First Autologous Transplant on Minimal Residual Disease Markers in Previously Untreated Myeloma Undergoing Initial Treatment With Velcade
2018年4月15日 更新者:Madan Jagasia, MD、Vanderbilt-Ingram Cancer Center
Impact of First Autologous Transplant on Minimal Residual Disease Markers in Previously Untreated Myeloma Undergoing Initial Treatment With Velcade Based Therapy
The purpose of this study is to study the MRD status after VELCADE based induction therapy (VELCADE, lenalidomide, dexamethasone or VELCADE, liposomal doxorubicin, dexamethasone) in patients with previously untreated multiple myeloma and study the impact of HDC and ASCT on MRD status post-transplant.
Our hypothesis is that MRD-status will continue to increase significantly at 3 months post-transplant and will validate that HDC and ASCT needs to be performed even when patients have achieved major response after induction therapy with novel agents.
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
36
阶段
- 阶段2
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
Tennessee
-
Memphis、Tennessee、美国、38104
- University of Tennessee Cancer Institute, Boston Baskin Cancer Group
-
Nashville、Tennessee、美国、37232
- Vanderbilt-Ingram Cancer Center
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 70年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
Confirmed Multiple Myeloma as defined below within 120 days of starting cycle 1:
- Bone marrow plasmacytosis with ≥ 10% plasma cells or sheets of plasma cells or biopsy proven plasmacytoma
- Presence of M protein in serum or urine or both. Conventional M spike, serum free light chains, or 24 hour urine study. Non-secretory myeloma is not eligible for this study.
- In addition patient must have one of the following organ dysfunction criteria
- Hypercalcemia
- Renal insufficiency
- Anemia
- Bone disease manifested by lytic lesion or osteoporosis (if osteoporosis is the only organ dysfunction criteria then BM should have ≥ 30% plasma cells)
- Confirmed Multiple myeloma as defined above within 90 days of starting cycle 1
- The following study assessments must be fulfilled and must be obtained with four weeks of starting cycle 1
- Hemoglobin > 7 g/dL, Platelet count > 75 X 10 to 9th power/L, and Absolute neutrophil count > 1 X 10 to 9th power/L
- Creatinine <2.5 mg/dL or calculated creatinine clearance > 30 ml/min/1.72 m2
- Bilirubin ≤ 1.5 mg/dL X ULN
- SGPT (ALT) and SGOT (AST) ≤ 2.5 times the upper limit of normal
- Ejection fraction ≥ 45% as measured by a MUGA scan or 2 D echocardiogram
- Pulmonary function tests show >60% predicted values for FVC, FEV1, and DLCO FEV1 must be > 1 liter.
- No prior systemic therapy with the exception of bisphosphonates for MM
- Prior glucocorticoid therapy for the treatment of multiple myeloma is not permitted EXCEPT if used in conjunction with palliative radiation to prevent vasogenic edema. In that case steroids should have been used for less than 7 days. Prior steroid use for non-malignant disorders is permitted and should have been restricted to less than the equivalent of prednisone 10 mg per day. Prior or concurrent topical or localized steroid therapy to treat non-malignant disorders is permitted
- Prior palliative and/ or localized radiation therapy is permitted provided at least 4 weeks have passed from date of last radiation therapy to starting cycle 1.
- Patients with prior solitary plasmacytoma treated with radiation therapy with curative intent are eligible if the disease has now progressed to active multiple myeloma and meeting all eligibility criteria for the protocol
- ECOG PS 0, 1 or 2
- For women of childbearing potential a negative serum pregnancy test is required within 4 weeks of starting cycle 1 and then every 4 weeks during the first 4 cycles of induction therapy
- Women of child bearing potential must be willing to refrain from sexual intercourse or willing to employ a dual method of contraception, one of which is highly effective (IUD, birth control pills, tubal ligation or partner's vasectomy) and another additional method (condom, diaphragm, or cervical cap) during the entire course of the study (start of therapy until 30 days after stem cell transplant).
- Sexually active males should be willing to use a condom (even if they have had a prior vasectomy) while having intercourse with any women during the course of the study (start of therapy until 30 days after stem cell transplant).
- Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.
Exclusion Criteria:
- Patients with smoldering myeloma or monoclonal gammopathy of unknown significance are not eligible
- Age > 70 years or < 18 years is not eligible
- Patient has > 1.5 × ULN Total Bilirubin
- Grade 2 or higher peripheral neuropathy due to ANY cause
- High index of suspicion of primary amyloid light chain (AL) amyloidosis.
- Patients with uncontrolled inter-current illness including uncontrolled hypertension, symptomatic congestive heart failure, unstable angina, uncontrolled cardiac arrhythmia, uncontrolled psychiatric illness or social situation that would limit compliance or a prior history of Steven Johnson syndrome
- Patients must not have a history of current or previous deep vein thrombosis or pulmonary embolism regardless of whether or not the patient is receiving anticoagulation therapy
- Female patients who are breastfeeding or pregnant.
- Patients known to be HIV positive
- Myocardial infarction within 6 months prior to enrollment or has New York Heart Association (NYHA) Class III or IV heart failure (see section 31.3), uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any ECG abnormality at Screening has to be documented by the investigator as not medically relevant.
- Patient has hypersensitivity to VELCADE, boron or mannitol.
- Patient has received other investigational drugs within 14 days before enrollment
- Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:VRD
VELCADE, Lenalidomide, Dexamethasone
|
1.3 mg/m2 by IV on days 1, 4, 8, 11 of each cycle
25 mg by mouth on days 1-4 of each cycle
20 mg the day before and the day after receiving VELCADE
At least one asprin 81 mg per day.
Other option per physician's choice
Zoledronic acid by IB or pamidronate by IV can be used as per standard of care.
40 mg by mouth on days 1-4, 8-11, and 15-18 of cycle 1 and days 1-4 on cycle 2-4
|
|
实验性的:VDD
VELCADE, liposomal doxorubicin, dexamethasone
|
1.3 mg/m2 by IV on days 1, 4, 8, 11 of each cycle
20 mg the day before and the day after receiving VELCADE
At least one asprin 81 mg per day.
Other option per physician's choice
40 mg by mouth on days 1-4, 8-11, and 15-18 of cycle 1 and days 1-4 on cycle 2-4
30 mg/m2 on day 4 of each cycle
|
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 |
|---|---|---|
|
The Percent of Patients With Minimal Residual Disease (MRD) Status Changing to Negative at Day 100 (Post-AHCT), Among Patients With MRD Positive at the End of Induction (EOI).
大体时间:6-months post ASCT
|
Patients were treated with induction therapy (VRD) followed by autologous hematopoietic cell transplant (AHCT).
MRD status of a patient with at least partial response was evaluated at the end of induction (EOI) and day 100 (post-AHCT).
MRD of a patient is measured by seven-color flow cytometry.
|
6-months post ASCT
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Progression Free Survival by MRD Status at Day 100.
大体时间:up to 7 years
|
Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
|
up to 7 years
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2010年11月1日
初级完成 (实际的)
2015年11月1日
研究完成 (实际的)
2018年3月1日
研究注册日期
首次提交
2010年10月4日
首先提交符合 QC 标准的
2010年10月5日
首次发布 (估计)
2010年10月6日
研究记录更新
最后更新发布 (实际的)
2018年5月15日
上次提交的符合 QC 标准的更新
2018年4月15日
最后验证
2018年4月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
- 病理过程
- 心血管疾病
- 血管疾病
- 免疫系统疾病
- 组织学类型的肿瘤
- 肿瘤
- 淋巴增生性疾病
- 免疫增生性疾病
- 血液病
- 出血性疾病
- 止血障碍
- 副蛋白血症
- 血液蛋白失调
- 肿瘤过程
- 多发性骨髓瘤
- 肿瘤,浆细胞
- 肿瘤,残留
- 药物的生理作用
- 药理作用的分子机制
- 自主代理
- 周围神经系统药物
- 酶抑制剂
- 抗炎药
- 抗肿瘤药
- 免疫因素
- 止吐药
- 胃肠道药物
- 糖皮质激素
- 荷尔蒙
- 激素、激素替代品和激素拮抗剂
- 抗肿瘤药,激素
- 蛋白酶抑制剂
- 拓扑异构酶 II 抑制剂
- 拓扑异构酶抑制剂
- 血管生成抑制剂
- 血管生成调节剂
- 生长物质
- 生长抑制剂
- 抗生素、抗肿瘤药
- 骨密度保护剂
- 地塞米松
- 醋酸地塞米松
- BB 1101
- 来那度胺
- 硼替佐米
- 阿霉素
- 脂质体阿霉素
- 双膦酸盐
其他研究编号
- VICC BMT 1020
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.