Tawalbeh Mohamed, Ibrahim Rewan M, Al-Saraireh Taif, Khreesha Lubna, Rawashdeh Baeth Al
Department of Special Surgery, Jordan University Hospital, School of Medicine, The University of Jordan, Amman, Jordan.
Medical Research Group of Egypt, Negida Academy, Arlington, MA, USA.
BMC Pharmacol Toxicol. 2025 Feb 4;26(1):26. doi: 10.1186/s40360-024-00829-4.
To evaluate the efficacy of the otoprotective transtympanic application of N-acetylcysteine in preventing chemotherapy-induced ototoxicity in patients subjected to platinum-based chemotherapy.
PubMed, Scopus, Web of Science, Cochrane Central, and ClinicalTrials.gov were searched for the following concepts: (("Acetylcysteine" [Mesh]) AND ("Ototoxicity" [Mesh]) AND ("Cisplatin" [Objective: To evaluate the efficacy of otoprotective transtympanic application of N-acetylcysteine in the prevention of chemotherapy-induced ototoxicity in patients subjected to platinum-based chemotherapy. [Mesh]).
Inclusion: randomized controlled trials, Exclusion: (1) case reports or case series; (2) thesis; (3) review articles; (4) conference abstracts; (5) animal studies; (6) non-english studies; (7) studies whose population was other than patients on platinum-based chemotherapy.
changes in hearing thresholds measured by pure tone tympanometry, covering high and low frequencies: 250, 500, 1000, 2000, 4000, and 8000 Hz. We used RevMan (Review Manager) version 5.3 to conduct the meta-analysis and GRADE to assess the quality of the evidence.
The literature search yielded 277 unique articles. After reviewing six full-text articles, three RCTs provided data available for meta-analysis. A total of 88 cisplatin-based chemotherapy candidates were included for final analysis. Hearing thresholds showed a significant threshold difference between the ear treated with N-acetylcysteine and the control ear (ear not treated with N-acetylcysteine), especially at high frequencies as high as 8000 Hz (pooled effect size - 10.67, 95% CI [-12.33, -9.02], P < 0.00001). The data favored the Nac group in all frequencies as well, at 4000 Hz (pooled effect size - 2.13, 95% CI [-3.49, -0.77], P = 0.002), at 2000 Hz (pooled effect size - 1.38, 95% CI [-2.69, -0.06], P = 0.04), at 1000 Hz (pooled effect size - 1.58, 95% CI [-2.63, -0.53], P = 0.003), at 500 Hz (pooled effect size - 1.58, 95% CI [-2.62, -0.54], P = 0.003), and at the low frequency of 250 after solving the heterogeneity (pooled effect size - 0.96, 95% CI [-2.88, 0.95], P = 0.32).
Current data justifies the transtympanic administration of N-acetylcysteine for otoprotection in chemotherapy patients, minimizing the enduring consequences of cisplatin-induced ototoxicity and auditory impairment. Given the results' emphasis on the Sarafraz et al. (2018) study, more randomized controlled trials are necessary with an expanded sample size and standardization of N-acetylcysteine concentration, study population, and assessed outcomes.
评估经鼓膜应用N-乙酰半胱氨酸预防铂类化疗患者化疗所致耳毒性的疗效。
检索了PubMed、Scopus、Web of Science、Cochrane Central和ClinicalTrials.gov,检索词如下:((“乙酰半胱氨酸”[医学主题词])AND(“耳毒性”[医学主题词])AND(“顺铂”[医学主题词])AND(“经鼓膜”[医学主题词])AND(“化疗”[医学主题词])AND(“预防”[医学主题词]))。
纳入标准:随机对照试验;排除标准:(1)病例报告或病例系列;(2)论文;(3)综述文章;(4)会议摘要;(5)动物研究;(6)非英文研究;(7)研究对象不是接受铂类化疗的患者的研究。
通过纯音鼓室图测量的听力阈值变化,涵盖高频和低频:250、500、1000、2000Hz、4000Hz和8000Hz。我们使用RevMan(综述管理器)5.3版进行荟萃分析,并使用GRADE评估证据质量。
文献检索共获得277篇独特文章。在查阅6篇全文文章后,3项随机对照试验提供了可用于荟萃分析的数据。最终分析共纳入88例接受顺铂化疗的患者。N-乙酰半胱氨酸治疗耳与对照耳(未用N-乙酰半胱氨酸治疗的耳)的听力阈值存在显著差异,尤其是在高达8000Hz的高频(合并效应量-10.67,95%可信区间[-12.33,-9.02],P<0.00001)。在所有频率下,数据也支持Nac组,在4000Hz(合并效应量-2.13,95%可信区间[-3.49,-0.77],P=0.002)、2000Hz(合并效应量-1.38,95%可信区间[-2.69,-0.06],P=0.04)、1000Hz(合并效应量-1.58,95%可信区间[-2.63,-0.53],P=0.003)、500Hz(合并效应量-1.58,95%可信区间[-2.62,-0.54],P=0.003)以及解决异质性后的低频250Hz(合并效应量-0.96,95%可信区间[-2.88,0.9],P=0.32)。
目前的数据证明经鼓膜给予N-乙酰半胱氨酸对化疗患者具有耳保护作用,可将顺铂所致耳毒性和听觉损伤的持久后果降至最低。鉴于结果强调了萨拉夫拉兹等人(2018年)的研究,有必要进行更多随机对照试验,扩大样本量,并对N-乙酰半胱氨酸浓度、研究人群和评估结果进行标准化。