Spiotto Michael T, Cao Hongyuan, Mell Loren, Toback F Gary
aDepartment of Radiation and Cellular Oncology, University of Chicago Medical Center bDepartment of Radiation Oncology, University of Illinois Hospital and Health Sciences System cDepartment of Health Studies dDepartment of Medicine, University of Chicago eDepartment of Radiation Oncology, University of California San Diego, San Diego, California, USA.
Anticancer Drugs. 2015 Mar;26(3):343-9. doi: 10.1097/CAD.0000000000000191.
Head and neck cancer patients undergoing chemoradiation experience considerable toxicities including acute kidney injury (AKI). However, it remains unclear what factors predispose patients to renal toxicity during treatment. Here, we assessed the predictors and outcomes of patients experiencing AKI during chemoradiation. We carried out a retrospective cohort study to assess the maximum changes in serum creatinine (Cr) in 173 patients with stage III-IV head and neck cancer treated with chemoradiation between 1999 and 2012. We defined AKI as Cr increases 26.5 µmol/l or more over the pretreatment baseline. AKI was associated with angiotensin-converting enzyme inhibitor (ACEI) use (33.0 vs. 11.0%; P=0.0004), but no other medications or comorbidities. On multivariate analysis, ACEI use, weight loss 10% or more of body weight, and performance status 70 or more predicted for Cr increments 26.5 µmol/l or more, whereas only ACEI use predicted for Cr increments of 44.2 µmol/l or greater. Furthermore, on multivariate analysis, AKI predicted for more interventions during radiotherapy including intravenous fluid use (P=0.0005) and hospitalizations (P=0.007), as well as long-term renal dysfunction (P<0.0001). Renal toxicity was not associated with worse locoregional control, progression-free survival, or overall survival. Renal toxicity during chemoradiation was associated with ACEI use alone or coupled with weight loss 10% or more of body weight during therapy. Our results suggest that actively managing ACEI use and intravascular volume status during chemoradiation may avoid AKI, minimize subsequent interventions, and reduce the risk for long-term renal dysfunction.
接受放化疗的头颈癌患者会经历包括急性肾损伤(AKI)在内的相当多的毒性反应。然而,目前尚不清楚哪些因素会使患者在治疗期间易发生肾毒性。在此,我们评估了放化疗期间发生AKI的患者的预测因素和预后情况。我们进行了一项回顾性队列研究,以评估1999年至2012年间接受放化疗的173例III-IV期头颈癌患者血清肌酐(Cr)的最大变化。我们将AKI定义为Cr较治疗前基线升高26.5µmol/l或更多。AKI与使用血管紧张素转换酶抑制剂(ACEI)有关(33.0%对11.0%;P=0.0004),但与其他药物或合并症无关。多因素分析显示,使用ACEI、体重减轻超过体重的10%以及体能状态为70或更高预测Cr升高26.5µmol/l或更多,而只有使用ACEI预测Cr升高44.2µmol/l或更高。此外,多因素分析显示,AKI预测放疗期间需要更多干预,包括使用静脉输液(P=0.0005)和住院(P=0.007),以及长期肾功能障碍(P<0.0001)。肾毒性与局部区域控制、无进展生存期或总生存期较差无关。放化疗期间的肾毒性与单独使用ACEI或与治疗期间体重减轻超过体重的10%有关。我们的结果表明,在放化疗期间积极管理ACEI的使用和血管内容量状态可能避免AKI,减少后续干预,并降低长期肾功能障碍的风险。