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
  • [1] SUBCUTANEOUS LOW-DOSE INTERLEUKIN-2 PLUS ALPHA-INTERFERON IN ADVANCED MALIGNANT-MELANOMA
    DEBRAUD, F
    BIGANZOLI, L
    BAJETTA, E
    COLLEONI, M
    ZAMPINO, MG
    TUMORI, 1993, 79 (03) : 187 - 190
  • [2] Response rates of patients with metastatic melanoma to high-dose intravenous interleukin-2 after prior exposure to alpha-interferon or low-dose interleukin-2
    Weinreich, DM
    Rosenberg, SA
    JOURNAL OF IMMUNOTHERAPY, 2002, 25 (02): : 185 - 187
  • [3] High-dose continuous infusion plus pulse interleukin-2 and famotidine in melanoma
    Quan, W
    Ramirez, M
    Taylor, WC
    Vinogradov, M
    Khan, N
    Jackson, S
    CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2004, 19 (06) : 770 - 775
  • [4] High-Dose Ipilimumab and High-Dose Interleukin-2 for Patients With Advanced Melanoma
    Silk, Ann W.
    Kaufman, Howard L.
    Curti, Brendan
    Mehnert, Janice M.
    Margolin, Kim
    McDermott, David
    Clark, Joseph
    Newman, Jenna
    Bommareddy, Praveen K.
    Denzin, Lisa
    Najmi, Saltanat
    Haider, Azra
    Shih, Weichung
    Kane, Michael P.
    Zloza, Andrew
    FRONTIERS IN ONCOLOGY, 2020, 9
  • [5] CHEMOIMMUNOTHERAPY OF ADVANCED MALIGNANT-MELANOMA - SEQUENTIAL ADMINISTRATION OF SUBCUTANEOUS INTERLEUKIN-2 AND INTERFERON-ALPHA AFTER INTRAVENOUS DACARBAZINE AND CARBOPLATIN OR INTRAVENOUS DACARBAZINE, CISPLATIN, CARMUSTINE AND TAMOXIFEN
    ATZPODIEN, J
    HANNINEN, EL
    KIRCHNER, H
    FRANZKE, A
    KORFER, A
    VOLKENANDT, M
    DUENSING, S
    SCHOMBURG, A
    CHAITCHIK, S
    POLIWODA, H
    EUROPEAN JOURNAL OF CANCER, 1995, 31A (06) : 876 - 881
  • [6] TREATMENT OF ADVANCED RENAL-CELL CANCER WITH SEQUENTIAL INTRAVENOUS RECOMBINANT INTERLEUKIN-2 AND SUBCUTANEOUS ALPHA-INTERFERON
    BESANA, C
    BORRI, A
    BUCCI, E
    CITTERIO, G
    DILUCCA, G
    FORTIS, C
    MATTEUCCI, P
    TOGNELLA, S
    TRESOLDI, M
    BAIOCCHI, C
    LANDONIO, G
    GHISLANDI, E
    RUGARLI, C
    EUROPEAN JOURNAL OF CANCER, 1994, 30A (09) : 1292 - 1298
  • [7] Administration of high-dose continuous infusion interleukin-2 to patients age 70 or over
    Quan, W
    Ramirez, M
    Taylor, C
    Quan, F
    Vinogradov, M
    Walker, P
    CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 2005, 20 (01) : 11 - 15
  • [8] LOW-DOSE CYCLOPHOSPHAMIDE, ALPHA-INTERFERON AND CONTINUOUS INFUSIONS OF INTERLEUKIN-2 IN ADVANCED RENAL-CELL CARCINOMA
    WERSALL, JP
    MASUCCI, G
    HJELM, AL
    RAGNHAMMAR, P
    FAGERBERG, J
    FRODIN, JE
    MERK, K
    LINDEMALM, C
    ERICSON, K
    KALIN, B
    MELLSTEDT, H
    MEDICAL ONCOLOGY AND TUMOR PHARMACOTHERAPY, 1993, 10 (03): : 103 - 111
  • [9] CARDIOTOXICITY AS A DOSE-LIMITING FACTOR IN A SCHEDULE OF HIGH-DOSE BOLUS THERAPY WITH INTERLEUKIN-2 AND ALPHA-INTERFERON - AN UNEXPECTEDLY FREQUENT COMPLICATION
    KRUIT, WH
    PUNT, KJ
    GOEY, SH
    DEMULDER, PH
    VANHOOGENHUYZE, DC
    HENZENLOGMANS, SC
    STOTER, G
    CANCER, 1994, 74 (10) : 2850 - 2856
  • [10] Subcutaneous low doses of interleukin-2 and recombinant interferon alpha with carboplatin and vinblastine in patients with advanced melanoma
    Bafaloukos, D
    Fountzilas, G
    Skarlos, D
    Pavlidis, N
    Bakoyiannis, C
    Karvounis, N
    Kosmidis, P
    ONCOLOGY, 1998, 55 (01) : 48 - 52