A combination of low-dose cyclophosphamide and colony-stimulating factors is more cost-effective than granulocyte-colony-stimulating factors alone in mobilizing peripheral blood stem and progenitor cells

被引:25
作者
Meisenberg, B [1 ]
Brehm, T [1 ]
Schmeckel, A [1 ]
Miller, W [1 ]
McMillan, R [1 ]
机构
[1] Scripps Clin & Res Fdn, Div Hematol & Oncol, Bone Marrow Transplant Program, La Jolla, CA 92037 USA
关键词
D O I
10.1046/j.1537-2995.1998.38298193107.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: The use of peripheral blood progenitor cells (PBPCs) instead of autologous bone marrow leads to more rapid engraftment following high-dose chemotherapy. Mobilization regimens differ with respect to toxicity, efficiency, and cost. STUDY DESIGN AND METHODS: Two cohorts of patients with breast cancer received one of two mobilization regimens: granulocyte-colony-stimulating factor (G-CSF) at 10 mu g per kg was given subcutaneously for 5 days, with leukapheresis begun an Day 6, or low-dose cyclophosphamide followed by sequential granulocyte-macrophage-CSF (GM-CSF) at 5 mu g per kg for 5 days and by G-CSF at 10 mu g per kg, with leukapheresis begun on Day 11. Results of CD34+ cell collection, engraftment, and costs of mobilization were determined. RESULTS: The combination chemotherapy and growth factor regimen was more efficient in mobilizing CD34+ cells. Sixty-six percent of patients reached a target 4 x 10(6) CD34+ cells per kg in a single leukapheresis session with the combination regimen, compared to 14 percent who received G-CSF alone (p<0.01). The mean number of leukapheresis sessions required to reach a target of 4 x 10(6) CD34+ cells per kg was 1.3 for the combination regimen and 2.7 for the regimen of G-CSF alone (p<0.01). One patient in the chemotherapy and growth factor group developed febrile neutropenia. Engraftment was similar in both cohorts of patients. The cost of mobilization, including all supplies and cryopreservation, was $7381 for the G-CSF regimen and $5508 for the chemotherapy regimen (p<0.05). This reduction was attributed to the lower number of leukapheresis and cryopreservation sessions, which outweighed the slight increase in expense for chemotherapy and growth factor in the combination regimen. CONCLUSION: This combination mobilization regimen allowed the predictable and efficient collection of CD34+ cells from the peripheral blood in a limited number of leukapheresis sessions, which reduced the cost of mobilization by approximately 25 percent.
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页码:209 / 215
页数:7
相关论文
共 23 条
[1]   FACTORS THAT INFLUENCE COLLECTION AND ENGRAFTMENT OF AUTOLOGOUS PERIPHERAL-BLOOD STEM-CELLS [J].
BENSINGER, W ;
APPELBAUM, F ;
ROWLEY, S ;
STORB, R ;
SANDERS, J ;
LILLEBY, K ;
GOOLEY, T ;
DEMIRER, T ;
SCHIFFMAN, K ;
WEAVER, C ;
CLIFT, R ;
CHAUNCEY, T ;
KLARNET, J ;
MONTGOMERY, P ;
PETERSDORF, S ;
WEIDEN, P ;
WITHERSPOON, R ;
BUCKNER, CD .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (10) :2547-2555
[2]  
CHAO NJ, 1993, BLOOD, V81, P2031
[3]   PERIPHERAL-BLOOD STEM-CELL COLLECTIONS AFTER PACLITAXEL, CYCLOPHOSPHAMIDE, AND RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR IN PATIENTS WITH BREAST AND OVARIAN-CANCER [J].
DEMIRER, T ;
ROWLEY, S ;
BUCKNER, CD ;
APPELBAUM, FR ;
LILLEBY, K ;
STORB, R ;
SCHIFFMAN, K ;
BENSINGER, WI .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (07) :1714-1719
[4]   When to harvest peripheral-blood stem cells after mobilization therapy: Prediction of CD34-positive cell yield by preceding day CD34-positive concentration in peripheral blood [J].
Elliott, C ;
Samson, DM ;
Armitage, S ;
Lyttelton, MP ;
McGuigan, D ;
Hargreaves, R ;
Giles, C ;
Abrahamson, G ;
Abboudi, Z ;
Brennan, M ;
Kanfer, EJ .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :970-973
[5]   SEQUENTIAL PROPHYLACTIC ORAL AND EMPIRIC ONCE-DAILY PARENTERAL ANTIBIOTICS FOR NEUTROPENIA AND FEVER AFTER HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS BONE-MARROW SUPPORT [J].
GILBERT, C ;
MEISENBERG, B ;
VREDENBURGH, J ;
ROSS, M ;
HUSSEIN, A ;
PERFECT, J ;
PETERS, WP .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (05) :1005-1011
[6]  
Goldschmidt H, 1996, BONE MARROW TRANSPL, V17, P691
[7]  
HO D, 1996, EXP HEMATOL, V24, P1460
[8]  
JAGANNATH S, 1996, BLOOD S1, V88, P3889
[9]   DEVELOPMENT OF A SIMPLIFIED SINGLE-APHERESIS APPROACH FOR PERIPHERAL-BLOOD PROGENITOR-CELL TRANSPLANTATION IN PREVIOUSLY TREATED PATIENTS WITH LYMPHOMA [J].
JONES, HM ;
JONES, SA ;
WATTS, MJ ;
KHWAJA, A ;
MILLS, W ;
FIELDING, A ;
GOLDSTONE, AH ;
LINCH, DC .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (08) :1693-1702
[10]  
LOBO F, 1991, BONE MARROW TRANSPL, V8, P389