Table 1

 Demographic, clinical, and biological data on 14 patients treated with rituximab for rheumatoid arthritis

CaseSex/age/duration of disease (y)No of prior DMARD/prior anti-TNF (Y/N)Non-articular involvement (Y/N)No of infusions × dose (mg)/No of MP pulses/concomitant ISAdverse event (Y/N)Efficacy RA/non-articular involvement (Y/N)Time to response (w)/follow up (m)DAS28 initial/last†Prednisone initial/last‡ (mg/d)RF initial/last (IU/ml) (n <20)Relapse (Y/N)/time to relapse (m)
*Evolution of neutropenia in patients 13 and 14 was described in a submitted case report.
†p<0.0002 between DAS28 value pre- and post-treatment using paired t test.
‡p<0.01 between prednisone dose pre- and post-treatment.
CPH, cyclophosphamide; DAS28, 28 joint disease activity score; DMARD, disease modifying antirheumatic drug; F, female; HQ, hydroxychloroquine; IS, immunosuppressants; lymph, lymphoma; m, months; M, male; MP, methylprednisolone; MTX, methotrexate; N, no; NA, not available; neg, negative; pos, positive; RA, rheumatoid arthritis; RF, rheumatoid factor (determined by nephelometry, except where stated “pos/neg”, when determined by latex); TNF, tumour necrosis factor; w, weeks; y, years; Y, yes; –, not relevant.
1F/48/48/YN4×375.m−2/HQNY4/65.9/2.915/10Pos/NAN
2M/83/33/YY/lymph4×375.m−2/4/MP (100)NY/Y6/5.57.6/2.412/9NAY/5.5
3F/42/1511/YN27×375.m−2/MTX,CPHNY16/158.3/3.610/10270/150Y/5
4F/47/24/YN2×1000/2/MP (100)/MTX+HQNY4/38.7/4.70/0240/122N
5F/68/183/NY/lymph8×1000/8/CHOPNY/Y4/245.3/2.73/0266/20N
6M/57/73/YN2×1000/CPHNY4/56/3.220/10938/441N
7F/41/85/YN2×1000/MTXNN–/46/5.210/1095/NA
8M/55/126/YN2×1000NY4/87.9/3.617.5/10Pos/negN
9F/48/75/NN2×1000/MTXNY8/124/1.810/2.5Neg/neg
10M/49/37/YN1×375.m−2/1/MP (100)Infusion relatedN–/3NA10/10Pos/pos
11F/68/345/YN4×375.m−2/4/MP (40)NY4/36.6/3.84/4NAN
12F/53/32/NN4×375.m−2/4/MP (40)NY6/66.5/2.24/020/20N
13*M/67/21/NY/Felty4×375.m−2NN/N–/66.6/6.715/15Neg/neg
14*M/53/42/NY/Felty4×375.m−2/MTXNY/N4/127.5/2.115/1060/14N