Bhat Zeenat Yousuf, Cadnapaphornchai Pravit, Ginsburg Kevin, Sivagnanam Milani, Chopra Shamit, Treadway Corey K, Lin Ho-Sheng, Yoo George, Sukari Ammar, Doshi Mona D
Wayne State University, School of Medicine, Detroit, Michigan, United States of America.
Patel Hospital, Civil Lines, Jalandhar City, Punjab, India.
PLoS One. 2015 Nov 10;10(11):e0142225. doi: 10.1371/journal.pone.0142225. eCollection 2015.
Acute kidney injury (AKI) is a well-known complication of cisplatin-based chemotherapy; however, its impact on long-term patient survival is unclear. We sought to determine the incidence and risk factors for development of cisplatin-associated AKI and its impact on long-term renal function and patient survival. We identified 233 patients who received 629 cycles of high-dose cisplatin (99±9mg/m2) for treatment of head and neck cancer between 2005 and 2011. These subjects were reviewed for development of AKI. Cisplatin nephrotoxicity (CN) was defined as persistent rise in serum creatinine, with a concomitant decline in serum magnesium and potassium, in absence of use of nephrotoxic agents and not reversed with hydration. All patients were hydrated per protocol and none had baseline glomerular filtration rate (GFR) via CKD-EPI<60mL/min/1.73m2. The patients were grouped based on development of AKI and were staged for levels of injury, per KDIGO-AKI definition. Renal function was assessed via serum creatinine and estimated glomerular filtration rate (eGFR) via CKD-EPI at baseline, 6- and 12-months. Patients with AKI were screened for the absence of nephrotoxic medication use and a temporal decline in serum potassium and magnesium levels. Logistic regression models were constructed to determine risk factors for cisplatin-associated AKI. Twelve-month renal function was compared among groups using ANOVA. Kaplan-Maier curves and Cox proportional hazard models were constructed to study its impact on patient survival. Of 233 patients, 158(68%) developed AKI; 77 (49%) developed stage I, 55 (35%) developed stage II, and 26 (16%) developed stage III AKI. Their serum potassium and magnesium levels correlated negatively with level of injury (p<0.05). African American race was a significant risk factor for cisplatin-associated AKI, OR 2.8 (95% CI 1.3 to 6.3) and 2.8 (95% CI 1.2 to 6.7) patients with stage III AKI had the lowest eGFR value at 12 months (p = 0.05) and long-term patient survival (HR 2.1; p<0.01) than patients with no or lower grades of AKI. Most common causes of death were recurrent cancer (44%) or secondary malignancy elsewhere (40%). Cisplatin-associated severe AKI occurs in 20% of the patients and has a negative impact on long-term renal function and patient survival. PEG tube placement may be protective and should be considered in high risk-patients.
急性肾损伤(AKI)是基于顺铂的化疗常见的并发症;然而,其对患者长期生存的影响尚不清楚。我们试图确定顺铂相关AKI的发生率、危险因素及其对长期肾功能和患者生存的影响。我们纳入了2005年至2011年间接受629个周期高剂量顺铂(99±9mg/m²)治疗头颈部癌的233例患者。对这些受试者进行了AKI发生情况的评估。顺铂肾毒性(CN)定义为血清肌酐持续升高,同时血清镁和钾水平下降,且未使用肾毒性药物且水化治疗不能逆转。所有患者均按方案进行水化治疗,且均无通过慢性肾脏病流行病学合作组(CKD-EPI)公式计算的基线肾小球滤过率(GFR)<60mL/min/1.73m²。根据AKI的发生情况对患者进行分组,并根据KDIGO-AKI定义对损伤程度进行分期。在基线、6个月和12个月时通过血清肌酐评估肾功能,并通过CKD-EPI公式估算肾小球滤过率(eGFR)。对发生AKI的患者筛查是否未使用肾毒性药物以及血清钾和镁水平是否随时间下降。构建逻辑回归模型以确定顺铂相关AKI的危险因素。使用方差分析比较各组12个月时的肾功能。构建Kaplan-Meier曲线和Cox比例风险模型以研究其对患者生存的影响。233例患者中,158例(68%)发生了AKI;77例(49%)为I期,55例(35%)为II期,26例(16%)为III期AKI。他们的血清钾和镁水平与损伤程度呈负相关(p<0.05)。非裔美国人种族是顺铂相关AKI的显著危险因素,比值比(OR)为2.8(95%置信区间[CI]为1.3至6.3),III期AKI患者在12个月时的eGFR值最低(p = 0.05),与未发生AKI或AKI分级较低的患者相比,长期患者生存风险比(HR)为2.1;p<0.01。最常见的死亡原因是癌症复发(44%)或其他部位的继发性恶性肿瘤(40%)。顺铂相关的严重AKI发生在20%的患者中,对长期肾功能和患者生存有负面影响。放置胃造口喂养管(PEG)可能具有保护作用,高危患者应考虑使用。