Lenalidomide or Observation in Treating Patients With Asymptomatic High-Risk Smoldering Multiple Myeloma
3期
进行中(已停止招募)
NCT01169337
| 适应症 | Light Chain Deposition Disease, Smoldering Multiple Myeloma |
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| 分期 | 3期 |
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| 申办方 | National Cancer Institute (NCI) |
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| 状态 | 进行中(已停止招募) |
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| 受试者人数 | 226 人 |
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| 干预(药物) | Clinical Observation, Lenalidomide, Quality-of-Life Assessment |
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| 开始日期 | 2011年1月24日 |
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| 完成日期 | 2019年1月25日 |
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| 结果公布日 | 2021年5月18日 |
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摘要
This randomized phase II/III trial studies how well lenalidomide works and compares it to observation in treating patients with asymptomatic high-risk asymptomatic (smoldering) multiple myeloma. Biological therapies such as lenalidomide, may stimulate the immune system in different ways and stop cancer cells from growing. Sometimes the cancer may not need treatment until it progresses. In this case, observation may be sufficient. It is not yet known whether lenalidomide is effective in treating patients with high-risk smoldering multiple myeloma than observation alone.
Proportion of Patients With Grade 3 Adverse Events That Effect Vital Organ Function or Any Grade 4 or Higher Non-hematologic Adverse Events (Phase II Primary Endpoint)
Assessed every 4 weeks while on treatment up to 24 weeks · proportion of participants
| Arm A (Lenalidomide; Phase II) | 0.056 proportion of participants |
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2-year Progression-free Survival (PFS) Rate (Phase III Primary Endpoint)
Assessed every 3 months for 2 years · proportion of participants
| Arm A (Lenalidomide; Phase III) | 0.93 proportion of participants |
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| Arm B (Observation; Phase III) | 0.76 proportion of participants |
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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。