Treating refractory advanced or metastatic urothelial carcinoma with interleukin-2: a phase II study

被引:9
作者
Kim, J
Millikan, RE
Smith, TL
Tu, SM
Pagliaro, LC
Logothetis, CJ
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
关键词
interleukin-2; urothelial carcinoma; immunotherapy; chemotherapy;
D O I
10.1016/S1078-1439(02)00207-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with refractory advanced or metastatic urothelial carcinoma derive only minor benefit from chemotherapy. Based on evidence that urothelial carcinoma may be associated with impaired immunological reactivity, we conducted a phase II trial of interleukin-2 (IL-2), a biologic response modifier, to assess its efficacy and toxicity in treating refractory advanced or metastatic urothelial carcinoma. Seventeen patients with urothelial carcinoma who had undergone no more than 1 cisplatin-containing chemotherapy regimen were treated with IL-2 at a dose of 3 x 10(6) IU/m(2)/day by continuous intravenous infusion for 4 consecutive days each week for 4 weeks. Cycles were to be repeated every 6 weeks until disease progression. Toxic effects could be assessed in all 17 patients and response in 13. The most common grade III and IV toxic effects included hypotension (13/17); anemia (6/17); thrombocytopenia (4/17); granulocytopenia (3/17); and, in 1 patient each, cardiac ischemia, bowel perforation, and an increase in creatinine level. One sudden death was assumed to be treatment related. Although we found no objective antitumor activity for IL-2, median patient survival was 10.5 months (95% confidence interval, 5.8 to 17.1 months), with a 15.9-month median survival for 3 patients with poor performance status and visceral metastases. Further clinical investigation of the biological effect of IL-2 in urothelial carcinoma may be warranted. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:21 / 26
页数:6
相关论文
共 44 条
[1]   Dendritic cells acquire antigen from apoptotic cells and induce class I restricted CTLs [J].
Albert, ML ;
Sauter, B ;
Bhardwaj, N .
NATURE, 1998, 392 (6671) :86-89
[2]   CANCER, CYTOKINES, AND CYTOTOXIC-CELLS - INTERLEUKIN-2 IN THE IMMUNOTHERAPY OF HUMAN NEOPLASMS [J].
ATZPODIEN, J ;
KIRCHNER, H .
KLINISCHE WOCHENSCHRIFT, 1990, 68 (01) :1-11
[3]  
CALIGIURI MA, 1993, SEMIN ONCOL, V20, P3
[4]   FUNCTIONAL CONSEQUENCES OF INTERLEUKIN-2 RECEPTOR EXPRESSION ON RESTING HUMAN-LYMPHOCYTES - IDENTIFICATION OF A NOVEL NATURAL-KILLER-CELL SUBSET WITH HIGH-AFFINITY RECEPTORS [J].
CALIGIURI, MA ;
ZMUIDZINAS, A ;
MANLEY, TJ ;
LEVINE, H ;
SMITH, KA ;
RITZ, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (05) :1509-1526
[5]   AUGMENTATION OF THE ANTI-TUMOR THERAPEUTIC EFFICACY OF LONG-TERM CULTURED LYMPHOCYTES-T BY INVIVO ADMINISTRATION OF PURIFIED INTERLEUKIN-2 [J].
CHEEVER, MA ;
GREENBERG, PD ;
FEFER, A ;
GILLIS, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1982, 155 (04) :968-980
[6]   METASTATIC RENAL-CANCER TREATED WITH INTERLEUKIN-2 AND LYMPHOKINE-ACTIVATED KILLER CELLS - A PHASE-II CLINICAL-TRIAL [J].
FISHER, RI ;
COLTMAN, CA ;
DOROSHOW, JH ;
RAYNER, AA ;
HAWKINS, MJ ;
MIER, JW ;
WIERNIK, P ;
MCMANNIS, JD ;
WEISS, GR ;
MARGOLIN, KA ;
GEMLO, BT ;
HOTH, DF ;
PARKINSON, DR ;
PAIETTA, E .
ANNALS OF INTERNAL MEDICINE, 1988, 108 (04) :518-523
[7]   DETERMINATION OF NUMBER OF PATIENTS REQUIRED IN A PRELIMINARY AND A FOLLOW-UP TRIAL OF A NEW CHEMOTHERAPEUTIC AGENT [J].
GEHAN, EA .
JOURNAL OF CHRONIC DISEASES, 1961, 13 (04) :346-&
[8]  
GRIMM E, 1982, ISOLATION CHARACTERI
[9]   LONG-TERM RESULTS WITH M-VAC FOR ADVANCED UROTHELIAL CANCER - HIGH RELAPSE RATE AND LOW SURVIVAL IN PATIENTS WITH A COMPLETE RESPONSE [J].
IGAWA, M ;
URAKAMI, S ;
SHIINA, H ;
ISHIBE, T ;
KADENA, H ;
USUI, T .
BRITISH JOURNAL OF UROLOGY, 1995, 76 (03) :321-324
[10]   A RANDOMIZED STUDY OF LOW-DOSE INTERLEUKIN-2 SUBCUTANEOUS IMMUNOTHERAPY VERSUS INTERLEUKIN-2 PLUS INTERFERON-ALPHA AS FIRST LINE THERAPY FOR METASTATIC RENAL-CELL CARCINOMA [J].
LISSONI, P ;
BARNI, S ;
ARDIZZOIA, A ;
ANDRES, M ;
SCARDINO, E ;
CARDELLINI, P ;
DELLABITTA, R ;
TANCINI, G .
TUMORI, 1993, 79 (06) :397-400