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Infantile ZFTA Fusion-Positive Tumor of the Posterior Fossa: Molecular Tumor Board.

作者信息

Paulson Vera A, Liu Yajuan J, Fang He, Browd Sam R, Hauptman Jason S, Wright Jason, Lockwood Christina M, Leary Sarah E S, Cole Bonnie L

机构信息

Department of Laboratory Medicine and Pathology, Genetics and Solid Tumor Laboratory, University of Washington, Seattle, WA.

Brotman Baty Institute for Precision Medicine, Seattle, WA.

出版信息

JCO Precis Oncol. 2023 Mar;7:e2200226. doi: 10.1200/PO.22.00226.

DOI:10.1200/PO.22.00226
PMID:36862968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10309551/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ca1/10309551/ee5c2a38e51e/po-7-e2200226-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ca1/10309551/67a13c439091/po-7-e2200226-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ca1/10309551/ee5c2a38e51e/po-7-e2200226-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ca1/10309551/67a13c439091/po-7-e2200226-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ca1/10309551/ee5c2a38e51e/po-7-e2200226-g002.jpg

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Neuro Oncol. 2021 Aug 2;23(8):1231-1251. doi: 10.1093/neuonc/noab106.
2
Temozolomide with irinotecan versus temozolomide, irinotecan plus bevacizumab for recurrent medulloblastoma of childhood: Report of a COG randomized Phase II screening trial.替莫唑胺联合伊立替康与替莫唑胺、伊立替康加贝伐珠单抗治疗儿童复发性髓母细胞瘤：COG 随机 II 期筛选试验报告。
Pediatr Blood Cancer. 2021 Aug;68(8):e29031. doi: 10.1002/pbc.29031. Epub 2021 Apr 12.
3
Infratentorial C11orf95-fused gliomas share histologic, immunophenotypic, and molecular characteristics of supratentorial RELA-fused ependymoma.
幕下C11orf95融合型胶质瘤具有幕上RELA融合型室管膜瘤的组织学、免疫表型和分子特征。
Acta Neuropathol. 2020 Dec;140(6):963-965. doi: 10.1007/s00401-020-02238-3. Epub 2020 Oct 24.
4
Ependymomas in infancy: underlying genetic alterations, histological features, and clinical outcome.婴儿期室管膜瘤：潜在的遗传改变、组织学特征和临床结局。
Childs Nerv Syst. 2020 Nov;36(11):2693-2700. doi: 10.1007/s00381-020-04655-x. Epub 2020 May 30.
5
Validation and implementation of a modular targeted capture assay for the detection of clinically significant molecular oncology alterations.用于检测具有临床意义的分子肿瘤学改变的模块化靶向捕获分析方法的验证与实施
Pract Lab Med. 2020 Feb 3;19:e00153. doi: 10.1016/j.plabm.2020.e00153. eCollection 2020 Mar.
6
Gene fusion analysis in renal cell carcinoma by FusionPlex RNA-sequencing and correlations of molecular findings with clinicopathological features.通过FusionPlex RNA测序对肾细胞癌进行基因融合分析以及分子结果与临床病理特征的相关性研究。
Genes Chromosomes Cancer. 2020 Jan;59(1):40-49. doi: 10.1002/gcc.22798. Epub 2019 Sep 2.
7
Extensive Molecular and Clinical Heterogeneity in Patients With Histologically Diagnosed CNS-PNET Treated as a Single Entity: A Report From the Children's Oncology Group Randomized ACNS0332 Trial.将组织学诊断为中枢神经系统原始神经外胚层肿瘤（CNS-PNET）的患者作为一个单一实体进行治疗时存在广泛的分子和临床异质性：儿童肿瘤学组随机ACNS0332试验报告
J Clin Oncol. 2018 Oct 17;36(34):JCO2017764720. doi: 10.1200/JCO.2017.76.4720.
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Practical implementation of DNA methylation and copy-number-based CNS tumor diagnostics: the Heidelberg experience.DNA 甲基化和基于拷贝数的中枢神经系统肿瘤诊断的实际应用：海德堡经验。
Acta Neuropathol. 2018 Aug;136(2):181-210. doi: 10.1007/s00401-018-1879-y. Epub 2018 Jul 2.
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