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用于癌症治疗的新型免疫治疗药物对肾脏的有害影响:一项系统综述。

Nephrological Detrimental Impacts Resulting From Novel Immunotherapy Drugs Used in the Treatment of Cancer: A Systematic Review.

作者信息

Jaiswal Amisha, Shergill Kainaat, Boppana Kusalik, Almansouri Naiela E, Bakkannavar Saloni, Faheem Youmna, Nath Tuheen Sankar

机构信息

Internal Medicine, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.

Surgery, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA.

出版信息

Cureus. 2024 Feb 19;16(2):e54487. doi: 10.7759/cureus.54487. eCollection 2024 Feb.

Abstract

The most recent advancements in cancer therapy center on efficiently and conveniently enhancing a patient's natural immune system. Immune checkpoint inhibitors (ICIs) are antibodies that target cytotoxic thymus (T) lymphocyte antigen-4 (CTLA-4) and its receptor. They function by stimulating T-cell activity against malignancies. Immune-related adverse events (irAEs) are a distinct class of inflammatory side effects that are specific to a given organ. Antineoplastic medications can impact any part of the kidney, leading to the development of proteinuria, hypertension, electrolyte abnormalities, glomerulonephritis, and both acute and chronic interstitial nephritis. We reviewed the scientific literature regarding kidney problems that can arise from chemotherapy and immunotherapy for neoplasms, such as various cancers, melanoma, non-small cell lung cancer, and colorectal cancer. We discussed the pathophysiology, associated risk factors, management, and safety measures for patients experiencing acute renal injury after a new immunotherapy medication treatment. Antineoplastic drugs have the potential to damage the renal tubules, glomeruli, parenchyma, and blood vessels, among other kidney tissues. This can result in a broad spectrum of complications, spanning from a rise in serum creatinine levels without symptoms to the development of acute kidney injury (AKI). The research examined a range of risk factors associated with acute kidney injury (AKI). These factors encompassed age, gender, preexisting medical conditions (such as diabetes, hypertension, and chronic kidney disease), and the medications that patients were taking at the beginning of the study, which included non-steroidal anti-inflammatory drugs, renin-angiotensin system inhibitors, allopurinol, diuretics, corticosteroids, and proton pump inhibitors. The data suggests that patients who were receiving baseline treatment with proton pump inhibitors (PPIs) or corticosteroids had a higher risk of mortality. This study serves as an illustration of the effective management of acute kidney injury and proteinuria linked to novel immunotherapy drugs like pembrolizumab. The approach involved the use of corticosteroids tailored to the patient's condition. Furthermore, it references the recommendations outlined in the Common Terminology Criteria for Adverse Events (CTCAE). Prompt recognition and effective management of these side effects are essential to optimizing outcomes for patients undergoing immunotherapy. Our results were refined and focused by utilizing Medical Subject Headings (MeSH) keywords in our search strategy. The MeSH keywords used were "renal side effects" OR "immunotherapy" OR "cancer treatment." The studies reviewed encompassed a total of 48,529 participants among the 21 studies examined.

摘要

癌症治疗的最新进展集中在高效且便捷地增强患者的天然免疫系统。免疫检查点抑制剂(ICIs)是靶向细胞毒性胸腺(T)淋巴细胞抗原4(CTLA-4)及其受体的抗体。它们通过刺激T细胞对抗恶性肿瘤的活性来发挥作用。免疫相关不良事件(irAEs)是一类特定于某个器官的独特炎症副作用。抗肿瘤药物可影响肾脏的任何部位,导致蛋白尿、高血压、电解质异常、肾小球肾炎以及急性和慢性间质性肾炎的发生。我们回顾了有关肿瘤化疗和免疫治疗可能引发的肾脏问题的科学文献,这些肿瘤包括各种癌症、黑色素瘤、非小细胞肺癌和结直肠癌。我们讨论了接受新型免疫治疗药物治疗后发生急性肾损伤的患者的病理生理学、相关危险因素、管理方法和安全措施。抗肿瘤药物有可能损害肾小管、肾小球、实质和血管等肾脏组织。这可能导致一系列并发症,从无症状的血清肌酐水平升高到急性肾损伤(AKI)的发生。该研究考察了一系列与急性肾损伤(AKI)相关的危险因素。这些因素包括年龄、性别、既往病史(如糖尿病、高血压和慢性肾病)以及研究开始时患者正在服用的药物,其中包括非甾体抗炎药、肾素 - 血管紧张素系统抑制剂、别嘌醇、利尿剂、皮质类固醇和质子泵抑制剂。数据表明,接受质子泵抑制剂(PPI)或皮质类固醇基线治疗的患者死亡率更高。这项研究展示了对与派姆单抗等新型免疫治疗药物相关的急性肾损伤和蛋白尿的有效管理。该方法涉及根据患者病情使用皮质类固醇。此外,它参考了《不良事件通用术语标准》(CTCAE)中概述的建议。对这些副作用的及时识别和有效管理对于优化接受免疫治疗患者的治疗效果至关重要。我们通过在搜索策略中使用医学主题词(MeSH)关键词来完善和聚焦我们的研究结果。所使用的MeSH关键词为“肾脏副作用”或“免疫治疗”或“癌症治疗”。在所审查的21项研究中,总共涵盖了48529名参与者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13ca/10954436/6e4d7887c1d3/cureus-0016-00000054487-i01.jpg

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