Study to Assess Various Sunitinib Schedules in Renal Cell Carcinoma (SURF)
Open Label, Randomised Multi-centre Phase II Study to Assess the Efficacy and Tolerability of Sunitinib by Dose Administration Regimen (Dose Modification or Dose Interruptions) in Patients With Advanced or Metastatic Renal Cell Carcinoma
Patients who are candidates for first line treatment with Sunitinib 50mg 4/6 regimen in accordance with the Marketing Authorisation who meet the inclusion/exclusion criteria will be offered participation in this study during the consultation as part of their usual care. The patients will be included before Sunitinib treatment is started. Thereafter, sunitinib is initiated 50 mg/day; regimen 4/6 (Marketing Authorisation Indication), 4 weeks "on " alternating with 2 weeks "off "
As soon as a dose or schedule adjustment is required, regardless of cause, the patient will be randomised 1/1:
- Either into arm A and will receive 37.5mg of Sunitinib per day by the 4/6 regimen (in accordance with the Marketing Authorisation); 4 weeks "on " alternating with 2 weeks "off "
- Or into arm B and will receive 50mg of Sunitinib per day by the 2/3 regimen (investigational arm); 2 weeks "on " alternating with 1 week "off "
調査の概要
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
研究場所
-
-
Franche-Comté
-
Besancon、Franche-Comté、フランス、25030
- CHU Besançon
-
-
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
Key Inclusion Criteria:
- Men or women over 18 years old
- Patients with local, advanced or inoperable or metastatic (MRCC) renal cell carcinoma who are starting first line treatment with Sunitinib 50mg (4/6 regimen) according to the Marketing Authorisation Indication
- Patients with histologically or cytologically confirmed renal cancer, clear cell variant or with a clear cell component
- Karnofsky performance status ≥ 70%
Adequate organ function:
- Absolute neutrophil (N) count ≥ 1 500 / µL
- Platelets ≥ 100 000 / µL
- Haemoglobin ≥ 10 g/dL
- Adjusted serum calcium ≤ 2.6 mmol/L
- Creatinine clearance ≥ 30 mL/min (by the MDRD formula)
- Total bilirubin ≤ 1.5 x ULN (upper limit of the normal range)
- AST ≤ 2.5 x ULN and ALT ≤ 2.5 x ULN OR AST and ALT ≤ 5 x ULN if liver abnormalities due to liver metastases AST = aspartate aminotransferase ALT = alanine aminotransferase
Key Exclusion Criteria:
- Renal carcinoma with no clear cell component.
- Previous systemic treatment for the RCC regardless of type (including targeted therapy, immunotherapy, chemotherapy, hormone or experimental therapy). Previous or concomitant treatment with a bisphosphonate or denosumab is allowed.
- Patients whose clinical state and comorbidities are not consistent with administration of Sunitinib at the initial dose of 50mg/day 4 weeks out of 6.
- Grade 3 haemorrhage within 4 weeks before starting treatment with Sunitinib (according to the NCI-CTCAE toxicity score version 3.0).
- The presence of a past history of cancer in the 3 years before inclusion into the study
- Major surgery within 4 weeks before sunitinib initiation
- Past history of symptomatic cerebral metastases, spinal cord compression or meningeal carcinomatosis. Patients with cerebral metastases discovered incidentally on imaging and who are asymptomatic are not excluded if these metastases have been treated (radiotherapy and/or surgery) with a period of at least 4 weeks between the end of treatment and inclusion into the study and no clinical or radiological signs of relapse, and corticosteroid dose is not exceeding 10mg/day of prednisone or equivalent. Subjects will be excluded if subjects have signs of grade ≥ 2 treatment-related complications.
- Any of the following features within 6 months of the administration of Sunitinib: myocardial infarction, severe/unstable angina, coronary artery/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack.
- Pulmonary embolism or deep vein thrombosis within 3 months of inclusion (unless it's stable, asymptomatic and treated with a low molecular weight heparin for at least 6 weeks before inclusion).
- Any known acute or chronic disorder (such as severe chronic obstructive pulmonary disease) which in the opinion of the investigator could impact on the patient's capacity to receive the study treatment or make interpretation of toxicity or adverse events difficult.
- Known HIV infection.
- History of chronic active hepatitis including subjects who are carriers of the hepatitis B (HBV) or hepatitis C (HCV) virus.
- Existence of uncontrolled infection.
- Uncontrolled hypertension defined as a blood pressure of > 150 mmHg systolic or > 100 mmHg diastolic despite optimal anti-hypertensive therapy (blood pressure must be controlled at inclusion).
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 |
|---|---|
|
アクティブコンパレータ:Arm A 4/6
Sunitinib 37.5 mg/day; regimen 4/6 (Marketing Authorisation Indication) 4 weeks "on " alternating with 2 weeks "off "
|
|
|
実験的:Arm B 2/3
Sunitinib 50 mg/day; regimen 2/3 (experimental arm) 2 weeks "on " alternating with 1 week "off "
|
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
MDT (median duration of treatment)
時間枠:12 mo
|
The primary objective of this study is to estimate the median duration of treatment in each treatment group (arm A vs arm B) calculated from sunitinib initiation.
|
12 mo
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
PFS (progression-free survival)
時間枠:12 months
|
To estimate progression-free survival in patients included in each of the groups and in the overall population included in this study.
|
12 months
|
|
OS (overall survival)
時間枠:30 months
|
To estimate overall survival in patients included in each of the groups and in the overall population included in this study.
|
30 months
|
|
duration of sunitinib post randomization
時間枠:12 months
|
Estimation of the time between date of randomization and sunitinib arrest (for any reason) in the two treatment arms.
|
12 months
|
|
time to randomization
時間枠:4 months
|
To estimate the time to randomization defined as the time between the date of sunitinib initiation and the date of randomization.
|
4 months
|
|
ORR (objective response rate)
時間枠:6 months
|
To measure the objective response rate according to RECIST 1.1 criteria.
|
6 months
|
|
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
時間枠:24 months
|
To assess safety profile before and after randomization.
|
24 months
|
|
QOL (quality of life)
時間枠:24 months
|
To assess health-related quality of life since sunitinib is started (before randomization, at the time of randomization and after randomization)
|
24 months
|
協力者と研究者
協力者
捜査官
- 主任研究者:antoine thiery-vuillemin, MD PhD、Centre Hospitalier Universitaire de Besancon
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (予想される)
研究の完了 (予想される)
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 (実際)
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。