Division of Nephrology, Medical University of South Carolina, Charleston, South Carolina; and.
Division of Nephrology, University of Virginia Health System, Charlottesville, Virginia.
Kidney360. 2020 Jan 13;1(2):141-150. doi: 10.34067/KID.0000952019. eCollection 2020 Feb 27.
Chemotherapeutic agents require precise dosing to ensure optimal efficacy and minimize complications. For those agents that are removed from the body by the kidney, accurate knowledge of GFR is critical. In addition, GFR needs to be determined rapidly, easily, and, if possible, with little additional cost. The ability to easily measure GFR also allows for rapid detection of nephrotoxicity. Current methodologies include direct clearance measurement of an indicator substance or estimation of creatinine clearance or GFR through regression equations that use a serum marker, such as creatinine or cystatin C. These methodologies all have shortfalls and limitations, some of which are specific to the patient with cancer. Newer methodologies that directly measure GFR are in clinical trials and offer the ability to rapidly and noninvasively provide accurate estimates of drug clearance as well as detection of nephrotoxicity. These methods offer the opportunity to refine drug dosing and improve outcomes.
化疗药物需要精确的剂量,以确保最佳疗效和最小化并发症。对于那些通过肾脏排出体外的药物,准确了解肾小球滤过率(GFR)至关重要。此外,GFR 需要快速、简便地确定,如果可能的话,还需要尽量降低额外成本。能够轻松测量 GFR 还可以快速检测到肾毒性。目前的方法包括直接清除测量指示剂物质,或通过回归方程估计肌酐清除率或 GFR,该回归方程使用血清标志物,如肌酐或胱抑素 C。这些方法都有缺点和局限性,其中一些是特定于癌症患者的。一些直接测量 GFR 的新方法正在临床试验中,这些方法提供了快速、非侵入性地提供药物清除率的准确估计值以及检测肾毒性的能力。这些方法提供了优化药物剂量和改善结果的机会。