Biology of Blood and Marrow Transplantation
Volume 17, Issue 5 , Pages 729-736, May 2011

Cost and Clinical Analysis of Autologous Hematopoietic Stem Cell Mobilization with G-CSF and Plerixafor Compared to G-CSF and Cyclophosphamide

  • Paul Shaughnessy

      Affiliations

    • Texas Transplant Institute, San Antonio, Texas
    • Corresponding Author InformationCorrespondence and reprint requests: Paul Shaughnessy, MD, Texas Transplant Institute, 7711 Louis Pasteur, Suite 704, San Antonio, TX 78229.
  • ,
  • Miguel Islas-Ohlmayer

      Affiliations

    • Texas Transplant Institute, San Antonio, Texas
  • ,
  • Julie Murphy

      Affiliations

    • Rocky Mountain Blood and Marrow Transplant Program, Denver, Colorado
  • ,
  • Maureen Hougham

      Affiliations

    • Texas Transplant Institute, San Antonio, Texas
  • ,
  • Jill MacPherson

      Affiliations

    • Texas Transplant Institute, San Antonio, Texas
  • ,
  • Kurt Winkler

      Affiliations

    • Texas Transplant Institute, San Antonio, Texas
  • ,
  • Matthew Silva

      Affiliations

    • Massachusetts College of Pharmacy and Health Sciences, Worcester, Massachusetts
  • ,
  • Michael Steinberg

      Affiliations

    • Massachusetts College of Pharmacy and Health Sciences, Worcester, Massachusetts
  • ,
  • Jeffrey Matous

      Affiliations

    • Rocky Mountain Blood and Marrow Transplant Program, Denver, Colorado
  • ,
  • Sheryl Selvey

      Affiliations

    • Massachusetts College of Pharmacy and Health Sciences, Worcester, Massachusetts
  • ,
  • Michael Maris

      Affiliations

    • Rocky Mountain Blood and Marrow Transplant Program, Denver, Colorado
  • ,
  • Peter A. McSweeney

      Affiliations

    • Rocky Mountain Blood and Marrow Transplant Program, Denver, Colorado

Received 21 July 2010; accepted 23 August 2010. published online 01 September 2010.

Plerixafor plus granulocyte-colony stimulating factor (G-CSF) has been shown to mobilize more CD34+ cells than G-CSF alone for autologous hematopoietic stem cell transplantation (HSCT). However, many centers use chemotherapy followed by G-CSF to mobilize CD34+ cells prior to HSCT. We performed a retrospective study of patients who participated in the expanded access program (EAP) of plerixafor and G-CSF for initial mobilization of CD34+ cells, and compared outcomes to matched historic controls mobilized with cyclophosphamide 3-5 g/m2 and G-CSF at 2 centers that participated in the EAP Control patients were matched for age, sex, disease, disease stage, and number of prior therapies. Mobilization costs were defined to be the costs of medical procedures, resource utilization, and medications. Median national CMS reimbursement rates were used to establish the costs of procedures, hospitalization, provider visits, apheresis, CD34+ cell processing and cryopreservation. Average sale price was used for G-CSF, plerixafor, cyclophosphamide, MESNA, antiemetics, and antimicrobials. A total of 33 patients from the EAP and 33 matched controls were studied. Two patients in the control group were hospitalized for neutropenic fever during the mobilization period. Apheresis started on the scheduled day in 33 (100%) study patients and in 29 (88%) control patients (P = 0.04). Sixteen (48%) control patients required weekend apheresis. There was no difference in number of CD34+ cells collected between the groups, and all patients proceeded to HSCT with no difference in engraftment outcomes. Median total cost of mobilization was not different between the plerixafor/G-CSF and control groups ($14,224 versus $18,824; P = .45). In conclusion, plerixafor/G-CSF and cyclophosphamide/G-CSF for upfront mobilization of CD34 cells resulted in similar numbers of cells collected, costs of mobilization, and clinical outcomes. Additionally, plerixafor/G-CSF mobilization resulted in more predictable days of collection, no weekend apheresis procedures, and no unscheduled hospital admissions.

Key Words: Plerixafor, Mobilization, Cost analysis, Autologous transplant

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.
 

 Financial disclosure: See Acknowledgments on page 736.

PII: S1083-8791(10)00367-8

doi:10.1016/j.bbmt.2010.08.018

Biology of Blood and Marrow Transplantation
Volume 17, Issue 5 , Pages 729-736, May 2011