SOMATOSTATIN ANALOG SANDOSTATIN AND INHIBITION OF TUMOR-GROWTH IN PATIENTS WITH METASTATIC ENDOCRINE GASTROENTEROPANCREATIC TUMORS

被引:76
作者
ARNOLD, R
NEUHAUS, C
BENNING, R
SCHWERK, WB
TRAUTMANN, ME
JOSEPH, K
BRUNS, C
机构
[1] UNIV MARBURG,DEPT RADIOL,W-3550 MARBURG,GERMANY
[2] SANDOZ LTD,PRECLIN RES,CH-4002 BASEL,SWITZERLAND
关键词
D O I
10.1007/BF01655111
中图分类号
R61 [外科手术学];
学科分类号
摘要
A prospective study was performed to determine the efficacy of octreotide (Sandostatin(R); SMS 201-995) 200 mug tid in controlling tumor growth. The study included 21 patients with metastasized endocrine GEP tumors: 6 gastrinomas, 8 carcinoid syndromes, 7 nonfunctioning tumors. Treatment was performed for 3 to 59 months (median 15 months). Evaluation of the response to octreotide was facilitated in 12 patients by a pretreatment observation period of 3 to 47 months (median 17 months) during which the natural growth behavior was determined. Based on the presence or absence of a control period prior to treatment, 5 patients were considered to be responders, 7 as questionable responders (no pretreatment phase available), and 9 as nonresponders. None of the 21 patients had documented shrinkage of the tumor mass. The most favorable response was tumor standstill. In all but one responder an escape to an initially favorable response occurred after 6 to 28 months (median 14 months). Proved inhibition of growth was paralleled by a reduction of serum and urine hormone parameters, whereas unaltered progression of tumor growth was observed also in the presence of hormone suppression. Tumor growth and hormone release was inhibited in the absence and presence of somatostatin receptors on the tumor. It is concluded that octreotide exerts a limited effect on metastatic GEP tumor growth. The evaluation of a response to octreotide is facilitated by an observation period prior to the drug that provides information on growth characteristics of the tumor. The presence of octreotide receptors does not predict the success of therapy.
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页码:511 / 519
页数:9
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