Pharmacokinetics of doxorubicin and etoposide in a morbidly obese pediatric patient
被引:16
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作者:
Ritzmo, Carina
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Karolinska Inst, Dept Woman & Child Hlth, Karolinska Pharm, Childhood Canc Res Unit, Stockholm, SwedenKarolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
Ritzmo, Carina
[2
]
Soderhall, Stefan
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Karolinska Inst, Dept Woman & Child Hlth, Karolinska Pharm, Childhood Canc Res Unit, Stockholm, SwedenKarolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
Soderhall, Stefan
[2
]
Karlen, Jonas
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机构:
Karolinska Inst, Dept Woman & Child Hlth, Karolinska Pharm, Childhood Canc Res Unit, Stockholm, SwedenKarolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
Karlen, Jonas
[2
]
Nygren, Helen
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Karolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, SwedenKarolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
Nygren, Helen
[1
]
Eksborg, Staffan
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Karolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
Karolinska Inst, Dept Woman & Child Hlth, Karolinska Pharm, Childhood Canc Res Unit, Stockholm, SwedenKarolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
Eksborg, Staffan
[1
,2
]
机构:
[1] Karolinska Univ Hosp, Karolinska Pharm, S-17176 Stockholm, Sweden
[2] Karolinska Inst, Dept Woman & Child Hlth, Karolinska Pharm, Childhood Canc Res Unit, Stockholm, Sweden
This case report presents the pharmacokinetics of doxorubicin and etoposide in a 14-year-old morbidly obese (body mass index: 46.3 kg/m(2)) male patient with Hodgkin disease. Dosing based on an adjusted body surface area resulted in a dose reduction by approximately 25% as compared to dosing based on actual body surface area. Plasma clearance of doxorubicin as well (is plasma clearance and elimination rate of eloposide for this patient was comparable to pharmacokinetic data from nonobese pediatric patients. The therapy was well tolerated without any specific toxicity and a complete response was obtained after 2 scheduled courses, with the patient in complele remission 25 months after end of treatment.