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临床试验/NCT00104780
NCT00104780Unknown2 期

A Phase II, Open Label, Multi-center Study of EP2101 Therapeutic Vaccine in Patients With Stage IIIB, Stage IV, or Recurrent Non-Small Cell Lung Cancer (NSCLC)

Epimmune18 个研究点 分布在 1 个国家开始时间: 2004年12月1日最近更新:
适应症

试验速览

阶段
2 期
发起方
试验地点
18
主要终点
Safety

研究概览

简要总结

RATIONALE: Vaccines made from peptides may make the body build an effective immune response to kill tumor cells.

PURPOSE: This phase II trial is studying how well vaccine therapy works in treating patients with stage IIIB, stage IV, or recurrent non-small cell lung cancer.

详细描述

OBJECTIVES:

Primary

  • Compare the overall survival of patients with HLA-A2-positive, stage IIIB or IV or recurrent non-small cell lung cancer (NSCLC) treated with vaccine therapy comprising EP-2101 emulsified in montanide ISA-51 with that of historical controls and patients with HLA-A2-negative, stage IIIB or IV or recurrent NSCLC who undergo observation only.
  • Determine the safety of this vaccine in these patients.

Secondary

  • Determine progression-free survival of patients treated with this vaccine.
  • Determine the frequency, magnitude, and breadth of cytotoxic and helper T-cell response to vaccine epitopes in patients treated with this vaccine.

研究设计

研究类型
Interventional
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

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed non-small cell lung cancer meeting 1 of the following stage criteria:
  • Stage IIIB disease
  • Stage IV disease
  • Recurrent disease
  • HLA-A2-positive disease
  • HLA-A2 negative patients are eligible to enroll in group II (observation) only
  • Measurable disease
  • Estimated tumor volume ≤ 125 cc
  • No CNS signs or symptoms of brain metastases
  • Brain metastases that are clinically stable for ≥ 2 months AND do not require anticonvulsants or systemic steroids are allowed
  • PATIENT CHARACTERISTICS:
  • 18 and over
  • Performance status
  • Life expectancy
  • At least 12 weeks
  • Hematopoietic
  • Hemoglobin ≥ 10 g/dL
  • Platelet count > 100,000/mm^3
  • WBC > 3,000/mm^3
  • Absolute neutrophil count > 1,500/mm^3
  • Absolute lymphocyte count > 500/mm^3
  • AST and ALT ≤ 2.5 times upper limit of normal (ULN) (5 times ULN for patients with liver involvement by tumor)
  • Bilirubin ≤ 2.0 mg/dL (3.0 mg/dL for patients with liver involvement by tumor)
  • Albumin ≥ 2.5 g/dL
  • Alkaline phosphatase ≤ 2.5 times ULN
  • No history of hepatitis B or C positivity
  • Creatinine ≤ 2 times ULN
  • Immunologic
  • No history of any of the following active conditions:
  • Systemic lupus erythematosus
  • Scleroderma
  • Connective tissue disease
  • Sjögren's syndrome
  • Multiple sclerosis
  • Rheumatoid arthritis
  • Inflammatory bowel disease
  • No history of HIV positivity
  • No history of serious adverse reaction, including anaphylaxis, or hypersensitivity to study vaccine or to any of its components
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 3 weeks after completion of study treatment
  • No other malignancy within the past 5 years except curatively excised nonmelanoma skin cancer or surgically cured carcinoma in situ of the cervix
  • No other acute medical condition that would preclude study treatment
  • No mental or psychiatric condition that would preclude study compliance
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy
  • More than 1 month since prior interferon therapy
  • More than 1 month since prior interleukin therapy
  • No prior cancer vaccine therapy, including participation in a vaccine study
  • 另有 9 项未显示

排除标准

  • 未提供

结局指标

主要结局

Safety

Comparison of overall survival with historical controls

次要结局

  • Progression-free survival
  • Frequency, magnitude, and breadth of cytotoxic and helper T-cell response to vaccine epitopes

研究者

发起方
Epimmune
申办方类型
Industry

研究点 (18)

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