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临床试验/NCT00322634
NCT00322634已完成不适用

Investigator Initiated Trial: Prospective Study of Clinical Predictors of Survival in Cancer Patients With Metastatic Solid Tumors

New Mexico Cancer Care Alliance5 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2006年2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
25
试验地点
5
主要终点
Disease Progression

研究概览

简要总结

The use of performance status and LDH in combination can predict patient survival more accurately than physician clinical impression or the patients' own feelings about their survival

详细描述

Patients with incurable cancer frequently ask their doctors for an estimate of survival. Such estimates can assist patients in making decisions about how best to spend their time and energy. Survival estimates are also required when considering patients with incurable cancer for experimental treatments. However, such estimates are difficult to make. There is some data to suggest that a simple clinical measure, the performance status, combined with a laboratory blood test, the LDH, may assist in making the survival estimate more realistic. This study is designed to test if this is the case, using patients with metastatic lung, breast, colorectal, prostate, or pancreatic cancer or patients with cancer of unknown primary who have exhausted life-prolonging therapy. These patients will be asked to consent to entering this study. Their performance status will be assessed by the Karnofsky and WHO scales, they will be asked to have their blood tested for LDH and they and their doctor will be asked to estimate their survival. After study entry they will be allowed to receive palliative radiotherapy, surgery or systemic therapy as indicated including protocol treatment. After study entry, the only other requirement is that the date of the patients death be reported so that the duration of survival can be compared with the doctors and patients estimate and correlated with the performance status and LDH.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients must be at least 18 years of age
  • All patients must have documented incurable metastatic cancer
  • All patients must have exhausted any treatments which are known to prolong survival in their disease, or have elected not to receive further life-prolonging therapy. Specifically, patients with the following are eligible:
  • Non-small cell lung cancer patients after third systemic therapy
  • Small cell lung cancer patients after second systemic therapy
  • Breast cancer patients after third cytotoxic therapy (does not include hormonal therapy)
  • Colorectal cancer patients after second systemic therapy
  • Hormone refractory prostate cancer patients after first cytotoxic therapy
  • Cancer of unknown primary
  • Pancreatic cancer patients after first systemic therapy
  • The use of systemic (chemotherapy, immunotherapy) or local treatments (XRT) for palliation of symptoms is allowed
  • Patients with a history of previous cancers are allowed
  • Patients with a history of other significant disease (e.g. heart disease, COPD, etc.) are allowed
  • All patients must sign informed consent

排除标准

  • Patients with acute or chronic leukemia, Hodgkin's disease, or non-Hodgkins lymphoma are excluded
  • Patients who do not sign informed consent are excluded

结局指标

主要结局

Disease Progression

时间窗: 2 years

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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