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临床试验/NCT00949312
NCT00949312Unknown不适用

Ultrastaging of Early Colon Cancer

Saint John's Cancer Institute2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
入组人数
26
试验地点
2
主要终点
Disease-free survival (time to local or distant recurrence after resection)

研究概览

简要总结

RATIONALE: Diagnostic procedures that look for micrometastases in lymph nodes removed during surgery for colon cancer may help doctors learn the extent of disease.

PURPOSE: This phase I trial is studying lymph nodes in patients with stage II colon cancer.

详细描述

OBJECTIVES:

  • Determine whether the immunohistochemical and molecular presence of micrometastases in ≥ 12 lymph nodes removed during en-bloc resection in patients with stage II colon cancer correlates with 3-year disease-free survival.
  • Evaluate the prognostic significance of molecular markers detected in the primary tumor and develop a microarray-based gene signature for stage II colon cancer.

OUTLINE: This is a multicenter study.

Tumor tissue and regional lymph node samples are collected during surgery for analysis of micrometastases and molecular markers by immunohistochemistry, qRT-PCR, MM qRT-PCR, qRDNA-PCR, and microarray profiling.

Patients are followed up periodically for 4 years after surgery.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All of the following inclusion criteria must be met in order for the subject to be eligible.
  • Subjects must have CC detected by proctosigmoidoscopy, flexible endoscopy, or gastrograffin/barium enema, with no evidence of distant metastases within 8 weeks of enrollment.
  • Subjects with CC must have a computerized tomography (CT; at a minimum - spiral (helical) CT with 5-mm contiguous reconstruction algorithms and adequate volume (based on site-specific protocols) of oral and intravenous contrast agents) of the abdomen and pelvis and a chest x-ray or CT of the chest per standard of care, within 8 weeks prior to enrollment to rule out distant metastases. Subjects with preoperative CT scans and testing showing non-specific or non-diagnostic (equivocal) abnormalities may be eligible pending intraoperative exploration.
  • Greater than 18 years of age
  • Subjects must have a performance status ≤ 2 on the ECOG/Zubrod scale.
  • Subject is able to give informed consent, and must be willing to be followed clinically or by phone/email/mail correspondence
  • Subject must have a life expectancy of greater than 5 years not including the disease/diagnosis of CC.
  • Subject must have clinical assessment conducted by phone unless patients follow up are part of the regular clinical visits.

排除标准

  • Any of the following criteria will exclude the subject from the study.
  • Subjects requiring emergent surgery (within 2 hours of presentation) to prevent a life-threatening situation or death such as those with a perforated colon, metabolically significant complete bowel obstruction or massive GI bleeding will be excluded. Subjects who do not require emergent surgery, such as those with occult bleeding or early or partial bowel obstruction will be permitted to enter.
  • Subjects with any history of Crohn's disease, chronic ulcerative colitis, or familial polyposis.
  • Discovery of distant metastases intra-operatively.
  • Subjects with history of another malignancy over the last three years (except for completely resected cervical, skin cancers or in-situ cancers - see Appendix B for a list of exempt cancers).
  • Pregnant and/or lactating women. Potentially childbearing subjects (pre-menopausal women) should undergo a pregnancy test within 7 days prior to surgery and after signing consent. Subjects found to be pregnant will be ineligible and withdrawn from the study.
  • Subjects should not be participating in another research protocol at the time of enrollment. Participation during follow-up is acceptable.
  • Systemic chemotherapy for node negative colon cancer.
  • Complete polypectomy by endoscopy
  • Less than 12 lymph nodes

结局指标

主要结局

Disease-free survival (time to local or distant recurrence after resection)

时间窗: 48 months

The event to be used for DFS is time to recurrence (local or distant) after resection of colon cancer

次要结局

  • Overall survival (time to death from colorectal cancer)(48 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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