Author/Authors :
Tsung-Yen Cheng، نويسنده , , Elizabeth Grubbs، نويسنده , , Omar Abdul-Wahab، نويسنده , , Szu-Yun Leu، نويسنده , , Chen-Fang Hung، نويسنده , , William Petros، نويسنده , , Thomas Aloia، نويسنده , , Randy Fedrau، نويسنده , , Scott Pruitt، نويسنده , , O. Michael Colvin، نويسنده , , Henry Friedman، نويسنده , , Douglas Tyler، نويسنده ,
Abstract :
Background
Hyperthermic isolated limb perfusion (HILP) with melphalan as treatment for locally recurrent or in-transit malignant melanoma is frequently performed but the principle for calculating drug dosage remains poorly understood.
Methods
This study examined the pharmacokinetic profile of 14 consecutive patients to determine what variables were associated with toxicity and tumor responses.
Results
Marked fourfold variability was noted in patient plasma melphalan concentrations. We defined a factor—the ratio of estimated limb volume (Vesti) to melphalan volume of distribution (Vss), Vesti/Vss—that was much more strongly correlated with acute regional toxicity than either area under concentration-time curve or peak plasma concentration. In addition, we found that AUX2 was the best correlate of tumor response.
Conclusions
Pharmacokinetic evaluation of prospective HILP trials is critical to not only understand response and toxicity outcomes but also to potentially improve the therapeutic index of regional perfusion.
Keywords :
Pharmacokinetics , limb perfusion , melphalan , Volume of distribution , melanoma