SMAC Mimetic LCL161 Alone or With Cyclophosphamide in Treating Patients With Relapsed or Refractory Multiple Myeloma
Phase II Study of LCL161 Alone and in Combination With Cyclophosphamide in Patients With Relapsed or Refractory Multiple Myeloma
研究概览
详细说明
PRIMARY OBJECTIVES:
I. To evaluate the confirmed overall response rate (>= partial response [PR]) to LCL161 (SMAC mimetic LCL161), used as a single agent, in patients with relapsed multiple myeloma (MM).
SECONDARY OBJECTIVES:
I. To estimate the confirmed overall response rate to LCL161 in combination with cyclophosphamide, when cyclophosphamide is added to LCL161 for lack of response or progression.
II. To estimate the overall survival and event-free survival of patients treated with LCL161 in combination with cyclophosphamide, when cyclophosphamide is added to LCL161 for lack of response or progression.
III. To evaluate the tolerability of LCL161 alone and in combination with cyclophosphamide in patients with relapsed MM.
TERTIARY OBJECTIVES:
I. To determine degradation of cellular inhibitor of apoptosis protein-1 (cIAP1) in peripheral blood mononuclear cells (PBMC), changes in serum cytokines, and changes in immune cell subsets by flow cytometry.
II. To correlate the effect of LCL161 with the presence of activating mutations of the nuclear factor kappa beta (NFKB) pathway.
III. To evaluate the pharmacokinetics (PK) of LCL161 alone, and LCL161 in combination with cyclophosphamide.
IV. To describe patient-reported health-related quality of life and symptoms.
OUTLINE:
Patients receive SMAC mimetic LCL161 orally (PO) once daily (QD) on days 1, 8, 15, and 22. Patients lacking a minor response by end of course 2 or partial response by end of course 4 may also receive cyclophosphamide PO QD on days 1, 8, 15, and 22 at the discretion of the treating physician. Patients taking cyclophosphamide with less than a 25% interval reduction in paraprotein receive SMAC mimetic LCL161 on days 2, 9, 16, and 23. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at 30 days and then every 6 months for 1 year.
研究类型
注册 (实际的)
阶段
- 阶段2
联系人和位置
学习地点
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Arizona
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Scottsdale、Arizona、美国、85259
- Mayo Clinic in Arizona
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Florida
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Jacksonville、Florida、美国、32224-9980
- Mayo Clinic in Florida
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Minnesota
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Rochester、Minnesota、美国、55905
- Mayo Clinic
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Relapsed or refractory multiple myeloma and has already received =< 4 standard treatment regimens; note: induction, transplant, consolidation, and maintenance is considered one regimen
- Have received prior therapy with an immunomodulatory agent, a proteosome inhibitor, and glucocorticoids
- Absolute neutrophil count (ANC) >= 1000/uL
- Untransfused platelet count >= 75,000/uL
- Aspartate aminotransferase (AST) =< 3 x upper limit of normal (ULN)
- Alanine aminotransferase (ALT) =< 3 x ULN
- Total bilirubin =< 1.5 mg/dL
- Serum creatinine =< 2.5 mg/dL
- Hemoglobin >= 8 g/dL
Measurable disease of multiple myeloma as defined by at least ONE of the following:
- Serum monoclonal protein >= 1.0 g/dL
- >= 200 mg of monoclonal protein in the urine on 24 hour electrophoresis
- Serum immunoglobulin free light chain >= 10 mg/dL AND abnormal serum immunoglobulin kappa to lambda free light chain ratio
- Monoclonal plasmacytosis >= 30% (evaluable disease)
- Measurable plasmacytoma that has not been radiated
- Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1, 2
- Willing and able to comply with scheduled visits, treatment plan and laboratory tests
- Able to swallow and retain oral medication
- Provide informed written consent
- Negative serum pregnancy test done =< 7 days prior to registration, for women of childbearing potential only
- Willing to provide all biological specimens as required by the protocol for correlative research purposes
- Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study)
- Mayo Clinic Arizona only: Willing to participate in associated biobanking study, 919-04; the patient must sign consent to enroll onto the mandatory companion biobanking study in order to participate in this treatment study
- Mayo Clinic Rochester and Florida only: Willing to participate in associated biobanking study, 521-93; the patient must sign consent to enroll onto the mandatory companion biobanking study in order to participate in this treatment study
Exclusion Criteria:
- Prior use of investigational drugs =< 14 days prior to registration
- Prior use of growth factors =< 14 days prior to registration
- Prior radiation therapy =< 14 days prior to registration
- Prior autologous stem cell transplant =< 12 weeks prior to registration
Any of the following:
- Pregnant women
- Nursing women
- Women of childbearing potential who are unwilling to employ adequate contraception while receiving treatment on this study and for 4 months after stopping treatment on this study
- Men who are unwilling to use a condom (even if they have undergone a prior vasectomy) while having intercourse with any woman, while receiving treatment on this study and for 4 months after stopping treatment on this study NOTE: Postmenopausal women are allowed to participate in this study; women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks ago; in the case of oophorectomy alone, a woman is considered to be of not child bearing potential only when her reproductive status has been confirmed by follow-up hormone level assessment
- Prior allogeneic transplant of any kind
- Known active infection requiring parenteral or oral anti-infective treatment
- Serious psychiatric illness, active alcoholism, or drug addiction that may hinder or confuse follow-up evaluation
- Known human immunodeficiency virus (HIV) or active hepatitis B or C viral infection
- Active autoimmune/inflammatory conditions requiring ongoing immunosuppressive therapy
Use of more than low dose corticosteroids (e.g., prednisone up to but no more than 10 mg PO QD or its equivalent) for symptom management and comorbid conditions, except for the following:
- Topical applications (e.g. rash)
- Inhaled sprays (e.g. obstructive airways diseases)
- Eye drops or local injections (e.g. intra-articular)
- Joint injections (e.g. arthritis) Doses of corticosteroid should be stable for at least 7 days prior to registration
- Any concurrent severe and/or uncontrolled medical conditions that could increase the patient's risk for toxicity while in the study or that could confound discrimination between disease- and study treatment-related toxicities
Impaired cardiac function or clinically significant cardiac diseases, including any of the following:
- History or presence of ventricular tachyarrhythmia
- Presence of unstable atrial fibrillation (ventricular response > 100 bpm) (NOTE: patients with stable atrial fibrillation are eligible, provided they do not meet any of the other cardiac exclusion criteria)
- Clinically significant resting bradycardia (< 50 bpm)
- Angina pectoris or acute myocardial infarction =< 3 months prior to registration
- Other clinically significant heart disease (e.g., symptomatic congestive heart failure; uncontrolled arrhythmia or hypertension; history of labile hypertension or poor compliance with an antihypertensive regimen)
- Currently receiving treatment with agents that are metabolized solely through cytochrome P450, family 3, subfamily A, polypeptide 4/5 (CYP3A4/5) and have a narrow therapeutic index or are strong cytochrome P450, family 2, subfamily C, polypeptide 8 (CYP2C8) inhibitors; or are receiving treatment with agents that carry a risk for QT prolongation and are CYP3A substrates; caution should be used in patients taking other CYP2C8- or CYP3A4/5-interacting agents
- Impaired gastrointestinal (GI) function or GI disease that may significantly alter the absorption of LCL161
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:Treatment (SMAC mimetic LCL161 and cyclophosphamide)
Patients receive SMAC mimetic LCL161 PO QD on days 1, 8, 15, and 22. Patients lacking a minor response by end of course 2 or partial response by end of course 4 may also receive cyclophosphamide PO QD on days 1, 8, 15, and 22 at the discretion of the treating physician.
Patients taking cyclophosphamide with less than a 25% interval reduction in paraprotein receive SMAC mimetic LCL161 on days 2, 9, 16, and 23.
Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
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相关研究
辅助研究
其他名称:
相关研究
给定采购订单
其他名称:
给定采购订单
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Confirmed Overall Response Rate (Stringent Complete Response [sCR], Complete Response [CR], Very Good Partial Response [VGPR], or Partial Response [PR]) With Single Agent SMAC Mimetic LCL161
大体时间:Up to 1 year
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The primary endpoint of this study is the confirmed overall response rate with single agent LCL161 (prior to initiation of cyclophosphamide).
A confirmed overall response is defined as sCR (CR as defined+Normal FLC ratio+Absence of clonal PCs by immunohistochemistry), CR (Negative immunofixation of serum and urine+Disappearance of any soft tissue plasmacytoma+<5% PCs in Bone Marrow+a normal FLC ratio), VGPR (Serum and urine M-component detectable by immunofixation but not on electrophoresis), or PR (If present at baseline, ≥ 50% reduction of serum M-protein and reduction in 24-hour urinary M-protein or to <200 mg/24hrs) noted as the objective status on two consecutive evaluations while receiving single agent LCL161.The rate (percentage) of successes will be estimated by the number of successes divided by the total number of evaluable patients times 100.
95% confidence intervals for the true success percentage will be calculated by the exact binomial method.
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Up to 1 year
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Combination Agent Response Rate
大体时间:Up to 1 year
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The overall response rate (percentage) with the addition of cyclophosphamide will be estimated by the number of patients who achieve a confirmed overall response at any time (with SMAC mimetic LCL161 plus cyclophosphamide) divided by the number of evaluable patients times 100.
95% confidence intervals for the true confirmed overall response rate will be calculated by the exact binomial method.
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Up to 1 year
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Event-free Survival
大体时间:From registration to disease progression while receiving SMAC mimetic LCL161 and cyclophosphamide, death due to any cause, or subsequent treatment for multiple myeloma, assessed up to 1 year
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The event-free survival time is defined as the time from registration to disease progression while receiving LCL161 and cyclophosphamide, death due to any cause, or subsequent treatment for multiple myeloma.
Date of progression will be defined as the date that the criteria for progressive disease were first met after initiation of cyclophosphamide.
If a patient goes off study treatment and never received cyclophosphamide, they will be censored on the date they went off study treatment.
If a patient initiates cyclophosphamide but later discontinues cyclophosphamide due to toxicity and continues LCL161 alone, disease progression on LCL161 alone will be considered an event in this case.
The distribution of event-free survival will be estimated using the method of Kaplan-Meier.
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From registration to disease progression while receiving SMAC mimetic LCL161 and cyclophosphamide, death due to any cause, or subsequent treatment for multiple myeloma, assessed up to 1 year
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Incidence of Toxicities Graded Using National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0 (All Treatment)
大体时间:Up to 30 days after the last day of study drug treatment
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The maximum grade for each type of adverse event, regardless of causality, will be recorded and reported for each patient, and frequency tables will be reviewed to determine adverse event patterns.
Additionally, the relationship of the adverse event(s) to the study treatment will be taken into consideration.
The percentage of patients with a maximum grade 3 or higher adverse event are reported below.
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Up to 30 days after the last day of study drug treatment
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Overall Survival
大体时间:From registration to death due to any cause, assessed up to 1 year
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Survival time is defined as the time from registration to death due to any cause.
The distribution of survival time will be estimated using the method of Kaplan-Meier.
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From registration to death due to any cause, assessed up to 1 year
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Activating Mutations of the NFKB Pathway
大体时间:Up to 1 year
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Continuous biomarker levels will be explored in a graphical manner including mean plots and plots of change and percent change from baseline and other summary measures.
Any potential relationships between the baseline level or change in the level of each biomarker and clinical outcome such as confirmed overall response, 6-month progression-free survival, and adverse event incidence will be further analyzed using Wilcoxon rank sum tests or logistic regression methods, as appropriate.
Association between a mutation status and confirmed overall response will be assessed using a chi-squared test.
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Up to 1 year
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Change in Patient-reported Outcomes (Quality of Life and Symptoms)
大体时间:Baseline up to 1 year
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Scale score trajectories over time will be examined using stream plots and mean plots with standard deviation error bars overall.
Changes from baseline at each cycle will be statistically tested using paired t-tests, and standardized response means (mean of the change from baseline scores at a given cycle, divided by the standard deviation of the change scores) will be interpreted (after applying Middel's adjustment) using Cohen's cut-offs.
Correlation between outcomes will employ Pearson and/or Spearman correlations at individual time points.
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Baseline up to 1 year
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Changes in Immune Cell Subsets
大体时间:Baseline up to 1 year
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Continuous biomarker levels will be explored in a graphical manner including mean plots and plots of change and percent change from baseline and other summary measures.
Any potential relationships between the baseline level or change in the level of each biomarker and clinical outcome such as confirmed overall response, 6-month progression-free survival, and adverse event incidence will be further analyzed using Wilcoxon rank sum tests or logistic regression methods, as appropriate.
Association between a mutation status and confirmed overall response will be assessed using a chi-squared test.
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Baseline up to 1 year
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Changes in Serum Cytokines
大体时间:Baseline up to 1 year
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Continuous biomarker levels will be explored in a graphical manner including mean plots and plots of change and percent change from baseline and other summary measures.
Any potential relationships between the baseline level or change in the level of each biomarker and clinical outcome such as confirmed overall response, 6-month progression-free survival, and adverse event incidence will be further analyzed using Wilcoxon rank sum tests or logistic regression methods, as appropriate.
Association between a mutation status and confirmed overall response will be assessed using a chi-squared test.
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Baseline up to 1 year
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Degradation of cIAP1 in PBMC
大体时间:Baseline up to 1 year
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Continuous biomarker levels will be explored in a graphical manner including mean plots and plots of change and percent change from baseline and other summary measures.
Any potential relationships between the baseline level or change in the level of each biomarker and clinical outcome such as confirmed overall response, 6-month progression-free survival, and adverse event incidence will be further analyzed using Wilcoxon rank sum tests or logistic regression methods, as appropriate.
Association between a mutation status and confirmed overall response will be assessed using a chi-squared test.
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Baseline up to 1 year
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合作者和调查者
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- MC1381 (其他标识符:Mayo Clinic)
- P30CA015083 (美国 NIH 拨款/合同)
- NCI-2013-01276 (注册表标识符:CTRP (Clinical Trial Reporting Program))
- CLCL161AUS01T
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