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. 2018 Jun 7;7(2):373–383. doi: 10.1007/s40120-018-0101-4

Table 2.

Biological and clinical follow-up of the NMOSD patients

Patient Rituximab follow-up (months) Rituximab infusions N Mean duration between 2 infusions (months) ARR with rituximab CD19 count before RTX (/MM3) Mean months for CD19+ CD27+ occurrence (min max) Mean rituximab concentration at retreatment (µg/mL) HACA (, D, +) ng/mL
1 AM 26 4 7.3 (6–8) 0 252 7.1 (6–7.9) 0 +
2 BG 44 4 9 (6–12.5) 0 200 8.8 (5.8–12.2) 0 D
3 CF 12 3 7.1 0 79 7 0 D
4 CP 60 4 18 (6–) 0 117 16 (6–11.3) 0
5 NY 23 3 8.3 0 619 8 0 +
6 PN 23 3 7.8 0 216 7.5 3.3 D
7 TMJ 66 6 11.4 (9–16.9) 0 120 11.1 (9–16.2) 0 D
8 SFA 36 5 6.9 (6–10.9) 0 210 6.5 (6–7.1) 0 D
9 AS 15 3 8.1 0 318 8 0 +
10 CM 34 2 0 151
11 DO 42 3 11.6 0 838 11.4 0
12 VE 36 3 13.5 0 225 13.2 0 D
13 OS 16 2 0 234
14 BM 24 4 6.4 (5.4–6.9) 0 213 6 (5.3–6.7) 0 D
15 SG 20 3 6 0 274 6 0
16 SN 29 3 10.8 0 301 10.5 0
17 GS 24 3 7.9 0 120 7.5 0

CD19+ CD27+ memory B cells were considered positive when below 0.05%. HACA-RTX Abs: human anti-chimeric antibodies to the murine fragments of RTX: (−) Negative = 0, (D) detectable < 10 UI/mL, (+) positive > 10 UI/mL. The RTX infusion was shortly administered with the CD19+ CD27+ re-emergence