ORAL TROFOSFAMIDE - AN ACTIVE-DRUG IN THE TREATMENT OF SOFT-TISSUE SARCOMA

被引:30
作者
BLOMQVIST, C
WIKLUND, T
PAJUNEN, M
VIROLAINEN, M
ELOMAA, I
机构
[1] Department of Radiotherapy and Oncology, University of Helsinki, FIN-Helsinki 29
关键词
SOFT-TISSUE SARCOMA; CHEMOTHERAPY TROFOSFAMIDE;
D O I
10.1007/BF00685858
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A total of 23 patients with metastatic sarcomas were treated with continuous oral trofosfamide, an alkylating agent structurally related to cyclophosphamide and ifosfamide. In all, 12 of the patients were chemotherapy-naive. Doses were escalated every 3rd week until the development of leukopenia of WHO grade 2. The treatment was well tolerated and produced little subjective toxicity. Leukopenia was the dose-limiting toxicity. The daily dose that produced grade 2 leukopenia was 200-250 mg in 65% of the patients. Three patients responded, all of whom had been treated with trofosfamide as first-line treatment.
引用
收藏
页码:263 / 265
页数:3
相关论文
共 16 条
[1]   RESPONSE TO IFOSFAMIDE AND MESNA - 124 PREVIOUSLY TREATED PATIENTS WITH METASTATIC OR UNRESECTABLE SARCOMA [J].
ANTMAN, KH ;
RYAN, L ;
ELIAS, A ;
SHERMAN, D ;
GRIER, HE .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (01) :126-131
[2]   TROFOSFAMIDE METABOLISM IN DIFFERENT SPECIES-IFOSFAMIDE IS THE PREDOMINANT METABOLITE [J].
BOOS, J ;
KUPKER, F ;
BLASCHKE, G ;
JURGENS, H .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1993, 33 (01) :71-76
[3]  
BRAMWELL VHC, 1993, CANCER CHEMOTH PHARM, V31, pS180
[4]  
BROCK N, 1989, CANCER RES, V49, P1
[5]  
BROCK N, 1973, MED MONATSSCHR, V27, P300
[6]  
DIRIX LY, 1989, SEMIN ONCOL, V16, P39
[7]   RESULTS OBTAINED WITH 2 NEW PHOSPHAMIDE DERIVATIVES [J].
DRINGS, P ;
ALLNER, R ;
BROCK, N ;
BURKERT, H ;
FISCHER, M ;
FOLSCH, E ;
GERHARTZ, H ;
GOTZKY, P ;
HOPPE, I ;
KANZLER, G ;
KLEIN, HO ;
MAINZER, K ;
OBRECHT, P ;
PALME, G ;
PAULISCH, H ;
RIEGG, H ;
SCHUBERT, JC ;
TRESKE, U ;
WEISE, W ;
WILLEMS, D ;
WILMANNS, H ;
WITTE, S ;
WOHLENBE.H .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1970, 95 (10) :491-&
[8]  
FALKSON G, 1978, S AFR MED J, V53, P886
[9]  
KUHBOCK J, 1983, 13TH P INT C CHEM VI, P21
[10]  
MILLER AB, 1981, CANCER, V47, P207, DOI 10.1002/1097-0142(19810101)47:1<207::AID-CNCR2820470134>3.0.CO