The doxorubicin-streptozotocin combination for the treatment of advanced well-differentiated pancreatic endocrine carcinoma: a judicious option?

被引:96
作者
Delaunoit, T
Ducreux, M
Boige, V
Dromain, C
Sabourin, JC
Duvillard, P
Schlumberger, M
de Baere, T
Rougier, P
Ruffie, P
Elias, D
Lasser, P
Baudin, E
机构
[1] Inst Gustave Roussy, Dept Gastroenterol, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Dept Radiol, F-94805 Villejuif, France
[3] Inst Gustave Roussy, Dept Pathol, F-94805 Villejuif, France
[4] Inst Gustave Roussy, Dept Endocrinol, F-94805 Villejuif, France
[5] Inst Gustave Roussy, Dept Intervent Radiol, F-94805 Villejuif, France
[6] Inst Gustave Roussy, Dept Med Oncol, F-94805 Villejuif, France
[7] Inst Gustave Roussy, Dept Surg, F-94805 Villejuif, France
关键词
neuroendocrine carcinoma; chemotherapy; pancreas;
D O I
10.1016/j.ejca.2003.09.035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Due to their rarity, only few trials have studied the role of the doxorubicin-streptozotocin (DS) combination in advanced well-differentiated pancreatic endocrine carcinomas (AWDPEC). However, the published results are inconsistent. We reviewed all AWDPEC (5-year period, 45 patients) treated in our institution with the DS combination for: objective response rate (ORR), progression-free survival, overall survival (OS) and toxicity. An ORR of 36% (95% Confidence Interval (CI) 22-49) was obtained, with 16 partial responses (PR). The mean duration of PR was of 19.7 months. Two and 3-year OS rates were 50.2 and 24.4%, respectively. Toxicities were mainly digestive (grade greater than or equal to3 vomiting, 13%) and haematological (grade greater than or equal to3 neutropenia, 24%). Previous systemic chemotherapy and malignant hepatomegaly were associated with a poorer ORR (P = 0.033, P = 0.016) and OS (P=0.008, P=0.045). Multivariate analysis demonstrated previous chemotherapy as the only independent predictive-factor for survival (P=0.013). In conclusion, our data confirm the sensitivity of AWDPEC to the DS combination, with an ORR of 36% and a remarkable median response duration of 19.7 months, and suggests that it could be considered as a valid option in first-line therapy. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:515 / 520
页数:6
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