Clinical Pharmacokinetics of Paclitaxel Monotherapy: An Updated Literature Review

被引:143
作者
Stage, Tore B. [1 ,2 ]
Bergmann, Troels K. [3 ,4 ]
Kroetz, Deanna L. [1 ]
机构
[1] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94143 USA
[2] Univ Southern Denmark, Dept Publ Hlth, Clin Pharmacol & Pharm, Odense, Denmark
[3] Odense Univ Hosp, Dept Clin Biochem & Pharmacol, Odense, Denmark
[4] Hosp South West Jutland, Hosp Pharm, Esbjerg, Denmark
基金
美国国家卫生研究院;
关键词
CELL LUNG-CANCER; ADVANCED SOLID TUMORS; METASTATIC BREAST-CANCER; ALBUMIN-BOUND PACLITAXEL; PHASE-I TRIAL; ADVANCED OVARIAN-CANCER; RECURRENT MALIGNANT GLIOMA; COLONY-STIMULATING FACTOR; P-GLYCOPROTEIN INHIBITOR; HIGH-DOSE PACLITAXEL;
D O I
10.1007/s40262-017-0563-z
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Paclitaxel is an anticancer agent efficacious in the treatment of ovarian, breast, and lung cancer. Due to a strong link between the pharmacokinetics and therapeutic efficacy of paclitaxel, we reviewed the literature on paclitaxel pharmacokinetics. Systematic data mining was performed to extract the maximum concentration (C-max), clearance (CL), and time of paclitaxel plasma concentration above 0.05 mu mol/L (T > 0.05 mu mol/L) following monotherapy of both the widely used cremophor-diluted paclitaxel and nanoparticle albumin-bound (nab-)paclitaxel. We identified a total of 53 studies yielding 121 aggregated pharmacokinetic profiles for paclitaxel monotherapy and extracted reported mean and median estimates of pharmacokinetic parameters. Paclitaxel has been studied formally at doses of 15-825 mg/m(2) and infused over 0.5-96 h; included studies examined both weekly and every 3-weeks dosing cycles. The most widely used dose of cremophor-diluted paclitaxel, 175 mg/m(2) given as a 3-h infusion, leads to an interstudy median C-max of 5.1 A mu mol/L [interquartile range (IQR) 4.5-5.7], CL of 12.0 L/h/m(2) (IQR 10.9-12.9), and T > 0.05 A mu mol/L of 23.8 h (IQR 21.5-26.8). Importantly, the significant interindividual variation widely reported in the literature is not reflected in these interstudy estimates of pharmacokinetic parameters. Cremophor-diluted paclitaxel pharmacokinetics are non-linear following short (< 6 h) but not long (> 24 h) infusions. A similar pattern of non-linearity was observed for nab-paclitaxel, although the number of studies was limited. The pharmacokinetics of paclitaxel monotherapy have been widely studied at numerous dose levels of the Cremophor EL (R) formulation, but are less well-characterized for the newer nab-paclitaxel formulation. In conclusion, paclitaxel pharmacokinetics are non-linear for short infusion times but not for longer infusions. Whether a similar conclusion can be drawn for nab-paclitaxel formulations requires further study.
引用
收藏
页码:7 / 19
页数:13
相关论文
共 115 条
  • [11] Impact of CYP2C8*3 on paclitaxel clearance: a population pharmacokinetic and pharmacogenomic study in 93 patients with ovarian cancer
    Bergmann, T. K.
    Brasch-Andersen, C.
    Green, H.
    Mirza, M.
    Pedersen, R. S.
    Nielsen, F.
    Skougaard, K.
    Wihl, J.
    Keldsen, N.
    Damkier, P.
    Friberg, L. E.
    Peterson, C.
    Vach, W.
    Karlsson, M. O.
    Brosen, K.
    [J]. PHARMACOGENOMICS JOURNAL, 2011, 11 (02) : 113 - 120
  • [12] Neurotoxicity and low paclitaxel clearance associated with concomitant clopidogrel therapy in a 60-year-old Caucasian woman with ovarian carcinoma
    Bergmann, Troels K.
    Filppula, Anne M.
    Launiainen, Terhi
    Nielsen, Flemming
    Backman, Janne T.
    Brosen, Kim
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2016, 81 (02) : 313 - 315
  • [13] Bhalla KN, 1999, CLIN CANCER RES, V5, P1723
  • [14] Initial paclitaxel improves outcome compared with CMFP combination chemotherapy as front-line therapy in untreated metastatic breast cancer
    Bishop, JF
    Dewar, J
    Toner, GC
    Smith, J
    Tattersall, MHN
    Olver, IN
    Ackland, S
    Kennedy, I
    Goldstein, D
    Gurney, H
    Walpole, E
    Levi, J
    Stephenson, J
    Canetta, R
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (08) : 2355 - 2364
  • [15] Bristol-Myers Squibb Company, 2011, SUMM PROD CHAR TAX P
  • [16] Brooks T, 2003, MOL CANCER THER, V2, P1195
  • [17] Brouwer E, 2000, DRUG METAB DISPOS, V28, P1141
  • [18] A PHASE-I TRIAL OF TAXOL GIVEN BY A 6-HOUR INTRAVENOUS-INFUSION
    BROWN, T
    HAVLIN, K
    WEISS, G
    CAGNOLA, J
    KOELLER, J
    KUHN, J
    RIZZO, J
    CRAIG, J
    PHILLIPS, J
    VONHOFF, D
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (07) : 1261 - 1267
  • [19] CALVERT AH, 1995, SEMIN ONCOL, V22, P91
  • [20] Phase II study of liposomal doxorubicin and weekly paclitaxel for recurrent Mullerian tumors
    Campos, SM
    Matulonis, UA
    Penson, RT
    Lee, H
    Berkowitz, RS
    Duska, LR
    Fuller, AF
    Wilson, KS
    Puchalski, TA
    Supko, JG
    Seiden, MV
    [J]. GYNECOLOGIC ONCOLOGY, 2003, 90 (03) : 610 - 618