Haematological malignancies developing in previously healthy individuals who received haematopoietic growth factors: report from the Research on Adverse Drug Events and Reports (RADAR) project

被引:112
作者
Bennett, Charles L.
Evens, Andrew M.
Andritsos, Leslie A.
Balasubramanian, Lakshmi
Mai, Mark
Fisher, Matthew J.
Kuzel, Timothy M.
Angelotta, Cara
Mckoy, June M.
Vose, Julie M.
Bierman, Philip J.
Kuter, David J.
Trifilio, Steven M.
Devine, Steven M.
Tallman, Martin S.
机构
[1] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Dept Med, Chicago, IL 60611 USA
[2] Washington Univ, Sch Med, St Louis, MO 63130 USA
[3] Harvard Univ, Sch Med, Boston, MA 02114 USA
[4] Univ Nebraska, Sch Med, Omaha, NE 68583 USA
关键词
haematopoietic growth factors; megakaryocyte growth and development factor; granulocyte colony-stimulating factor; Research on Adverse Drug Events and Reports;
D O I
10.1111/j.1365-2141.2006.06312.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pegylated recombinant human megakaryocyte growth and development factor (PEG-rHuMGDF) and granulocyte colony-stimulating factor (G-CSF) promote haematopoietic progenitor cell maturation. We reviewed the findings for healthy volunteers/donors who developed haematological malignancies following PEG-rHuMGDF or G-CSF administration. Information was reviewed for three of 538 volunteers who received PEG-rHuMGDF in clinical trials and two of 200 donors who underwent G-CSF mobilised stem cell harvesting procedures for sibling stem cell transplants. Mantle cell, diffuse large B-cell lymphoma and chronic lymphocytic leukaemia were diagnosed 1-5 years after PEG-rHuMGDF exposure among three volunteers. For one patient, thrombocytopenia due to autoantibodies to PEG-rHuMGDF developed shortly after PEG-rHuMGDF administration and persisted until chemotherapy was administered. All three achieved complete remission, although one patient relapsed. Acute myeloid leukaemia was diagnosed 4 and 5 years after G-CSF mobilisation in two donors who underwent peripheral blood stem cell donation for sibling allogeneic haematopoietic stem cell transplantation. Following intensive chemotherapy, one died from acute leukaemia and the second is in complete remission. Controversy exists over the appropriateness of administering haematopoietic growth factors to healthy individuals. While a causal relationship with haematological malignancies cannot be demonstrated, long-term follow-up among healthy individuals who receive haematopoietic growth factors is needed.
引用
收藏
页码:642 / 650
页数:9
相关论文
共 43 条
[1]   Long-term follow-up of granulocyte colony-stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy [J].
Ancliff, PJ ;
Gale, RE ;
Liesner, R ;
Hann, I ;
Linch, DC .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 120 (04) :685-690
[2]   Long-term follow-up of normal peripheral blood progenitor cell donors treated with filgrastim:: no evidence of increased risk of leukemia development [J].
Anderlini, P ;
Chan, FA ;
Champlin, RE ;
Körbling, M ;
Strom, SS .
BONE MARROW TRANSPLANTATION, 2002, 30 (10) :661-663
[3]   Splenic rupture after granulocyte-colony-stimulating factor mobilization in a peripheral blood progenitor cell donor [J].
Balaguer, H ;
Galmes, A ;
Ventayol, G ;
Bargay, J ;
Besalduch, J .
TRANSFUSION, 2004, 44 (08) :1260-1261
[4]   Development of pancytopenia with neutralizing antibodies to thrombopoietin after multicycle chemotherapy supported by megakaryocyte growth and development factor [J].
Basser, RL ;
O'Flaherty, E ;
Green, M ;
Edmonds, M ;
Nichol, J ;
Menchaca, DM ;
Cohen, B ;
Begley, CG .
BLOOD, 2002, 99 (07) :2599-2602
[5]   The Rresearch on Adverse Drug Events and Reports (RADAR) project [J].
Bennett, CL ;
Nebeker, JR ;
Lyons, EA ;
Samore, MH ;
Feldman, MD ;
McKoy, JM ;
Carson, KR ;
Belknap, SM ;
Trifilio, SM ;
Schumock, GT ;
Yarnold, PR ;
Davidson, CJ ;
Evens, AM ;
Kuzel, TM ;
Parada, JP ;
Cournoyer, D ;
West, DP ;
Sartor, O ;
Tallman, MS ;
Raisch, DW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (17) :2131-2140
[6]  
BORTIN MM, 1987, BLOOD, V70, P227
[7]   Health, economic, and quality-of-life effects of erythropoietin and granulocyte colony-stimulating factor for the treatment of myelodysplastic syndromes:: a randomized, controlled trial [J].
Casadevall, N ;
Durieux, P ;
Dubois, S ;
Hemery, F ;
Lepage, E ;
Quarré, MC ;
Damaj, G ;
Giraudier, S ;
Guerci, A ;
Laurent, G ;
Dombret, H ;
Chomienne, C ;
Ribrag, V ;
Stamatoullas, A ;
Marie, JP ;
Vekhoff, A ;
Maloisel, F ;
Navarro, R ;
Dreyfus, F ;
Fenaux, P .
BLOOD, 2004, 104 (02) :321-327
[8]   Three to six year follow-up of normal donors who received recombinant human granulocyte colony-stimulating factor [J].
Cavallaro, AM ;
Lilleby, K ;
Majolino, I ;
Storb, R ;
Appelbaum, FR ;
Rowley, SD ;
Bensinger, WI .
BONE MARROW TRANSPLANTATION, 2000, 25 (01) :85-89
[9]   Splenic rupture in a parental donor undergoing peripheral blood progenitor cell mobilization [J].
Dincer, AP ;
Gottschall, J ;
Margolis, DA .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2004, 26 (11) :761-763
[10]   A CONTROLLED-STUDY OF RECOMBINANT HUMAN GRANULOCYTE-COLONY-STIMULATING FACTOR IN ELDERLY PATIENTS AFTER TREATMENT FOR ACUTE MYELOGENOUS LEUKEMIA [J].
DOMBRET, H ;
CHASTANG, C ;
FENAUX, P ;
REIFFERS, J ;
BORDESSOULE, D ;
BOUABDALLAH, R ;
MANDELLI, F ;
FERRANT, A ;
AUZANNEAU, G ;
TILLY, H ;
YVER, A ;
DEGOS, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (25) :1678-1683