T-Cell Prolymphocytic Leukemia: Diagnosis, Pathogenesis, and Treatment.
ATM
BH3 mimetic
JAK
STAT
T-cell receptor
T-prolymphocytic leukemia (T-PLL)
TCL1A
alemtuzumab
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
28 Jul 2023
28 Jul 2023
Historique:
received:
19
06
2023
revised:
20
07
2023
accepted:
26
07
2023
medline:
14
8
2023
pubmed:
12
8
2023
entrez:
12
8
2023
Statut:
epublish
Résumé
T-cell prolymphocytic leukemia (T-PLL) is a rare and aggressive neoplasm of mature T-cells. Most patients with T-PLL present with lymphocytosis, anemia, thrombocytopenia, and hepatosplenomegaly. Correct identification of T-PLL is essential because treatment for this disease is distinct from that of other T-cell neoplasms. In 2019, the T-PLL International Study Group (TPLL-ISG) established criteria for the diagnosis, staging, and assessment of response to treatment of T-PLL with the goal of harmonizing research efforts and supporting clinical decision-making. T-PLL pathogenesis is commonly driven by T-cell leukemia 1 (
Identifiants
pubmed: 37569479
pii: ijms241512106
doi: 10.3390/ijms241512106
pmc: PMC10419310
pii:
doi:
Substances chimiques
Alemtuzumab
3A189DH42V
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NCI NIH HHS
ID : R01 CA265929
Pays : United States
Organisme : NIH HHS
ID : R01CA265929
Pays : United States
Organisme : NIH HHS
ID : R37CA233476
Pays : United States
Organisme : NIH HHS
ID : R01CA236722
Pays : United States
Organisme : NCI NIH HHS
ID : R37 CA233476
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA236722
Pays : United States
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