培美曲塞致非小细胞肺癌肾毒性的回顾性研究

Sharat Venkat Reddy Kallem, P. Harichandana, C. Bhavya, N. K. Thota
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摘要

背景:培美曲塞(PEM)是一种新一代多靶向抗叶酸药物,已被证明对多种人类癌症具有广谱疗效,包括NSCLC和间皮瘤。剂量限制性血液学毒性是最严重的副作用之一。PEM肾毒性是众所周知的,但它的发生被认为是罕见的。目的探讨培美曲塞对非小细胞肺癌患者的肾毒性。方法:在非小细胞肺癌患者中,我们记录了对pemen引起的肾毒性的回顾性回顾。2012 - 2019年,我院共收治NSCLC患者327例。其中,134名患者被诊断为2个或更多的化疗周期。这些患者中有60人被诊断为基于培美曲塞和铂的联合抗肿瘤药物。其他人则被排除在研究之外,并被要求接受其他潜在肾损伤原因的检测。结果:采用合适的统计学方法,对数据进行分析,发现培美曲塞重复化疗周期可导致可逆性急性肾损伤。根据我们的研究结果,我们可以了解培美曲塞对非小细胞肺癌患者肾毒性的严重程度。患者多为一、二期肾毒性,以男性居多。大多数患者年龄在40岁以上,化疗周期也在4个以上。结论:这表明PEM可以延长生存期,但急性或慢性肾衰竭是这一成就的代价。总之,培美曲塞治疗的患者应常规控制肾毒性。在培美曲塞的每个周期前,应测量肌酐清除率。患者在治疗过程中需要充足的水分。还应检查患者是否同时服用药物,检查任何肾毒性症状并停用药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A retrospective study on pemetrexed induced nephrotoxicity in non-small cell lung carcinoma patients
Background: Pemetrexed (PEM) is a new-generation multitargeted antifolate agent that has been shown to have broadspectrum efficacy in a variety of human cancers, including NSCLC and mesothelioma. Dose-limiting hematologic toxicities are among the most serious side effects. PEM nephrotoxicity is well-known, but its occurrence is thought to be rare. Aim was to determine nephrotoxicity induced due to pemetrexed in non-small cell lung cancer patients. Methods: In patients with the NSCLC, we record a retrospective review on PEMinduced renal toxicity. A total of 327 NSCLC patients were treated in our hospital between 2012 and 2019. Of these, 134 patients were diagnosed with 2 or more chemotherapy cycles. 60 of these patients have been diagnosed with combination of antineoplastic drugs based on pemetrexed and platinum. Others were removed from the study and were also required to be tested for other potential causes of renal injury. Results: Suitable statistical tools were used and data was analysed which showed that repeated chemo cycles of pemetrexed leads to the reversible acute kidney injury. With the results from our study we can understand the severity of nephrotoxicity induced with pemetrexed in patients with non-small cell lung cancer. Most of the patients were in the first and second stages of nephrotoxicity and most of them were male. Majority of the patients were also above 40 years of age and also endured more than 4 chemo cycles. Conclusions: It shows that PEM allows longer survival, but acute or chronic kidney failure is the price for this achievement. In conclusion, renal toxicity should be controlled routinely in patients treated with pemetrexed. Before each cycle of pemetrexed, creatinine clearance should be measured. Patients need to be well hydrated during treatment. The patient should also be tested for concomitant medications, and any nephrotoxic symptoms should be reviewed and those drugs removed.
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