Seminars in Hematology
Volume 49, Issue 1 , Pages 15-24, January 2012

Late Pulmonary Complications After Allogeneic Hematopoietic Stem Cell Transplantation: Diagnosis, Monitoring, Prevention, and Treatment

  • Andrea Bacigalupo

      Affiliations

    • Unità Operativa Ematologia 2, Azienda Ospedaliera Universitaria “San Martino”, Genova, Italy
    • Corresponding Author InformationAddress correspondence to Andrea Bacigalupo, MD, Unità Operativa Ematologia 2, Azienda Ospedaliera Universitaria “San Martino”, Largo Rosanna Benzi, 10, 16132 Genova, Italy
  • ,
  • Jason Chien

      Affiliations

    • Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA
  • ,
  • Giovanni Barisione

      Affiliations

    • Unità Operativa Medicina Preventiva e del Lavoro, Laboratorio di Fisiopatologia Respiratoria, Azienda Ospedaliera Universitaria “San Martino”, Genova, Italy
  • ,
  • Steven Pavletic

      Affiliations

    • Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD

Bronchiolitis obliterans syndrome (BOS) is a life-threatening complication that occurs among recipients of allogeneic lung and hematopoietic stem cell transplantation (allo-HSCT). BOS usually occurs within the first 2 years but may develop as late as 5 years after allo-HSCT. Recent prevalence estimates suggest that BOS is likely underdiagnosed in the clinical setting and that 14% of all long-term survivors with chronic graft-versus-host disease (GVHD) may develop BOS. It is difficult to diagnose and once respiratory symptoms appear, most allo-HSCT recipients show severe airflow obstruction. This may be due, at least in part, to the low sensitivity of standard spirometry in detecting small airways obstruction and lack of formal recommendations for screening for this complication. The prognosis of BOS is poor with reported 5-year survival of about 15%. A key obstacle in advancing clinical research in BOS is the lack of diagnostic and therapeutic response standards, making interpretation of survival and treatment results between studies difficult. This situation has significantly improved due to the introduction of the National Institutes of Health (NIH) criteria, which provide investigators with common definitions for studying BOS and for assessing the effects of therapeutic interventions. Future advances in the therapy of BOS may need to include development of better early intervention strategies based on identification of reliable early biological markers of the disease. It would be also important to improve understanding of the biological heterogeneity of this devastating complication after allo-HSCT.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 This work was supported by Associazione Italiana Ricerca contro il Cancro (A.I.R.C.), Milano, and Fondazione Ricerca Trapianto di Midollo Osseo (FA-RI.T.M.O.), Genova, Italy

 Conflict of interest: the authors have no conflict of interest to declare

PII: S0037-1963(11)00099-0

doi:10.1053/j.seminhematol.2011.10.005

Seminars in Hematology
Volume 49, Issue 1 , Pages 15-24, January 2012