Prediction of response to treatment in superficial bladder carcinoma through pattern of interleukin-2 gene expression

被引:83
作者
Kaempfer, R
Gerez, L
Farbstein, H
Madar, L
Hirschman, O
Nussinovich, R
Shapiro, A
机构
[1] HADASSAH UNIV HOSP,DEPT UROL,IL-91120 JERUSALEM,ISRAEL
[2] ISRAEL CANC RES FUND,BIOSTAT & DATA MANAGEMENT CTR,GIVAT SHMUEL,ISRAEL
关键词
D O I
10.1200/JCO.1996.14.6.1778
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Superficial bladder carcinoma, treated by resection and intravesical administration of bacillus Calmette-Guerin (BCG), yields a remission rate that approaches 70%, We examined whether expression of interleukin-2 (IL-2) or interferon-gamma (IFN-gamma) genes can serve to predict response. Patients and Methods: During BCG treatment, we analyzed induction of IL-2 and IFN-gamma mRNA in peripheral-blood mononuclear cells (PBMC) from 73 patients: 51 with papillary tumors and 22 with carcinoma-in-situ (CIS). Results were correlated with remission, relapse, or tumor persistence over a 4-year follow-up period. Results: Independent of tumor type, induction of IL-2 mRNA was observed for patients who responded with remission, but not far those who relapsed (P = .0001). Multivariate logistic analysis showed that inducibility of IL-2 mRNA is the discriminating parameter, which yields a predictive value of 97% for remission, Of 23 patients with relapse/persistence, 22 lacked inducibility of IL-2 mRNA (sensitivity, 95.6%), while 35 of 50 patients ire remission exhibited inducibility (specificity, 70%), For patients with carcinoma-in-situ, in which remission or failure depends solely on response to BCG, sensitivity and specificity were 88% and 86%, respectively; for patients with papillary tumors, they were 100% and 64%. IFN-gamma mRNA, by contrast, was clearly inducible in PBMC from all patients (P = .51), The disease-free interval increased progressively with inducibility of IL-2 mRNA; this trend was highly significant (P = .0001). Conclusion: IL-2 gene expression is essential for mounting an antitumor response in superficial bladder carcinoma, Inducibility of IL-2 mRNA is an independent prognostic parameter and useful predictive indicator of remission versus relapse. (C) 1996 by American Society of Clinical Oncology.
引用
收藏
页码:1778 / 1786
页数:9
相关论文
共 39 条
[11]   DEFECT IN LECTIN-INDUCED INTERLEUKIN-2 PRODUCTION BY PERIPHERAL-BLOOD LYMPHOCYTES OF PATIENTS WITH INVASIVE URINARY-BLADDER CARCINOMA [J].
BUBENIK, J ;
KIELER, J ;
TROMHOLT, V ;
HERMANN, G ;
JANDLOVA, T .
IMMUNOLOGY LETTERS, 1988, 18 (02) :115-118
[12]   A REPRODUCIBLE MICROANALYTICAL METHOD FOR THE DETECTION OF SPECIFIC RNA SEQUENCES BY DOT BLOT HYBRIDIZATION [J].
CHELEY, S ;
ANDERSON, R .
ANALYTICAL BIOCHEMISTRY, 1984, 137 (01) :15-19
[13]   REGRESSION OF BLADDER-TUMORS IN MICE TREATED WITH INTERLEUKIN-2 GENE-MODIFIED TUMOR-CELLS [J].
CONNOR, J ;
BANNERJI, R ;
SAITO, S ;
HESTON, W ;
FAIR, W ;
GILBOA, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (04) :1127-1134
[14]   LONG-TERM FOLLOW-UP OF PATIENTS TREATED WITH 1 OR 2, 6-WEEK COURSES OF INTRAVESICAL BACILLUS CALMETTE-GUERIN - ANALYSIS OF POSSIBLE PREDICTORS OF RESPONSE FREE OF TUMOR [J].
COPLEN, DE ;
MARCUS, MD ;
MYERS, JA ;
RATLIFF, TL ;
CATALONA, WJ .
JOURNAL OF UROLOGY, 1990, 144 (03) :652-657
[15]  
CORNELL R, 1984, STAT METHODS CANC ST
[16]   PRESENCE OF INTERLEUKIN-2 IN URINE OF SUPERFICIAL BLADDER-CANCER PATIENTS AFTER INTRAVESICAL TREATMENT WITH BACILLUS CALMETTE-GUERIN [J].
DEJONG, WH ;
DEBOER, EC ;
VANDERMEIJDEN, APM ;
VEGT, P ;
STEERENBERG, PA ;
DEBRUYNE, FMJ ;
RUITENBERG, EJ .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1990, 31 (03) :182-186
[17]   CONTROL OF BIOLOGICALLY-ACTIVE INTERLEUKIN-2 MESSENGER-RNA FORMATION IN INDUCED HUMAN-LYMPHOCYTES [J].
EFRAT, S ;
KAEMPFER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (09) :2601-2605
[18]  
EFRAT S, 1982, NATURE, V297, P236, DOI 10.1038/297236a0
[19]   SUPERINDUCTION OF HUMAN INTERLEUKIN-2 MESSENGER-RNA BY INHIBITORS OF TRANSLATION [J].
EFRAT, S ;
ZELIG, S ;
YAGEN, B ;
KAEMPFER, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 123 (02) :842-848
[20]  
FLEISCHMANN JD, 1989, CANCER, V64, P1447, DOI 10.1002/1097-0142(19891001)64:7<1447::AID-CNCR2820640715>3.0.CO