NCT03285035Unknown不适用
Quality of Life Assessment in Patients Receiving Cryotherapy in Addition to Chemotherapy for Palliation of Unresectable Esophageal or Gastroesophageal Cancer
适应症
试验速览
- 阶段
- 不适用
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Change in baseline quality of life (QOL) assessment using a modified EORTC QLQ-OES18 at 6 months compared to baseline
研究概览
简要总结
Cryoablation combined with chemotherapy on the quality of life of patients with non resectable esophageal or gastroesophageal cancer.
详细描述
This is a single arm prospective study to determine the effect of cryoablation combined with chemotherapy on the quality of life of patients with non resectable esophageal or gastroesophageal cancer.
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 99 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Has esophageal or gastroesophageal cancer and will be receiving chemotherapy
- •Dysphagia score of 1, 2, 3 or
- •Age ≥18 years old
- •American Society of Anesthesiologists (ASA) Physical Status Classification ≤ 4
- •Deemed not a candidate for esophageal cancer surgical resection
- •Female subjects must be either post-menopausal, surgically sterilized, or willing to use an acceptable method of birth control (i.e., total abstinence, birth control pills, an intrauterine device (IUD), diaphragm, progesterone injections or implants, or condoms plus a spermicide) for the duration of the study
排除标准
- •Eastern Cooperative Oncology Group (ECOG) performance status greater than 2
- •Patient who received radiation treatment in the prior 8 weeks
- •Known brain metastases causing cranial nerve deficits which can cause dysphagia
- •Inability to undergo an esophagogastroduodenoscopy (EGD)
- •Pregnant or nursing
- •Surgery or anatomy where capacity of stomach is reduced making cryotherapy contraindicated
- •Patients with tracheoesophageal fistula
结局指标
主要结局
Change in baseline quality of life (QOL) assessment using a modified EORTC QLQ-OES18 at 6 months compared to baseline
时间窗: 6 months
次要结局
- Number of participants requiring alternative treatments for dysphagia palliation such as stenting, photodynamic therapy or brachytherapy and stenting(1 year)
- Subjective Global Assessment scale of nutritonal status will be determined at baseline and approximately 3 month intervals.(1 year)
- Immunoassays will be obtained before and after treatment(1 year)
- Tumor length in centimeters, endoscopist estimated luminal diameter and endoscopist subjective assessment of size as compared to the prior endoscopy will be determined(1 to 12 weeks)
- Number of participants with adverse events as assessed by CTCAE 4.03.(30 days)
- Survival while on cryotherapy and systemic chemotherapy will be measured.(1 year)
- Change in baseline quality of life (QOL) assessment using a modified EORTC QLQ-OES18 at 1 to 2 weeks compared to baseline(1 year)
- Change in dysphagia score using the 5 point Likert scale at 1 to 2 weeks post-procedure compared to baseline(1 to 2 weeks)
- local tumor control will be compared to systemic tumor control(1 year)
研究者
研究点 (1)
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