The High-Affinity CXCR4 Antagonist BKT140 Is Safe and Induces a Robust Mobilization of Human CD34+ Cells in Patients with Multiple Myeloma

被引:81
作者
Peled, Amnon [4 ]
Abraham, Michal [5 ]
Avivi, Irit [6 ,7 ]
Rowe, Jacob M. [6 ,7 ]
Beider, Katia [1 ,2 ,3 ]
Wald, Hanna [5 ]
Tiomkin, Lena [5 ]
Ribakovsky, Lena [1 ,2 ,3 ]
Riback, Yossi [5 ]
Ramati, Yaron [5 ]
Aviel, Sigal [5 ]
Galun, Eithan [4 ]
Shaw, Howard Laurence [5 ]
Eizenberg, Orly [5 ]
Hardan, Izhar [1 ,2 ,3 ]
Shimoni, Avichai [1 ,2 ,3 ]
Nagler, Arnon [1 ,2 ,3 ]
机构
[1] Chaim Sheba Med Ctr, Div Hematol, IL-52621 Tel Hashomer, Israel
[2] Chaim Sheba Med Ctr, BMT, IL-52621 Tel Hashomer, Israel
[3] Tel Aviv Univ, Tel Hashomer, Israel
[4] Hebrew Univ Hosp, Goldyne Savad Inst Gene Therapy, Jerusalem, Israel
[5] Biokine Therapeut Ltd, Ness Ziona, Israel
[6] Rambam Med Ctr, Dept Hematol & Bone Marrow Transplantat, Haifa, Israel
[7] Technion Israel Inst Technol, Haifa, Israel
关键词
HEMATOPOIETIC STEM-CELLS; HIGH-DOSE CHEMOTHERAPY; LENALIDOMIDE THERAPY; TRANSPLANTATION; PLERIXAFOR; COLLECTION; NUMBERS; RESCUE; IMPACT; PET;
D O I
10.1158/1078-0432.CCR-13-1302
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: CXCR4 plays an important role in the retention of stem cells within the bone marrow. BKT140 (4F-benzoyl-TN14003) is a 14-residue bio stable synthetic peptide, which binds CXCR4 with a greater affinity compared with plerixafor (4 vs. 84 nmol/L). Studies in mice demonstrated the efficient and superior mobilization and transplantation of stem cells collected with GCSF-BKT140, compared with those obtained when using stem cells obtained with each one of these mobilizing agent alone. These results have served as a platform for the present clinical phase I study. Experimental Design: Eighteen patients with multiple myeloma who were preparing for their first autologous stem cell transplantation were included. Patients received a standard multiple myeloma mobilization regimen, consisting of 3 to 4 g/m(2) cyclophosphamide (day 0), followed by granulocyte colony-stimulating factor (G-CSF) at 5 mu g/kg/d starting on day 5 and administered between 8 and 10 pm until the end of stem cell collection. A single injection of BKT140 (0.006, 0.03, 0.1, 0.3, and 0.9 mg/kg) was administered subcutaneously on day 10 in the early morning, followed by G-CSF 12 hours later. Results: BKT140 was well tolerated at all concentrations, and none of the patients developed grade 3 and 4 toxicity. A single administration of BKT140 at the highest dose, 0.9 mg/kg, resulted in a robust mobilization and collection of CD34(+) cells (20.6 +/- 6.9 x 10(6) /kg), which were obtained through a single apheresis. All transplanted patients received similar to 5.3 x 10(6) CD34(+) cells/kg, which rapidly engrafted (n = 17). The median time to neutrophil and platelet recovery was 12 and 14 days, respectively, at the highest dose (0.9 mg/kg). Conclusions: When combined with G-CSF, BKT140 is a safe and efficient stem cell mobilizer that enabled the collection of a high number of CD34(+) cells in 1 and 2 aphaeresis procedures, resulting in successful engraftment. (C) 2013 AACR.
引用
收藏
页码:469 / 479
页数:11
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