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Real-World Outcomes of Patients with Primary CNS Lymphoma (PCNSL): A Report from the Australasian Lymphoma Alliance (ALA).

Authors :
Tatarczuch M.
Lewis K.L.
Gunjur A.
Shaw B.
Poon M.
Paul E.
Ku M.
Wong M.
Beekman A.
Krigstein M.
Di Ciaccio P.R.
Wight J.
Coombes C.
Gilbertson M.
Tey A.
Shortt J.
Nagarajan C.
Latimer M.
Talaulikar D.
Hamad N.
Ratnasingam S.
Cochrane T.
Hawkes E.
Cheah C.Y.
Opat S.
Gregory G.P.
Tatarczuch M.
Lewis K.L.
Gunjur A.
Shaw B.
Poon M.
Paul E.
Ku M.
Wong M.
Beekman A.
Krigstein M.
Di Ciaccio P.R.
Wight J.
Coombes C.
Gilbertson M.
Tey A.
Shortt J.
Nagarajan C.
Latimer M.
Talaulikar D.
Hamad N.
Ratnasingam S.
Cochrane T.
Hawkes E.
Cheah C.Y.
Opat S.
Gregory G.P.
Publication Year :
2021

Abstract

Aim: Primary Central Nervous System Lymphoma (PCNSL) [i.e. diffuse large B-cell lymphoma of the CNS] is a rare and poor-prognosis disease occurring predominantly in older patients (median age >60 years old). Prospective studies of two commonly used chemoimmunotherapy (CIT) protocols, MATRix and MPV/Ara-C (+/- rituximab), have reported 2-year PFS and OS of 57-61% and 69-81% respectively. Our aim was to evaluate registry-reported outcomes of frontline CIT strategies employed at Australasian sites. Method(s): A retrospective study of consecutive, immunocompetent, adult PCNSL patients (WHO criteria: 2017) treated with curative-intent CIT, from 10 sites (9 Australian, 1 Singaporean) between 1 st January 2009 and 31 st December 2018 (i.e. ten-year period). Overall survival (OS) and progression-free survival (PFS) were calculated using the Kaplan-Meier (log-rank) method. Univariate associations were derived using a Cox model with variables p<0.10 entered stepwise into a multivariate model. Result(s): Data was collected on 207 patients, 189 of whom met WHO diagnostic criteria for PCNSL (i.e. diffuse large B-cell lymphoma of the CNS). We excluded patients with insufficient data (6), non-DLBCL histology (6), secondary PCNSL (3) and post-transplant lymphoproliferative disorder (3). Of these, 176 (93%) received curative-intent CIT. The majority (66%) were over 65 years of age (median: 65, range: 25-87); ECOG performance status was >= 2 in 31% (data not available for 14% of patients). The majority were male (55%) and had deep structure involvement (64%). International Extranodal Lymphoma Study Group (IELSG) risk criteria could not be calculated in many patients due to missing data (predominantly LDH and CSF protein). CSF involvement was rare (n=23, 13%) but data was only available for 60% of patients. Of the 159 with documented renal function, 26% had renal impairment (defined as Cockroft-Gault creatinine clearance <60ml/min or eGFR <90ml/min). Five CIT regimens were used: MATRi

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1305135308
Document Type :
Electronic Resource