Abstract
Thirteen children with refractory or recurrent Hodgkin's lymphoma (HL) received high-dose chemotherapy and autologous hematopoietic stem cell transplant (ASCT). After hematologic recovery, 10 patients were given interferon-α (IFN-α) as adjuvant therapy, starting at a dose of 0.5 × 106 U/m2 subcutaneously, three times a week. The dose was escalated as tolerated. Patients were treated for a median of 12 (4–24) months. Transient myelosuppression was the most common toxicity and led to temporary treatment interruption in five patients. The IFN-α dose was increased in nine patients, to a median final dose of 3.5 × 106 U/m2/week. With a median follow-up of 67 (range 25–114) months, nine of the 10 patients are alive and in continuous remission. One patient relapsed. Three patients were not treated with IFN-α initially, two because of rapidly progressive disease. One patient received IFN-α for treatment of relapse after transplant, and is alive in remission 10 years later. IFN-α has activity in children with advanced HL, and prolonged, low-dose treatment given after ASCT can be tolerated. Its therapeutic effect as a post-transplant adjuvant warrants further investigation.
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Petropoulos, D., Worth, L., Mullen, C. et al. Interferon-α after autologous stem cell transplantation in pediatric patients with advanced Hodgkin's lymphoma. Bone Marrow Transplant 38, 345–349 (2006). https://doi.org/10.1038/sj.bmt.1705458
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DOI: https://doi.org/10.1038/sj.bmt.1705458
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