Octreotide versus octreotide plus interferon-alpha in endocrine gastroenteropancreatic tumors:: A randomized trial

被引:196
作者
Arnold, R
Rinke, A
Klose, KJ
Müller, HH
Wied, M
Zamzow, K
Schmidt, C
Schade-Brittinger, C
Barth, P
Moll, R
Koller, M
Unterhalt, M
Hiddemann, W
Schmidt-Lauber, M
Pavel, M
Arnold, CN
机构
[1] Univ Marburg, Dept Internal Med, Div Gastroenterol & Endocrinol, D-35043 Marburg, Germany
[2] Univ Marburg, Dept Radiol, D-35043 Marburg, Germany
[3] Univ Marburg, Inst Med Biometry & Epidemiol, D-35043 Marburg, Germany
[4] Univ Marburg, Dept Pathol, D-35043 Marburg, Germany
[5] Univ Marburg, Inst Theoret Surg, D-35043 Marburg, Germany
[6] Univ Munich, Dept Internal Med 3, Munich, Germany
[7] Civ Hosp, Oldenburg, Germany
[8] Univ Erlangen Nurnberg, Dept Internal Med, Erlangen, Germany
[9] Albrecht Ludwig Univ, Dept Internal Med, Freiburg, Germany
关键词
D O I
10.1016/S1542-3565(05)00481-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: The effect of octreotide plus interferon-alpha versus octreotide monotherapy on the primary study end points of time to treatment failure (progression, death, stop of study treatment) and long-term survival was investigated in patients with progressive metastatic neuroendocrine foregut (mainly pancreatic) and midgut tumors. Methods: One hundred nine of 125 registered patients were randomized starting in January 1995, and 105 patients (51 monotherapy, 54 combination treatment) were finally analyzed in March 2000. Tumor growth was assessed at 3-month intervals by computed tomography or magnetic resonance imaging. Long-term survival was studied up to April 2004 in all analyzed patients and in 9 patients not randomized because of stable disease. Results: Partial tumor regression occurred in 2.9%, 1.9%, and 5.7% and stabilization of tumor growth in 44.8%, 27.6%, and :15.2% at 3, 6, and 12 months, respectively, with no significant differences between both treatment arms. In March 2000, 9.15% of patients were in treatment. Time to treatment failure and long-term survival did not differ significantly between the 2 groups, with a median survival of 32 and 54 months for the octreotide and the combination groups, respectively. Survival was longer in patients not randomized because of stable disease (median, 68 months) and in those with low nuclear Ki-67. A trend toward longer survival was shown for patients with slow spontaneous tumor growth before randomization. Patients responding to treatment lived longer than unresponsive patients. Conclusions: Combination treatment was not superior to monotherapy concerning progression-free and long-term survival. Patients responding to treatment and those with slow spontaneous tumor growth had a survival advantage.
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页码:761 / 771
页数:11
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