2006
DOI: 10.1080/10428190500398849
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Safety of fractionated dose of rituximab in renal failure patients receiving hemodialysis

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Cited by 4 publications
(6 citation statements)
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“…Pharmacokinetic studies on rituximab in patients with end-stage renal disease demonstrated that this agent is not eliminated by dialysis [11]. Similarly, the use of vincristine is safe in severe renal failure (<30 ml/min), with no need for dose adjustment [8].…”
Section: Discussionmentioning
confidence: 99%
“…Pharmacokinetic studies on rituximab in patients with end-stage renal disease demonstrated that this agent is not eliminated by dialysis [11]. Similarly, the use of vincristine is safe in severe renal failure (<30 ml/min), with no need for dose adjustment [8].…”
Section: Discussionmentioning
confidence: 99%
“…The commonest etiology of acquired FVIII: C inhibitor in nonhemophilia patients is idiopathic. [6][7][8] The fact that rituximab is a 145 kDa molecule, suggests that no dose adjustment is needed in patients on HD. Systemic lupus erythematosus contributes to about 6.2% 2-4 of such cases.…”
Section: Discussionmentioning
confidence: 99%
“…The experience on this issue is limited. [6][7][8] The fact that rituximab is a 145 kDa molecule, suggests that no dose adjustment is needed in patients on HD. Because, angio-edema has been reported during infusion of rituximab, we recommend that the dose be given on non-HD days due to a theoretical risk of higher incidence in some patients who may have reaction to certain dialyzers.…”
Section: Discussionmentioning
confidence: 99%
“…This agent does not require dose modification in the renal setting; however, it could be responsible for acute and often severe fluid retention (ATRA syndrome), thus requiring careful management and accurate water balance monitoring [78,79]. The novel proteasome inhibitor bortezomib [80], which is used in the management of MM and in selected cases of others HM, and the monoclonal antibody rituximab [81,82], which represents an essential agent for the treatment of most lymphoproliferative disorders, have been safely administered at full doses to patients with RI and to those on HD. Of note, sustained therapeutic serum levels of rituximab comparable with patients with normal renal function were achieved after the infusion of this agent after HD, and no rituximab clearance into the dialysate was found.…”
Section: Reviewmentioning
confidence: 99%
“…Full dose [81,82] Expert Review of Anticancer Therapy Downloaded from informahealthcare.com by University of Cincinnati on 12/08/14…”
Section: Acute Leukemiasmentioning
confidence: 99%