Ixabepilone in Treating Patients With Relapsed or Refractory Aggressive Non-Hodgkin's Lymphoma
A Phase II Study of Epothilone B Analog BMS-247550 (NSC 710428) in Patients With Relapsed Aggressive Non-Hodgkin's Lymphomas
調査の概要
状態
介入・治療
詳細な説明
OBJECTIVES:
I. Determine the objective overall response rate of patients with relapsed or refractory aggressive non-Hodgkin's lymphoma treated with BMS-247550 (ixabepilone).
II. Determine the safety and toxicity of this drug in these patients. III. Determine the duration of response, overall survival, and time to progression in patients treated with this drug.
OUTLINE: This is a multi-center study.
Patients receive ixabepilone intravenously (IV) over 1 hour on days 1, 8, and 15. Courses repeat every 28 days in the absence of disease progression, unacceptable toxicity, or if the patient becomes a candidate for stem cell transplantation.
Patients are followed every 8 weeks until disease progression.
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
-
-
Illinois
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Chicago、Illinois、アメリカ、60637
- University of Chicago
-
-
Texas
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Houston、Texas、アメリカ、77030
- M D 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 confirmed aggressive non-Hodgkin's lymphoma of 1 of the following cellular types:
- Grade III follicular center
- Diffuse large B-cell
- Mantle cell
- Primary mediastinal B-cell
- Burkitt's
- High-grade B-cell (Burkitt-like)
Anaplastic large cell of 1 of the following subtypes:
- CD30-positive
- T-cell
- Null cell
- Hodgkin's-like
Relapsed or refractory disease after prior standard chemotherapy, meeting criteria for 1of the following cohorts:
- Cohort 1 (relapsed but chemosensitive): Prior complete response (CR) or partial response (PR) lasting at least 4 weeks after the most recent prior therapy
Cohort 2 (refractory): Stable disease or less than a PR after the most recent prior therapy
- No progressive disease after the most recent prior therapy
Measurable disease
- At least 1 bidimensionally measurable lesion at least 10 mm by conventional techniques or clinical exam
Ineligible for or unwilling to undergo hematopoietic stem cell transplantation
- Patients requiring debulking prior to transplant allowed
No known CNS involvement by lymphoma
- Prior CNS disease that has been successfully treated in patients with relapsed disease exclusively outside of the CNS may be allowed by the principal investigator
- Performance status - ECOG 0-2
- More than 3 months
- WBC at least 3,000/mm^3
- Absolute neutrophil count at least 1,200/mm^3
- Platelet count at least 100,000/mm^3
- Bilirubin no greater than 1.5 mg/dL
- AST/ALT no greater than 2.5 times upper limit of normal
- Creatinine no greater than 1.5 mg/dL
- Creatinine clearance at least 60 mL/min
- No symptomatic congestive heart failure
- No unstable angina pectoris
- No cardiac arrhythmia
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- No prior allergic reaction or hypersensitivity to compounds containing Cremophor EL or agents of similar chemical or biological composition to BMS-247550
- No peripheral neuropathy grade 2 or greater
- No other currently active malignancy except nonmelanoma skin cancer or carcinoma in situ of the cervix (previously treated malignancy allowed if considered to be at less than 30% risk of relapse)
- No ongoing or active infection
- No psychiatric illness or social situation that would preclude study compliance
- No other concurrent uncontrolled illness
- No colony-stimulating factors (CSFs) within 24 hours of study chemotherapy
- No CSFs during first course of study therapy
- No concurrent filgrastim-SD/01
- No concurrent immunotherapy
- See Disease Characteristics
- At least 4 weeks since prior cytotoxic chemotherapy (6 weeks for nitrosoureas or mitomycin)
- No other concurrent chemotherapy
- No concurrent hormonal therapy
- At least 4 weeks since prior radiotherapy
- No concurrent therapeutic radiotherapy
- At least 4 weeks since prior surgery
- Recovered from prior therapy
- At least 7 days since prior cimetidine
- No concurrent cimetidine
- No concurrent combination antiretroviral therapy for HIV-positive patients
- No other concurrent investigational agents
- No other concurrent anticancer medications
- No concurrent unconventional therapies, food, or vitamin supplements containing Hypericum perforatum
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:Treatment (chemotherapy)
Patients receive ixabepilone IV over 1 hour on days 1, 8, and 15.
Courses repeat every 28 days in the absence of disease progression, unacceptable toxicity, or if the patient becomes a candidate for stem cell transplantation.
|
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 |
|---|---|---|
|
Objective Overall Response Rate
時間枠:up to 3 years
|
The 1999 international response criteria (http://www.ncbi.nlm.nih.gov/pubmed/10561185) as published by Cheson was used for the definition of target lesions and CT scans were used for response assessment.
CR(complete response)/CRu(unconfirmed complete response) requires disappearance of all target lesions; PR (partial response) requires >=50% decrease in the sum of the products of the greatest diameters; Overall Response (OR)=CR/CRu+PR.
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up to 3 years
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Safety and Toxicity of Ixabepilone
時間枠:up to 3 years
|
Number of patients experiencing adverse event grade 3 or above.
Grade was determined by the National Cancer Institute Common Toxicity Criteria (CTC) version 2.0.
Adverse events possibly, probably, or definitely attributed to use of ixabepilone.
|
up to 3 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Duration of Response
時間枠:up to 3 years
|
Duration of response was measured from the time measurement criteria are met for CR(complete response)/CRu(unconfirmed complete response)/PR(partial response), whichever was first recorded, until the first date that PD(progressive disease) was objectively documented.
According to the 1999 international response criteria as published by Cheson, CR/CRu is defined as the disappearance of all target lesions; PR is defined as >=50% decrease in the sum of the products of the greatest diameters; PD is defined as >=50% increase from nadir in the sum of the products of the greatest diameters of any previously identified abnormal node for PRs or nonresponders, or appearance of any new lesion during or at the end of therapy.
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up to 3 years
|
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Overall Survival
時間枠:up to 3 years
|
Defined as the time from the first day of therapy to the date of death.
If the patient was lost to follow-up, survival was censored on the last date the patient was known to be alive.
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up to 3 years
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Time to Progression
時間枠:up to 3 years
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Defined as the time from the first day of treatment until the date PD(progressive disease) or death is first reported.
Patients who died without a reported prior progression was considered to have progressed on the day of their death.
Patients who did not progress was censored at the day of their last tumor assessment.
According to the 1999 international response criteria as published by Cheson, progression/progressive disease is defined as >=50% increase from nadir in the sum of the products of the greatest diameters of any previously identified abnormal node for PRs or nonresponders, or appearance of any new lesion during or at the end of therapy.
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up to 3 years
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協力者と研究者
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
その他の研究ID番号
- NCI-2009-00031 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
- N01CM62201 (米国 NIH グラント/契約)
- N01CM62202 (米国 NIH グラント/契約)
- P30CA014599 (米国 NIH グラント/契約)
- NCI-5913
- UCCRC-NCI-5913
- CDR0000285683
- UCCRC-11965B
- 11965B (その他の識別子:University of Chicago)
- 5913 (CTEP)
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