No substantial benefit from transplantation reported for a high-risk leukaemia subtype

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Checking for minimal residual disease early in treatment can help some young high-risk leukaemia patients avoid bone marrow transplantation without compromising their long-term survival.

A St. Jude Children’s Research Hospital investigator led the international retrospective analysis that is published in the Journal of Clinical Oncology.

The study involved children and adolescents with hypodiploid acute lymphoblastic leukaemia (ALL).

This high-risk subtype accounts for about 2 percent of paediatric ALL cases. It is characterised by a poor prognosis and leukaemic cells with 25 to 44 chromosomes rather than the usual 46.

The historically poor prognosis has prompted many leukaemia specialists to advocate for treating these patients with intensive chemotherapy followed by allogeneic bone marrow transplantation.

Transplantation, however, carries its own short- and long-term health risks.

The largest study yet of children and adolescents with hypodiploid ALL found that transplantation did not significantly improve survival compared to chemotherapy alone.

However, contemporary risk-directed therapy–with dose intensity based on early treatment response determined by measuring minimal residual disease levels in bone marrow following remission induction chemotherapy–was more closely associated with better patient outcomes.

“This study confirms our earlier observation that patients with hypodiploid ALL who have no evidence of minimal residual disease after remission induction therapy should not be transplanted,” said first and corresponding author Ching-Hon Pui, M.D., chair of the St. Jude Department of Oncology.

“We recommend continued treatment with intensive chemotherapy.”

Remission induction therapy encompasses the first four to six weeks of chemotherapy.

Minimal residual disease (MRD) negative patients are defined as having fewer than 1 leukaemic cell in 10,000 white blood cells in bone marrow.

Overall, 58 percent of patients in the study became long-term survivors.

Disease-free, long-term survival rates were 75 percent for the 87 patients who were MRD negative after remission-induction chemotherapy.

Survival rates were similar, 74 percent, for hypodiploid patients with 44 rather than fewer chromosomes.

The study included data from 306 hypodiploid ALL patients who were enrolled on 16 different protocols of national study groups or major institutions between 1997 and 2013.

Questions remain about how to improve outcomes for patients with fewer than 44 chromosomes with minimal residual disease following induction therapy.

This analysis found that compared to intensive chemotherapy alone, transplantation did not provide a significant survival advantage for patients with fewer than 44 chromosomes.

Adjusted five-year overall survival was 57.7 percent for the 186 patients treated with chemotherapy alone versus 68.9 percent for the 42 patients treated with both chemotherapy and bone marrow transplantation.

Pui said the difference was not significant, particularly considering the long-term health risks, including second cancers, associated with transplant-related radiation.

He said additional studies are warranted for treating hypodiploid ALL with immuno- or cellular therapies, which do not involve radiation.

Researchers said the growth of precision medicines holds promise for improved outcomes for patients with hypodiploid ALL and other high-risk subtypes.

The list of promising possible treatments includes chimeric antigen receptor-modified T cells, genetically modified antibodies and inhibitors targeting cell signalling pathways that drive proliferation.


Source:St Jude Children’s Research Hospital

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The ONA Editor curates oncology news, views and reviews from Australia and around the world for our readers. In aggregated content, original sources will be acknowledged in the article footer.

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