Plerixafor for Autologous Peripheral Blood Stem Cell Mobilization in Patients Previously Treated with Fludarabine or Lenalidomide

被引:40
作者
Malard, Florent [1 ,2 ]
Kroeger, Nicolaus [3 ]
Gabriel, Ian H. [4 ]
Huebel, Kai [5 ]
Apperley, Jane F. [4 ]
Basak, Grzegorz W. [6 ]
Douglas, Kenneth W. [7 ]
Geraldes, Catarina [8 ]
Jaksic, Ozren [9 ]
Koristek, Zdenek [10 ]
Lanza, Francesco [11 ]
Lemoli, Roberto [12 ]
Mikala, Gabor [13 ]
Selleslag, Dominik [14 ]
Worel, Nina
Mohty, Mohamad [1 ,2 ]
Duarte, Rafael F. [15 ]
机构
[1] CHU Nantes, Serv Hematol Clin, F-44093 Nantes, France
[2] Univ Nantes, CI2C, INSERM, CRNCA UMR 892, Nantes, France
[3] Univ Hosp Hamburg Eppendorf, Hamburg, Germany
[4] Univ London Imperial Coll Sci Technol & Med, Dept Haematol, London, England
[5] Univ Hosp Cologne, Dept Internal Med 1, Cologne, Germany
[6] Med Univ Warsaw, Dept Hematol Oncol & Internal Dis, Warsaw, Poland
[7] Beatson W Scotland Canc Ctr, HPC Transplant Programme, Glasgow, Lanark, Scotland
[8] Hosp Univ, Coimbra, Portugal
[9] Dubrava Univ Hosp, Zagreb, Croatia
[10] Fak MU & FN Brno, Int Hematoonkol Klin Lekarske, Brno, Czech Republic
[11] Cremona Hosp, Sect Hematol, Cremona, Italy
[12] Univ Bologna, Inst Hematol, Dept Hematol & Oncol Sci L&A Seragnoli, Bologna, Italy
[13] St Laszlo Hosp, Dept Haematol & SCT, Budapest, Hungary
[14] Algemeen Ziekenhuis St Jan, Brugge, Belgium
[15] IDIBELL, Catalan Inst Oncol, Barcelona, Spain
关键词
Autologous stem cell mobilization; Plerixafor; Salvage mobilization; Fludarabine; CHRONIC LYMPHOCYTIC-LEUKEMIA; BONE-MARROW-TRANSPLANTATION; MULTIPLE-MYELOMA; THERAPY; IMPACT; CHEMOTHERAPY; LYMPHOMA; CLL;
D O I
10.1016/j.bbmt.2011.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fludarabine and lenalidomide are essential drugs in the front-line treatment of non-Hodgkin lymphoma (NHL) and multiple myeloma (MM), respectively. Data suggests that fludarabine and lenalidomide therapy may have a deleterious effect on stem cell mobilization. In the European compassionate use program, 48 patients (median age 57 years) previously treated with fludarabine (median 5 cycles; range: 1-7 cycles) were given plerixafor plus granulocyte colony-stimulating factor (G-CSF) for remobilization following a primary mobilization attempt. The overall median number of CD34(+) cells collected was 2.3 x 10(6)/kg (range: 0.3-13.4). The minimum required number of CD34(+) cells (>= 2.0 x 10(6)/kg) was collected from 58% of patients in a median of 2 days. Thirty-five patients (median age = 57 years) previously treated with lenalidomide (median 5 cycles; range: 1-10 cycles) were given plerixafor plus G-CSF for remobilization. The overall median number of CD34(+) cells collected was 3.4 x 10(6)/kg (range: 1.1-14.8). The minimum required number of CD34(+) cells (>= 2.0 x 10(6) per kg) was collected from 69% of patients in a median of 2 days. In conclusion, salvage mobilization with plerixafor plus G-CSF is successful in the majority of patients with MM previously treated with lenalidomide. In fludarabine-exposed patients, only 58% of patients will achieve successful salvage mobilization with plerixafor plus G-CSF, suggesting the need for novel mobilization regimens algorithms in this subgroup of patients.
引用
收藏
页码:314 / 317
页数:4
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