Anti-GM-CSF monoclonal antibody therapy for refractory acute leukemia

被引:4
作者
Bouabdallah, R [1 ]
Olive, D [1 ]
Meyer, P [1 ]
Lopez, M [1 ]
Sainty, D [1 ]
Hirn, M [1 ]
Mannoni, P [1 ]
Fougereau, E [1 ]
Gastaut, JA [1 ]
Maraninchi, D [1 ]
机构
[1] Inst J Paoli I Calmettes, Dept Haematol, F-13009 Marseille, France
关键词
acute leukemia; monoclonal antibody; GM-CSF;
D O I
10.3109/10428199809057566
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Several phase I trials and pilot studies using Monoclonal Antibody (MoAb) have been performed in B-cell neoplasms, but this approach has not until now been extensively tested in myeloid leukemias. Recently, we evaluated the use of anti-Granulocyte-Macrophage Colony-Stimulating Factor MoAb (Anti-GM-CSF MoAb) in acute myeloid leukemia (AML). Eight patients fulfilled inclusion criteria and received a single course of Anti-GM-CSF MoAb infusion during 5 to 15 days. Anti-GM-CSF MoAb was well tolerated and was detectable in pharmacokinetics studies. Using Human Anti-Rat Antibodies (HARA), we also observed an immunological response to the MoAb. Despite sufficient levels detected in the serum and biological activity of Anti-GM-CSF MoAb in vivo, no anti-leukemic effect was noted, except for one patient who had a decrease of 50% in the marrow blast cell mass. These observations indicate that leukemic proliferation in vivo involves a complex network spanning many mechanisms, and inhibition of leukemia is not effective if only one of these key targets is attacked. The development of these new approaches may be more effective in the future.
引用
收藏
页码:539 / 549
页数:11
相关论文
共 34 条
[21]  
RITZ J, 1981, BLOOD, V58, P141
[22]   CONSTITUTIVE UNCOUPLING OF PATHWAYS OF GENE-EXPRESSION THAT CONTROL GROWTH AND DIFFERENTIATION IN MYELOID-LEUKEMIA - A MODEL FOR THE ORIGIN AND PROGRESSION OF MALIGNANCY [J].
SACHS, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (10) :6152-6156
[23]  
SACHS L, 1990, CANCER-AM CANCER SOC, V65, P2196, DOI 10.1002/1097-0142(19900515)65:10<2196::AID-CNCR2820651006>3.0.CO
[24]  
2-Y
[25]  
SAELAND S, 1988, BLOOD, V72, P1580
[26]   A PHASE-I TRIAL OF MONOCLONAL-ANTIBODY M195 IN ACUTE MYELOGENOUS LEUKEMIA - SPECIFIC BONE-MARROW TARGETING AND INTERNALIZATION OF RADIONUCLIDE [J].
SCHEINBERG, DA ;
LOVETT, D ;
DIVGI, CR ;
GRAHAM, MC ;
BERMAN, E ;
PENTLOW, K ;
FEIRT, N ;
FINN, RD ;
CLARKSON, BD ;
GEE, TS ;
LARSON, SM ;
OETTGEN, HF ;
OLD, LJ .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (03) :478-490
[27]   HUMAN RECOMBINANT GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR - A MULTILINEAGE HEMATOPOIETIN [J].
SIEFF, CA ;
EMERSON, SG ;
DONAHUE, RE ;
NATHAN, DG ;
WANG, EA ;
WONG, GG ;
CLARK, SC .
SCIENCE, 1985, 230 (4730) :1171-1173
[28]   RECOMBINANT HUMAN GRANULOCYTE COLONY-STIMULATING FACTOR - EFFECTS ON NORMAL AND LEUKEMIC MYELOID CELLS [J].
SOUZA, LM ;
BOONE, TC ;
GABRILOVE, J ;
LAI, PH ;
ZSEBO, KM ;
MURDOCK, DC ;
CHAZIN, VR ;
BRUSZEWSKI, J ;
LU, H ;
CHEN, KK ;
BARENDT, J ;
PLATZER, E ;
MOORE, MAS ;
MERTELSMANN, R ;
WELTE, K .
SCIENCE, 1986, 232 (4746) :61-65
[29]  
SPORN MB, 1985, CANCER SURV, V4, P627
[30]   THE MULTICHAIN INTERLEUKIN-2 RECEPTOR - A TARGET FOR IMMUNOTHERAPY [J].
WALDMANN, TA ;
PASTAN, IH ;
GANSOW, OA ;
JUNGHANS, RP .
ANNALS OF INTERNAL MEDICINE, 1992, 116 (02) :148-160