Diffuse large B‐cell lymphoma at risk of secondary CNS involvement: The inefficacy of intravenous high‐dose methotrexate CNS prophylaxis and the importance of baseline cerebrospinal fluid analysis
High‐dose intravenous methotrexate (HD‐MTX) CNS prophylaxis in high‐risk diffuse large B cell lymphoma (DLBCL) remains controversial. We describe real‐world CNS relapse incidence following baseline cerebrospinal fluid (CSF) analysis to exclude asymptomatic leptomeningeal involvement in newly diagnos...
Gespeichert in:
Veröffentlicht in: | American journal of hematology 2023-07, Vol.98 (7), p.1070-1079 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | High‐dose intravenous methotrexate (HD‐MTX) CNS prophylaxis in high‐risk diffuse large B cell lymphoma (DLBCL) remains controversial. We describe real‐world CNS relapse incidence following baseline cerebrospinal fluid (CSF) analysis to exclude asymptomatic leptomeningeal involvement in newly diagnosed high‐risk DLBCL patients with versus without single‐route HD‐MTX CNS prophylaxis. Consecutively diagnosed high‐risk systemic DLBCL patients without leptomeningeal involvement by CSF analysis (noCNS) were identified retrospectively. Five‐year CNS relapse incidence and survival outcomes were examined, as stratified by receipt of HD‐MTX prophylaxis. Secondary analysis of survival outcomes in patients with synchronous leptomeningeal involvement (CNSinv) by CSF analysis at diagnosis were compared with the noCNS group. No significant difference in 5‐year CNS relapse incidence was observed following HD‐MTX prophylaxis versus no prophylaxis (total n = 445) despite similar CNS‐IPI risk; 6.2% versus 5.6%, adjusted HR 1.08 (95% CI 0.41–2.85), p = .88; nor in 5‐year progression free survival (PFS) or overall survival (OS) risk. Of CNSinv patients, 93.3% had ≥1 extranodal site. Increased CNS relapse/progression risk (5‐year risk; HR 10.7 [95% CI 5.35–21.37], p |
---|---|
ISSN: | 0361-8609 1096-8652 |
DOI: | 10.1002/ajh.26953 |