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Hematopoietic stem cell transplantation for pediatric patients with non-anaplastic peripheral T-cell lymphoma. An EBMT pediatric diseases working party study

  • Olga Moser,
  • Maud Ngoya,
  • Jacques-Emmanuel Galimard,
  • Arnaud Dalissier,
  • Jean Hugues Dalle,
  • Krzysztof Kalwak,
  • Wilhelm Wössmann,
  • Birgit Burkhardt,
  • Marc Bierings,
  • Marta Gonzalez-Vicent,
  • Lucía López Corral,
  • Karin Mellgren,
  • Andishe Attarbaschi,
  • Jean Henri Bourhis,
  • Kristina Carlson,
  • Selim Corbacioglu,
  • Katarzyna Drabko,
  • Mikael Sundin,
  • Jacek Toporski,
  • Gunnar Cario,
  • Udo Kontny

摘要

Peripheral T-cell lymphomas (PTCL) other than anaplastic large-cell lymphoma are rare in children, and the role of hematopoietic stem cell transplantation (HSCT) has not been clarified yet. In a retrospective analysis of registry-data of the European Society for Blood and Marrow Transplantation we analyzed 55 patients aged < 18 years who received allogeneic (N = 46) or autologous (N = 9) HSCT for PTCL. Median age at HSCT was 13.9 years; 33 patients (60%) were in first remission, and 6 (19%) in progression at HSCT. Conditioning was myeloablative in 87% of the allogeneic HSCTs and in 27 (58.7%) based on total body irradiation. After allogeneic HSCT the 5-year overall- and progression-free survival was 58.9% (95% CI 42.7–71.9) and 52.6% (95% CI 36.8–66.1), respectively. 5-year relapse incidence was 27.6% (95% CI 15.1–41.6), the non-relapse mortality rate was 19.8% (95% CI 9.7–32.6). Five of the six patients with progression at HSCT died. Seven of nine patients after autologous HSCT were alive and disease-free at last follow-up. Our data suggest a role of allogeneic HSCT in consolidation-treatment of patients with high-risk disease, who reach at least partial remission after primary- or relapse-therapy, whereas patients with therapy-refractory or progressive disease prior to transplantation do not profit from HSCT.