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. 2019 Jun 26;85(9):2002–2010. doi: 10.1111/bcp.13991

Table 3.

Pharmacokinetic studies of rituximab using pharmacokinetic modelling

Study Year Disease Nonlinear elimination Antigen mass V1 (L) CL (L/day) T½‐β (days)
Regazzi 2005 FL 2.98 0.208 22.4
Blasco 2008 DLBCL 1.77 0.117 94.1
Muller 2012 DLBCL 3.88 0.226 53.9
Rozman 2017 DLBCL Time‐varying Disease progression on kdes 4.62 0.252 40.3
Tout 2017 DLBCL Tumour volume on V1 and V2 6.4 0.55 12.8
Gota 2016 DLBCL 0.95 0.141 11.2
Candelaria 2018 DLBCL 3.19 0.3 21.2
Li 2012 CLL Time‐varying 4.15 0.171 26.7
Tout 2016 CLL TMDD Circulating CD20 on kdeg 3.08 0.137 31.3
Ng 2006 RA 2.98 0.257 20.2
Lioger 2017 RA Time‐varying CD19 count on k10 4 0.44 18.5
Puisset 2013 Plasma‐pheresis 2.48 0.15936 22.8

All pharmacokinetic models were bicompartmental.

FL: follicular lymphoma; DLBCL, diffuse large B‐cell lymphoma; CLL: chronic lymphocytic leukaemia; RA, rheumatoid arthritis; TMDD, target‐mediated drug disposition; V1, V2: central and peripheral volumes of distribution; CL: clearance; k10: first‐order elimination rate constant; kdes: time‐varying elimination rate; kdeg: second‐order target‐mediated elimination rate; T½‐β: elimination half‐life.