DEVELOPMENT OF A MARROW TRANSPLANT REGIMEN FOR ACUTE-LEUKEMIA USING TARGETED HEMATOPOIETIC IRRADIATION DELIVERED BY I-131-LABELED ANTI-CD45 ANTIBODY, COMBINED WITH CYCLOPHOSPHAMIDE AND TOTAL-BODY IRRADIATION

被引:122
作者
MATTHEWS, DC
APPELBAUM, FR
EARY, JF
FISHER, DR
DURACK, LD
BUSH, SA
HUI, TE
MARTIN, PJ
MITCHELL, D
PRESS, OW
BADGER, CC
STORB, R
NELP, WB
BERNSTEIN, ID
机构
[1] UNIV WASHINGTON, DEPT PEDIAT, SEATTLE, WA USA
[2] UNIV WASHINGTON, DEPT MED, SEATTLE, WA USA
[3] UNIV WASHINGTON, DEPT RADIOL, SEATTLE, WA USA
[4] PACIFIC NW LAB, RICHLAND, WA USA
关键词
D O I
10.1182/blood.V85.4.1122.bloodjournal8541122
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In an attempt to decrease the relapse rate after bone marrow transplantation (BMT) for advanced acute leukemia, we initiated studies using (131)-labeled anti-CD45 antibody (BC8) to deliver radiation specifically to hematopoietic tissues, followed by a standard transplant preparative regimen. Biodistribution studies were performed in 23 patients using 0.5 mg/kg trace I-131-labeled BC8 antibody. The BC8 antibody was cleared rapidly from plasma with an initial disappearance half-time of 1.5 +/- 0.2 hours, presumably reflecting rapid antigen-specific binding. The mean radiation absorbed doses (cGy/mCi I-131 administered) were as follows: marrow, 7.1 +/- 0.8; spleen, 10.8 +/- 1.4; liver, 2.7 +/- 0.2; lungs, 2.1 +/- 0.1; kidneys, 0.7 +/- 0.1; and total body, 0.4 +/- 0.03. Patients with acute myelogenous leukemia (AML) in relapse had a higher marrow dose (11.4 cGy/mCi) than those in remission (5.2 cGy/mCi; P = .001) because of higher uptake and longer retention of radionuclide in marrow, Twenty patients were treated with a dose of I-131 estimated to deliver 3.5 Gy (level 1) to 7 Gy (level 3) to liver, with marrow doses of 4 to 30 Gy and spleen doses of 7 to 60 Gy, followed by 120 mg/kg cyclophosphamide (CY) and 12 Gy total body irradiation (TBI). Nine of 13 patients with AML or refractory anemia with excess blasts (RAEB) and two of seven with acute lymphocytic leukemia (ALL) are alive disease-free at 8 to 41 months (median, 17 months) after BMT, Toxicity has not been measurably greater than that of CY/TBI alone, and the maximum tolerated dose has not been reached. This study demonstrates that with the use of (131)-BC8 substantially greater doses of radiation can be delivered to hematopoietic tissues as compared with liver, lung, or kidney, which may improve the efficacy of marrow transplantation. (C) 1995 by The American Society of Hematology.
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页码:1122 / 1131
页数:10
相关论文
共 42 条
[11]  
DENARDO GL, 1990, CANCER RES, V50, pS1014
[12]  
EARY JF, 1990, J NUCL MED, V31, P1257
[13]  
ECKERMANN KF, 1994, J NUCL MED, V35, pP112
[14]  
FISHER DR, 1991, ANTIBODY IMMUNOCONJ, V4, P655
[15]   TARGETING, DOSIMETRY, AND RADIOIMMUNOTHERAPY OF B-CELL LYMPHOMAS WITH IODINE-131-LABELED LL2 MONOCLONAL-ANTIBODY [J].
GOLDENBERG, DM ;
HOROWITZ, JA ;
SHARKEY, RM ;
HALL, TC ;
MURTHY, S ;
GOLDENBERG, H ;
LEE, RE ;
STEIN, R ;
SIEGEL, JA ;
IZON, DO ;
BURGER, K ;
SWAYNE, LC ;
BELISLE, E ;
HANSEN, HJ ;
PINSKY, CM .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (04) :548-564
[16]  
HUNEKE RB, 1992, CANCER RES, V52, P5818
[17]   RADIOIMMUNOTHERAPY OF B-CELL LYMPHOMA WITH [I-131] ANTI-B1 (ANTI-CD20) ANTIBODY [J].
KAMINSKI, MS ;
ZASADNY, KR ;
FRANCIS, IR ;
MILIK, AW ;
ROSS, CW ;
MOON, SD ;
CRAWFORD, SM ;
BURGESS, JM ;
PETRY, NA ;
BUTCHKO, GM ;
GLENN, SD ;
WAHL, RL .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (07) :459-465
[18]  
KNOX SJ, 1990, CANCER RES, V50, P4935
[19]   ISOTOPIC IMMUNOGLOBULIN - A NEW SYSTEMIC THERAPY FOR ADVANCED HODGKINS-DISEASE [J].
LENHARD, RE ;
ORDER, SE ;
SPUNBERG, JJ ;
ASBELL, SO ;
LEIBEL, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1985, 3 (10) :1296-1300
[20]   BIODISTRIBUTION STUDIES OF ANTI-THY 1.2 IGM IMMUNOCONJUGATES - IMPLICATIONS FOR RADIOIMMUNOTHERAPY [J].
MACKLIS, RM ;
KAPLAN, WD ;
FERRARA, JLM ;
KINSEY, BM ;
KASSIS, AI ;
BURAKOFF, SJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1988, 15 (02) :383-389