ACTIVITY OF 2',2'-DIFLUORODEOXYCYTIDINE (GEMCITABINE) AGAINST HUMAN TUMOR COLONY-FORMING-UNITS

被引:28
作者
HANAUSKE, AR
DEGEN, D
MARSHALL, MH
HILSENBECK, SG
GRINDEY, GB
VONHOFF, DD
机构
[1] UNIV TEXAS,HLTH SCI CTR,DEPT MED,DIV ONCOL,7703 FLOYD CURL DR,SAN ANTONIO,TX 78284
[2] TECH UNIV MUNICH,KLINIKUM RECHTS ISAR,HAMATOL & ONKOL ABT,W-8000 MUNICH 80,GERMANY
[3] ELI LILLY RES LABS,INDIANAPOLIS,IN
关键词
2'; 2'-DIFLUORODEOXYCYTIDINE; GEMCITABINE; GROWTH MODULATION; TUMOR COLONY FORMING UNITS;
D O I
10.1097/00001813-199204000-00012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
2',2'-Difluorodeoxycytidine (LY 188011, Gemcitabine) is a novel pyrimidine antimetabolite with promising activity in preclinical models for leukemia and solid tumors. Phase I clinical trials with the agent are ongoing. In order to better define types of tumors with clinical sensitivity to Gemcitabine (to help target phase II trials), we have studied the antitumor effects of this agent against a variety of freshly explanted human tumor specimens using an in vitro capillary soft agar cloning system. Final concentrations of 2.0-200-mu-g/ml were used for short-term (1 h) and continuous incubations experiments. Using a short-term incubation, 94/215 (44%) tumor specimens were evaluable for the determination of antitumor activity. The most common tumor types studied included colorectal, breast, non-small cell lung, ovarian cancer, kidney and melanoma. A concentration-dependent increase in the frequency of inhibited tumor specimens was noted (2-mu-g/ml: 6/94 specimens, 20-mu-g/ml: 13/94 specimens, 200-mu-g/ml: 33/94 specimens; p < 0.0001). A similar increase in tumor growth inhibition was found using a continuous incubation (2-mu-g/ml: 0/14 specimens, 20-mu-g/ml: 1/14 specimens, 200-mu-g/ml: 7/14 specimens; p < 0.001). We conclude that Gemcitabine is an active antitumor agent against tumor colony forming units from a variety of human malignancies if sufficiently high concentrations can be achieved. The agent should be evaluated for Phase II clinical activity against those tumor types.
引用
收藏
页码:143 / 146
页数:4
相关论文
共 15 条
[1]  
ABBRUZZESE J, 1991, P AN M AM SOC CLIN, V10, P147
[2]   A PHASE-I CLINICAL, PLASMA, AND CELLULAR PHARMACOLOGY STUDY OF GEMCITABINE [J].
ABBRUZZESE, JL ;
GRUNEWALD, R ;
WEEKS, EA ;
GRAVEL, D ;
ADAMS, T ;
NOWAK, B ;
MINEISHI, S ;
TARASSOFF, P ;
SATTERLEE, W ;
RABER, MN ;
PLUNKETT, W .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (03) :491-498
[3]  
ANDERSON H, 1991, P AN M AM SOC CLIN, V10, P247
[4]   COMPARISON OF ANTINEOPLASTIC ACTIVITY OF 2',2'-DIFLUORODEOXYCYTIDINE AND CYTOSINE-ARABINOSIDE AGAINST HUMAN MYELOID AND LYMPHOID LEUKEMIC-CELLS [J].
BOUFFARD, DY ;
MOMPARLER, LF ;
MOMPARLER, RL .
ANTI-CANCER DRUGS, 1991, 2 (01) :49-55
[5]  
BRAAKHUIS BJM, 1991, CANCER RES, V51, P211
[6]  
BROWN T, 1991, P AN M AM SOC CLIN, V10, P115
[7]  
CASPER ES, 1991, P AN M AM SOC CLIN, V10, P143
[8]  
GANDHI V, 1990, CANCER RES, V50, P3675
[9]  
GRUNEWALD R, 1990, CANCER RES, V50, P6823
[10]  
Hanauske A R, 1985, Curr Probl Cancer, V9, P1, DOI 10.1016/S0147-0272(85)80026-X