Vaccine Therapy in Treating Patients With Stage III, Stage IV, or Relapsed Non-Small Cell Lung Cancer Treated With First-Line Chemotherapy
Novel Tumor Vaccine gp96-Ig Fusion Protein in Advanced (Stage IIIB), Relapsed or Metastatic (Stage IV) Non-Small Cell Lung Cancer (NSCLC) Patients Who Have Failed First Line Chemotherapy
RATIONALE: Vaccines made from a person's tumor cells may help the body build an effective immune response to kill non-small cell lung cancer cells.
PURPOSE: This phase I trial is studying the effects of gp96-Ig vaccine therapy in treating patients with stage III, stage IV, or relapsed non-small cell lung cancer treated with first-line chemotherapy.
調査の概要
詳細な説明
Overall Goals:
- to evaluate the safety and induction of anti-tumor immunity by administration of an immunogenic human tumor cell vaccine, and assess immune response in relation to clinical outcome.
Primary Aim:
- to evaluate the safety of administering a heat shock protein gp96-Ig-secreting allogeneic tumor cell-vaccine (gp96-Ig vaccine) in patients with advanced NSCLC.
Secondary Aims:
- to study the immune response to vaccination,
- to monitor clinical responses and
- to recommend a dose-schedule combination for further testing in an initial Phase II trial of vaccine efficacy.
研究の種類
入学 (実際)
段階
- フェーズ 1
連絡先と場所
研究場所
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Florida
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Miami、Florida、アメリカ、33136
- University of Miami Sylvester Comprehensive Cancer Center
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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
Inclusion Criteria
- Histologically confirmed NSCLC (squamous, adeno-, large cell anaplastic, bronchoalveolar, and non-small cell carcinoma NOS): stage IIIB with malignant pleural effusion, stage IV, or recurrent disease.
- At least one site of bi-dimensionally measurable disease.
- Metastasis if present and treated must be stable by CT scan or MRI for at least 8 weeks.
- Patient must have received and failed at least one line of chemotherapy.
- Age >= 18 years.
- ECOG performance status 0-2.
- Life expectancy >= 3 months.
Laboratory parameters:
- Hemoglobin levels >= 10.0 (transfusions allowed if necessary).
- ANC >= 1,500.
- Platelets >= 100k.
- Creatinine clearance >= 50 ml/min.
- Total and direct bilirubin: < 2.5 X upper institution limit for normal.
- Liver function tests: AST, ALT, and AlkP < 2.5 X upper institution limit for normal.
- Signed informed consent.
- Autopsy consent - although not a requirement for study entry, patients who consent to participate in study will be made aware of the critical importance of a post-mortem examination in the event of the patient's death after receiving therapy with this experimental vaccine. Therefore, pre-treatment written agreement to autopsy will be sought from the patient, or verbal agreement to autopsy will be sought in the presence of the next of kin or other family members.
Exclusion Criteria
- Active or symptomatic cardiac disease such as congestive heart failure, angina pectoris or recent myocardial infarction. Patients with history of these conditions who are stable taking cardiac medications will also be excluded.
- Pregnant or lactating women (negative test for pregnancy is required of women of childbearing potential).
- Known HIV infection.
- Uncontrolled or untreated brain or spinal cord metastases.
- Active infection.
- Concomitant steroid or other immunosuppressive therapy.
- Other active malignancies present within the past three years, except for basal and/or squamous cell carcinoma(s) or in situ cervical cancer.
- Alcohol or chemical abuse.
- Meningeal carcinomatosis.
- Chemotherapy, radiation therapy, or other anti-tumor therapy during the last four weeks.
- Prior biologic response modifier therapy.
- Refusal in fertile men or women to use effective birth control measures during and for six months after the completion of treatment on study.
- Immune deficiency syndromes, including the following: rheumatoid arthritis, systemic lupus erythematosus, Sjogren's disease, sarcoidosis, vasculitis, polymyositis, glomerulonephritis.
Compromised lung function:
- FeV1 < 30% of the predicted value, or
- DLCO < 30% of the predicted value, or
- PCO2 > 45 mmHg.
- Any patient enrolled on study whose respiratory symptoms have experienced marked deterioration not related to a known cause, such as pneumonia, congestive heart failure, or pulmonary embolism, will have a repeat PFT evaluation, and if the above parameter values for FeV1, DLCO, or PCO2 are seen, will be excluded from further treatment.
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
- 割り当て:非ランダム化
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:DS-1: gp96-ig Dose Schedule 1
Dose Schedule 1 (DS-1): Ad100-gp96Ig-HLA A1 Vaccine 4x10^7 cells bi-weekly, maximum 9 vaccines/patient;
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Dose Schedule 1 (DS-1): 4x10^7 cells bi-weekly, maximum 9 vaccines/patient; Dose Schedule 2 (DS-2): 2X10^7 cells weekly, maximum 18 vaccines/patient; Dose Schedule 3 (DS-3): 1x10^7 cells twice weekly, maximum 36 vaccines/patient
他の名前:
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実験的:DS-2: gp96-ig Dose Schedule 3
Dose Schedule 2 (DS-2): Ad100-gp96Ig-HLA A1 Vaccine 2X10^7 cells weekly, maximum 18 vaccines/patient;
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Dose Schedule 1 (DS-1): 4x10^7 cells bi-weekly, maximum 9 vaccines/patient; Dose Schedule 2 (DS-2): 2X10^7 cells weekly, maximum 18 vaccines/patient; Dose Schedule 3 (DS-3): 1x10^7 cells twice weekly, maximum 36 vaccines/patient
他の名前:
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実験的:DS-3: gp96-ig Dose Schedule 3
Dose Schedule 3 (DS-3): Ad100-gp96Ig-HLA A1 Vaccine 1x10^7 cells twice weekly, maximum 36 vaccines/patient
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Dose Schedule 1 (DS-1): 4x10^7 cells bi-weekly, maximum 9 vaccines/patient; Dose Schedule 2 (DS-2): 2X10^7 cells weekly, maximum 18 vaccines/patient; Dose Schedule 3 (DS-3): 1x10^7 cells twice weekly, maximum 36 vaccines/patient
他の名前:
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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 |
時間枠 |
|---|---|
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Safety
時間枠:6, 12, 18, 24, and 36 months post enrollment
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6, 12, 18, 24, and 36 months post enrollment
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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Immunologic response: CD8, CD4 and NK response
時間枠:Baseline, Day 1 Week1, Day 1 Week 13, Day 1 Week 19
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Baseline, Day 1 Week1, Day 1 Week 13, Day 1 Week 19
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協力者と研究者
スポンサー
捜査官
- スタディチェア:Luis E. Raez, MD, FACP、University of Miami Sylvester Comprehensive Cancer Center
出版物と役立つリンク
一般刊行物
- Raez LE, Cassileth PA, Schlesselman JJ, Sridhar K, Padmanabhan S, Fisher EZ, Baldie PA, Podack ER. Allogeneic vaccination with a B7.1 HLA-A gene-modified adenocarcinoma cell line in patients with advanced non-small-cell lung cancer. J Clin Oncol. 2004 Jul 15;22(14):2800-7. doi: 10.1200/JCO.2004.10.197.
- Raez LE, Podack ER, CD8 T cell response in a phase I study of therapeutic vaccination of advanced NSCLC with allogeneic tumor cells secreting endoplasmic reticulum-chaperone gp96-Ig-peptide complexes. Advances in Lung Cancer 2(1): 9-18, 2013 doi:10.4236/alc.2013.21002
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
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
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