Biology of Blood and Marrow Transplantation
Volume 12, Issue 2 , Pages 217-225, February 2006

Tacrolimus and Mycophenolate Mofetil after Nonmyeloablative Matched-Sibling Donor Allogeneic Stem-Cell Transplantations Conditioned with Fludarabine and Low-Dose Total Body Irradiation

  • Yago Nieto

      Affiliations

    • Bone Marrow Transplant Programs, University of Navarra, Pamplona, Spain
    • Corresponding Author InformationCorrespondence and reprint requests: Yago Nieto, MD, Clínica Universitaria de Navarra, Avda Pío XII-36, Pamplona 31080, Spain
  • ,
  • Nigel Patton

      Affiliations

    • Canterbury Health Laboratories, Christchurch, New Zealand
  • ,
  • Timothy Hawkins

      Affiliations

    • Auckland City Hospital, Auckland, New Zealand
  • ,
  • Ruth Spearing

      Affiliations

    • Canterbury Health Laboratories, Christchurch, New Zealand
  • ,
  • Scott I. Bearman

      Affiliations

    • Rocky Mountain Cancer Center, Denver, Colorado
  • ,
  • Roy B. Jones

      Affiliations

    • M.D. Anderson Cancer Center, Houston, Texas
  • ,
  • Elizabeth J. Shpall

      Affiliations

    • M.D. Anderson Cancer Center, Houston, Texas
  • ,
  • Rachel Rabinovitch

      Affiliations

    • Department of Radiation Oncology, University of Colorado
  • ,
  • Chan Zeng

      Affiliations

    • Department of Biostatistics, University of Colorado
  • ,
  • Anna Barón

      Affiliations

    • Department of Biostatistics, University of Colorado
  • ,
  • Peter A. McSweeney

      Affiliations

    • Rocky Mountain Cancer Center, Denver, Colorado

Received 7 September 2005; accepted 6 October 2005.

Abstract 

We evaluated tacrolimus/mycophenolate mofetil (MMF) for graft-versus-host disease (GVHD) prophylaxis after a nonmyeloablative stem cell transplantation (NST) from a matched sibling donor (MSD). Thirty-two patients (median age, 57 years) with advanced hematologic malignancies, who were poor candidates for a conventional myeloablative transplantation, received fludarabine (30 mg/m2, day −4 to day −2), total-body irradiation (TBI) (200 cGy, day 0), infusion of donor peripheral blood progenitor cells (day 0), oral tacrolimus 0.06 mg/kg twice daily (from day 3), and oral MMF at 15 mg/kg twice daily (days 0-+27). Tacrolimus was tapered from day +100 to day +180 in those patients with indolent malignancies (n = 25), and from day +35 to day +56 in those with aggressive tumors (n = 7). Regimen toxicities and myelosuppression were mild, allowing 75% of patients to have entirely outpatient transplantations. One patient (3%) experienced a nonfatal graft rejection. Rates of grades II-IV and III-IV acute GVHD were 15.6% and 3%, respectively. Acute GVHD was diagnosed at median day +78 (range, days +31-+84). Extensive chronic GVHD was observed in 10 of 24 evaluable patients (41.6%) at a median onset of day +198 (range, days +128-+277), either spontaneously (n = 5) or elicited after tumor progression (n = 5). Five patients experienced transplantation-related mortality (TRM) (15.6%) from either acute GVHD-related multiorgan failure (MOF) (n = 3) or infectious complications (n = 2). At median follow-up of 19 months (range, 2-41 months), the overall survival, progression-free survival, and disease-free survival rates are 62.5%, 50%, and 40%, respectively. In conclusion, the use of tacrolimus/MMF after MSD NST is associated with encouraging rates of GVHD control.

Key words:  Tacrolimus , Mycophenolate mofetil , Graft-versus-host disease , Nonmyeloablative transplantation , Matched sibling donor

 

PII: S1083-8791(05)00682-8

doi:10.1016/j.bbmt.2005.10.012

Biology of Blood and Marrow Transplantation
Volume 12, Issue 2 , Pages 217-225, February 2006