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Home / Health Conditions / Clinical Trials / New Ready-Made Treatment for Acute Myeloid Leukemia Presented at AACR Chicago

New Ready-Made Treatment for Acute Myeloid Leukemia Presented at AACR Chicago

New Ready-Made Treatment for Acute Myeloid Leukemia Presented at AACR Chicago

Scientists have developed a new, ready-made way to fight blood cancers that looks promising. Imagine having cancer-fighting cells already prepared and waiting, ready to be given to patients who need them. The results were presented at the American Association for Cancer Research’s (AACR) meeting in Chicago.

How This New Therapy Works: Unleashing Natural Killer Cells

This new treatment uses special cells from our body’s defense system, called “natural killer cells” or “NK cells.” These NK cells have been trained in the lab to find and destroy cancer cells in the blood. In a recent study, this treatment helped several people with a serious blood cancer called AML (acute myeloid leukemia) get much better – in some cases, the cancer completely disappeared!

One of the lead doctors, Dr. Stephen Strickland Jr., was very encouraged by how well it worked for these patients. He hopes this could be a new and important option for people with AML, where finding good treatments can be tough. “The deep and durable responses observed in patients for whom we have follow-up data are impressive,” Dr. Strickland said in a press release. “We are hopeful this can be a new type of treatment for AML patients where the unmet medical need is extremely high.”

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Comparing to Existing Treatments: The Advantage of “Off-the-Shelf” Therapy

You might have heard of another type of cell therapy called “CAR T-cell therapy.” That’s when doctors take a patient’s own immune cells (T-cells), teach them to fight their specific cancer, and then put them back in. It’s like giving your own army special training.

But this process can take time in the lab, which can be a problem for people with fast-moving cancers like AML. Also, sometimes their own T-cells aren’t strong enough to be trained properly.

That’s where this new CAR NK-cell therapy is different. Instead of using the patient’s own cells, these NK cells can come from healthy donors. Think of it as having a supply of healthy fighters ready to go. These NK cells can be made ahead of time and stored, so they can be given to patients quickly, instead of needing a personalized treatment made just for them.

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The Science Behind SENTI-202: Smart Targeting of Cancer Cells

In this study, the scientists tested a specific version of this CAR NK-cell therapy called SENTI-202. These NK cells were designed to recognize two different signals found on leukemia cells. This helps them find and kill cancer cells that have either of these signals.

These NK cells also have a built-in safety system. It’s like they have a special code that tells them not to attack healthy cells that might also have one of these signals. This “smart targeting” helps them focus on the cancer cells and leave the healthy ones alone.

Patients Show Significant Improvement

The early results from the first nine patients who received this treatment after other treatments didn’t work or the cancer came back are exciting. After getting some initial treatment to prepare their bodies, they received the SENTI-202. For four of these patients, there was no sign of cancer left in their blood! Another patient also had a very good response and was considered “leukemia-free.”

Dr. Strickland said that it’s usually hard to find targets that are only on cancer cells and not on healthy ones. But this new technology, which can recognize multiple targets on cancer while avoiding healthy cells, could be a big step forward in making these kinds of treatments easier to use.

More Research Is Coming

It’s important to remember that these are just early results, and scientists are still studying this treatment in clinical trials to make sure it’s safe and it works well. But this new approach offers hope for a faster and simpler way to fight serious blood cancers.

By Taylyn Washington-Harmon | Published April 29, 2025

April 29, 2025 by Taylyn Washington-Harmon

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