CONTINUOUS INTRAVENOUS-INFUSION OF HIGH-DOSE RECOMBINANT INTERLEUKIN-2 FOR ACUTE MYELOID-LEUKEMIA - A PHASE-II STUDY

被引:57
作者
LIM, SH
NEWLAND, AC
KELSEY, S
BELL, A
OFFERMAN, E
RIST, C
GOZZARD, D
BAREFORD, D
SMITH, MP
GOLDSTONE, AH
机构
[1] UNIV LONDON UNIV COLL,DEPT HAEMATOL,LONDON WC1E 6BT,ENGLAND
[2] ROYAL LONDON HOSP,DEPT HAEMATOL,LONDON,ENGLAND
[3] ROYAL VICTORIA HOSP,DEPT HAEMATOL,BOURNEMOUTH,DORSET,ENGLAND
[4] QUEEN MARY HOSP,DEPT HAEMATOL,SIDCUP,ENGLAND
[5] WORTHING DIST HOSP,DEPT HAEMATOL,WORTHING,ENGLAND
[6] GLEN CLWYD HOSP,DEPT HAEMATOL,CLWYD,WALES
[7] DUDLEY RD GEN HOSP,DEPT HAEMATOL,BIRMINGHAM B18 7QH,W MIDLANDS,ENGLAND
关键词
ACUTE MYELOID LEUKEMIA; RECOMBINANT INTERLEUKIN-2;
D O I
10.1007/BF01741555
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A group of 13 patients with acute myeloid leukaemia of differing disease status were treated with continuous intravenous infusion of high-dose recombinant interleukin-2 (rIL-2). There was up-regulation of the cellular cytotoxic functions in all these patients following the rIL-2 therapy, with increase in the natural killer (NK) activity, lectin-dependent cellular cytotoxicity, induction of cytotoxicity-linked cytoplasmic serine esterase and lymphocyte activation. However, the clinical response to rIL-2 in these patients was disappointing, especially in patients treated in frank relapse. Although 1 patient treated in early second relapse achieved a third complete remission, the duration of the remission was brief and lasted only 6 months. Adverse reactions among these patients were common. Whether or not lymphokine-activated killer cells are needed to improve the response rate over rIL-2 alone in these patients deserves further investigation.
引用
收藏
页码:337 / 342
页数:6
相关论文
共 26 条
[1]  
ADLER A, 1988, BLOOD, V71, P709
[2]  
BARRETT AJ, 1989, NOV GRANTH M LEUK RE
[3]  
BERAN M, 1983, BLOOD, V61, P596
[4]   TREATMENT OF ACUTE MYELOGENOUS LEUKEMIA - A PROSPECTIVE CONTROLLED TRIAL OF BONE-MARROW TRANSPLANTATION VERSUS CONSOLIDATION CHEMOTHERAPY [J].
CHAMPLIN, RE ;
HO, WG ;
GALE, RP ;
WINSTON, D ;
SELCH, M ;
MITSUYASU, R ;
LENARSKY, C ;
ELASHOFF, R ;
ZIGHELBOIM, J ;
FEIG, SA .
ANNALS OF INTERNAL MEDICINE, 1985, 102 (03) :285-291
[5]  
FLETCHER M, 1987, LYMPHOKINE RES, V6, P45
[6]  
FOA R, 1990, BONE MARROW TRANSPL, V6, P98
[7]   INTERLEUKIN-2 DOES NOT PROMOTE THE INVITRO AND INVIVO PROLIFERATION AND GROWTH OF HUMAN ACUTE-LEUKEMIA CELLS OF MYELOID AND LYMPHOID ORIGIN [J].
FOA, R ;
CARETTO, P ;
FIERRO, MT ;
BONFERRONI, M ;
CARDONA, S ;
GUARINI, A ;
LISTA, P ;
PEGORARO, L ;
MANDELLI, F ;
FORNI, G ;
GAVOSTO, F .
BRITISH JOURNAL OF HAEMATOLOGY, 1990, 75 (01) :34-40
[8]   LONG-TERM CULTURE OF TUMOR-SPECIFIC CYTOTOXIC T-CELLS [J].
GILLIS, S ;
SMITH, KA .
NATURE, 1977, 268 (5616) :154-156
[9]   LYMPHOKINE-ACTIVATED KILLER CELL PHENOMENON - LYSIS OF NATURAL KILLER-RESISTANT FRESH SOLID TUMOR-CELLS BY INTERLEUKIN 2-ACTIVATED AUTOLOGOUS HUMAN PERIPHERAL-BLOOD LYMPHOCYTES [J].
GRIMM, EA ;
MAZUMDER, A ;
ZHANG, HZ ;
ROSENBERG, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (06) :1823-1841
[10]   INTERLEUKIN-2 AUGMENTS NATURAL-KILLER CELL-ACTIVITY [J].
HENNEY, CS ;
KURIBAYASHI, K ;
KERN, DE ;
GILLIS, S .
NATURE, 1981, 291 (5813) :335-338