Treating pediatric acute lymphoblastic leukemia with CAR T-cell therapy, a feasible global option that is both effective and safe.

‘International multisite clinical trial results show that CAR T-cell therapy a feasible, safe and effective treatment approach for pediatric acute lymphoblastic leukemia.’

Pulsipher, who is also Chair of the Pediatric Blood and Marrow Transplant Consortium, worked with Grupp and the paper's primary author, Shannon Maude from CHOP, as well as investigators from the US, Canada, Europe, Japan, and Australia to organize and run the trial, teaming with Novartis, the industry sponsor of the trial. The study was conducted at 25 sites in 11 countries. 




The New England Journal paper reports on 75 evaluable patients between 3 to 21 years of age with relapsed or treatment refractory B-cell ALL. 61% of these patients had relapsed after allogeneic hematopoietic stem cell transplantation, an intensive therapy intended to be curative and whose failure leaves few remaining options. For comparison, the paper cites another FDA-approved therapy for the treatment of children with relapsed or refractory ALL; it produced a response rate of 20% with a median overall survival time of 13 weeks.
"Previously, for patients who relapsed after transplant or did not respond to treatment - there wasn't much else we had to offer them and often, they went to hospice," said Pulsipher. "Now, instead of sending them to hospice - we treat them with CAR-T-cells, make them better, then send them home."
The updated analysis showed an overall remission rate of 81% within 3 months of treatment. All patients who responded to therapy showed no minimal residual disease by flow cytometry - the most sensitive means of analysis. Overall survival was 90% at 6 months and 76% at 12 months. The median length of remission was not reached, with tisagenlecleucel remaining in the blood for up to 20 months.
"CAR-T therapy is truly a game changer for pediatric leukemia," said Alan S. Wayne, MD, director of the Children's Center for Cancer and Blood Diseases at CHLA. "We are pleased to be one of a small number of institutions able to offer this new treatment to children for whom conventional therapies have failed."
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