London: An experimental study involving only 16 patients with untreatable cancers, had their immune system redesigned to attack their own tumours in what is being called a “leap forward” in carcinoma treatment.
The results were presented at a meeting of the Society for Immunotherapy of Cancer and published simultaneously in the journal Nature.
The study and the results are being called “powerful” demonstration of the potential of new technology, the BBC reported, however, adding it is too early to fully assess the therapy’s effectiveness, besides its expensive and time-consuming.
As per the report, for the unique study each person had a treatment developed just for them, which targeted the specific weak spots in their tumour.
The work focuses on a part of the immune system called T-cells, which patrol the body and inspect other cells for problems.
They use proteins – called receptors – to effectively sniff out signs of infection or deviant cells that have become cancerous.
Cancers can be tricky for T-cells to spot. A virus is distinctly different to the human body, but cancers are more subtle because they are a corrupted version of our own cells.
The idea of the therapy is to boost levels of these cancer-spotting T-cells. It has to be tailored to each patient as each tumour is unique.
Explaining how it works, the report said: The researchers scoured patient’s blood for rare T-cells that already had receptors which could sniff out their cancer
Next, they then harvested other T-cells that could not find the cancer and redesigned them. Their original receptors, which may find other problems or infections, were replaced with those from the cancer-searching T-cells.
Finally, these modified T-cells were then put back into the patient to seek out the tumour.
Transforming T-cells into a form that can hunt cancer requires considerable genetic manipulation to both remove the genetic instructions for building their old receptors, and give them the instructions for the new ones.
It was made possible by tremendous advances in the gene-editing technology Crispr, whose developers won the Nobel Prize for Chemistry in 2020.
Crispr acts like a pair of molecular scissors – allowing scientists to easily manipulate DNA.
The trial involved people with colon, breast or lung cancers that had failed to respond to other treatments.
The study was designed to test the safety and feasibility of the technology, and showed the modified cells were finding their way into the tumour.
The disease continued to get worse in 11 patients, but stabilised in the other five. However, it will take larger studies to work out the correct dose and how effective it really is.
“This is a leap forward in developing a personalised treatment for cancer,” said Dr Antoni Ribas, one of the researchers at the University of California, Los Angeles, who tested the approach developed by the company Pact Pharma.
Dr Manel Juan, head of the immunology service at Clinic Hospital in Barcelona, told BBC: “It opens the door to using this personalised [approach] in many types of cancer and potentially in many other diseases.”
Dr Astero Klampatsa, from the Institute of Cancer Research, London, said the study was “important” but warned that the “time, labour and expense involved” were “huge”.
