A Phase I/II Study of Liposomal Doxorubicin (Doxil)/Melphalan/Bortezomib (Velcade) in Relapsed/Refractory Multiple Myeloma (DMV)
調査の概要
研究の種類
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究場所
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California
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San Francisco、California、アメリカ、94143
- University of California San Francisco
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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:
- Previously diagnosed with multiple myeloma; Durie-Salmon Stage I, II, or III based on standard criteria
- Progressive disease, defined as 25% increase in serum M-protein or Bence Jones protein (an absolute increase of 0.5 gram/dL serum M-protein or at least 200 mg/24 hours of urine light chain excretion). For non-secretory multiple myeloma, progressive disease is defined as bone marrow biopsy with >25% increase in plasma cells or an absolute increase of at least 10% over prior known level. Alternatively, development of new or worsening of existing lytic bone lesions or soft tissue plasmacytomas, or hypercalcemia or relapse from CR.
- 18 year or older and willing and able to comply with the protocol requirements.
- Patient has signed informed consent.
- Unless a female patient is post-menopausal or surgically sterilized, must be willing to use an acceptable method of birth control (hormonal contraceptive, intrauterine device, diaphragm, with spermicide, condom with spermicide, or abstinence) for the duration of the study.
- Male patient must agree to use an acceptable method for contraception for the duration of the study.
- ECOG performance Status of < or equal to 2.
- Life expectancy is at least 3 months.
Initial Required Laboratory Values within 14 days of baseline i.e. Cycle 1, Day 1 (note that renal insufficiency, including dialysis dependence is permissable):
- ANC>1,000uL without the use of colony stimulating factors
- Platelets >50,000/L without transfusion support 7 days before the test
- Bilirubin < or equal to 2.0 mg/dL
- AST < or equal to 4 x upper limit of normal
Prior therapy: Patient must have had at least 2 prior therapeutic regimens as defined below for treatment of multiple myeloma
- Biologic therapy:
Prior nonmyeloablative transplantation allowed provided patient does not have significant graft-versus-host disease and is off aggressive immunosuppressive therapy for at least 30 days. Low dose immunosuppression is allowed (i.e. Prednisone at dose < or equal to 10 mg daily, low dose tacrolimus (subtherapeutic levels) or other agents with equivalent low-dose immunosuppression).
- Chemotherapy:
- Mobilization with chemotherapy followed by either single or tandem autologous transplantation is counted as 1 prior regimen.
- Mobilization with chemotherapy followed by autologous and subsequent nonmyeloablative allogenic transplantation is counted as 1 prior regimen.
- Any combination of drugs given concurrently is counted as a single regimen.
Exclusion Criteria:
- Pregnant or breast-feeding
- History of allergic reaction to compounds containing boron or mannitol.
- Active uncontrolled viral (including HIV), bacterial, or fungal infection.
- Grade III or IV toxicity due to previous anti-neoplastic therapy (except alopecia).
- Grade > or equal to 2 motor or sensory neuropathy as defined by the NCI Common Toxicity Criteria (NCI CTC):
- Grade 2: Either mild objective weakness or objective sensory loss/parasthesia (including tingling) that interferes with function, but not interfering with ADLs.
- Grade 3: Objective weakness or sensory loss/parasthesia interfering with ADLs.
- Grade 4: Paralysis or permanent sensory loss that interferes with function.
- Myocardial infarction within 6 months of enrollment or New York Heart Association (NYHA) Class III or IV heart failure, uncontrolled angina, severe uncontrolled arrhythmias, or electrocardiographic evidence of acute ischemia.
- For any patients whose lifetime cumulative doxorubicin dose exceeds 400 mg/m(2), patients with LVEF < or equal to 35% by MUGA are excluded. In other patients, MUGA is not required but if performed, LVEF must be > or equal to 35%.
- Concurrent administration of liposomal doxorubicin, melphalan, and bortezomib (single or two drug combinations of these are permissable).
- Less than 3 weeks since most recent chemotherapy or concurrent chemotherapy.
- Use of corticosteroids (>10 mg prednisone/day or equivalent).
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)
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 |
|---|---|
|
--To evaluate the safety and tolerability of four dose levels of liposomal doxorubicin, melphalan, and bortezomib in patients with relapsed/refractory MM and to identify a maximum tolerated dose of this combination.
時間枠:6 years
|
6 years
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
--To determine the efficacy of DMV therapy --Tabulate all the toxicities of DMV at the MTD by NCI criteria
時間枠:6 years
|
6 years
|
協力者と研究者
捜査官
- 主任研究者:Thomas G. Martin, M.D.、University of California, San Francisco
出版物と役立つリンク
便利なリンク
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
その他の研究ID番号
- UC-2408
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
米国で製造され、米国から輸出された製品。
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