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临床试验/NCT02103010
NCT02103010已完成不适用

Predictive Modelling for Patient Stratification According to Treatment-related Toxicity and Survival After Chemoradiation for Head and Neck Cancer

University Hospital, Ghent2 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2014年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
2
主要终点
Change in dysphagia

研究概览

简要总结

Radiotherapy is an integral component of the current multimodality treatment approach in locally advanced head and neck cancer (HNC). There is growing evidence that more aggressive treatment regimens improve tumour control and survival. However, intensified treatment is at the expense of increased toxicity, in particular severe acute mucositis. In addition and of increasing importance, late and irreversible treatment-related side effects, including xerostomia and swallowing dysfunction, occur in a considerable proportion of patients and negatively affect quality of life.

High-risk human papilloma virus (HPV), specifically HPV type-16, is implicated as the causative factor in a proportion of HNC, especially those of the oropharynx. HPV-related cancers respond well to chemoradiotherapy compared to HNC related to tobacco and alcohol. Furthermore, the incidence of HPV-related oropharyngeal cancer is rising in Western countries. Given the significant toxicity associated with concurrent chemoradiotherapy, subsets of patients could be managed differently.

The first objective of the project is to develop predictive models for radiation-induced dysphagia and xerostomia in HNC patients. Clinical characteristics, treatment parameters, dose-volume effects on healthy tissues and whole-genome genetic data will be considered. The second objective of the project is to study the prognostic value of HPV status together with a panel of tumour biomarkers in oropharyngeal cancer patients. The overall aim of the project is to stratify patients according to the risks (side-effects) and benefits (survival) of cancer treatment using the developed risk models. Clustering patients into different risk categories may aid treatment decision making reducing therapy toxicity without compromising survival.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

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

入选标准

  • Histologically confirmed squamous cell carcinoma of oral cavity, oropharynx, hypopharynx and larynx. Histologically confirmed cervical lymph node metastases of unknown primary cancer (CUP). For prognosis part of the study: only histologically confirmed squamous cell carcinoma of the oropharynx
  • Stages : Tany N1-3, T3-4 N0, T1-2 N0, if prophylactic neck irradiation is performed
  • Multidisciplinary decision of curative radiotherapy or radiochemotherapy
  • Karnofsky performance status ≥ 70%
  • Age ≥ 18 years old
  • Gender : male - female
  • Informed consent obtained, signed and dated before start of radiotherapy

排除标准

  • Treatment combined with brachytherapy
  • Treatment combined with cetuximab or other targeted agents
  • Prior irradiation to the head and neck region
  • History of prior malignancies, except for cured non-melanoma skin cancer, curatively treated in-situ carcinoma of the cervix or other cancer curatively treated and with no evidence of disease at least 5 years
  • Distant metastases
  • Pregnant or lactating women
  • Mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study
  • Patients unlikely to comply with the protocol, i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study

结局指标

主要结局

Change in dysphagia

时间窗: during radiotherapy and at 6/12/18/24 months after the end of radiotherapy

Dysphagia during radiotherapy and at 6/12/18/24 months after the end of radiotherapy using the CTCAE (Common Terminology Criteria for Adverse Events) v4.0 scale.

change in xerostomia

时间窗: during radiotherapy and at 6/12/18/24 months after the end of radiotherapy

xerostomia during radiotherapy and at 6/12/18/24 months after the end of radiotherapy using the CTCAE (Common Terminology Criteria for Adverse Events) v4.0 scale

change in progression-free survival

时间窗: up to three years after study start

appearance of distant metastasis

时间窗: up to three years after study start

change in overall survival

时间窗: up to three years after study start

change in disease specific survival

时间窗: up to three years after study start

次要结局

  • Change in weight loss(during radiotherapy and at 6/12/18/24 months after the end of radiotherapy)
  • change of Quality of life(pre-radiotherapy, at the last day of radiotherapy and post-radiotherapy (12/24 months))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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