Department of Hospital Pharmacy, Nagoya University Hospital, Nagoya, Japan.
Department of Clinical Oncology and Chemotherapy, Nagoya University Hospital, Nagoya, Japan.
Nagoya J Med Sci. 2022 Aug;84(3):547-553. doi: 10.18999/nagjms.84.3.547.
Although the Cockcroft-Gault equation is still used for the dose adjustment of many drugs that have been approved prior to creatinine standardization, the clinical impact of standardized creatinine in the dose adjustment of capecitabine is poorly understood. We focused on patients with borderline renal function and evaluated the tolerability and safety of capecitabine in patients who received capecitabine plus oxaliplatin (Cape-Ox). We retrospectively identified patients with resected colorectal cancer who had received adjuvant therapy with Cape-Ox regimen. Creatinine clearance (CrCL) was calculated by the Cockcroft-Gault equation with standardized creatinine measured using enzymatic methods, and adjusted CrCL was estimated by adding 0.2 (mg/dL) to the serum creatinine in the equation. We defined patients with "pseudo-normal" renal function as those who had an adjusted CrCL of ≤50 mL/min in patients with normal renal function (CrCL >50 mL/min). We evaluated the tolerability and grade 2 or severer adverse events of capecitabine treatment. One hundred four patients had normal and 10 had impaired renal function (CrCL <50 mL/min). Among the 104 patients with normal renal function, 23 (22.1%) had pseudo-normal renal function. Seventeen patients completed the eight cycles of Cape-Ox therapy without treatment delay or dose reduction, and all of them had truly normal renal function. The patients with pseudo-normal renal function were more likely to have grade 2 or severer thrombocytopenia than those with truly normal renal function. We should recognize correctly the clinical impact of standardized creatinine in the treatment of borderline renal function with Cape-Ox regimen in patients.
虽然 Cockcroft-Gault 方程仍被用于调整许多在肌酐标准化之前获得批准的药物的剂量,但标准化肌酐对卡培他滨剂量调整的临床影响尚未被充分了解。我们专注于肾功能临界的患者,并评估了 Cape-Ox 方案中接受卡培他滨加奥沙利铂(Cape-Ox)治疗的患者的卡培他滨的耐受性和安全性。我们回顾性地确定了接受 Cape-Ox 方案辅助治疗的结直肠癌患者。采用酶法测定标准化肌酐后,通过 Cockcroft-Gault 方程计算肌酐清除率(CrCL),并通过在方程中血清肌酐值上加 0.2(mg/dL)来估计调整后的 CrCL。我们将“假性正常”肾功能定义为肾功能正常(CrCL>50mL/min)患者中调整后的 CrCL≤50mL/min 的患者。我们评估了卡培他滨治疗的耐受性和 2 级或更严重的不良事件。104 例患者肾功能正常,10 例患者肾功能受损(CrCL<50mL/min)。在 104 例肾功能正常的患者中,23 例(22.1%)存在假性正常肾功能。17 例患者完成了 8 个周期的 Cape-Ox 治疗,无治疗延迟或剂量减少,且所有患者均具有真正的正常肾功能。假性正常肾功能的患者发生 2 级或更严重血小板减少症的可能性高于真正正常肾功能的患者。我们应正确认识标准化肌酐在 Cape-Ox 方案治疗临界肾功能患者中的临床影响。