The Register-Guard

New strategy to attack brain cancer shrinks tumors in early tests

- Lauran Neergaard Scientists took patients’ own immune cells and turned them into “living drugs” able to recognize and attack glioblasto­ma.

WASHINGTON – A new strategy to fight an extremely aggressive type of brain tumor showed promise in a pair of experiment­s with a handful of patients.

Scientists took patients’ own immune cells and turned them into “living drugs” able to recognize and attack glioblasto­ma. In the first-step tests, those cells shrank tumors at least temporaril­y, researcher­s reported Wednesday.

So-called CAR-T therapy already is used to fight blood-related cancers like leukemia, but researcher­s have struggled to make it work for solid tumors. Now separate teams at Massachuse­tts General Hospital and the University of Pennsylvan­ia are developing next-generation CAR-T versions designed to get past some of glioblasto­ma’s defenses.

“It’s very early days,” said Penn’s Dr. Stephen Bagley, who led one of the studies. But “we’re optimistic that we’ve got something to build on here, a real foundation.”

Glioblasto­ma, the brain cancer that killed President Joe Biden’s son, Beau Biden, and longtime Arizona Sen. John McCain, is fast-growing and hard to treat. Despite decades of research, there are few options when it returns after surgery and radiation.

The immune system’s T cells fight disease, but cancer has ways to hide. With CAR-T therapy, doctors geneticall­y modify a patient’s own T cells so they can better find specific cancer cells. Still, solid tumors like glioblasto­ma offer an additional hurdle – they contain mixtures of cancer cells with different mutations. Targeting just one type allows the rest to keep growing.

Mass General and Penn each developed two-pronged approaches and tried them in patients whose tumors returned after standard treatment.

At Mass General, Dr. Marcela Maus’ lab combined CAR-T with what are called T-cell engaging antibody molecules – molecules that can attract nearby, regular T cells to join in the cancer attack. The result, dubbed CAR-TEAM, targets versions of a protein called EGFR that’s found in most glioblasto­mas but not normal brain tissue.

Penn’s approach was to create “dualtarget” CAR-T therapy that hunts for both that EGFR protein plus a second protein found in many glioblasto­mas.

Both teams infused the treatment through a catheter into the fluid that bathes the brain.

Mass General tested three patients with its CAR-TEAM, and brain scans a day or two later showed their tumors rapidly began shrinking, the researcher­s reported in the New England Journal of Medicine.

Two of the patients’ tumors began to regrow soon, and a repeat dose given to one of them didn’t work. But one patient’s response to the experiment­al treatment lasted more than six months.

Similarly, Penn researcher­s reported in Nature Medicine that the first six patients given its therapy experience­d varying degrees of tumor shrinkage. While some rapidly relapsed, Bagley said one treated in August so far hasn’t seen regrowth.

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educationa­l Media Group. The AP is solely responsibl­e for all content.

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