TP53 DNA binding domain mutational status and rituximabbased treatment are independent prognostic factors for pediatric Burkitt lymphoma patients stratification

Haematologica. 2024 Sep 1;109(9):3031-3036. doi: 10.3324/haematol.2023.284868.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adolescent
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Burkitt Lymphoma* / diagnosis
  • Burkitt Lymphoma* / drug therapy
  • Burkitt Lymphoma* / genetics
  • Burkitt Lymphoma* / mortality
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Male
  • Mutation*
  • Prognosis
  • Rituximab* / therapeutic use
  • Tumor Suppressor Protein p53* / genetics

Substances

  • Rituximab
  • Tumor Suppressor Protein p53
  • TP53 protein, human

Grants and funding

Funding: This work was supported by Fondazione Città della Speranza, Padova, Italy (Grant 21/03 to LM); AIRC, Milano, Italy (Investigator Grant - IG 2018 #21385 to LM). This work was also supported by the Comitato Assistenza Socio-Sanitaria in Oncoematologia Pediatrica (CASOP), Padova, Italy, and the Associazione Italiana contro le Leucemie-Linfomi e Mieloma (AIL), Rovigo, Italy