How I treat bronchiolitis obliterans syndrome after hematopoietic stem cell transplantation

Blood. 2017 Jan 26;129(4):448-455. doi: 10.1182/blood-2016-08-693507. Epub 2016 Nov 16.

Abstract

In past years, a diagnosis of bronchiolitis obliterans syndrome (BOS) after allogeneic hematopoietic cell transplant (HCT) conferred nearly universal mortality secondary to lack of consensus for diagnostic criteria, poorly understood disease pathogenesis, and very few studies of therapeutic or supportive care interventions. Recently, however, progress has been made in these areas: revised consensus diagnostic guidelines are now available, supportive care has improved, there is greater understanding of potential mechanisms of disease, and prospective trials are being conducted. This article describes these advances and provides suggestions to optimize therapy for patients with BOS after HCT.

Publication types

  • Case Reports
  • Review
  • Research Support, N.I.H., Intramural

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Bronchiolitis Obliterans / drug therapy*
  • Bronchiolitis Obliterans / etiology
  • Bronchiolitis Obliterans / pathology
  • Child, Preschool
  • Drug Monitoring
  • Female
  • Graft vs Host Disease / drug therapy
  • Graft vs Host Disease / etiology
  • Graft vs Host Disease / pathology
  • Graft vs Host Disease / prevention & control*
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Leukemia / immunology
  • Leukemia / pathology
  • Leukemia / therapy
  • Male
  • Practice Guidelines as Topic
  • Respiratory Function Tests
  • Risk Factors
  • Syndrome
  • Transplantation, Homologous

Substances

  • Antineoplastic Agents
  • Immunosuppressive Agents