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临床试验/NCT00004922
NCT00004922已完成2 期

A Phase II Clinical Trial of Irinotecan (CPT-11) in Patients With Advanced High Grade Neuroendocrine Tumors

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家开始时间: 1999年6月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
试验地点
1

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

PURPOSE: Phase II trial to study the effectiveness of irinotecan in treating patients who have advanced neuroendocrine tumors.

详细描述

OBJECTIVES:

  • Determine the efficacy of irinotecan in terms of tumor response, time to tumor progression, and survival in patients with advanced high grade neuroendocrine tumors.
  • Evaluate the dose limiting and nondose limiting toxicities of this treatment regimen in this patient population.

OUTLINE: Patients receive irinotecan IV over 90 minutes once weekly for 4 weeks. Treatment repeats every 6 weeks in the absence of disease progression or unacceptable toxicity.

Patients are followed until death.

PROJECTED ACCRUAL: A total of 10-31 patients will be accrued for this study.

研究设计

研究类型
Interventional
主要目的
Treatment

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

  • DISEASE CHARACTERISTICS:
  • Histologically proven metastatic or unresectable high grade neuroendocrine tumor including:
  • Small cell carcinoma
  • Large cell neuroendocrine carcinoma
  • Other high grade neuroendocrine carcinomas without specification to cell size
  • No lung only involvement without any other primary site
  • No primary small cell lung cancer with or without metastases
  • Bidimensionally measurable disease with at least one lesion measuring at least 1 cm by 1 cm
  • High grade tumor indicated by at least one of the following:
  • Growth pattern suggestive of neuroendocrine differentiation
  • Mitotic rate greater than 15 mitoses per 10 hpf
  • Presence of abundant necrosis
  • Immunohistochemical evidence of neuroendocrine differentiation by positive staining for chromogranin, synaptophysin, or neuron specific enolase if no classic microscopic appearance of small cell carcinoma
  • No low grade neuroendocrine tumors (e.g., carcinoid tumors, pancreatic endocrine tumors) and atypical tumors
  • PATIENT CHARACTERISTICS:
  • 18 and over
  • Performance status:
  • Karnofsky 70-100%
  • Life expectancy:
  • Not specified
  • Hematopoietic:
  • WBC at least 3,500/mm^3
  • Granulocyte count at least 1,500/mm^3
  • Platelet count at least 75,000/mm^3
  • Bilirubin no greater than upper limit of normal (ULN)
  • SGOT no greater than 5 times ULN
  • Creatinine no greater than 2.0 mg/dL
  • Cardiovascular:
  • No myocardial infarction within the past 6 months
  • No uncontrolled congestive heart failure requiring therapy
  • No active or uncontrolled infection
  • HIV negative
  • No psychiatric or other disorder that would preclude study
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy
  • Not specified
  • Chemotherapy
  • No more than 2 prior chemotherapy regimens
  • No prior camptothecins
  • Endocrine therapy
  • Not specified
  • Radiotherapy
  • Not specified
  • Not specified

排除标准

  • 未提供

研究者

申办方类型
Other

研究点 (1)

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