ESCALATED THERAPY FOR REFRACTORY UROTHELIAL TUMORS - METHOTREXATE-VINBLASTINE-DOXORUBICIN-CISPLATIN PLUS UNGLYCOSYLATED RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR

被引:121
作者
LOGOTHETIS, CJ
DEXEUS, FH
SELLA, A
AMATO, RJ
KILBOURN, RG
FINN, L
GUTTERMAN, JU
机构
[1] Department of Medical Oncology, Section of Genitourinary Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX
关键词
D O I
10.1093/jnci/82.8.667
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thirty-two assessable patients with metastatic urothelial tumors refractory to standard chemotherapy with methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC) were treated with escalated doses of MVAC plus unglycosylated recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF). Results of this phase I trial revealed that escalated MVAC (30 mg of methotrexate/m2,4 mg of vinblastine/m2, 60 mg of doxorubicin/m2, and 100 mg of cisplatin/m2) can be tolerated by heavily pretreated patients. The side effects of rhGM-CSF are dose- and schedule-dependent. The maximum tolerated dose is 250 μg/m2 per day as a single dose administered subcutaneously (SC) for 10 consecutive days. This dose is well tolerated in outpatients, resulting in only modest fever and few side effects. The same dose delivered as a continuous infusion or a higher dose delivered either as a continuous infusion or SC caused significant side effects. For phase II trials, the starting dose of rhGM-CSF when combined with escalated MVAC is 120 μg/m2 per day SC for 10 consecutive days. Forty percent of the treated patients responded, seven (23%) with complete remission and five (17%) with partial remission. This response rate is higher than anticipated from such a modest dosage escalation in chemotherapy-refractory patients. ]J Natl Cancer Inst 82: 667-672,1990[ © 1990 Oxford University Press.
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页码:667 / 672
页数:6
相关论文
共 12 条
[1]  
BURGESS AW, 1987, BLOOD, V69, P43
[2]   A DOSE AND TIME RESPONSE ANALYSIS OF THE TREATMENT OF HODGKINS-DISEASE WITH MOPP CHEMOTHERAPY [J].
CARDE, P ;
MACKINTOSH, FR ;
ROSENBERG, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1983, 1 (02) :146-153
[3]   STIMULATION OF HEMATOPOIESIS IN PRIMATES BY CONTINUOUS INFUSION OF RECOMBINANT HUMAN GM-CSF [J].
DONAHUE, RE ;
WANG, EA ;
STONE, DK ;
KAMEN, R ;
WONG, GG ;
SEHGAL, PK ;
NATHAN, DG ;
CLARK, SC .
NATURE, 1986, 321 (6073) :872-875
[4]   DOSE - A CRITICAL FACTOR IN CANCER-CHEMOTHERAPY [J].
FREI, E ;
CANELLOS, GP .
AMERICAN JOURNAL OF MEDICINE, 1980, 69 (04) :585-594
[5]   EFFECT OF GRANULOCYTE COLONY-STIMULATING FACTOR ON NEUTROPENIA AND ASSOCIATED MORBIDITY DUE TO CHEMOTHERAPY FOR TRANSITIONAL-CELL CARCINOMA OF THE UROTHELIUM [J].
GABRILOVE, JL ;
JAKUBOWSKI, A ;
SCHER, H ;
STERNBERG, C ;
WONG, G ;
GROUS, J ;
YAGODA, A ;
FAIN, K ;
MOORE, MAS ;
CLARKSON, B ;
OETTGEN, HF ;
ALTON, K ;
WELTE, K ;
SOUZA, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (22) :1414-1422
[6]   CISPLATIN, METHOTREXATE, AND VINBLASTINE (CMV) - AN EFFECTIVE CHEMOTHERAPY REGIMEN FOR METASTATIC TRANSITIONAL CELL-CARCINOMA OF THE URINARY-TRACT - A NORTHERN-CALIFORNIA-ONCOLOGY-GROUP STUDY [J].
HARKER, WG ;
MEYERS, FJ ;
FREIHA, FS ;
PALMER, JM ;
SHORTLIFFE, LD ;
HANNIGAN, JF ;
MCWHIRTER, KM ;
TORTI, FM .
JOURNAL OF CLINICAL ONCOLOGY, 1985, 3 (11) :1463-1470
[7]   DOSE INTENSITY ANALYSIS OF CHEMOTHERAPY REGIMENS IN OVARIAN-CARCINOMA [J].
LEVIN, L ;
HRYNIUK, WM .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (05) :756-767
[8]   RECOMBINANT HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR INDUCES SECRETION OF AUTOINHIBITORY MONOKINES BY U-937 CELLS [J].
LINDEMANN, A ;
RIEDEL, D ;
OSTER, W ;
MERTELSMANN, R ;
HERRMANN, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (03) :369-374
[9]  
LOGOTHETIS CJ, 1989, J UROL, V141
[10]   PRELIMINARY-RESULTS OF M-VAC (METHOTREXATE, VINBLASTINE, DOXORUBICIN AND CISPLATIN) FOR TRANSITIONAL CELL-CARCINOMA OF THE UROTHELIUM [J].
STERNBERG, CN ;
YAGODA, A ;
SCHER, HI ;
WATSON, RC ;
AHMED, T ;
WEISELBERG, LR ;
GELLER, N ;
HOLLANDER, PS ;
HERR, HW ;
SOGANI, PC ;
MORSE, MJ ;
WHITMORE, WF .
JOURNAL OF UROLOGY, 1985, 133 (03) :403-407