Early findings from a small clinical trial provide evidence that a new cellular immunotherapy approach may be effective in treating metastatic solid tumours.

In the trial, researchers from the National Institutes of Health (NIH) genetically engineered normal white blood cells, known as lymphocytes, from each patient to produce receptors that recognise and attack their specific cancer cells.

These initial findings are from people with metastatic colourectal cancer who had already undergone multiple earlier treatments.

The personalised immunotherapy shrank tumours in several patients and was able to keep the tumours from regrowing for up to seven months.

The findings were published July 11, 2024, in Nature Medicine.

One form of cellular immunotherapy, chimeric antigen receptor (CAR) T-cell therapy, has already been shown to be effective against some blood cancers, and another, called tumour-infiltrating lymphocyte (TIL) therapy, has proven to be effective against metastatic melanoma.

However, to date, a cellular therapy that’s effective against any other solid cancers has been elusive, according to Steven A. Rosenberg, M.D., Ph.D., of NCI’s Center for Cancer Research (CCR), who co-led the study with Maria Parkhurst, Ph.D., of CCR’s Surgery Branch. 

“The fact that we can take a growing metastatic solid cancer and get it to regress shows that the new cellular immunotherapy approach has promise,” Dr. Rosenberg said. “However, it’s important to understand that these findings are preliminary and that the approach needs to be further refined and tested in more types of solid cancers.”

The new approach overcomes two challenges in cellular immunotherapy: how to produce large numbers of T cells that can recognise cancer cells specifically, and how to boost the ability of modified T cells to multiply once they’ve been returned to the patient. 

For each patient in the study, Dr. Rosenberg and his colleagues collected lymphocytes present in the patient’s tumours.

They then used sophisticated molecular characterisation techniques to identify and isolate receptors on those lymphocytes, called T-cell receptors, that recognised specific changes in each patient’s tumour.

After genetically sequencing those receptors, they then used a retrovirus to insert the genes for the receptor into normal lymphocytes collected from each patient’s circulating blood. 

The genetically modified lymphocytes were then multiplied into the hundreds of millions in the laboratory and infused back into the patients, where they expressed the tumour-specific T-cell receptors and continued to multiply.

“By taking the natural T-cell receptors that are present in a very small number of cells and putting them into normal lymphocytes for which we have enormous numbers—a million in every thimbleful of blood—we can generate as many cancer-fighting cells as we want,” Dr. Rosenberg explained. 

As part of a larger phase 2 trial, seven patients with metastatic colon cancer were treated with the experimental personalised cellular immunotherapy.

All seven received several doses of the immunotherapy drug pembrolizumab before the cell therapy and another immunotherapy drug called IL-2 afterward.

Three patients had substantial shrinkage of metastatic tumours in the liver, lung, and lymph nodes that lasted for four to seven months.

The median time to disease progression was 4.6 months. 

Dr. Rosenberg noted that, of the three patients who responded to the treatment, two had received T-cell receptors derived from cytotoxic T cells, which are primarily responsible for killing diseased cells.

Dr. Rosenberg said his research team is exploring how to put the T cell receptors into subtypes of normal lymphocytes to improve their reactivity. 

Colon cancer is just one of many solid tumours the researchers are studying.

The trial is still ongoing and includes patients with different types of solid cancers. 

“It's just the very beginning of converting normal lymphocytes into cells capable of treating the common solid cancers,” Dr. Rosenberg said. “What this study shows is that it's possible. Once you know it’s possible, you work to improve it.”

Source: NIH/National Cancer Institute