ERCC1 Targeted Trial (ET)
A Multicentre, Randomised, Phase III Trial of Platinum-based Chemotherapy Versus Non-platinum Chemotherapy, After ERCC1 Stratification, in Patients With Advanced/Metastatic Non-small Cell Lung Cancer
調査の概要
詳細な説明
TRIAL OBJECTIVES
Primary objective
The trial will have two main objectives:
- To detect an improvement in survival for ERCC1+ve patients treated with a non-platinum chemotherapy compared to platinum-based treatment.
- To establish non-inferiority or improvement in survival for ERCC1-ve patients treated with a platinum-based chemotherapy compared to non-platinum treatment.
Secondary objectives
- To examine progression-free survival, response rate and quality of life between the two treatment regimens, according to ERCC1 status.
- To investigate whether the treatment effect differs according to histology (squamous vs. nonsquamous);gender (males vs. females); performance status
- To undertake a cost-effectiveness analysis based on all patients, and according to ERCC1 status.
研究の種類
入学 (実際)
段階
- フェーズ 3
連絡先と場所
研究場所
-
-
-
London、イギリス
- University College London Hospitals
-
-
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
- Histological confirmation of non-squamous NSCLC
- Have a tissue biopsy available for sending to the central laboratory to determine ERCC1 status
- Presentation with stage IIIb (not amenable to curative treatment) or IV disease - staging scans must be no more than 28 days prior to registration. Patients with relapsed NSCLC must not have received prior chemotherapy or biological therapy (previous surgery or radical radiotherapy allowed)
- At least one measurable lesion according to Response Evaluation Criteria in Solid Tumours
- Either sex, at least 18 years of age
- ECOG performance status 0-1
- Estimated life expectancy of at least 8 weeks
Adequate bone marrow function as evidenced by the following (assessed within 14 days of registration):
- Absolute neutrophil count (ANC) ≥1.5 × 109/L
- Platelet count ≥100 × 109/L
- Haemoglobin ≥9 g/dL
Adequate liver function as evidenced by the following (assessed within 14 days of registration):
- Total bilirubin ≤ 1.5 x upper limit of normal (ULN)
- Aspartate transaminase (AST) ≤3 × ULN or ≤5 × ULN is acceptable with liver metastases
- Alanine transaminase (ALT) ≤3 × ULN
Adequate renal function as evidenced by the following (assessed within 14 days of registration):
- GFR > 60ml/min as measured by creatinine clearance through EDTA. Alternatively, the Cockcroft and Gault formula may be used to estimate GFR, but if < 60 ml/min then EDTA should be performed.
- Previous palliative radiotherapy to non-target metastatic lesions is allowed for pain relief prior to starting chemotherapy
- Patients with stable brain metastases will be allowed to enrol. Stable brain metastases being defined as no progression of brain metastases 28 days after treatment as documented by a CT scan/MRI of the brain. Patients with incidentally discovered asymptomatic brain metastases may be enrolled and treated with trial chemotherapy without prior brain irradiation if deemed feasible by the treating physician
- Signed informed consent form
- Use of effective contraception during, and for 6 months after trial treatment by patients of reproductive potential and partners of reproductive potential. Patients who receive aprepitant (anti-emetic) must be willing to use an alternative or back-up method to hormonal contraceptives as aprepitant may reduce their efficacy. Female patients with childbearing potential must have a negative serum pregnancy test prior to registration.
EXCLUSION CRITERIA
- Cytologically or clinically diagnosed NSCLC
- Evidence of significant medical condition or laboratory finding which, in the opinion of the treating physician or chief investigator, makes it undesirable for the patient to participate in the trial
- Presence of uncontrolled brain or leptomeningeal metastases thought to require immediate radiotherapy
- Presence of clinically significant third-space fluid collections (for example, ascites or pleural effusions) that cannot be controlled by drainage or other procedures prior to trial entry
- Yellow fever vaccination received within the 30 days previous to study entry
- Unable to interrupt aspirin or other NSAIDs (for pemetrexed arms of the trial)
- Unable or unwilling to take vitamin B12 and folic acid (for pemetrexed arms of the trial)
- A history of prior malignant tumour, unless the patient has been without evidence of disease for at least 3 years or the tumour was a non-melanoma skin tumour or early cervical cancer
- Pregnant or lactating women
- Inability to comply with protocol or trial procedures
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:ランダム化
- 介入モデル:並列代入
- 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 |
|---|---|
|
実験的:Platinum Arm
Cisplatin (IMP) / Pemetrexed (IMP)
|
|
|
実験的:Non Platinum Arm
Paclitaxel (IMP) / Pemetrexed (IMP)
|
|
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 |
|---|---|
|
Overall Survival
時間枠:Dec 2014
|
Dec 2014
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Time to progression
時間枠:Dec 2014
|
Dec 2014
|
協力者と研究者
捜査官
- 主任研究者:Siow M. Lee, MD, PhD, FRCP、Cancer Research UK
研究記録日
主要日程の研究
研究開始
一次修了 (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
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- ISRCTN02370070
- CRUK-UCL-ET
- EUDRACT-2007-007639-17
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。