low-grade smoldering meningitis, because you’re actually putting immune cells in the spinal fluid, and they’re active, and they’re not supposed to be there.”
To combat this, he believes that patients will fare better when treated earlier when the tumors are smaller.
Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
Fake Weight Loss Drugs: Growing Threat to Consumer Health
October 25th 2024In this episode of the Pharmaceutical Executive podcast, UpScriptHealth's Peter Ax, Founder and CEO, and George Jones, Chief Operations Officer, discuss the issue of counterfeit weight loss drugs, the potential health risks associated with them, increasing access to legitimate weight loss medications and more.
Johnson & Johnson Seeks FDA Approval for Subcutaneous Tremfya Regimen for Ulcerative Colitis
November 22nd 2024Johnson & Johnson has submitted a supplemental Biologics License Application to the FDA for a subcutaneous induction regimen of Tremfya for adults with moderately to severely active ulcerative colitis based on positive Phase III ASTRO trial results.