Table 1.
Patient characteristics
Demographicsn = 47
Median age, yr (range) 58 (34–70) 
Gender, n 28 male; 19 female 
Stage 
 Stage III 3 (6%) 
 Stage IV 44 (94%) 
ECOG PS 
 0 35 (74%) 
 1 11 (23%) 
 2 1 (2%) 
Treatment received 
 R-CHOP 7 (15%) 
 R-HyperCVAD 15 (32%) 
 R-CHOP/R-DHAP 23 (49%) 
 Dose-adjusted R-EPOCH 1 (2%) 
 R-Bendamustine 1 (2%) 
Response to immunochemotherapy 
 PR 5 (11%) 
 CR 42 (89%) 
MIPI 
 Low risk 26 (55%) 
 Intermediate risk 15 (32%) 
 High risk 6 (13%) 
Ki-67 
 ≥30% 18 (38%) 
 ≤30% 22 (47%) 
 Unknown 7 (15%) 
B-MIPI 
 Low risk 8 (17%) 
 Intermediate risk 20 (43%) 
 High risk 12 (26%) 
 Unknown 7 (15%) 
Demographicsn = 47
Median age, yr (range) 58 (34–70) 
Gender, n 28 male; 19 female 
Stage 
 Stage III 3 (6%) 
 Stage IV 44 (94%) 
ECOG PS 
 0 35 (74%) 
 1 11 (23%) 
 2 1 (2%) 
Treatment received 
 R-CHOP 7 (15%) 
 R-HyperCVAD 15 (32%) 
 R-CHOP/R-DHAP 23 (49%) 
 Dose-adjusted R-EPOCH 1 (2%) 
 R-Bendamustine 1 (2%) 
Response to immunochemotherapy 
 PR 5 (11%) 
 CR 42 (89%) 
MIPI 
 Low risk 26 (55%) 
 Intermediate risk 15 (32%) 
 High risk 6 (13%) 
Ki-67 
 ≥30% 18 (38%) 
 ≤30% 22 (47%) 
 Unknown 7 (15%) 
B-MIPI 
 Low risk 8 (17%) 
 Intermediate risk 20 (43%) 
 High risk 12 (26%) 
 Unknown 7 (15%) 

Data are presented as n (%) unless specified otherwise. ECOG PS, Eastern Cooperative Oncology Group performance status; R-HyperCVAD, rituximab, cyclophosphamide, vincristine, doxorubicin, and dexamethasone; R-DHAP, rituximab, dexamethasone, cytarabine, and cisplatin; R-EPOCH, rituximab, etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin; PR, partial response; CR, complete response.

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