Which dose of busulfan is best?

@article{JohnsonDavis2010WhichDO,
  title={Which dose of busulfan is best?},
  author={Kamisha L. Johnson-Davis and Gwendolyn A McMillin and Joetta M Juenke and Clyde D Ford and Finn Bo Petersen},
  journal={Clinical chemistry},
  year={2010},
  volume={56 7},
  pages={
          1061-4
        }
}
A 24-year-old woman with advanced Hodgkin disease received the standard dosing protocol for busulfan/cyclophosphamide before allogeneic hematopoietic stem cell transplantation (HSCT)1 from a matched unrelated donor. The target area under the plasma concentration vs time curve (AUC) for busulfan was set at 950 μmol · L−1 · min−1, near the low end of the therapeutic interval of 900–1350 μmol · L−1 · min−1. The patient’s body mass index (BMI) was 45.5 kg/m2 (height, 170.2 cm; weight, 132.0 kg), so… 
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References

SHOWING 1-10 OF 11 REFERENCES
Individualizing high-dose oral busulfan: prospective dose adjustment in a pediatric population undergoing allogeneic stem cell transplantation for advanced hematologic malignancies
TLDR
The feasibility of adjusting the oral BU dose in individual pediatric patients is demonstrated and toxicity associated with BU seemed to be reduced, but the overall regimen-related toxicity (RRT) remains substantial and reflected the effects of all agents used in the preparative regimen.
THERAPEUTIC MONITORING OF BUSULFAN IN PEDIATRIC BONE MARROW TRANSPLANTATION
TLDR
The data suggest that it may be reasonable to recommend a busulfan dose of 1.2 mg/kg to achieve the accepted therapeutic target in children undergoing BMT.
Intravenous busulfan in adults prior to haematopoietic stem cell transplantation: a population pharmacokinetic study
TLDR
A limited sampling strategy based on a Bayesian methodology was developed and validated on an independent dataset: AUCs obtained from one to two samplings were demonstrated to be reliably estimated and no dose adjustment is required in obese patients when using a AIBW- or BSA-based dose calculation.
Chronopharmacology of high-dose busulfan in children.
TLDR
The circadian changes in busulfan trough plasma levels observed at the steady state were not related to the occurrence of HVOD in these children with solid tumors, since this rhythm was stable from day 2 to day 4, it should not compromise dose adjustment.
Busulfan disposition: the role of therapeutic monitoring in bone marrow transplantation induction regimens.
  • L. Grochow
  • Medicine, Biology
    Seminars in oncology
  • 1993
TLDR
It is suggested that therapeutic monitoring can play an important role in decreasing the toxicity of BMT preparative regimens and may improve treatment efficacy by identifying patients who are not receiving adequate drug exposure.
Association of busulfan area under the curve with veno-occlusive disease following BMT.
TLDR
Routine pharmacotherapeutic monitoring of busulfan is recommended with further study to evaluate the impact of earlier and greater overall dose reduction in patients with high initial busulfans exposures.
The effect of metronidazole on busulfan pharmacokinetics in patients undergoing hematopoietic stem cell transplantation
TLDR
It is concluded that metronidazole should not be administered simultaneously with Bu to avoid the high plasma levels of Bu, which may lead to severe toxicity and/or treatment related mortality.
Pharmacokinetic and metabolic studies of high-dose busulphan in adults
TLDR
Sulolane, 3-hydroxysulpholane and tetrahydrothiophene 1-oxide were identified as urinary metabolites of busulphan in man for the first time and suggest that busulfan may increase its own metabolic rate on repeated treatment.
The impact of obesity and disease on busulfan oral clearance in adults.
TLDR
Routine dosing on the basis of BSA or AIBW in adults and adolescents does not require a specific accommodation for the obese, however, dosing based on BSA may be improved by considering CL/F differences in certain diseases.
Adverse Effects of Voriconazole: Analysis of the French Pharmacovigilance Database
TLDR
Most AOEs found in this study are well documented in the literature, except for cardiac complications, which are rarely reported, and clinicians should be aware of potential interactions between voriconazole and other drugs metabolized through this pathway.
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