Pharmacokinetics in children
The following kinetic parameters have been observed for bortezomib in the treatment of ALL (after a dose of 1.3 mg/m², n=3) [Horton 2007]:
Cmax: 63 ng/ml
t½: 725 min
Cl: 38 ml/hour/m²
dose recommendation of formulary compared to licensed use (on-label versus off-label)
No information is present at this moment.
Available formulations
No information is present at this moment.
Dosages
| Acute alloantibody-mediated kidney rejection (acute AMR) |
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| Recurrent/refractory ALL |
- Intravenous
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6 months
up to
18 years
The dosage and dosing frequency of oncological agents depend on the condition and are very much subject to new insights. Oncological drugs are often used in combinations. For these reasons, please refer to the detailed treatment protocols (see www.skion.nl); no dose recommendations have been included.
Treatment by or after consultations with a paediatric specialist (oncology) who has experience using bortezomib for this indication
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Renal impaiment in children > 3 months
GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects
No information is present at this moment.
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Contra-indications
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Warnings & precautions in children
As of yet there is insufficient evidence to include the indication thrombotic thrombocytopenia purpura. Treatment by a paediatric specialist (haematologist) who has experience with using bortezomib for this indication.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
OTHER ANTINEOPLASTIC AGENTS
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| MONOKLONALE ANTILICHAMEN |
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L01XC11
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L01XC18
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L01XC18
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| Other antineoplastic agents |
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L01XX01
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L01XX02
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L01XX05
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L01XX23
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L01XX24
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L01XX14
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| Antineoplastic cell and gene therapy |
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L01XL04
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References
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Claes DJ et al., Protective immunity and use of bortezomib for antibody-mediated rejection in a pediatric kidney transplant recipient., Pediatr Transplant., 2014, Jun;18(4), E100-5
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Nguyen S et al. 2014, Efficacy of bortezomib for reducing donor-specific antibodies in children and adolescents on a steroid minimization regimen., Pediatr Transplant., 2014, Aug;18(5), 463-8
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Twombley K et al., Acute antibody-mediated rejection in pediatric kidney transplants: a single center experience., Pediatr Transplant., 2013, Nov;17(7):, E149-55
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Westphal S et al. , Successful treatment of severe ABO antibody-mediated rejection using bortezomib: a case report. , Transplant Proc., 2013, Apr;45(3), 1213-5
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Messinger YH et al, Bortezomib with chemotherapy is highly active in advanced B-precursor acute lymphoblastic leukemia: Therapeutic Advances in Childhood Leukemia & Lymphoma (TACL) Study., Blood, 2012, Jul 12;120(2), 285-90
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Horton TM et al., A phase 1 study of the proteasome inhibitor bortezomib in pediatric patients with refractory leukemia: a Children's Oncology Group study., Clin Cancer Res., 2007, Mar 1;13(5), 1516-22
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Kizilbash S et al., Bortezomib in the treatment of antibody-mediated rejection in pediatric kidney transplant recipients: A multicenter Midwest Pediatric Nephrology Consortium study, Pediatr Transplant., 2017, Jan 16
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Westphal S et al., Successful treatment of severe ABO antibody-mediated rejection using bortezomib: a case report., Transplant Proc., 2013, Apr;45(3), 1213-5
Therapeutic Drug Monitoring
Overdose