Recombinant human thrombopoietin augments mobilization of peripheral blood progenitor cells for autologous transplantation

被引:30
作者
Linker, C
Anderlini, P
Herzig, R
Christiansen, N
Somlo, G
Bensinger, W
Fay, J
Lynch, JP
Goodnough, LT
Ashby, M
Benyunes, MC
Jones, DV
Yang, TA
Miller, LL
Weaver, C
机构
[1] Univ Calif San Francisco, Dept Hematol Oncol, San Francisco, CA 94143 USA
[2] Univ Texas, MD Anderson Canc Ctr, Houston, TX 77030 USA
[3] Univ Louisville, Louisville, KY 40292 USA
[4] Univ S Carolina, Columbia, SC 29208 USA
[5] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[6] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[7] Baylor Univ, Med Ctr, Dallas, TX USA
[8] Natalie Warren Bryant Canc Ctr, Tulsa, OK USA
[9] Washington Univ, Sch Med, St Louis, MO USA
[10] Genentech Inc, San Francisco, CA 94080 USA
[11] Pharmacia Corp, Peapack, NJ USA
[12] Response Oncol Inc, Memphis, TN USA
关键词
thrombopoietin; mobilization;
D O I
10.1016/S1083-8791(03)00101-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study assessed the ability of various schedules of recombinant human thrombopoietin (rhTPO) to enhance mobilization of peripheral blood progenitor cells (PBPCs) in 134 patients with cancer undergoing high-dose chemotherapy and autologous PBPC transplantation. Patients received the study drug on days 1, 3, and 5 before initiation of granulocyte colony-stimulating factor (G-CSF) 10 mug/kg/day on day 5 and pheresis starting on day 9. Randomly assigned treatments on days 1, 3, and 5 were: group 1 (n=27) placebo, placebo, rhTPO 1.5 mug/kg; group 2 (n=27) rhTPO 1.5 mug/kg, placebo, placebo; groups 3 (n=28) and 4 (n=22) rhTPO 0.5 mug/kg on all 3 treatment days; and group 5 (n=30) placebo on all 3 treatment days. After high-dose chemotherapy and PBPC transplantation, groups I through 4 received rhTPO 1.5 mug/kg days 0, +2, +4, and +6 with either G-CSF 5 mug/kg/day (groups 1-3) or granulocyte-macrophage colony-stimulating factor 250 mug/m(2)/day (group 4). Group S received placebo plus G-CSF 5 mug/kg/day. The addition of rhTPO to G-CSF increased median CD34(+) cell yield/pheresis in cohorts in which rhTPO was started before day 5, with higher yields in groups 2 (2.67 x 10(6)/kg) and groups 3 and 4 (3.10 x 10(6)/kg) than in group 1 (1.86 x 10(6)/kg) or group 5 (1.65 x 10(6)/kg) (P=.006 across groups). Comparing rhTPO to placebo, higher percentages of patients achieved the minimum yield of CD34(+) greater than or equal to2 x 10(6)/kg (92% v 75%; P=.050) as well as the target yield of CD34(+) greater than or equal to5 x 10(6)/kg (73% v 46%; P=.041). rhTPO-treated patients required fewer phereses to achieve minimum (P=.011) and target (P=.015) CD34(+) cell values. rhTPO given after transplantation did not speed platelet recovery. No neutralizing antibodies were observed. We conclude that rhTPO can safely enhance mobilization of PBPC, reduce the number of leukapheresis, and allow more patients to meet minimal cell yield requirements to receive high-dose chemotherapy with PBPC transplantation. (C) 2003 American Society for Blood and Marrow Transplantation.
引用
收藏
页码:405 / 413
页数:9
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