Uveal Melanomas with SF3B1 Mutations: A Distinct Subclass Associated with Late-Onset Metastases

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• 作者：Serdar Yavuzyigitoglu ; MD¹ ; ² ; ^&lowast ; ; Anna E. Koopmans ; MD ; PhD¹ ; ² ; ^&lowast ; ; Robert M. Verdijk ; MD ; PhD³ ; Jolanda Vaarwater ; BSc¹ ; ² ; Bert Eussen ; BSc² ; Alice van Bodegom ; BSc¹ ; ² ; Dion Paridaens ; MD ; PhD⁴ ; Emine Kiliç ; MD ; PhD¹ ; Annelies de Klein ; PhD² ; ^{a.deklein@erasmusmc.nl" class="auth_mail" title="E-mail the corresponding author} ; on behalf of the Rotterdam Ocular Melanoma Study Group
• 关键词：BAP1 ; BRCA-associated protein 1 ; DFS ; disease-free survival ; EIF1AX ; eukaryotic translation initiation factor 1A ; GNAQ ; Guanine nucleotide-binding protein G(q) subunit alpha ; GNA11 ; Guanine nucleotide-binding protein G(q) subunit alpha 11 ; HR ; hazard ratio ; SF3B1 ; splicing factor 3 subunit B1 ; UM ; uveal melanoma
• 刊名：Ophthalmology
• 出版年：2016
• 出版时间：May 2016
• 年：2016
• 卷：123
• 期：5
• 页码：1118-1128
• 全文大小：1273 K

文摘

To investigate the prevalence and prognostic value of SF3B1 and EIF1AX mutations in uveal melanoma (UM) patients.

Design

Case series.

Participants

Cohort of 151 patients diagnosed with and treated for UM.

Methods

SF3B1 and EIF1AX mutations in primary tumors were investigated using whole-exome sequencing (n = 25) and Sanger sequencing (n = 151). For the detection of BAP1 mutations, a previously reported cohort of 90 patients was extended using BAP1 sequencing or immunohistochemistry.

Main Outcome Measures

The status of SF3B1, EIF1AX, and BAP1 in tumors of patients were correlated to clinical, histopathologic, and genetic parameters. Survival analyses were performed for patients whose tumors had SF3B1, EIF1AX, and BAP1 mutations.

Results

Patients with tumors harboring EIF1AX mutations rarely demonstrated metastases (2 of 28 patients) and overall had a longer disease-free survival (DFS; 190.1 vs. 100.2 months; P < 0.001). Within the patient group with disomy 3, UM patients with an SF3B1 mutation had an increased metastatic risk compared with those without an SF3B1 mutation (DFS, 132.8 vs. 174.4 months; P = 0.008). Patients with such a mutation were more prone to demonstrate late metastases (median, 8.2 years; range, 23–145 months). Patients with UM and loss of BAP1 expression had a significantly decreased survival (DFS, 69.0 vs. 147.9 months; P < 0.001).

Conclusions

According to our data, patients with UM can be classified into 3 groups, of which EIF1AX-mutated tumors and tumors without BAP1, SF3B1, or EIF1AX mutations are associated with prolonged survival and low metastatic risk, SF3B1-mutated tumors are associated with late metastasis, and tumors with an aberrant BAP1 are associated with an early metastatic risk and rapid decline in patient DFS.