THE FEASIBILITY OF REPETITIVE COURSES OF HIGH-DOSE CONTINUOUS INTRAVENOUS-INFUSION INTERLEUKIN-2 AND SUBCUTANEOUS ALPHA-INTERFERON WITH POLYCHEMOTHERAPY IN ADVANCED MALIGNANT-MELANOMA

被引:3
|
作者
FOPPOLI, M
CITTERIO, G
POLASTRI, D
GUERRIERI, R
机构
[1] Divisione di Medicina II, Ospedale S. Raffaele, 20132 Milano
来源
TUMORI JOURNAL | 1995年 / 81卷 / 02期
关键词
MELANOMA; INTERLEUKIN-2; COMBINED IMMUNOTHERAPY;
D O I
10.1177/030089169508100206
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims and background: A Phase I study of repetitive courses of chemotherapy (carmustine, cis-platinum, dacarbazine) and immunotherapy (continuous intravenous infusion recombinant interleukin-2 (rlL-2) and subcutaneous (sc) alpha-interferon 2b) plus tamoxifen was performed in order to establish a more efficaciuous way to sequence this kind of treatment for advanced malignant melanoma. Study design: Patients who had measurable metastatic melanoma, a Karnofsky performance status greater than or equal to 80, and no clinically significant hematologic or cardiac disfunction were considered eligible. Treatment consisted of BCNU, 150 mg/m(2) i.v. day 1 in alternating cycles; DTIC, 220 mg/m(2) i.v. days 1, 2 and 3; CDDP, 25 mg/m(2) i.v. days 1,2 and 3; tamoxifen 10 mg twice/day per os continuously; rIL-2, 18x10(6) IU/m(2)/day continuous i.v. infusion days 5-8 (96 h) and days 19-22 (96 h); alpha-interferon (IFN) s.c. 3x10(6) U day 12, 6x10(6) U day 14, 9x10(6) U days 16, 19, 21, 23, 26, and 28 (from cycle 2, 9x10(6) U days 2, 5, 7, 9, 12, 14, 16, 19, 21, 23, 26, and 28). Two consecutive cycles were planned until response evaluation. Results: Three patients were treated according with the protocol; none of them was able to respect the planned dose-intensity schedule. The given dose intensity/planned dose intensity ratios were as follows: DTIC, 0.74 (range, 0.70-0.80); CDDP, 0.77 (0.72-0.80); BCNU, 0.77 (0.72-0.80); rlL-2, 0.65 (0.36-0.80); alpha-IFN, 0.01 (0-0.03); tameoxifen, 1.0. Systemic side effects of rlL-2 and myelotoxicity were the main reasons for treatment delay and/or dose-reduction, and for the long period of hospital care. Conclusions: We conclude that the treatment schedule is not feasible. However, since we believe that combined chemo-immunotherapy is a potentially active treatment in metastatic malignant melanoma, we have modified it in order to make it more feasible and consequently efficacious.
引用
收藏
页码:102 / 106
页数:5
相关论文
共 39 条
  • [11] A phase II study of dacarbazine, cisplatin, interferon-alpha and high-dose interleukin-2 in 'poor-risk' metastatic melanoma
    Proebstle, TM
    Scheibenbogen, C
    Sterry, W
    Keilholz, U
    EUROPEAN JOURNAL OF CANCER, 1996, 32A (09) : 1530 - 1533
  • [12] High-dose continuous infusion plus pulse interleukin-2 and famotidine in metastatic kidney cancer
    Quan, W
    Ramirez, M
    Taylor, C
    Vinogradov, M
    Quan, F
    Khan, N
    CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2005, 20 (01) : 36 - 40
  • [13] A PHASE-II TRIAL OF CONCOMITANT HUMAN INTERLEUKIN-2 AND INTERFERON-ALPHA-2A IN PATIENTS WITH DISSEMINATED MALIGNANT-MELANOMA
    WHITEHEAD, RP
    FIGLIN, R
    CITRON, ML
    PFILE, J
    MOLDAWER, N
    PATEL, D
    JONES, G
    LEVITT, D
    ZEFFREN, J
    JOURNAL OF IMMUNOTHERAPY, 1993, 13 (02) : 117 - 121
  • [14] PHASE-II STUDY OF CONTINUOUS INTRAVENOUS-INFUSION OF RECOMBINANT INTERLEUKIN-2 IN PATIENTS WITH ADVANCED RENAL-CELL CARCINOMA
    LOPEZ, M
    CARPANO, S
    CANCRINI, A
    MARCELLINI, M
    DELMEDICO, P
    RINALDI, M
    VICI, P
    PAOLETTI, G
    DILAURO, L
    ANNALS OF ONCOLOGY, 1993, 4 (08) : 689 - 691
  • [15] Correlation between development of pulmonary edema and response of pulmonary metastases of metastatic melanoma and kidney cancer to high-dose continuous-infusion interleukin-2
    Quan, WDY
    Khan, N
    Ramirez, M
    Taylor, WC
    Quan, F
    Vinogradov, M
    Walker, P
    CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2005, 20 (02) : 151 - 154
  • [16] Cyclosporine A, alpha-interferon and interleukin-2 following chemotherapy with BCNU, DTIC, cisplatin, and tamoxifen: A phase II study in advanced melanoma
    Feun, L
    Marini, A
    Moffat, F
    Savaraj, N
    Hurley, J
    Mazumder, A
    CANCER INVESTIGATION, 2005, 23 (01) : 3 - 8
  • [17] A phase II study of interferon alpha and low-dose subcutaneous interleukin-2 in advanced renal cell carcinoma
    Piga, A
    Giordani, P
    Quattrone, A
    Giulioni, M
    DeSignoribus, G
    Antognoli, S
    Cellerino, R
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 1997, 44 (06) : 348 - 351
  • [18] A PHASE-I STUDY OF HIGH-DOSE INTERLEUKIN-2 IN COMBINATION WITH INTERFERON-ALPHA-2B
    SZNOL, M
    MIER, JW
    SPARANO, J
    GAYNOR, ER
    WEISS, GR
    MARGOLIN, KA
    BAR, MH
    HAWKINS, MJ
    ATKINS, MB
    DUTCHER, JP
    FISHER, RI
    BOLDT, DH
    DOROSHOW, JH
    LOUIE, A
    ARONSON, FR
    JOURNAL OF BIOLOGICAL RESPONSE MODIFIERS, 1990, 9 (06): : 529 - 537
  • [19] A PHASE-II STUDY OF COMBINED ADMINISTRATION OF DACARBAZINE AND CARBOPLATIN WITH HOME THERAPY OF RECOMBINANT INTERLEUKIN-2 AND INTERFERON-ALPHA-2A IN PATIENTS WITH ADVANCED MALIGNANT-MELANOMA
    RON, IG
    MORDISH, Y
    EISENTHAL, A
    SKORNICK, Y
    INBAR, MJ
    CHAITCHIK, S
    CANCER IMMUNOLOGY IMMUNOTHERAPY, 1994, 38 (06) : 379 - 384
  • [20] DAILY ALTERNATING ADMINISTRATION OF HIGH-DOSE INTERFERON-ALPHA-2B AND INTERLEUKIN-2 BOLUS INFUSION IN METASTATIC RENAL-CELL CANCER - A PHASE-II STUDY
    BERGMANN, L
    FENCHEL, K
    WEIDMANN, E
    ENZINGER, HM
    JAHN, B
    JONAS, D
    MITROU, PS
    CANCER, 1993, 72 (05) : 1733 - 1742