Basrah肿瘤中心接受顺铂治疗的癌症患者的耳毒性:一项队列研究

Hasanain Al-Ali, J. Al-Asadi, Abdulrazzaq Alrubaye, H. Ali
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引用次数: 0

摘要

背景:顺铂是一种广泛应用于多种肿瘤治疗的化疗药物。然而,已报道了顺铂的进行性不可逆副作用,包括耳毒性。方法:2015年4月1日至8月30日进行队列研究,研究顺铂化疗与感觉神经性听力损失(耳毒性的主要和最重要标志)之间的关系。队列组包括接受顺铂治疗的癌症患者,而接受卡铂治疗的患者为对照组。顺铂和卡铂属于烷基化铂类化疗药物,用于治疗各种恶性实体肿瘤。通过问卷收集数据,包括与社会人口特征、当前和过去病史有关的信息。在化疗开始时和一个月后使用纯音测听法评估听力损失。结果:患者总数50例,男女比例1:1,平均年龄49.7±14.7岁(18-80岁),其中顺铂27例,平均年龄50.3±13.5岁;卡铂23例,平均年龄51.9±15.1岁,年龄差异无统计学意义(P=0.695)。使用顺铂与感觉神经性听力损失之间的高度显著相关(RR, 5.13;P <0.001)。没有发现听力损失与社会人口学特征或其他临床状况有显著关联。结论:耳毒性是癌症患者顺铂化疗的重要临床后遗症。建议将来进行更大样本量的研究,以评估和预防顺铂引起的耳毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ototoxicity in Cancer Patients on Cisplatin Therapy Attending Basrah Oncology Centre: A Cohort Study
  Background: Cisplatin is a chemotherapeutic agent that is used extensively for the treatment of a broad spectrum of tumors. However, progressive irreversible side effects of Cisplatin, including ototoxicity, have been reported. Methods: A cohort study was implemented from 1 April to 30 August 2015 to study the association between Cisplatin chemotherapy and sensory-neural hearing loss as the major and most important sign of ototoxicity. The cohort group included cancer patients treated with Cisplatin, while patients on Carboplatin were the control group. Cisplatin and Carboplatin belong to alkylating platinum chemotherapy drugs, which are used to treat various malignant solid tumors. Data collection was done through a questionnaire, including information related to sociodemographic characteristics and current and past medical history. Hearing loss was assessed using pure tone audiometry at the time of starting chemotherapy and one month later. Results: The total number of patients was 50, with male to female ratio 1:1 and a mean age of 49.7±14.7 (range 18–80 years): 27 patients were on Cisplatin with a mean age of 50.3±13.5 and 23 patients were on Carboplatin chemotherapy with a mean age of 51.9±15.1 with no significant difference in age (P=0.695). A highly significant association between Cisplatin use and sensory-neural hearing loss (RR, 5.13; P <0.001) was noted. No significant association was found between hearing loss and sociodemographic characteristics or other clinical conditions. Conclusions: Ototoxicity represents a significant clinical sequel of Cisplatin chemotherapy in patients with cancer. A future study using a larger sample size aiming at the evaluation and prevention of Cisplatin induced ototoxicity is recommended.  
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