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. Author manuscript; available in PMC: 2017 Dec 1.
Published in final edited form as: Int J Cancer. 2016 Aug 18;139(11):2519–2528. doi: 10.1002/ijc.30372

Table 1.

Demographics, DLBCL Characteristics, and Oncologic Treatment in the HCV-Infected Cases and Uninfected Controls

Characteristic Cases (N=76)
No. of Patients (%)
Controls (N=228)
No. of Patients (%)
p
Age, years [median (IQR)] 59 (53-63) 59 (53-64) Matched
Sex N = 76 N = 228 Matched
 Male 53 (70) 159 (70)
 Female 23 (30) 69 (30)
Race N = 75 N = 225 0.01
 White 51 (68) 175 (78)
 Black 14 (19) 9 (4)
 Hispanic 6 (8) 33 (15)
 Other* 4 (5) 8 (3)
Transformation of DLBCL N = 76 N = 228 0.28
 De novo DLBCL 55 (72) 178 (78)
 Transformed DLBCL 21 (28) 50 (22)
DLBCL subtype N = 54 N = 198 0.39
 GCB 30 (56) 123 (62)
 Non-GCB 24 (44) 75 (38)
Ann Arbor stage N = 75 N = 228 Matched
 1-2 15 (20) 45 (20)
 3-4 60 (80) 183 (80)
ECOG score N = 62 N = 207 0.13
 0-1 44 (71) 165 (80)
 2-4 18 (29) 42 (20)
IPI score N = 58 N = 205 0.37
 Low risk (0-1) 21(36) 63 (31)
 Intermediate risk (2-3) 24 (41) 106 (51)
 High risk (4-5) 13 (23) 36 (18)
Presence of B symptoms 24/73 (33) 82/219 (38) 0.47
Extra nodal involvement 60/76 (79) 164/228 (72) 0.07
Upper GI and splenic involvement 32/76 (42) 54/228 (24) 0.004
Para-aortic lymph node involvement 44/76 (58) 110/218 (50) 0.24
Bone marrow involvement 27/74 (36) 61/228 (27) 0.08
Cirrhosis at DLBCL diagnosis 18/76 (24) 4/220 (2) <0.0001
First-line CT N = 75 N = 228 0.91
 R-CHOP 54 (72) 165 (72)
 Other§ 21 (28) 63 (28)
Second-line CT N = 33 N = 105 0.55
 R-ICE 19 (58) 64 (61)
 Other 14 (42) 41 (39)
Radiotherapy 18/74 (24) 62/228 (27) 0.55
HCT 16/74 (22) 66/228 (29) 0.15
Mortality/survival N = 76 N = 228 0.79
 Dead 30 (39) 94 (41)
Cause of death N = 26 N = 71 --
 Refractory DLBCL 15 (58) 45 (63)
 Liver failure 2 (8) 0
 Infections other than HCV 4 (15) 9 (13)
 Others# 5 (19) 17 (24)

DLBCL indicates diffuse large B-cell lymphoma; GCB, germinal center B-cell; ECOG, Eastern Cooperative Oncology Group; IPI, International Prognostic Index; GI, gastrointestinal; CT, chemotherapy; R-CHOP, rituximab-cyclophosphamide, doxorubicin, vincristine, and prednisone; R-ICE, rituximab-ifosfamide, carboplatin, and etoposide; HCT, hematopoietic stem cell transplantation; HCV, hepatitis C virus.

*

Asian or Pacific Islander.

According to composite or discordant biopsy results (lymph node and bone marrow biopsies) or a previous history of indolent lymphoma.

Stomach, liver, and/or pancreas.

§

Rituximab-etoposide, prednisone, Oncovin (vincristine), cyclophosphamide, and hydroxydaunorubicin (doxorubicin) (R-EPOCH); rituximab-cyclophosphamide, vincristine, doxorubicin (Adriamycin), and dexamethasone (R-hyper-CVAD); or CHOP. Only three patients did not receive rituximab.

Rituximab-etoposide, methylprednisolone, cytarabine, and cisplatin (R-ESHAP); rituximab-gemcitabine and oxaliplatin (R-GEMOX); rituximab-dexamethasone, cytarabine, and cisplatin (R-DHAP); or rituximab-mesna, ifosfamide, novantrone, and etoposide (R-MINE).

Bulky disease at the level of hepatic hilum (n=1), septic shock with multiorgan failure (n=1).

#

Myocardial infarction, tamponade, or other cancers.