Page 137 - 《中国药房》2021年第1期
P. 137

[31]  ZHAO C,HAN SY,LI PP,et al. Pharmacokinetics of gefi-  centrations of dasatinib have a clinical impact on the fre-
             tinib:roles of drug metabolizing enzymes and transpor-  quency of dasatinib dose reduction and interruption in
             ters[J]. Curr Drug Deliv,2017,14(2):282-288.       chronic myeloid leukemia:an analysis of the DARIA 01
        [32]  KOBAYASHI H,SATO K,NIIOKA T,et al. Effects of     study[J]. Int J Clin Oncol,2018,23(5):980-988.
             polymorphisms in CYP2D6 and ABC transporters and  [45]  MIURA M. Therapeutic drug monitoring of imatinib,nilo-
             side effects induced by gefitinib on the pharmacokinetics  tinib,and dasatinib for patients with chronic myeloid leu-
             of the gefitinib metabolite,O-desmethyl gefitinib[J]. Med  kemia[J]. Biol Pharm Bull,2015,38(5):645-654.
             Oncol,2016. DOI:10.1007/s12032-016-0773-5.    [46]  HOŘÍNKOVÁ J,ŠÍMA M,SLANAŘ O. Pharmacokine-
        [33]  ZHAO YY,LI S,ZHANG Y,et al. The relationship be-  tics of dasatinib[J]. Prague Medical Report,2019,120(2):
             tween drug exposure and clinical outcomes of non-small  52-63.
             cell lung cancer patients treated with gefitinib[J]. Med On-  [47]  张昕怡,侯珂,贾月萍,等.治疗药物监测指导下达沙替尼
             col,2011,28(3):697-702.                            个体化给药的病例分析[J].中国临床药理学杂志,2020,
        [34]  XIN S,ZHAO YY,WANG XD,et al. The Dissociation of  36(3):341-343.
             geftinib trough concentration and clinical outcome in  [48]  JOHNSON FM,AGRAWAL S,BURRIS H,et al. Phase 1
             NSCLC patients with EGFR sensitive mutations[J]. Sci  pharmacokinetic and drug-interaction study of dasatinib in
             Rep,2015. DOI:10.1038/srep12675.                   patients with advanced solid tumors[J]. Cancer,2010,116
        [35]  YASUMURO O,UCHIDA S,KASHIWAGURA Y,et al.          (6):1582-1591.
             Changes in gefitinib,erlotinib and osimertinib pharmaco-  [49]  LEVÊQUE D,BECKER G,BILGER K,et al. Clinical
             kinetics under various gastric pH levels following oral ad-  pharmacokinetics and pharmacodynamics of dasatinib[J].
             ministration of omeprazole and vonoprazan in rats[J]. Xe-  Clin Pharmacokinet,2020,59(7):849-856.
             nobiotica,2018,48(11):1106-1112.              [50]  TAKAHASHI N,MIURA M,NIIOKA T,et al. Influence
        [36]  MAI HX,HUANG J,ZHANG YY,et al. In-vivo relation   of H2-receptor antagonists and proton pump inhibitors on
             between plasma concentration of sorafenib and its safety  dasatinib pharmacokinetics in Japanese leukemia pa-
             in Chinese patients with metastatic renal cell carcinoma:a  tients[J]. Cancer Chemother Pharmacol,2012,69(4):
             single-center clinical study[J]. Oncotarget,2017,8(26):  999-1004.
             43458-43469.                                  [51]  MIURA M,TAKAHASHI N. Routine therapeutic drug
        [37]  史蕤,李然,赵冰清,等.索拉非尼血药浓度与疗效和不良                        monitoring of tyrosine kinase inhibitors by HPLC-UV or
             反应的关系以及在肝细胞癌治疗应用[J].中国临床药理                         LC-MS/MS methods[J]. Drug Metab Pharmacokinet,
             学杂志,2015,31(17):1793-1795.                         2016,31(1):12-20.
        [38]  THOMAS S,THANKAPPAN AP,PADMA UD. Thera-      [52]  MOTZER RJ,HOOSEN S,BELLO CL,et al. Sunitinib
             peutic drug monitoring of sorafenib in hepatocellular car-  malate for the treatment of solid tumours:a review of cur-
             cinoma patients[J]. Ther Drug Monit,2020,42(2):345-  rent clinical data[J]. Expert Opin Investig Drugs,2006,15
             347.                                               (5):553-561.
        [39]  KAWAHARA D,OZAWA S,KIMURA T,et al. Clinical  [53]  MENDEL DB,LAIRD AD,XIN X,et al. In vivo antitu-
             pharmacokinetics and pharmacodynamics of transarterial  mor activity of SU11248,a novel tyrosine kinase inhibitor
             chemoembolization and targeted therapies in hepatocellu-  targeting vascular endothelial growth factor and plate-
             lar carcinoma[J]. Phys Med,2016,32(4):557-561.     let-derived growth factor receptors:determination of a
        [40]  BA HL,MBATCHI L,GATTACCECA F,et al. Pharmaco-     pharmacokinetic/pharmacodynamic relationship[J]. Clin
             genetics and pharmacokinetics modeling of unexpected  Cancer Res,2003,9(1):327-337.
             and extremely severe toxicities after sorafenib intake[J].  [54]  WESTERDIJK K,KRENS SD,VAN DER GRAAF WT,
             Pharmacogenomics,2020,21(3):173-179.               et al. The relationship between sunitinib exposure and
        [41]  KARBOWNIK A,SOBAŃSKA K,GRABOWSKI T,et             both efficacy and toxicity in real-world patients with renal
             al. In vivo assessment of the drug interaction between  cell carcinoma and gastrointestinal stromal tumour[J]. Br
             sorafenib and paracetamol in rats[J]. Cancer Chemother  J Clin Pharmacol,2020. DOI:10.1111/bcp.14332.
             Pharmacol,2020,85(6):1039-1048.               [55]  HOUK BE,BELLO CL,POLAND B,et al. Relationship
        [42]  徐怀友,束超,邵凤,等. LC-MS/MS 法测定人血浆中达                    between exposure to sunitinib and efficacy and tolerability
             沙替尼的浓度及两种片剂的生物等效性研究[J].中国药                         endpoints in patients with cancer:results of a pharmacoki-
             房,2016,27(8):1051-1054.                            netic/pharmacodynamic Meta-analysis[J]. Cancer Che-
        [43]  CHRISTOPHER LJ,CUI DH,WU CY,et al. Metabolism     mother Pharmacol,2010,66(2):357-371.
             and disposition of dasatinib after oral administration to hu-  [56]  RAHAVENDRAN SV,PITHAVALA YK,BELLO C,
             mans[J]. Drug Metab Dispos,2008,36(7):1357-1364.   et al. Comparison of clinical drug-drug interaction study
        [44]  MIZUTA S,SAWA M,TSURUMI H,et al. Plasma con-      results for sunitinib and axitinib with an in silico tool[J].


        中国药房    2021年第32卷第1期                                               China Pharmacy 2021 Vol. 32 No. 1  ·127 ·
   132   133   134   135   136   137   138   139   140   141   142