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Idiopathic Pneumonia Syndrome and Thrombotic Microangiopathy Following Nonmyeloablative Haploidentical Peripheral Blood Stem Cell Transplantation and Posttransplant Cyclophosphamide: A Case Report.

Abstract
Posttransplant high-dose cyclophosphamide (pT-HDCy) following T-cell-replete haploidentical bone marrow (BM) transplantation has been successfully utilized to control alloreactivity, mainly in ameliorating graft-versus-host disease (GVHD) and graft rejection. Recently, peripheral blood stem cells (PBSCs) have also been suggested to be a feasible and effective graft alternative to BM in the same setting. We report a case with refractory Hodgkin lymphoma treated with haploidentical PBSC transplantation with nonmyeloablative conditioning and pT-HDCy. Although engraftment with complete donor chimerism was achieved without classical GVHD, the patient suffered from idiopathic pneumonia syndrome followed by thrombotic microangiopathy. Although idiopathic pneumonia syndrome and thrombotic microangiopathy improved after treatment, the patient's lymphoma rapidly progressed nonetheless. This outcome may suggest that the alloreactivity against the classical GVHD targets is successfully eradicated by pT-HDCy, but alloreactivity against the lungs and endothelial cells is differentially preserved when utilizing granulocyte colony-stimulating factor-mobilized PBSCs as the graft source. The graft-versus-Hodgkin lymphoma effect was not observed in our patient.
AuthorsWei-Hsin Liu, Wei-Ting Chen, Li-Hua Fang, Rong-Long Chen
JournalMedicine (Medicine (Baltimore)) Vol. 94 Issue 29 Pg. e1200 (Jul 2015) ISSN: 1536-5964 [Electronic] United States
PMID26200635 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Granulocyte Colony-Stimulating Factor
  • Cyclophosphamide
Topics
  • Adolescent
  • Cyclophosphamide (administration & dosage)
  • Female
  • Granulocyte Colony-Stimulating Factor (pharmacology)
  • Hodgkin Disease (therapy)
  • Humans
  • Peripheral Blood Stem Cell Transplantation (adverse effects, methods)
  • Pneumonia (etiology)
  • Syndrome
  • Thrombotic Microangiopathies (etiology)

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