Cetuximab and Lenalidomide in Head and Neck
Phase II Study of Cetuximab and Lenalidomide in Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck
研究概览
详细说明
To study specific FcRIIIa polymorphisms and their correlation with clinical outcome in subjects treated with cetuximab and lenalidomide. There is evidence with cetuximab in CRC, trastuzumab in breast cancer and rituximab with follicular lymphoma, that FcRIIIa polymorphisms correlate with clinical response to antibody therapy and clinical outcome. It is our hypothesis that patients with SCCHN will have clinical outcomes to cetuximab and lenalidomide that correlate with patient FcRIIIa genotype.
Secondary:
To evaluate the safety and toxicity profile of the combination of cetuximab and lenalidomide given to treat subjects with SCCHN.
To study FcRIIIa polymorphisms and the correlation with the ability of NK cells to mediate ADCC against SCCHN. It is our hypothesis that NK cells from patients with advanced SCCHN can mediate ADCC against SCCHN cell lines in the presence of cetuximab and lenalidomide and that the efficiency of ADCC correlates with FcRIIIa polymorphisms.
To evaluate the ability of NK cells to induce ADCC expression of specific activation markers on the NK cell surface. It is our hypothesis that NK cells that induce ADCC will express specific activation markers that are predictive of efficiency of ADCC.
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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Illinois
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Chicago、Illinois、美国、60637
- The University of Chicago
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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:
- Understand and voluntarily sign an informed consent form.
- Age ≥18 years at the time of signing the informed consent form.
- Able to adhere to the study visit schedule and other protocol requirements.
- Recurrent or metastatic squamous cell or undifferentiated carcinoma of the head and neck that is not amenable to curative therapy. Patients who are candidates for local or locoregional therapy should not be deprived of proven beneficial palliative therapies.
- All previous cancer therapy, including radiation, hormonal therapy, EGFR inhibitors, and surgery, must have been discontinued at least 4 weeks prior to treatment in this study.
- ECOG performance status of 0-1 at study entry.
Laboratory test results within these ranges:
- Absolute neutrophil count to ≥ 1000/mm³
- Platelet count ≥ 100,000/mm³
- Calculated creatinine clearance ≥ 50ml/min by Cockcroft-Gault estimation
- Total bilirubin < 1.5 x ULN
- AST (SGOT) and ALT (SGPT) < 3 x ULN or < 5 x ULN if hepatic metastases are present.
- Disease free of prior malignancies for < 3 years with exception of currently treated basal cell, squamous cell carcinoma of the skin, or carcinoma "in-situ" of the cervix or breast. Patients with malignancies diagnosed less than 3 years prior to study entry are eligible if the first cancer was no greater than stage I and did not recur. Patients with malignancies diagnosed less than 3 years prior to study entry must have the diagnosis of recurrent or metastatic squamous cell carcinoma of the head and neck confirmed pathologically.
- All study participants must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist®.
- Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days prior to and again within 24 hours of prescribing lenalidomide (prescriptions must be filled within 7 days) and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy. See Appendix: Risks of Fetal Exposure, Pregnancy Testing Guidelines and Acceptable Birth Control Methods.
- Able to take aspirin (81 or 325 mg) daily as prophylactic anticoagulation (patients intolerant to ASA may use warfarin or low molecular weight heparin).
- Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded), with minimum lesion size ≥ 2 cm on conventional measurement techniques or ≥ 1 cm on spiral computed tomography (CT) scan. Lesions that can be measured clinically must be at least 1 cm in greatest dimension by caliper measurement.
Exclusion Criteria:
- Primary head and neck carcinomas of the salivary gland, skin, or thyroid regardless of pathology
- Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the informed consent form.
- Pregnant or breast feeding females. (Lactating females must agree not to breast feed while taking lenalidomide).
- Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study.
- Use of any other experimental drug or therapy within 28 days of baseline.
- Prior therapy with lenalidomide for squamous cell carcinoma of the head and neck
- Known hypersensitivity to thalidomide.
- The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs.
- Concurrent use of other anti-cancer agents or treatments.
- Known positive for HIV or infectious hepatitis, type B or C.
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:Sub Group 1
All Subjects Enrolled in the Trial
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The treatment of Head and Neck Cancer with Cetuximab and Lenalidomide
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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 |
|---|---|---|
|
Correlate the Presence of Specific Fc RIIIa Polymorphisms With Progression-free Survival in Subjects Receiving Cetuximab and Lenalidomide for SCCHN.
大体时间:24 months
|
Progression-free survival (PFS) was defined as time from date of the first treatment dose administered to the earlier of disease progression or death from any cause.
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.
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24 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Number of Participants With Fatigue Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Maculopapular Rash Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Constipation Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Anemia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Anorexia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Nausea Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Hypoalbuminemia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Lymphopenia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Oral Mucositis Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Pain Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Vomiting Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With White Blood Cell Decreased Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Diarrhea Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Hyponatremia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Neutropenia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Headache Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Hypokalemia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Hypophosphatemia Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Thrombocytopenia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Acneiform Rash Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Hyperglycemia Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Alkaline Phosphatase Increased Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Aspartate Aminotransferase Increased Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Xerostomia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 3
|
24 months
|
|
Number of Participants With Fever Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Hypocalcaemia Related to Cetuximab/Lenalidomide
大体时间:24 months
|
Toxicity was scored according to NCI/CTC version 4
|
24 months
|
|
Number of Participants With Neck Pain Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Peripheral Sensory Neuropathy Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Alanine Aminotransferase Increased Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Back Pain Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Dyspnea Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Weight Loss Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Blood Bilirubin Increased Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Infusion Related Reaction Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With C. Diff Infection Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Febrile Neutropenia Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
|
Number of Participants With Lymphocyte Count Increased Related to Cetuximab/Lenalidomide
大体时间:24 month
|
Toxicity was scored according to NCI/CTC version 4
|
24 month
|
合作者和调查者
出版物和有用的链接
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 (估计)
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
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