The Molecular Landscape of Primary CNS Lymphomas (PCNSLs) in Children and Young Adults

Author:

Shi Zhi-Feng12,Li Kay Ka-Wai3,Liu Anthony Pak-Yin45ORCID,Chung Nellie Yuk-Fei3,Wong Sze-Ching3,Chen Hong6,Woo Peter Yat-Ming7,Chan Danny Tat-Ming7,Mao Ying12ORCID,Ng Ho-Keung23ORCID

Affiliation:

1. Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai 200040, China

2. Hong Kong and Shanghai Brain Consortium (HSBC), Hong Kong, China

3. Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong, China

4. Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, China

5. Department of Paediatrics and Adolescent Medicine, Hong Kong Children’s Hospital, Hong Kong, China

6. Department of Pathology, Huashan Hospital, Fudan University, Shanghai 200040, China

7. Division of Neurosurgery, Department of Surgery, The Chinese University of Hong Kong, Shatin, Hong Kong, China

Abstract

Pediatric brain tumors are often noted to be different from their adult counterparts in terms of molecular features. Primary CNS lymphomas (PCNSLs) are mostly found in elderly adults and are uncommon in children and teenagers. There has only been scanty information about the molecular features of PCNSLs at a young age. We examined PCNSLs in 34 young patients aged between 7 and 39 years for gene rearrangements of BCl2, BCL6, CCND1, IRF4, IGH, IGL, IGK, and MYC, homozygous deletions (HD) of CDKN2A, and HLA by FISH. Sequencing was performed using WES, panel target sequencing, or Sanger sequencing due to the small amount of available tissues. The median OS was 97.5 months and longer than that for older patients with PCNSLs. Overall, only 14 instances of gene rearrangement were found (5%), and patients with any gene rearrangement were significantly older (p = 0.029). CDKN2A HD was associated with a shorter OS (p < 0.001). Only 10/31 (32%) showed MYD88 mutations, which were not prognostically significant, and only three of them were L265P mutations. CARD11 mutations were found in 8/24 (33%) cases only. Immunophenotypically, the cases were predominantly GCB, in contrast to older adults (61%). In summary, we showed that molecular findings identified in the PCNSLs of the older patients were only sparingly present in pediatric and young adult patients.

Funder

National Natural Science Foundation of China

Shanghai Municipal Health Commission, China

Children’s Cancer Foundation, Hong Kong

Publisher

MDPI AG

Reference66 articles.

1. Deckert, M., Batchelor, T., Ferry, J.A., Hoang-Xuan, K., Nagane, M., Paulus, M., and Weller, M. (2021). WHO Classification of Tumours, Central Nervous System Tumours, the WHO Classification of Tumours Editorial Board, IRAC. [5th ed.]. Chapter 10.

2. A genetically distinct pediatric subtype of primary CNS large B-cell lymphoma is associated with favorable clinical outcome;Guney;Blood Adv.,2022

3. Molecular and clinical diversity in primary central nervous system lymphoma;Kirasic;Ann. Oncol.,2023

4. Primary central nervous system lymphoma in children;Abla;Neurosurg. Focus,2006

5. The mutational pattern of primary lymphoma of the central nervous system determined by whole-exome sequencing;Vater;Leukemia,2015

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3