Clinical significance of cyclooxygenase-2 (COX-2) in multiple myeloma

被引:0
|
作者
Trojan, A
Tinguely, M
Vallet, S
Seifert, B
Jenni, B
Zippelius, A
Witzens-Harig, M
Mechtersheimer, G
Ho, AD
Goldschmidt, H
Jäger, D
Boccadoro, M
Ladetto, M
机构
[1] CHU Vaudois, Ctr Pluridisciplinaire Oncol, CH-1011 Lausanne, Switzerland
[2] Univ Turin, Div Ematol, Turin, Italy
[3] Univ Zurich, Inst Clin Pathol, Zurich, Switzerland
[4] Univ Zurich, Dept Biostat, Zurich, Switzerland
[5] Univ Zurich Hosp, Dept Oncol, CH-8091 Zurich, Switzerland
[6] Univ Heidelberg, Med Klin 5, Heidelberg, Germany
[7] Univ Heidelberg, Dept Pathol, D-6900 Heidelberg, Germany
[8] Univ Heidelberg, Natl Zentrum Tumorekrankungen, Heidelberg, Germany
关键词
multiple myeloma; cyclooxygenase-2 (COX-2); immunohistochemistry; prognosis;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several biological and clinical considerations suggest the involvement of cyclooxygenase-2 (COX-2), the key enzyme of prostaglandin (PG) synthesis, in the pathogenesis and progression of haematological malignancies. Despite the wealth of data concerning COX-2 expression, only limited information is available on multiple myeloma (MM). Using standard immunohistochemistry we therefore evaluated COX-2 protein expression in samples from 57 patients with a primary diagnosis of MM. Time to progression and a variety of clinicopathological features were evaluated by the Kaplan-Meier method and the Cox regression model. In addition, COX-2 expression was evaluated by staining bone marrow from healthy donors and 11 patients with MGUS. Overall, 31 MM samples (54%) expressed COX-2. Positivity for COX-2 was unrelated to stage or clinical or molecular features of the disease. However, patients with COX-2 positive tumours experienced a significantly shorter time to progression (17 vs 30 months, p = 0.037). In summary, COX-2 is frequently expressed in MM and correlates with shorter progression-free survival.
引用
收藏
页码:400 / 403
页数:4
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