Marked variability of melphalan plasma drug levels during regional hyperthermic isolated limb perfusion

被引:22
作者
Cheng, TY
Grubbs, E
Abdul-Wahab, O
Leu, SY
Hung, CF
Petros, W
Aloia, T
Fedrau, R
Pruitt, S
Colvin, M
Friedman, H
Tyler, D
机构
[1] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[3] Sun Yat Sen Canc Ctr, Koo Fdn, Div Gen Surg, Taipei, Taiwan
[4] W Virginia Univ, Sch Pharm, Dept Basic Pharmaceut Sci, Morgantown, WV 26506 USA
[5] W Virginia Univ, Ctr Canc, Dept Basic Pharmaceut Sci, Morgantown, WV 26506 USA
关键词
pharmacokinetics; limb perfusion; melphalan; volume of distribution; melanoma;
D O I
10.1016/j.amjsurg.2003.07.019
中图分类号
R61 [外科手术学];
学科分类号
摘要
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. (C) 2003 Excerpta Medica, Inc. All rights reserved.
引用
收藏
页码:460 / 467
页数:8
相关论文
共 33 条
[1]
MODIFIED EXTRACTION AND CHROMATOGRAPHY FOR THE MEASUREMENT OF PLASMA MELPHALAN BY ION-PAIR HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
ADAIR, CG ;
BURNS, DT ;
CROCKARD, AD ;
DESAI, ZR ;
HARRIOTT, M .
JOURNAL OF CHROMATOGRAPHY, 1984, 336 (02) :429-433
[2]
ALOIA T, 2001, P SOC SURG ONCOL
[3]
Atkinson Jr AJ, 2001, PRINCIPLES CLIN PHAR
[4]
BENCKHUIJSEN C, 1986, J PHARMACOL EXP THER, V237, P583
[5]
BODDIE AW, 1992, P ASCO, V11, P351
[6]
BRIELE HA, 1985, CANCER RES, V45, P1885
[7]
DIFILIPPO F, 1989, CANCER, V63, P2551
[8]
Fraker DJ., 1998, CUTANEOUS MELANOMA, P281
[9]
GEXFABRY M, 1994, PHARMACOKINETICS DRU, P507
[10]
IMPORTANCE TISSUE DISTRIBUTION IN PHARMACOKINETICS [J].
GILLETTE, JR .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1973, 1 (06) :497-520