Predictors of Outcome in Adenoid Cystic Carcinoma of Salivary Glands A Clinicopathologic Study With Correlation Between MYB Fusion and Protein Expression

被引:1
|
作者
Xu, Bin [1 ]
Drill, Esther [3 ]
Ho, Allen [4 ]
Ho, Alan [2 ]
Dunn, Lara [2 ]
Prieto-Granada, Carlos Nicolas [1 ]
Chan, Timothy [2 ]
Ganly, Ian [4 ]
Ghossein, Ronald [1 ]
Katabi, Nora [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
adenoid cystic carcinoma; prognosis; histology; MYB immunohistochemistry; MYB-NFIB fusion; HIGH-GRADE TRANSFORMATION; LYMPH-NODE METASTASIS; CLINICAL-COURSE; HEAD; NECK; NFIB; REARRANGEMENTS; RECURRENCE; SURVIVAL; INVASION;
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Adenoid cystic carcinoma (ACC) is the second most common salivary gland malignancy and it has a high rate of recurrences and a poor long-term prognosis. Our aim was to assess the prognostic factors in ACC and study MYB-NFIB fusion and MYB protein expression in a large retrospective cohort of 135 patients with a median follow-up of 6.3 years. The 5- and 10-year local recurrence-free survival (RFS) rate of 94% and 78%, 5- and 10-year distant metastasis survival rate of 77% and 58%, and 5- and 10-year RFS of 66% and 44%. The following features were identified as adverse prognostic factors of RFS on univariate analysis: large tumor size, solid growth pattern, increased mitoses, positive margin, American Joint Committee on Cancer clinical staging, high-grade transformation, vascular invasion, nuclear atypia, open chromatin, prominent nucleoli, and tumor necrosis. However, on multivariate analysis, only increased mitoses (>= 5/10 high-power fields), any solid growth pattern, and advanced American Joint Committee on Cancer TNM staging were independent adverse predictors for RFS. MYB immunoexpression and MYB-NFIB translocation were common findings in ACC, occurring in 72% and 59% of the tested ACCs, respectively. The sensitivity and specificity of MYB immunohistochemistry in detecting MYB-NFIB fusion was relatively low at 78% sensitivity and 50% specificity. The high prevalence of alterations leading to high expression of the MYB transcription factor family suggests that targeted approaches developed to suppress the expression of these oncogenic transcription factors and/or the transcriptional activity of these proteins would be a rational therapeutic approach to investigate in ACC.
引用
收藏
页码:1422 / 1432
页数:11
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