PHASE-II EVALUATION OF RECOMBINANT INTERFERON-ALPHA-2A AND CONTINUOUS INFUSION FLUOROURACIL IN PREVIOUSLY UNTREATED METASTATIC COLORECTAL ADENOCARCINOMA

被引:0
作者
PAZDUR, R
AJANI, JA
PATT, YZ
GOMEZ, J
BREADY, B
LEVIN, B
机构
[1] UNIV TEXAS,DIV PHARM,HOUSTON,TX 77030
[2] SW INT MED,EL PASO,TX
关键词
COLON CANCER; COLORECTAL CARCINOMA; 5-FLUOROURACIL; INTERFERON; INTERFERON-ALPHA-2A;
D O I
10.1002/1097-0142(19930215)71:4<1214::AID-CNCR2820710407>3.0.CO;2-T
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Thirty-nine patients with advanced measurable metastatic colorectal carcinoma were entered in a clinical trial of recombinant alpha-2a-interferon (ralpha-2a-IFN) and continuous-infusion 5-fluorouracil (5-FU). Patients had not been treated previously with chemotherapy and had bidimensionally measurable disease. Methods. A course of therapy consisted of a 5-day continuous infusion of 5-FU, 750 mg/m2/day, with ralpha-2a-IFN, 9 x 10(6) IU, subcutaneously, on days 1, 3 and 5 of the 5-FU infusion. A course of therapy was repeated every 15 days, and patients were examined for response after receiving four courses of therapy. Results. One patient had a complete response, and 11 patients experienced partial responses, for an overall response rate of 31% (95% confidence interval [CI], 17-48%). The median duration of response was 7.5 months (range, 2-13 months). Fifty-two percent of the patients entered in this trial are alive at time of this writing, with a median follow-up duration of 12.2 months (range, 6-24 months). Grade 3-4 toxicities included mucositis (nine patients), diarrhea (two patients), granulocytopenia (two patients), and fatigue (three patients). Conclusion. This regimen of 5-FU with ralpha-2a-IFN administration does not appear to be superior to previously published schedules of 5-FU with ralpha-2a-IFN or to other methods that modulate 5-FU.
引用
收藏
页码:1214 / 1218
页数:5
相关论文
共 26 条
  • [1] TREATMENT OF ADVANCED COLORECTAL-CANCER
    ABBRUZZESE, JL
    LEVIN, B
    [J]. HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1989, 3 (01) : 135 - 153
  • [2] CHU E, 1990, CANCER RES, V50, P5834
  • [3] ELIAS L, 1988, CANCER RES, V48, P4868
  • [4] INTERFERON EFFECTS UPON FLUOROURACIL METABOLISM BY HL-60 CELLS
    ELIAS, L
    SANDOVAL, JM
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) : 867 - 874
  • [5] A PILOT-STUDY OF INTERFERON ALFA-2A IN COMBINATION WITH FLUOROURACIL PLUS HIGH-DOSE LEUCOVORIN IN METASTATIC GASTROINTESTINAL CARCINOMA
    GREM, JL
    MCATEE, N
    MURPHY, RF
    BALIS, FM
    STEINBERG, SM
    HAMILTON, JM
    SORENSEN, JM
    SARTOR, O
    KRAMER, BS
    GOLDSTEIN, LJ
    GAY, LM
    CAUBO, KM
    GOLDSPIEL, B
    ALLEGRA, CJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (10) : 1811 - 1820
  • [6] GREM JL, 1990, CANC CHEMOTHERAPY PR, P180
  • [7] KEMENY N, 1990, CANCER, V66, P2470, DOI 10.1002/1097-0142(19901215)66:12<2470::AID-CNCR2820661205>3.0.CO
  • [8] 2-Y
  • [9] A PROSPECTIVE RANDOMIZED COMPARISON OF CONTINUOUS INFUSION FLUOROURACIL WITH A CONVENTIONAL BOLUS SCHEDULE IN METASTATIC COLORECTAL-CARCINOMA - A MID-ATLANTIC ONCOLOGY PROGRAM STUDY
    LOKICH, JJ
    AHLGREN, JD
    GULLO, JJ
    PHILIPS, JA
    FRYER, JG
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (04) : 425 - 432
  • [10] MAYER RJ, 1991, SEMIN ONCOL, V18, P62