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Natural killer cell therapy in children with relapsed leukemia.
Rubnitz, Jeffrey E; Inaba, Hiroto; Kang, Guolian; Gan, Kwan; Hartford, Christine; Triplett, Brandon M; Dallas, Mari; Shook, David; Gruber, Tanja; Pui, Ching-Hon; Leung, Wing.
Afiliação
  • Rubnitz JE; Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Inaba H; Department of Pediatrics, University of Tennessee Health Science Center, College of, Medicine, Memphis, Tennessee.
  • Kang G; Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Gan K; Department of Pediatrics, University of Tennessee Health Science Center, College of, Medicine, Memphis, Tennessee.
  • Hartford C; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Triplett BM; Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Dallas M; Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Shook D; Department of Pediatrics, University of Tennessee Health Science Center, College of, Medicine, Memphis, Tennessee.
  • Gruber T; Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee.
  • Pui CH; Department of Pediatrics, University of Tennessee Health Science Center, College of, Medicine, Memphis, Tennessee.
  • Leung W; Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee.
Pediatr Blood Cancer ; 62(8): 1468-72, 2015 Aug.
Article em En | MEDLINE | ID: mdl-25925135
BACKGROUND: Novel therapies are needed for children with relapsed or refractory leukemia. We therefore tested the safety and feasibility of haploidentical natural killer cell therapy in this patient population. PROCEDURE: Twenty-nine children who had relapsed or refractory leukemia were treated with chemotherapy followed by the infusion of haploidentical NK cells. Cohort 1 included 14 children who had not undergone prior allogeneic hematopoietic cell transplantation (HCT), whereas Cohort 2 included 15 children with leukemia that had relapsed after HCT. RESULTS: Twenty-six (90%) NK donors were KIR mismatched (14 with one KIR and 12 with 2 KIRs). The peak NK chimerism levels were >10% donor in 87% of the evaluable recipients. In Cohort 1, 10 had responsive disease and 12 proceeded to HCT thereafter. Currently, 5 (36%) are alive without leukemia. In Cohort 2, 10 had responsive disease after NK therapy and successfully proceeded to second HCT. At present, 4 (27%) are alive and leukemia-free. The NK cell infusions and the IL-2 injections were well-tolerated. CONCLUSIONS: NK cell therapy is safe, feasible, and should be further investigated in patients with chemotherapy-resistant leukemia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Matadoras Naturais / Leucemia / Imunoterapia Adotiva / Recidiva Local de Neoplasia Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Matadoras Naturais / Leucemia / Imunoterapia Adotiva / Recidiva Local de Neoplasia Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article