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临床试验/NCT01238185
NCT01238185已完成1 期

Oral Topical Cyclooxygenase Inhibitor (Aspirin) Mouthwash for Treatment of Oral Dysplasia

Institute of Head and Neck Studies and Education, United Kingdom4 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2010年2月1日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
40
试验地点
4
主要终点
COX-1 and COX-2 protein expression as assessed by immunohistochemistry and quantified by immunoblotting to determine whether COX inhibition in oral dysplasia tissues is actually possible by use of the mouthwash formulation

研究概览

简要总结

RATIONALE: Aspirin mouthwash may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

PURPOSE: This phase I trial is studying the side effects and best dose of aspirin mouthwash in treating patients with oral leukoplakia.

详细描述

OBJECTIVES:

  • To determine if oral topical acetylsalicylic acid mouthwash achieves modulation of COX-1, COX-2, and prostaglandin in oral dysplasia tissues in patients with oral leukoplakia.
  • To determine if this drug achieves alteration of histopathology and gene and protein expression in tissue.
  • To determine if this drug achieves aspirin-induced tissue changes relating to altered tumor biology.
  • To assess local and general tolerability and safety of this drug in these patients.

OUTLINE: All patients undergo tissue biopsy for histological diagnosis. Patients without a histological diagnosis of precancerous oral dysplasia undergo routine follow-up. Patients with a histological diagnosis of precancerous oral dysplasia are sequentially allocated to 1 of 4 treatment groups.

  • Group 1: Patients receive acetylsalicylic acid mouthwash (one 75 mg tablet dissolved in 250 mL of water) twice daily for 4-6 weeks, gargling for 60 seconds then expectorate it fully, before planned definitive surgical excision.
  • Group 2: Patients receive acetylsalicylic acid mouthwash (two 75 mg tablets of acetylsalicylic acid dissolved in 250 mL of water) twice daily for 4-6 weeks, gargling for 60 seconds then expectorate it fully, before planned definitive surgical excision.
  • Group 3: Patients receive acetylsalicylic acid mouthwash (one 300 mg tablet of acetylsalicylic acid dissolved in 250 mL of water) twice daily for 4-6 weeks, gargling for 60 seconds then expectorate it fully, before planned definitive surgical excision.
  • Group 4: Patients receive acetylsalicylic acid mouthwash (one 300 mg tablet of acetylsalicylic acid dissolved in 250 mL of water) three times daily for 4-6 weeks, gargling for 60 seconds then expectorate it fully, before planned definitive surgical excision.

At the time of definitive surgical excision, the patient is asked to gargle with the last dose of acetylsalicylic acid mouthwash just before being anesthetized. A small biopsy of the dysplasia lesion is taken and examined for immediate effects of the acetylsalicylic acid mouthwash on the dysplasia lesion. The surgically excised tissue is treated in the same way as the initial biopsy tissue (i.e., half being used for routine histology to confirm the diagnosis and the other half for research purposes). Tissue samples are analyzed via enzyme immunosorbent assay, qRT-PCR, immunoblotting, ELISA, immunohistochemistry, gene array analysis, and microvessel density analysis.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • DISEASE CHARACTERISTICS:
  • Clinically diagnosed oral leukoplakia requiring a tissue biopsy for histological diagnosis
  • Attending the outpatient clinic
  • PATIENT CHARACTERISTICS:
  • Not nursing
  • No known or suspected sensitivity to aspirin or other nonsteroidal anti-inflammatory drugs
  • No diagnosis of asthma or angioedema
  • No contraindications, including any of the following:
  • Active peptic ulceration or a history of peptic ulceration
  • Hemophilia or a history of bleeding disorders
  • Gout or a history of gout
  • PRIOR CONCURRENT THERAPY:
  • No concurrent regular use of aspirin for heart disease or other reasons
  • No other concurrent nonsteroidal anti-inflammatory drugs

排除标准

  • 未提供

结局指标

主要结局

COX-1 and COX-2 protein expression as assessed by immunohistochemistry and quantified by immunoblotting to determine whether COX inhibition in oral dysplasia tissues is actually possible by use of the mouthwash formulation

PGE2 levels as assessed by enzyme immunosorbent assay

COX-1 and COX-2 mRNA as assessed by qRT-PCR

次要结局

  • Protein expression as assessed by ELISA and immunohistochemistry for VEGFA
  • Tolerability and possible oral and other adverse effects using a questionnaire
  • VEGF mRNA expression as assessed by qRT-PCR
  • Global gene response of dysplastic tissue as assessed by Affymetrix gene expression microarrays
  • Comparison of WHO histological grade and clinical size of dysplastic lesions before and after treatment and assessment of proliferating cell nuclear antigen

研究者

发起方
Institute of Head and Neck Studies and Education, United Kingdom
申办方类型
Other

研究点 (4)

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