Accelerated regression of brain metastases in patients receiving whole brain radiation and the topoisomerase II inhibitor, lucanthone

被引:28
作者
Del Rowe, JD
Bello, J
Mitnick, R
Sood, B
Filippi, C
Moran, J
Freeman, K
Mendez, F
Bases, R
机构
[1] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Radiat Oncol, Bronx, NY 10467 USA
[2] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Radiol, Bronx, NY 10467 USA
[3] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Nucl Med, Bronx, NY 10467 USA
[4] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Epidemiol & Social Med, Bronx, NY 10467 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 1999年 / 43卷 / 01期
关键词
lucanthone; topoisomerase II; blood-brain barrier;
D O I
10.1016/S0360-3016(98)00374-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine if lucanthone crossed the blood-brain barrier in experimental animals; and to determine accelerated tumor regression of human brain metastases treated jointly with lucanthone and whole brain radiation. Methods and Materials: The organ distribution of H-3 lucanthone in mice and I-125 lucanthone in rats was determined to learn if lucanthone crossed the blood-brain barrier. Size determinations were made of patients' brain metastases from magnetic resonance images or by computed tomography before and after treatment with 30 GS' whole brain radiation alone or with lucanthone. Results: The time course of lucanthone's distribution in brain was identical to that in muscle and heart after intraperitoneal or intravenous administration in experimental animals. Lucanthone, therefore, readily crossed the blood-brain barrier in experimental animals. Conclusion: Compared with radiation alone, the tumor regression in patients with brain metastases treated with lucanthone and radiation was accelerated, approaching significance using a permutation test at p = 0.0536. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:89 / 93
页数:5
相关论文
共 10 条
[1]  
BASES R, 1970, CANCER RES, V30, P2007
[2]   DNA INTERCALATING AGENTS AS ADJUVANTS IN RADIATION-THERAPY [J].
BASES, R .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1978, 4 (3-4) :345-346
[3]   Topoisomerase inhibition by lucanthone, an adjuvant in radiation therapy [J].
Bases, RE ;
Mendez, F .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1997, 37 (05) :1133-1137
[4]  
BLAIR D M, 1958, Bull World Health Organ, V18, P989
[5]  
Hirschberg E., 1974, ANTIBIOTICS-BASEL, P274
[6]  
HOLLANDER M, 1973, NONPARAMETRIC STAT M, P244
[7]   ABASIC SITES STIMULATE DOUBLE-STRANDED DNA CLEAVAGE MEDIATED BY TOPOISOMERASE-II - DNA LESIONS AS ENDOGENOUS TOPOISOMERASE-II POISONS [J].
KINGMA, PS ;
CORBETT, AH ;
BURCHAM, PC ;
MARNETT, LJ ;
OSHEROFF, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :21441-21444
[8]   EFFECT OF LUCANTHONE (MIRACIL-D) ON SUBLETHAL RADIATION-DAMAGE IN CHINESE-HAMSTER CELLS [J].
LEEPER, DB ;
KARAMUZ, JE ;
BLANNET, JD .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1978, 4 (3-4) :219-227
[9]   LUCANTHONE AS A RADIOSENSITIZING AGENT IN TREATMENT OF CARCINOMA OF CERVIX [J].
NOBLER, MP ;
SCHER, AJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1978, 4 (11-1) :1039-1044
[10]   ADJUVANT EFFECT OF LUCANTHONE (MIRACIL-D) IN CLINICAL RADIATION-THERAPY [J].
TURNER, S ;
BASES, R ;
PEARLMAN, A ;
NOBLER, M ;
KABAKOW, B .
RADIOLOGY, 1975, 114 (03) :729-731