EFFECTS OF AMSACRINE IN COMBINATION WITH OTHER ANTICANCER AGENTS IN HUMAN ACUTE LYMPHOBLASTIC-LEUKEMIA CELLS IN CULTURE

被引:32
作者
KANO, Y
SAKAMOTO, S
KASAHARA, T
AKUTSU, M
INOUE, Y
MIURA, Y
机构
[1] TOCHIGI CANC CTR,DIV SURG,UTSUNOMIYA,TOCHIGI 320,JAPAN
[2] JICHI MED SCH,DEPT MED,DIV HEMATOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
[3] JICHI MED SCH,DEPT PARASITOL,MINAMI KAWACHI,TOCHIGI 32904,JAPAN
关键词
AMSACRINE; DRUG COMBINATION;
D O I
10.1016/0145-2126(91)90112-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Effects of amsacrine in combination with other anticancer agents at ID80 were evaluated by cell growth assay using a human T-cell leukemia cell line (MOLT-3). The data were analyzed with the aid of an improved isobologram, using the concept of an envelope of additivity. A supra-additive effect was observed for amsacrine in combination with cytosine arabinoside and mitoxantrone. An additive effect was observed in its combinations with bleomycin, CPT-11, cisplatin, daunorubicin, doxorubicin, etoposide, 5-fluorouracil, homoharringtonine, mitomycin C, or vincristine. 6-Mercaptopurine had an additive effect with amsacrine at ID80 but a sub-additive to protective effect at ID90. A sub-additive to protective effect was shown for amsacrine in combination with methotrexate. These data suggest that cytosine arabinoside and mitoxantrone are the best of the anticancer agents we studied for use in combination with amsacrine. Bleomycin, cisplatin, CPT-11, doxorubicin, cytosine arabinoside, homoharringtonine, mitomycin C, and vincristine also yielded favorable results when administrated simultaneously with amsacrine. Simultaneous administration of amsacrine with 6-mercaptopurine and methotrexate is not appropriate. If amsacrine is combined with 6-mercaptopurine and methotrexate, other suitable schedules should be explored. These results may provide a rationale for the design of clinical protocols combining amsacrine with other anticancer agents.
引用
收藏
页码:1059 / 1066
页数:8
相关论文
共 44 条
[1]  
ABRAMS RA, 1986, CANCER TREAT REP, V70, P535
[2]  
ARLIN ZA, 1985, CANCER TREAT REP, V69, P1001
[3]  
ARLIN ZA, 1982, BLOOD, V60, P1224
[4]  
BAJETTA E, 1985, CANCER TREAT REP, V69, P965
[5]   EFFECT OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE (ARA-C) ON NUCLEAR TOPOISOMERASE-II ACTIVITY AND ON THE DNA CLEAVAGE AND CYTO-TOXICITY PRODUCED BY 4'-(9-ACRIDINYLAMINO)METHANESULFON-META-ANISIDIDE (META-AMSA) AND ETOPOSIDE IN META-AMSA-SENSITIVE AND META-AMSA-RESISTANT HUMAN-LEUKEMIA CELLSD [J].
BAKIC, M ;
CHAN, D ;
ANDERSSON, BS ;
BERAN, M ;
SILBERMAN, L ;
ESTEY, E ;
RICKETTS, L ;
ZWELLING, LA .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (23) :4067-4077
[6]   CRITERIA FOR ANALYZING INTERACTIONS BETWEEN BIOLOGICALLY-ACTIVE AGENTS [J].
BERENBAUM, MC .
ADVANCES IN CANCER RESEARCH, 1981, 35 :269-335
[7]   ACUTE LEUKEMIAS - ANALYSIS OF 322 CASES AND REEVIEW OF LITERATURE [J].
BOGGS, DR ;
CARTWRIGHT, GE ;
WINTROBE, MM .
MEDICINE, 1962, 41 (03) :163-+
[8]  
CABANILLAS F, 1981, BLOOD, V57, P614
[9]   ADRIAMYCIN - REVIEW [J].
CARTER, SK .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1975, 55 (06) :1265-1274
[10]  
CLARKSON B, 1970, Cancer, V25, P279, DOI 10.1002/1097-0142(197002)25:2<279::AID-CNCR2820250205>3.0.CO