Tumor Drug Penetration Measurements Could Be the Neglected Piece of the Personalized Cancer Treatment Puzzle

被引:54
作者
Bartelink, Imke H. [1 ,2 ,13 ]
Jones, Ella F. [3 ]
Shahidi-Latham, Sheerin K. [4 ]
Lee, Pei Rong Evelyn [5 ]
Zheng, Yanan [2 ]
Vicini, Paolo [6 ]
van't Veer, Laura [5 ]
Wolf, Denise [5 ]
Iagaru, Andrei [7 ]
Kroetz, Deanna L. [8 ]
Prideaux, Brendan [9 ]
Cilliers, Cornelius [10 ,11 ]
Thurber, Greg M. [10 ,11 ]
Wimana, Zena [12 ]
Gebhart, Geraldine [12 ]
机构
[1] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[2] Medlmmune, Clin Pharmacol Pharmacometr & DMPK CPD, San Francisco, CA 94080 USA
[3] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA
[4] Genentech Inc, Drug Metab & Pharmacokinet, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Lab Med, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[6] Medlmmune, Clin Pharmacol Pharmacometr & DMPK CPD, Cambridge, England
[7] Stanford Hlth Care, Div Nucl Med & Mol Imaging, Stanford, CA USA
[8] Univ Calif San Francisco, Sch Pharm, Dept Bioengn & Therapeut Sci BTS, San Francisco, CA 94143 USA
[9] Rutgers State Univ, Publ Hlth Res Inst, Rutgers New Jersey Med Sch, New Brunswick, NJ USA
[10] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[11] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
[12] Univ Libre Bruxelles, Inst Jules Bordet, Brussels, Belgium
[13] Vrije Univ Amsterdam, Dept Clin Pharmacol & Pharm, Amsterdam UMC, Amsterdam, Netherlands
关键词
RECEPTOR RADIONUCLIDE THERAPY; BREAST-CANCER; PHASE-I; SOLID TUMORS; POPULATION PHARMACOKINETICS; MONOCLONAL-ANTIBODIES; DNA-ADDUCTS; IMMUNE; TISSUE; PET;
D O I
10.1002/cpt.1211
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Precision medicine aims to use patient genomic, epigenomic, specific drug dose, and other data to define disease patterns that may potentially lead to an improved treatment outcome. Personalized dosing regimens based on tumor drug penetration can play a critical role in this approach. State-of-the-art techniques to measure tumor drug penetration focus on systemic exposure, tissue penetration, cellular or molecular engagement, and expression of pharmacological activity. Using in silico methods, this information can be integrated to bridge the gap between the therapeutic regimen and the pharmacological link with clinical outcome. These methodologies are described, and challenges ahead are discussed. Supported by many examples, this review shows how the combination of these techniques provides enhanced patient-specific information on drug accessibility at the tumor tissue level, target binding, and downstream pharmacology. Our vision of how to apply tumor drug penetration measurements offers a roadmap for the clinical implementation of precision dosing.
引用
收藏
页码:148 / 163
页数:16
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