Long-term results of continuous treatment with recombinant interferon-alpha in patients with metastatic carcinoid tumors - An antiangiogenic effect?

被引:0
作者
Dirix, LY
Vermeulen, PB
Fierens, H
DeSchepper, B
Corthouts, B
VanOosterom, AT
机构
[1] UNIV ANTWERP HOSP, DEPT RADIOL, B-2650 EDEGEM, BELGIUM
[2] UNIV ANTWERP HOSP, DEPT GASTROENTEROL, B-2650 EDEGEM, BELGIUM
[3] MED INST ST AUGUSTINUS, DEPT MED ONCOL, ANTWERP, BELGIUM
[4] MED INST ST AUGUSTINUS, DEPT GASTROENTEROL, ANTWERP, BELGIUM
关键词
angiogenesis; carcinoid tumors; interferon-alpha neuron-specific enolase;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study investigated the efficacy of long-term continuous and dose-escalated interferon-alpha (IFN) treatment in patients with progressive carcinoid tumors, In this single-institution, phase II study 16 chemotherapy-naive, eligible patients were entered, Interferon treatment consisted on 5 MIU IFN three times weekly s.c. until radiologic progression, In case of progression the dose was increased to 10 MIU. Radiologic and biochemical evaluation was done monthly and thereafter 3 monthly, We have treated 16 patients of whom 15 are evaluable for tumor response, Calculated by standard response criteria, three patients experienced a partial response, Another three had an important minor response. Median response duration was 24 months (range 18-51 months), Biochemical responses were observed in nine out of 12 patients with an elevated 5-hydroxyindoleacetic acid excretion. The serum neuron-specific enolase proved a reliable marker for both response end progression, In the one patient progressive after 3 months, a dose increment to 10 MIU was without effect. In patients initially not progressing or responding to 5 MIU, escalation to 10 MIU had a short lasting beneficial effect in three cases. The radiological characteristics and the kinetics of these responses are compatible with an anti-angiogenic effect of IFN, This study of IFN in carcinoid tumors confirms the activity in this disease. Our results demonstrate the necessity of initiating treatment only in radiologically progressive patients and continuing this treatment until progression, We feel that currently the activity of IFN in metastatic carcinoid tumors compares favorably with that of systemic chemotherapy in patients with progressive disease.
引用
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页码:175 / 181
页数:7
相关论文
共 33 条
[1]  
ABERG K, 1989, EUR J CANCER CLIN ON, V25, P1475
[2]  
ANDERSSON T, 1990, CANCER RES, V50, P3413
[3]  
BEAUCHAMP RD, 1991, CANCER RES, V51, P5253
[4]   RECOMBINANT INTERFERON-ALPHA-2B IN PATIENTS WITH METASTATIC APUDOMAS - EFFECT ON TUMORS AND TUMOR-MARKERS [J].
BIESMA, B ;
WILLEMSE, PHB ;
MULDER, NH ;
VERSCHUEREN, RCJ ;
KEMA, IP ;
DEBRUIJN, HWA ;
POSTMUS, PE ;
SLEIJFER, DT ;
DEVRIES, EGE .
BRITISH JOURNAL OF CANCER, 1992, 66 (05) :850-855
[5]   PRODUCTION OF BASIC FIBROBLAST GROWTH-FACTOR BY GASTRIC CARCINOID-TUMORS AND THEIR PUTATIVE CELLS OF ORIGIN [J].
BORDI, C ;
FALCHETTI, A ;
BUFFA, R ;
AZZONI, C ;
DADDA, T ;
CARUANA, P ;
RINDI, G ;
BRANDI, ML .
HUMAN PATHOLOGY, 1994, 25 (02) :175-180
[6]   A PHASE-II TRIAL OF DACARBAZINE, FLUOROURACIL AND EPIRUBICIN IN PATIENTS WITH NEUROENDOCRINE TUMORS - A STUDY BY THE ITALIAN TRIALS IN MEDICAL ONCOLOGY (ITMO) GROUP [J].
DIBARTOLOMEO, M ;
BAJETTA, E ;
BOCHICCHIO, AM ;
CARNAGHI, C ;
SOMMA, L ;
MAZZAFERRO, V ;
VISINI, M ;
GEBBIA, V ;
TUMOLO, S ;
BALLATORE, P .
ANNALS OF ONCOLOGY, 1995, 6 (01) :77-79
[7]   TREATMENT OF METASTATIC CARCINOID-TUMORS AND THE CARCINOID-SYNDROME WITH RECOMBINANT INTERFERON ALPHA [J].
DOBERAUER, C ;
MENGELKOCH, B ;
KLOKE, O ;
WANDL, U ;
NIEDERLE, N .
ACTA ONCOLOGICA, 1991, 30 (05) :603-605
[8]   DEVELOPMENT OF TYPE-1 DIABETES-MELLITUS DURING INTERFERON-ALFA THERAPY FOR CHRONIC HCV HEPATITIS [J].
FABRIS, P ;
BETTERLE, C ;
FLOREANI, A ;
GREGGIO, NA ;
DELAZZARI, F ;
NACCARATO, R ;
CHIARAMONTE, M .
LANCET, 1992, 340 (8818) :548-548
[9]   INCREASED SERUM LEVELS OF BASIC FIBROBLAST GROWTH-FACTOR IN PATIENTS WITH RENAL-CELL CARCINOMA [J].
FUJIMOTO, K ;
ICHIMORI, Y ;
KAKIZOE, T ;
OKAJIMA, E ;
SAKAMOTO, H ;
SUGIMURA, T ;
TERADA, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 180 (01) :386-392
[10]  
GOODWIN JD, 1975, CANCER, V36, P560