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How I treat bronchiolitis obliterans syndrome after hematopoietic stem cell transplantation

Journal

BLOOD
Volume 129, Issue 4, Pages 448-455

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2016-08-693507

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Funding

  1. intramural research program of the National Institutes of Health, National Cancer Institute

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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.

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