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临床试验/NCT02075112
NCT02075112已完成1 期

A Pilot Study of Soy Isoflavone, Genistein, in Combination With Radiation Therapy and Cisplatin in Locally Advanced Squamous Cell Carcinoma of the Head and Neck

Emory University2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2013年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
24
试验地点
2
主要终点
Percentage of patients with grade 2 or higher xerostomia at 1 year post-treatment

研究概览

简要总结

The purpose of this study is to determine if soy supplementation during chemotherapy and radiation therapy will decrease side effects caused by treatment. Long-lasting dry mouth is a side effect of the standard treatment, and we are testing whether soy supplementation during treatment may reduce this symptom and other side effects of chemoradiation.

详细描述

Concurrent chemoradiation is the standard of care for locally advanced squamous cell carcinoma of the head and neck (SCCHN). Improving the outcome for patients with this disease remains a major challenge.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • Biopsy proven squamous cell carcinoma of the head and neck (SCCHN)
  • Primary disease site involving the oropharynx
  • Clinical stage III or IV
  • Karnofsky Performance Status (KPS) ≥ 70
  • Adequate bone marrow, kidney, and hepatic function (no laboratory value > 2 times the normal limit)
  • Amylase (0-160 U/L) and lipase (0-130 U/L) levels within 1.5 times the range of normal

排除标准

  • Prior history of SCCHN
  • Prior history of radiation to the head and neck region
  • KPS < 70
  • Soy allergy
  • Contraindication to cisplatin chemotherapy or plans to alter or reduce cisplatin therapy
  • Any head and neck cancer of non-squamous histology
  • Any head and neck subsite other than oropharynx (including unknown primary site)
  • Patients who are pregnant or lactating
  • Patients who may benefit from surgical resection

研究组 & 干预措施

Soy isoflavone

Experimental

Study treatment: Soy isoflavone in combination with radiation therapy & cisplatin

干预措施: Soy isoflavone (Drug)

Soy isoflavone

Experimental

Study treatment: Soy isoflavone in combination with radiation therapy & cisplatin

干预措施: Radiation (Radiation)

Soy isoflavone

Experimental

Study treatment: Soy isoflavone in combination with radiation therapy & cisplatin

干预措施: Cisplatin (Drug)

结局指标

主要结局

Percentage of patients with grade 2 or higher xerostomia at 1 year post-treatment

时间窗: 1 year after treatment completion

The primary outcome of this study is the percentage of patients with symptomatic (grade 2 or higher) xerostomia at 1 year post-treatment, assessed by the Late Effects of Normal Tissues (LENT)/Subjective, Objective, Management, Analytic (SOMA) method.

次要结局

  • Exploratory biomarker studies: changes in interleukin 6(3 and 6 months post-treatment)
  • Exploratory biomarker studies: changes in vascular endothelial growth factor(3 and 6 months post-treatment)
  • Exploratory biomarker studies: changes in isoprostanes levels(3 and 6 months post-treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kristin Higgins, MD

Principal Investigator

Emory University

研究点 (2)

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