4.6 Article

Recurrent Somatic Chromosomal Abnormalities in Relapsed Extraocular Retinoblastoma

期刊

CANCERS
卷 13, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13040673

关键词

extraocular retinoblastoma; copy number alteration; genomic; metastasis; BCOR mutations

类别

资金

  1. Agencia Nacional de Promocion Cientifica y Tecnologica [PIDC 2014-0043]
  2. Fondation Nelia et Amadeo Barletta
  3. Fundacion Leo Messi
  4. Fund for Ophthalmic Knowledge, NY, Instituto Nacional del Cancer (National Cancer Institute), Argentina
  5. Fundacion Natalie Dafne Flexer de Ayuda al Nino con Cancer
  6. Fundacion Garrahan
  7. Instituto Oncologico Herny Moore

向作者/读者索取更多资源

Relapse of retinoblastoma outside the eye is a rare event in developed countries but remains the main cause of death in patients worldwide. A study of 23 cases from different countries revealed a characteristic pattern of chromosomal copy number alterations in these patients, providing valuable guidance for future clinical management. Previously underrecognized CNAs such as 11q deletions, 17q gains, 19q loss, and BCOR alterations were found to be more common in extraocular retinoblastoma, potentially indicating a more aggressive tumor phenotype that requires careful consideration in patient management.
Simple Summary Relapse outside the eye of retinoblastoma (the most common eye cancer in children) is an uncommon event in developed countries, however it is the main cause of death in patients with retinoblastoma worldwide. The genomic features of this population are not known. We studied 23 cases from four countries and found a characteristic pattern in chromosomal copy number alterations that could help guide future clinical management of these patients. Most reports about copy number alterations (CNA) in retinoblastoma relate to patients with intraocular disease and features of children with extraocular relapse remain unknown, so we aimed to describe the CNA in this population. We evaluated 23 patients and 27 specimens from 4 centers. Seventeen cases had extraocular relapse after initial enucleation and six cases after an initial preservation attempt. We performed an analysis of CNA and BCOR gene alteration by SNP array (Single Nucleotide Polymorfism array), whole-exome sequencing, IMPACT panel and CGH array (Array-based comparative genomic hybridization). All cases presented CNA at a higher prevalence than those reported in previously published studies for intraocular cases. CNA previously reported for intraocular retinoblastoma were found at a high frequency in our cohort: gains in 1q (69.5%), 2p (60.9%) and 6p (86.9%), and 16q loss (78.2%). Other, previously less-recognized, CNA were found including loss of 11q (34.8%), gain of 17q (56.5%), loss of 19q (30.4%) and BCOR alterations were present in 72.7% of our cases. A high number of CNA including 11q deletions, 17q gains, 19q loss, and BCOR alterations, are more common in extraocular retinoblastoma. Identification of these features may be correlated with a more aggressive tumor warranting consideration for patient management.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据