Phase II Trial of FOLFOX6, Bevacizumab and Cetuximab in Patients With Colorectal Cancer
調査の概要
状態
詳細な説明
PRIMARY OBJECTIVES:
I. To determine the safety, feasibility of administration, response rates and progression free survival among chemotherapy naïve patients with advanced colorectal cancer treated with FOLFOX6 plus bevacizumab and cetuximab (FBC).
II. To determine the survival of patients with advanced colorectal cancer treated with FBC.
III. To determine the safety of the current regimen in selected patients who have had prior MoAb therapy.
OUTLINE: This is a multicenter study.
Patients receive cetuximab IV over 60-120 minutes on day 1 in weeks 1-8. Patients also receive bevacizumab IV over 30-90 minutes, oxaliplatin IV over 2 hours, and leucovorin calcium IV over 2 hours on day 1, and fluorouracil IV continuously over 48 hours on days 1 and 2 of weeks 1, 3, 5, and 7. Courses repeat every 8 weeks in the absence of disease progression or unacceptable toxicity.
Patients are followed for survival.
PROJECTED ACCRUAL: A total of 40-67 patients will be accrued for this study.
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
-
-
New York
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Bronx、New York、アメリカ、10467-2490
- Montefiore Medical 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 adenocarcinoma of the colon or rectum which is beyond the scope of surgical resection (MEDRA code:"Colorectal neoplasms malignant","Colorectal cancer stage IV","10010035")
- Measurable disease,
- Life expectancy of greater than 3 months
- ECOG performance status =< 1
- Leukocytes >= 3,500/uL
- Absolute neutrophil count >= 1,500/uL
- Platelets >= 150,000/uL
- Total bilirubin within normal institutional limits
- AST(SGOT)/ALT(SGPT) =< 2.5 X institutional upper limit of normal
- Creatinine within normal institutional limits
- Patients may not have received prior therapy with bevacizumab or cetuximab
- Ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
- Patients who have had radiotherapy within 4 weeks prior to entering the study or those who have not recovered from adverse events due to radiotherapy administered more than 4 weeks earlier
- Patients may not be receiving any other investigational agents
- Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to any of the agents used in the study
- Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
- Pregnant or lactating women
- Serious or non-healing wound, ulcer or bone fracture
Invasive procedures defined as follows:
- Major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to Day 1 therapy
- Anticipation of need for major surgical procedures during the course of the study
- Core biopsy within 7 days prior to D1 therapy
If a patient is on full-dose anticoagulants, the following criteria should be met for enrollment:
- The subject must have an in-range INR (usually between 2 and 3) on a stable dose of warfarin or on stable dose of LMW heparin
- The subject must not have active bleeding or pathological conditions that carry high risk of bleeding (e.g. tumor involving major vessels, known varices)
- Active infection requiring parental antibiotics on D1
- Proteinuria at baseline; subjects unexpectedly discovered to have >= 1+ proteinuria will undergo a 24-hour urine collection, which will be < 1000 mg protein/ 24 hours to be allowed participation in the study
- No currently active second malignancy other than non-melanoma skin cancer or carcinoma in-situ of the cervix; patients are not considered to have a "currently active" malignancy if they have completed therapy and have no evidence of recurrence for at least 5 years
Patients with clinically significant cardiovascular disease:
- Uncontrolled hypertension
- Myocardial infarction or unstable angina < 6 months prior to registration
- New York heart association grade II or greater congestive heart failure, serious cardiac arrhythmia requiring medication, unstable angina pectoris
- Grade II or greater peripheral vascular disease
- CVA within 6 months of study entry
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 |
|---|---|
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実験的:Treatment (combination chemotherapy)
Patients receive cetuximab IV over 60-120 minutes on day 1 in weeks 1-8.
Patients also receive bevacizumab IV over 30-90 minutes, oxaliplatin IV over 2 hours, and leucovorin calcium IV over 2 hours on day 1, and fluorouracil IV continuously over 48 hours on days 1 and 2 of weeks 1, 3, 5, and 7. Courses repeat every 8 weeks in the absence of disease progression or unacceptable toxicity.
|
与えられた IV
他の名前:
与えられた IV
他の名前:
与えられた IV
他の名前:
与えられた IV
他の名前:
与えられた IV
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Severe Adverse Event (SAE) Rate
時間枠:The duration of the study
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The primary objective is to evaluate safety in all treated patients specifically the rate of serious adverse events which were defined as grade 5 events, grade 4 hemorrhage or thrombosis or bowel perforation
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The duration of the study
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Progression Free Survival Rate
時間枠:From randomization to the first documented disease progression
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From randomization to the first documented disease progression
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協力者と研究者
捜査官
- 主任研究者:Allyson Ocean、Montefiore Medical Center
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
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
本研究に関する用語
追加の関連 MeSH 用語
- 消化器系疾患
- 病理学的プロセス
- 組織型別の新生物
- 新生物
- 部位別新生物
- がん
- 新生物、腺および上皮
- 疾患の属性
- 消化器腫瘍
- 消化器系腫瘍
- 消化器疾患
- 結腸疾患
- 腸の病気
- 腸の腫瘍
- 直腸疾患
- 結腸直腸腫瘍
- 新生物、嚢胞性、粘液性、および漿液性
- 再発
- 腺癌
- 直腸腫瘍
- 嚢胞腺癌
- 結腸新生物
- 腺癌、粘液
- 薬の生理作用
- 薬理作用の分子機構
- 代謝拮抗薬、抗腫瘍薬
- 代謝拮抗剤
- 抗悪性腫瘍薬
- 免疫抑制剤
- 免疫学的要因
- 保護剤
- 血管新生阻害剤
- 血管新生調節剤
- 成長物質
- 成長阻害剤
- 微量栄養素
- ビタミン
- 解毒剤
- ビタミンB複合体
- 抗体
- フルオロウラシル
- オキサリプラチン
- 免疫グロブリン
- ベバシズマブ
- ロイコボリン
- レボルコボリン
- 抗体、モノクローナル
- 抗悪性腫瘍剤、免疫
- セツキシマブ
その他の研究ID番号
- NCI-2012-03006
- N01CM62201 (米国 NIH グラント/契約)
- N01CM62204 (米国 NIH グラント/契約)
- NCI-6490 (その他の識別子:CTEP ID)
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。