Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/9550
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dc.contributor.authorUittenboogaard, Aniek-
dc.contributor.authorVelde, Mirjam van de-
dc.contributor.authorHeijden, Lisa van de-
dc.contributor.authorMukuhi, Leah-
dc.contributor.authorVries, Niels de-
dc.contributor.authorLangat, Sandra-
dc.contributor.authorOlbara, Gilbert-
dc.contributor.authorHuitema, Alwin D. R-
dc.contributor.authorVik, Terry-
dc.contributor.authorKaspers, Gertjan-
dc.contributor.authorNjuguna, Festus-
dc.date.accessioned2025-02-20T08:54:42Z-
dc.date.available2025-02-20T08:54:42Z-
dc.date.issued2024-06-10-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/9550-
dc.description.abstractThe low incidence of vincristine-induced peripheral neuropathy (VIPN) in Kenyan children may result from low vincristine exposure. We studied vincristine expo- sure in Kenyan children and dose-escalated in case of low vincristine exposure (NCT05844670). Average vincristine exposure was high. Individual vincristine expo- sure was assessed with a previously developed nomogram. A 20% dose increase was recommended for participants with low exposure and no VIPN, hyperbilirubinemia, or malnutrition. None of the 15 participants developed VIPN. Low vincristine exposure was seen in one participant: a dose increase was implemented without side effects. In conclusion, the participants did not develop VIPN despite having high vincristine exposure.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectIndividualized dosing,en_US
dc.subjectPediatric oncologyen_US
dc.subjectPharmacokineticsen_US
dc.subjectVincristineen_US
dc.titleVincristine exposure in Kenyan children with cancer: CHAPATI feasibility studyen_US
dc.typeArticleen_US
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