Table 1.

Baseline patient, disease, and transplant characteristics

Patient characteristicsFrequency (%) n = 102*
Age 
 <60 y 63 (62) 
 ≥60 y 39 (38) 
Gender 
 Female 40 (39) 
 Male 62 (61) 
KPS at transplant* 
 ≥90 69 (69) 
 70-80 31 (31) 
Stage at diagnosis* 
 Stage 1/2 22 (22) 
 Stage 3/4 78 (78) 
IPI at transplant 
 >2 34 (33) 
 ≤2 68 (67) 
LDH at transplant* 
 High 40 (40) 
 Normal 61 (60) 
CNS involvement site 
 Leptomeningeal 35 (34) 
 Parenchymal 31 (30) 
 Leptomeningeal and parenchymal 11 (11) 
 CSF only 8 (8) 
 Other 17 (17) 
Extent of disease prior to transplant 
 CNS alone 24 (24) 
 CNS and systemic 68 (69) 
 Systemic alone 7 (7) 
Prior lines of therapy 
 ≤2 68 (67) 
 >2 34 (33) 
Time from diagnosis to transplant 
 >18 mo 49 (48) 
 ≤18 mo 53 (52) 
Disease status at transplant 
 CR/CRu 76 (75) 
 Not remission 26 (25) 
CNS directed therapy before transplant*  
 MTX-based regimen 28 (30) 
 ARA-C–based regimen 21 (23) 
 MTX- and ARA-C–based regimen 30 (32) 
 Intrathecal alone 14 (15) 
Conditioning regimen§ 
 BEAM +/− rituximab 54 (53) 
 Thiotepa-based 25 (24) 
 GBM-based 18 (18) 
 Other 5 (5) 
Patient characteristicsFrequency (%) n = 102*
Age 
 <60 y 63 (62) 
 ≥60 y 39 (38) 
Gender 
 Female 40 (39) 
 Male 62 (61) 
KPS at transplant* 
 ≥90 69 (69) 
 70-80 31 (31) 
Stage at diagnosis* 
 Stage 1/2 22 (22) 
 Stage 3/4 78 (78) 
IPI at transplant 
 >2 34 (33) 
 ≤2 68 (67) 
LDH at transplant* 
 High 40 (40) 
 Normal 61 (60) 
CNS involvement site 
 Leptomeningeal 35 (34) 
 Parenchymal 31 (30) 
 Leptomeningeal and parenchymal 11 (11) 
 CSF only 8 (8) 
 Other 17 (17) 
Extent of disease prior to transplant 
 CNS alone 24 (24) 
 CNS and systemic 68 (69) 
 Systemic alone 7 (7) 
Prior lines of therapy 
 ≤2 68 (67) 
 >2 34 (33) 
Time from diagnosis to transplant 
 >18 mo 49 (48) 
 ≤18 mo 53 (52) 
Disease status at transplant 
 CR/CRu 76 (75) 
 Not remission 26 (25) 
CNS directed therapy before transplant*  
 MTX-based regimen 28 (30) 
 ARA-C–based regimen 21 (23) 
 MTX- and ARA-C–based regimen 30 (32) 
 Intrathecal alone 14 (15) 
Conditioning regimen§ 
 BEAM +/− rituximab 54 (53) 
 Thiotepa-based 25 (24) 
 GBM-based 18 (18) 
 Other 5 (5) 

ARA-C, cytarabine; CR, complete response; CRu, complete response uncertain; CSF, cerebrospinal fluid; GBM, gemcitabine, busulphan, melphalan; IPI, international prognostic index; KPS, Karnofsky performance scale; MTX, methotrexate.

*

Numbers do not add up for a total of 102 in some subgroups because of missing information, unless otherwise specified.

Included patients with isolated neurolymphomatosis, intramedullary spinal dissemination, and others not otherwise classified such as epidural with nerve root or spine involvement.

Disease involvement prior to salvage therapy for relapsed patients and at presentation for patients who underwent upfront consolidation with transplant.

§

BEAM and GBM-based conditioning were given as previously described (references 18,–20). Thiotepa-based regimens included BCNU/thiotepa plus or minus rituximab (n = 17) and thiotepa/busulfan/cyclophosphamide plus or minus rituximab (n = 8). Five patients received “other” less commonly used regimens.

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