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临床试验/NCT05330169
NCT05330169已完成不适用

Prospective Observational Cohort Study to Evaluate Hearing Toxicity Before and After Chemoradiotherapy in Patients With Nasopharyngeal Carcinoma

Guangxi Medical University1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2022年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200
试验地点
1
主要终点
The ratio of distortion product otoacoustic emission(DPOAE) failure

研究概览

简要总结

This observational cohort study was aimed to evaluate the hearing toxicity at multiple time points from baseline to 1 year after radical chemoradiotherapy among nasopharyngeal carcinoma patients.

详细描述

With the development of radiotherapeutic techniques and equipment as well as advances in treatment modalities, the 5-year overall survival of patients with non-disseminated NPC has exceeded 80%. However, the incidence of hearing toxicity did not decrease significantly compared with the past. The hearing loss remains the second most common toxicity after xerostomia. Audiometry, acoustic impedance testing, eustachian tube pressure measurements, and distortion product otoacoustic emissions will be used to compare hearing before treatment and up to 1 year after radical chemoradiotherapy. The related factors affecting the hearing of NPC patients will also be investigated and explored.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically confirmed non-keratinizing nasopharyngeal carcinoma(WHO II/III).
  • About to undergo radical chemoradiotherapy with intensity-modulated radiotherapy (IMRT).
  • Eastern Cooperative Oncology Group performance status≤
  • Adequate marrow function: neutrocyte count≥1.5×10e9/L, hemoglobin
  • ≥90g/L, and platelet count≥100×10e9/L.
  • Alanine Aminotransferase (ALT)/Aspartate Aminotransferase (AST)
  • ≤2.5×upper limit of normal (ULN), and bilirubin≤ 1.5×ULN.
  • Adequate renal function: creatinine clearance rate≥ 60 ml/min (Cockcroft-Gault formula).
  • Patients must be informed of the investigational nature of this study and give written informed consent.

排除标准

  • Age > 60 or <
  • Receiving additional targeted therapy or immunotherapy except for radiotherapy and chemotherapy.
  • With a condition that could cause hearing impairment, such as ear canal cerumen blockage, ear canal foreign body blockage, cholesteatoma, tympanic membrane perforation, cholesteatoma otitis media, middle ear granulation tissue growth, inner ear labyrinthitis, sudden nerve deafness, Meniere's disease, acoustic neuroma, and so on.
  • Patients who received aminoglycoside antibiotics or macrocyclic lipid antibiotics (such as streptomycin, gentamicin, kanamycin, neomycin, tobramycin, minocycline, erythromycin, roxithromycin, etc.) orally or intravenously within 30 days before treatment.
  • Patients with hearing loss at the baseline(except for those with conductive hearing loss diagnosed by at least two deputy chief physicians as nasopharyngeal carcinoma-related)
  • Patients who received additional treatment during the observation period due to disease progression.
  • Pregnant or breastfeeding.
  • Patients with prior malignancy who have received systemic chemotherapy or head and neck radiotherapy.
  • Any other condition, including symptomatic heart failure, unstable angina, myocardial infarction, active infection requiring systemic therapy, mental illness or domestic/social factors, deemed by the investigator to be likely to interfere with a patient's ability to sign informed consent, cooperate and participate in the study, or interferes with the interpretation of the results.

结局指标

主要结局

The ratio of distortion product otoacoustic emission(DPOAE) failure

时间窗: up to 16 months

We will use distortion product otoacoustic emission(DPOAE) to access the hearing before treatment and serially up to 1 year after radical chemoradiotherapy.

Hearing level (decibel)

时间窗: up to 16 months

We will use pure tone audiometry to access the hearing level (decibel) before treatment and serially up to 1 year after radical chemoradiotherapy.

次要结局

  • The ratio of Eustachian tube dysfuction(ETD)(up to 16 months)
  • Tympanogram type(up to 16 months)

研究者

发起方
Guangxi Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kai Hu

professor

Guangxi Medical University

研究点 (1)

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