Sunitinib Scheduling in Metastatic Renal Cell Carcinoma (mRCC)
A Phase II Study of Alternative Sunitinib Scheduling in Patients With Metastatic Renal Cell Carcinoma (mRCC)
調査の概要
詳細な説明
Study Drug Administration:
If you are found to be eligible to take part in this study, you will take sunitinib capsules by mouth every day for 2 weeks, followed by 1 week in which you do not receive any study drug. This will then be repeated every 3 weeks.
Every 6 weeks will be 1 study cycle.
If you have any side effects tell the study doctor right away. The study doctor may change your dose of the study drug.
Study Visits:
Every day during the first week, and then at least 1 time each week during the study, your blood pressure will be checked (either at home, at the clinic, or by your local doctor). You will need to write down your blood pressure in a blood pressure diary each time you check it and bring the diary with you to each clinic visit.
On Day 1 of Cycle 1:
- You will have a physical exam.
- Blood (about 3-4 tablespoons) will be drawn for routine and biomarker testing.
- You will fill out a questionnaire about the quality of your life and about how you are feeling. This should take about 5 minutes.
On Day 42 of every cycle:
- You will have a physical exam.
- Blood (about 3-4 tablespoons) will be drawn for routine tests.
On Day 42 of every even-numbered cycle (Cycles 2, 4, 6, and so on):
- You will have a CT scan of your chest, abdomen, and pelvis.
- Blood (about 1 tablespoon) will be drawn to check your thyroid function.
- Blood (about 2 tablespoons) will be drawn for biomarker testing. (Cycles 2 , 4, and 6 only)
- You will fill out the questionnaire about the quality of your life and about how you are feeling. (Cycles 2 , 4, and 6 only)
At any time that the doctor thinks it is needed, additional blood (about 1 tablespoon) may be drawn to check your thyroid function, and you may need to have a bone scan and CT scan or MRI of the brain to check the status of the disease.
Length of Study:
You may continue taking the study drug for as long as the study doctor thinks it is in your best interest. You will be taken off treatment if the disease gets worse, intolerable side effects occur, or if you are unable to follow study directions.
Your participation in this study will be over after the follow-up visit. However, the study team may perform a medical record review or follow-up call to check on how you are doing. If you are called, this should last about 5-10 minutes.
End-of-Treatment Visit:
After you are no longer receiving the study drug, you will have an end-of-treatment visit. You will have a physical exam and blood (about 3-4 tablespoons) will be drawn for routine and biomarker testing.
End-of- Treatment Follow-Up Visit:
About 30 days after your end-of-treatment visit you will have a follow-up visit and the following procedures will be performed:
- You will have a physical exam.
- Blood (about 3-4 tablespoons) will be drawn for routine tests.
- You will have CT scans of your chest, abdomen and pelvis to check the status of the disease.
This is an investigational study. Sunitinib is FDA approved and commercially available to treat advanced kidney cancer. The dosing schedule being used on this study is investigational.
Up to 60 participants will be enrolled in this study. Up to 60 may take part at MD Anderson.
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
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California
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Stanford、California、アメリカ、94305
- Stanford University Medical Center
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North Carolina
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Chapel Hill、North Carolina、アメリカ、27514
- Lineberger Cancer Center
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Ohio
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Cleveland、Ohio、アメリカ、44195
- Cleveland Clinic Taussig Cancer Institute
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Pennsylvania
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Philadelphia、Pennsylvania、アメリカ、19111-2497
- Fox Chase Cancer Center
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Texas
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Houston、Texas、アメリカ、77030
- University of Texas MD Anderson 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 or cytologically-confirmed metastatic renal cell carcinoma of clear cell histology. Prior nephrectomy is not a requirement for eligibility
- Age >/=18 years
- Measurable or evaluable metastatic disease per RECIST v 1
- ECOG performance status 0-1
- Normal organ and bone marrow function as defined by: Serum aspartate transaminase (AST) or serum glutamic oxaloacetic transaminase (SGOT) and serum alanine transaminase (ALT) or serum glutamic pyruvic transaminase (SGPT) </= 2.5 x laboratory upper limit of normal (ULN); Total serum bilirubin </= 2.0 x ULN; Absolute neutrophil count (ANC) >/= 1500/µL; Platelets >/= 100,000/µL; Hemoglobin >/= 9.0 g/dL (transfusion permitted); Serum calcium </= 12.0 mg/dL; Serum creatinine </= 2.5 mg/dL
- Patients with a history of deep venous thromboembolism or pulmonary embolism on treatment with anticoagulation are eligible for the study.
- Subjects must have the ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
- Prior treatment with sunitinib or any other systemic therapy in the metastatic setting (prior neo/adjuvant therapy will be allowed if completed > 6 months prior to registration and therapy not discontinued for toxicity)
- Uncontrolled hypertension (defined as blood pressure >140/90 mm Hg not controlled with anti-hypertensives)
- Prior intraabdominal, intrathoracic, vascular, spinal or intracranial surgery or radiation therapy within 4 weeks of starting treatment
- History of or known brain metastases, spinal cord compression, or carcinomatous meningitis
- New York Heart Association (NYHA) grade II or greater congestive heart failure
- Current treatment on another therapeutic clinical trial
- Any of the following within the preceding 6 months- myocardial infarction, severe/unstable angina, severe peripheral vascular disease (claudication) or procedure on peripheral vasculature, coronary/peripheral artery bypass, graft, cerebrovascular accident or transient ischemic attack, clinically significant bleeding
- Pregnant or breastfeeding women are excluded from this study because there is an unknown, but potential risk for adverse events in nursing infants secondary to treatment of the mother with sunitinib. Breastfeeding must be discontinued if the mother is treated with sunitinib
- Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness
- HIV-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with sunitinib. In addition, these patients are at increased risk of lethal infections when treated with marrow suppressive 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
- 割り当て：なし
- 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 |
|---|---|
|
実験的：Sunitinib
Sunitinib starting dose 50 mg by mouth daily given for 2 weeks "on" followed by 1 week "off". 1 cycle is 6 weeks.
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Starting dose: 50 mg by mouth daily given for 2 weeks "on" followed by 1 week "off". 1 cycle is 6 weeks.
他の名前：
Questionnaire completion on Day 1 of Cycle 1, and on Day 35 of Cycles 2, 4, and 6.
他の名前：
|
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 |
|---|---|---|
|
Rate of Toxicity
時間枠：Participants were monitored for toxicities for 30 days after treatment was discontinued; total treatment duration approximately 34 months
|
Determine the number of participants who experience a specific, treatment-related adverse events at a grade three, four or five: fatigue, hand-foot syndrome, and/or diarrhea.
Adverse events as defined by the Common Terminology Criteria for Adverse Events (CTCAE) version 4
|
Participants were monitored for toxicities for 30 days after treatment was discontinued; total treatment duration approximately 34 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Progression-Free Survival (PFS)
時間枠：17 months
|
Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
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17 months
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The Number and Percentage of Participants Who Experienced a Grade 3, 4, or 5 Adverse Event
時間枠：Participants were monitored for toxicities for 30 days after treatment was discontinued or until death, whichever occurred first.
|
Adverse events as defined by Common Terminology Criteria for Adverse Events (CTCAE) version 4
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Participants were monitored for toxicities for 30 days after treatment was discontinued or until death, whichever occurred first.
|
|
Dose Reductions and Treatment Discontinuations Due to Unacceptable Toxicities
時間枠：2 years
|
Reported as the number and percentage of participants who underwent one or more dose reductions, as well as, the number and percentage of participants whose treatment ended.
|
2 years
|
|
Changes in Participant Reported Outcomes in the Functional Assessment of Cancer Therapy-General (FACT-G)
時間枠：36 weeks from the start of treatment
|
Participants completed FACT-G suveys evaluating quality of life at weeks 0, 12, 24, and 36.
The score range is from 0 to 180 with higher scores reflecting a better quality of life.
The results were reported for each time point for all participants and then broken into two groups: participants with a grade 3 toxicity and participants without a grade 3 toxicity.
The total number of surveys changes as the weeks progress.
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36 weeks from the start of treatment
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Changes in Circulating DNA Levels With Antiangiogenic Treatment
時間枠：Not applicable due data not generated due to timing and budgetary issues
|
Not applicable due data not generated due to timing and budgetary issues
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協力者と研究者
協力者
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始 (実際)
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 (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
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
- 2013-0944
- NCI-2014-01908 (レジストリ識別子：NCI CTRP)
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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