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The Molecular Landscape of Primary CNS Lymphomas (PCNSLs) in Children and Young Adults.
Shi, Zhi-Feng; Li, Kay Ka-Wai; Liu, Anthony Pak-Yin; Chung, Nellie Yuk-Fei; Wong, Sze-Ching; Chen, Hong; Woo, Peter Yat-Ming; Chan, Danny Tat-Ming; Mao, Ying; Ng, Ho-Keung.
Afiliación
  • Shi ZF; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai 200040, China.
  • Li KK; Hong Kong and Shanghai Brain Consortium (HSBC), Hong Kong, China.
  • Liu AP; Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
  • Chung NY; Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong, China.
  • Wong SC; Department of Paediatrics and Adolescent Medicine, Hong Kong Children's Hospital, Hong Kong, China.
  • Chen H; Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
  • Woo PY; Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
  • Chan DT; Department of Pathology, Huashan Hospital, Fudan University, Shanghai 200040, China.
  • Mao Y; Division of Neurosurgery, Department of Surgery, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
  • Ng HK; Division of Neurosurgery, Department of Surgery, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
Cancers (Basel) ; 16(9)2024 Apr 29.
Article en En | MEDLINE | ID: mdl-38730692
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: China
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