Peripheral T-Cell Lymphomas Involving the Central Nervous System: A Report From the Czech Lymphoma Study Group Registry
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
35646641
PubMed Central
PMC9133472
DOI
10.3389/fonc.2022.874462
Knihovny.cz E-zdroje
- Klíčová slova
- CNS prophylaxis, central nervous system, leptomeningeal infiltration, methotrexate, peripheral T-cell lymphoma,
- Publikační typ
- časopisecké články MeSH
INTRODUCTION: We analyzed the incidence, risk factors of central nervous system (CNS) relapse, and outcome of CNS involvement in patients with peripheral T-cell lymphomas (PTCL) from the Czech Lymphoma Study Group Registry NiHiL (Clinical Trial gov. NCT03199066). MATERIALS AND METHODS: Out of 1,040 patients with PTCL, we identified 29 patients (2.79%) with CNS involvement: 2 patients with primary CNS T cell lymphoma, 11 patients with CNS and systemic disease at diagnosis, and 16 patients (1.54%) at CNS relapse. The most common histology with CNS disease was PTCL, not otherwise specified. Progression-free survival (PFS) was defined as the time interval from diagnosis to progression or death. PFS-2 was defined as the interval from the date of a new relapse until the next relapse. RESULTS: Patients with testicular involvement received intrathecal prophylaxis with methotrexate. High-dose methotrexate-based treatment was administered in 44.8% of patients with CNS disease. Median follow-up was 71.3 months. The difference between the median PFS of 1,027 patients without initial CNS disease (32.6 months) and 11 patients with initial CNS and systemic disease (4.8 months) was significant (p = 0.04). The difference between the median PFS2 in CNS relapses (10.1 months) and 493 relapses outside of CNS (9.1 months) was not significant (p = 0.6). Risk factors for CNS relapses included the following: involvement of more than one extranodal site (p = 0.008), soft tissue involvement (p = 0.003), testicular involvement (p = 0.046), and the presence of B symptoms (p = 0.035). The difference between the median OS of 1,027 patients without initial CNS disease (46.0 months) and 11 patients with initial CNS and systemic disease (18.2 months) was significant (p = 0.02). The median OS2 in CNS relapses was 11.8 months and that in relapses outside of CNS was 21.3 months. CNS involvement was not associated with a significantly worse OS compared to relapsed/refractory patients without CNS involvement (p = 0.1). CONCLUSIONS: The incidence of CNS disease at the time of diagnosis and at relapse in PTCL is low and usually associated with other systemic involvement. The prognosis of PTCL with initial CNS involvement is significantly worse when compared to patients without CNS disease at diagnosis. The outcome of CNS relapse is comparable with relapsed PTCL outside of CNS. The optimal treatment is not defined yet.
1st Department of Medicine 1st Faculty of Medicine Charles University Prague Czechia
Department of Clinical Hematology University Hospital Pilsen Czechia
Department of Haemato Oncology Faculty of Medicine and Dentistry Palacky University Olomouc Czechia
Department of Hemato Oncology University Hospital and Faculty of Medicine Ostrava Czechia
Department of Internal Medicine Hematology 3rd Faculty of Medicine Charles University Prague Czechia
Department of Internal Medicine Hematology and Oncology University Hospital Brno Brno Czechia
Institute of Haematology and Blood Transfusion Prague Czechia
Institute of Pathology and Molecular Medicine University Hospital Motol Prague Czechia
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ClinicalTrials.gov
NCT03199066