RADIOIMMUNOTHERAPY OF INTERLEUKIN-2R-ALPHA-EXPRESSING ADULT T-CELL LEUKEMIA WITH YTTRIUM-90-LABELED ANTI-TAC

被引:202
作者
WALDMANN, TA
WHITE, JD
CARRASQUILLO, JA
REYNOLDS, JC
PAIK, CH
GANSOW, OA
BRECHBIEL, MW
JAFFE, ES
FLEISHER, TA
GOLDMAN, CK
TOP, LE
BAMFORD, R
ZAKNOEN, S
ROESSLER, E
KASTENSPORTES, C
ENGLAND, R
LITOU, H
JOHNSON, JA
JACKSONWHITE, T
MANNS, A
HANCHARD, B
JUNGHANS, RP
NELSON, DL
机构
[1] NCI,RADIAT ONCOL BRANCH,BETHESDA,MD 20892
[2] NCI,VIRAL EPIDEMIOL BRANCH,BETHESDA,MD 20892
[3] NIH,DEPT CLIN PATHOL,BETHESDA,MD 20892
[4] NIH,WARREN G MAGNUSON CLIN CTR,DEPT NUCL MED,BETHESDA,MD 20892
[5] UNIV W INDIES,DEPT PATHOL,KINGSTON 7,JAMAICA
关键词
D O I
10.1182/blood.V86.11.4063.bloodjournal86114063
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adult T-cell leukemia (ATL) is a malignancy of mature lymphocytes caused by the retrovirus human T-cell lymphotropic virus-I. It is an aggressive leukemia with a median survival time of 9 months; no chemotherapy regimen appears successful in inducing long-term disease-free survival. The scientific basis of the present study is that ATL cells express high-affinity interleukin-2 receptors identified by the anti-Tac monoclonal antibody, whereas normal resting cells do not. To exploit this difference, we administered anti-Tac armed with Yttrium-90 (Y-90) to 18 patients with ATL initially (first 9 patients) in a phase I dose-escalation trial and subsequently (second group of 9 patients) in a phase II trial involving a uniform 10-mCi dose of Y-90-labeled anti-Tac. Patients undergoing a remission were permitted to receive up to eight additional doses. At the 5- to 15-mCi doses used. 9 of 16 evaluable patients responded to Y-90 anti-Tac with a partial (7 patients) or complete (2 patients) remission. The responses observed represent improved efficacy in terms of length of remission when compared with previous results with unmodified anti-Tac. Clinically meaningful (greater than or equal to grade 3) toxicity was largely limited to the hematopoietic system. In conclusion, radioimmunotherapy with Y-90 anti-Tac directed toward the IL-2R expressed on ATL cells may provide a useful approach for treatment of this aggressive malignancy. This is a US government work. There are no restrictions on its use.
引用
收藏
页码:4063 / 4075
页数:13
相关论文
共 60 条
[1]  
ANASETTI C, 1994, BLOOD, V84, P1320
[2]  
[Anonymous], ANTIBODIES RADIODIAG
[3]  
ARTEAGA CL, 1994, CANCER RES, V54, P3758
[4]   YTTRIUM-90-LABELED ANTIFERRITIN FOLLOWED BY HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS BONE-MARROW TRANSPLANTATION FOR POOR-PROGNOSIS HODGKINS-DISEASE [J].
BIERMAN, PJ ;
VOSE, JM ;
LEICHNER, PK ;
QUADRI, SM ;
ARMITAGE, JO ;
KLEIN, JL ;
ABRAMS, RA ;
DICKE, KA ;
VRIESENDORP, HM .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (04) :698-703
[5]   BACKBONE-SUBSTITUTED DTPA LIGANDS FOR Y-90 RADIOIMMUNOTHERAPY [J].
BRECHBIEL, MW ;
GANSOW, OA .
BIOCONJUGATE CHEMISTRY, 1991, 2 (03) :187-194
[6]   ANTI-TAC-H, A HUMANIZED ANTIBODY TO THE INTERLEUKIN-2 RECEPTOR, PROLONGS PRIMATE CARDIAC ALLOGRAFT SURVIVAL [J].
BROWN, PS ;
PARENTEAU, GL ;
DIRBAS, FM ;
GARSIA, RJ ;
GOLDMAN, CK ;
BUKOWSKI, MA ;
JUNGHANS, RP ;
QUEEN, C ;
HAKIMI, J ;
BENJAMIN, WR ;
CLARK, RE ;
WALDMANN, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (07) :2663-2667
[7]  
CARRASQUILLO JA, IN PRESS PRINCIPALS
[8]  
DUKE RC, 1986, LYMPHOKINE RES, V5, P289
[9]  
FAN Z, 1993, CANCER RES, V53, P4637
[10]  
GHETIE MA, 1994, BLOOD, V83, P1329