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US approval for breakthrough cancer gene therapy

The US Food and Drug Administration described the approval as 'a historic action'
The US Food and Drug Administration described the approval as 'a historic action'

A treatment that uses a patient's own immune cells to fight leukemia has received approval in the United States, the first time any gene therapy has done so.

The move is seen as opening a new era in the fight against cancer.

The breakthrough treatment is made by Novartis and is called Kymriah, or tisagenlecleucel.

This type of immunotherapy is known as Chimeric Antigen Receptor T Cell or CAR-T cell therapy.

It was approved by the US Food and Drug Administration for children and young adult patients up to 25 years old with a form of acute lymphoblastic leukemia.

The FDA described the approval as "a historic action" that would usher "in a new approach to the treatment of cancer and other serious and life-threatening diseases".

Studies have shown that 83% of patients responded to the one-time only treatment, achieving remission within three months.

The treatment is not a pill or a form of chemotherapy. It uses a patient's own immune cells, called T-cells, along with white blood cells.

These cells are removed from a patient, sent to a lab, reprogrammed, and then returned to the patient.