Expression of Bcl-2 in gastrointestinal stromal tumors - Correlation with progression-free survival in 81 patients treated with imatinib mesylate

被引:35
作者
Steinert, DM
Oyarzo, M
Wang, XM
Choi, HS
Thall, PF
Medeiros, LJ
Raymond, AK
Benjamin, RS
Zhang, W
Trent, JC
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Sarcoma Med Oncol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Biostat & Appl Math, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
关键词
gastrointestinal stromal tumor (GIST); apoptosis; sarcoma; clinicopathologic; survival;
D O I
10.1002/cncr.21781
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The natural history of gastrointestinal stromal tumor (GIST) has been revolutionized by imatinib mesylate (imatinib) therapy. Before imatinib, Bcl-2 expression in GIST was associated With a worse prognosis or added no additional prognostic value. To the authors' knowledge, the current study is the first to evaluate Bcl-2 expression in pre-imatinib GIST tissue samples as a prognostic marker of progression-free survival (PFS) time in patients treated with imatinib. METHODS. The cases of 81 patients with GIST who were evaluated between December 15, 2000 and September 1, 2001 were retrospectively reviewed. Clinicopathologic variables were reviewed. GIST cell morphology and patterns of Bcl-2 expression were described. The methods of Kaplan-Meier and the Cox proportionat hazards regression model were used for statistical analysis. RESULTS. Sixty-one (75%) patients had tumors that expressed Bcl-2, and 20 (25%) patients had tumors; that were negative for Bcl-2. All epithelioid tumors (n = 12) expressed Bcl-2 and tumours with mixed morphology exhibited Bcl-2 expression in the epithelioid component. A trend toward longer PFS for patients whose tumors expressed Bcl-2 at a greater immunohistochemical intensity was observed (20.6 mos for no Bcl-2 expression: 28.3 mos for 1++Bcl-2 expression; 31.9 mos for 1.5++Bcl-2 expression; 40.8 mos for 2++Bcl-2 expresssion; and 35.9 mos for 3++Bcl-2 expression). CONCLUSIONS. in contrast to Studies performed in the preimatinib era, in which Bcl-2 was found to be a negative prognostic indicator, the Current study Suggests a trend toward better PPS with increasing Bcl-2 expression level in GISTs from patients Subsequently treated with imatinib. Larger Studies may help elucidate the influence of Bcl-2 expression oil PFS after therapy with imatinib.
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收藏
页码:1617 / 1623
页数:7
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