Biology of Blood and Marrow Transplantation
Volume 10, Issue 4 , Pages 276-282, April 2004

A randomized trial of amifostine and carmustine-containing chemotherapy to assess lung-protective effects

  • Roy B Jones

      Affiliations

    • M.D. Anderson Cancer Center, Houston, Texas, USA
    • Corresponding Author InformationCorrespondence and reprint requests: Roy B. Jones, MD, PhD, Department of Blood and Marrow Transplantation, M.D. Anderson Cancer Center, 1515 Holcombe Blvd. 423, Houston, TX 77030 USA
  • ,
  • Keith E Stockerl-Goldstein

      Affiliations

    • Stanford University Medical Center, Palo Alto, California, USA
  • ,
  • Jared Klein

      Affiliations

    • Karmanos Cancer Center, Detroit, Michigan, USA
  • ,
  • James Murphy

      Affiliations

    • National Jewish Medical and Research Center, Denver, Colorado, USA
  • ,
  • Karl G Blume

      Affiliations

    • Stanford University Medical Center, Palo Alto, California, USA
  • ,
  • Roger Dansey

      Affiliations

    • Karmanos Cancer Center, Detroit, Michigan, USA
  • ,
  • Charles Martinez

      Affiliations

    • M.D. Anderson Cancer Center, Houston, Texas, USA
  • ,
  • Steven Matthes

      Affiliations

    • M.D. Anderson Cancer Center, Houston, Texas, USA
  • ,
  • Yago Nieto

      Affiliations

    • University of Colorado Health Sciences Center, Denver, Colorado, USA

Received 11 November 2003; accepted 21 January 2004.

Abstract 

We conducted a randomized, double blind, placebo-controlled multi-institutional trial to assess the ability of amifostine to protect patients against acute lung injury associated with cyclophosphamide/cisplatin/carmustine (BCNU) (STAMP I), a BCNU-containing high dose chemotherapy regimen used with hematopoietic cell transplantation. Amifostine was administered in a dose of 740 mg/m2 for 2 doses preceding administration of BCNU, the presumed pulmonary-toxic component of the regimen. The trial was stopped after 79 patients were randomized and a planned interim analysis demonstrated that it was unlikely that pulmonary cytoprotection would be detected with further accrual. We conclude that amifostine, used in the dose and schedule we tested, does not reduce the incidence of acute lung injury produced by STAMP I. Further, we suggest that amifostine use with BCNU in other contexts and with clinically achievable doses is unlikely to protect the lung from BCNU-associated acute injury.

Keywords:  Amifostine, Acute lung injury, Hematopoietic cell transplantation, BCNU

 

PII: S1083-8791(04)00046-1

doi:10.1016/j.bbmt.2004.01.001

Biology of Blood and Marrow Transplantation
Volume 10, Issue 4 , Pages 276-282, April 2004