Denileukin Diftitox in Treating Patients With Metastatic Melanoma or Metastatic Kidney Cancer
Phase II Evaluation of Denileukin Diftitox in Patients With Metastatic Melanoma or Metastatic Kidney Cancer
RATIONALE: Denileukin diftitox may be able to make the body build an immune response to kill tumor cells.
PURPOSE: This phase II trial is studying how well denileukin diftitox works in treating patients with metastatic melanoma or metastatic kidney cancer.
調査の概要
詳細な説明
OBJECTIVES:
Primary
- Determine the clinical response in patients with metastatic melanoma or metastatic kidney cancer treated with denileukin diftitox.
Secondary
- Determine whether changes occur in levels of CD4-positive CD25-positive lymphocytes in the peripheral blood of these patients before and after treatment with this drug.
- Determine the toxicity profile of this drug in these patients.
OUTLINE: Patients are stratified according to disease type (metastatic melanoma vs metastatic kidney cancer).
Patients receive denileukin diftitox IV over 1 hour on days 1-5, 21-25, 42-46, and 63-67. Treatment repeats every 84 days (12 weeks) for up to a maximum total of 5 courses in the absence of disease progression, autoimmune ocular toxicity attributable to denileukin diftitox, or any other unacceptable toxicity. At any time during therapy, patients achieving a complete response receive 1 additional course of therapy after the complete response.
PROJECTED ACCRUAL: A total of 10-96 patients (5-48 per stratum) will be accrued for this study within 3-4 years.
研究の種類
段階
- フェーズ2
連絡先と場所
研究場所
-
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Maryland
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Bethesda、Maryland、アメリカ、20892-1182
- Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support
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Bethesda、Maryland、アメリカ、20892
- NCI - Center for Cancer Research
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
DISEASE CHARACTERISTICS:
Diagnosis of 1 of the following:
- Melanoma
- Kidney cancer
- Metastatic disease
- Measurable disease
- Documented disease progression while receiving standard therapy
- No resectable local or regional disease
PATIENT CHARACTERISTICS:
Age
- 16 and over
Performance status
- ECOG 0-2
Life expectancy
- More than 3 months
Hematopoietic
- WBC ≥ 3,000/mm^3
- Platelet count ≥ 90,000/mm^3
- Lymphocyte count ≥ 500/mm^3
- No concurrent coagulation disorders
Hepatic
- Bilirubin ≤ 2.0 mg/dL (< 3.0 mg/dL for patients with Gilbert's syndrome)
- AST and ALT < 3 times normal
- Albumin ≥ 2.5 g/dL
- Hepatitis B surface antigen negative
- Hepatitis C antibody negative
Renal
- Creatinine ≤ 2.0 mg/dL
Cardiovascular
- Normal thallium stress test*
- No prior myocardial infarction
- No history of severe coronary artery disease
- No major medical illness of the cardiovascular system NOTE: *For patients > 50 years of age OR who have a history of cardiovascular disease
Pulmonary
- No major medical illness of the respiratory system
Immunologic
- HIV negative
- No active systemic infection
- No presence of opportunistic infections
- No primary or secondary immunodeficiency
- No autoimmune disease
- No other known immunodeficiency
Other
- No sensitivity to denileukin diftitox or any of its components (e.g., diphtheria toxin, interleukin-2, or excipients)
- Willing to undergo leukapheresis
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
PRIOR CONCURRENT THERAPY:
Biologic therapy
- Prior treatment with interleukin-2 allowed provided the patient's disease status required this therapy
Chemotherapy
- Recovered from prior chemotherapy
Endocrine therapy
- No concurrent systemic steroids
Radiotherapy
- Recovered from prior radiotherapy
Surgery
- Not specified
Other
- More than 3 weeks since prior systemic anticancer therapy
- No other concurrent systemic anticancer therapy
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- マスキング:なし(オープンラベル)
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
|---|
|
臨床反応
|
二次結果の測定
結果測定 |
|---|
|
毒性
|
|
Changes in levels of CD4-positive CD25-positive lymphocytes in the peripheral blood
|
協力者と研究者
研究記録日
主要日程の研究
研究開始
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。