Symptom Burden in Head and Neck Cancer
A Study of Reducing the Symptom Burden Produced by Chemoradiation Treatment for Head and Neck Cancer
研究概览
详细说明
The Study Drugs:
It is not known which study drug or combination of study drugs is better at reducing side effects patients may experience during chemoradiation therapy. For this reason, researchers have chosen 3 study drugs that may help to reduce side effects such as fatigue, pain, sleep disturbance, difficulty swallowing, and lack of appetite. The study drugs will be tested alone and in combination with each other.
- Armodafinil is designed to prevent excessive sleepiness.
- Bupropion and minocycline each may reduce inflammation, which may help to reduce other symptoms. Bupropion is a drug for depression. Minocycline is an antibiotic (a drug to treat infection).
Study Groups:
If you agree to take part in this study, you will be randomly assigned (as in the roll of dice) to 1 of 8 groups. You may be assigned to receive no study drugs, 1 study drug, a combination of 2, or all 3 of the study drugs.
During this study, you may receive 1 or more placebos. A placebo looks like the study drug(s) but has no active ingredients. There is a chance that you will be in a group that does not receive any study drugs at all. The study drugs are being tested to learn if they can help control symptoms. All participants will be able to receive standard care for head and neck cancer outside of the study.
Neither you nor the study staff will know if you are receiving the study drugs and/or the placebo(s). However, if needed for your safety, the study staff will be able to find out which study drug(s) you are receiving.
Study Drug Administration:
You will take the study drugs/placebos 2 times every day for up to 10 weeks. You will take 1 or more study drug(s) or placebos by mouth each time, as instructed by the study doctor. If you have trouble swallowing the study drugs/placebos, they can be crushed just before taking them. You will be given information sheets on how to take the study drugs/placebos.
You will be given a daily diary to write down when you take the study drugs/placebos. You should bring your study drugs/placebos to the clinic to every study visit. You should also bring your diary to every study visit.
Symptom Questionnaire:
Throughout the study, you will be asked to fill out a symptom questionnaire. You will be asked about symptoms you may be experiencing and how they may be interfering with your daily activities. When you are in the clinic, the questionnaire can be completed by paper and pen with the study staff or by entering your answers into a computer. When you are away from the clinic, the questionnaire may be completed either through a phone call with the study staff or through a phone call from the interactive voice response (IVR) system. The symptom questionnaire will take up to 5 minutes each time. The study staff will give you the information you need to complete the questionnaire through the IVR system.
During Weeks 1-10, you will complete the symptom questionnaire 2 times a week. During Weeks 11-16, you will complete the symptom questionnaire 1 time a week.
If you would like, you can fill out a paper version of the questionnaire instead of using the phone system.
Study Visits:
Before you begin chemoradiation:
- You will fill out 6 questionnaires about pain and other symptoms, your mood, your tobacco and alcohol use, and the quality of your life. This should take about 15 minutes.
- You will have a blood coagulation test, called PT-INR, to make sure your blood clots normally.
- If you are a woman who is able to become pregnant, you will have a urine pregnancy test. The study staff will give you the pregnancy test kit at your scheduled visit, and will review and record the results of the test before your study prescriptions are filled by the pharmacy. This will also be done at about Weeks 4 and 7, at the first follow-up visit after radiation treatment, and 30 days after the study drugs are stopped.
At about Week 4 of chemoradiation:
- You will fill out 1 quality-of-life questionnaire. This should take about 2-3 minutes.
- You will be asked three questions about smoking after the start of chemoradiation therapy.
- You will have a blood coagulation test, called PT-INR, to make sure your blood clots normally.
During the last week of chemoradiation (about Week 7):
-You will fill out 3 questionnaires about your symptoms, mood, and quality of life. This should take about 10 minutes.
After about Week 7, the study staff will call you 2 times per week to check on you until Week 10. This phone call should last only a few minutes. If you have experienced several side effects from chemoradiation, this phone call may take longer.
At about Week 10 and at your first follow-up visit after your chemoradiation treatment:
- You will fill out 3 questionnaires about your symptoms, mood, and quality of life.
- You will fill out 2 questionnaires that ask about your smoking history and changes in your tobacco use during the study. This will take a few minutes.
- You will be asked to fill out another questionnaire that asks about your satisfaction with the study drug(s). For example, you will be asked if you thought the study drugs helped to control the symptoms, if you would recommend the study drugs to other patients, and if you had problems taking the study drugs. This will take a few minutes.
- In addition, at your first follow-up visit after your chemoradiation treatment, you will have a blood coagulation test, called PT INR, to make sure your blood clots normally.
Length of Study:
You will take the study drug(s)/placebo for up to 10 weeks, if the doctor thinks it is in your best interest. You will fill out the symptom questionnaires by phone until 16 weeks. You will no longer be able to take the study drug(s)/placebo if you experience intolerable side effects.
This is an investigational study. Armodafinil is FDA approved and commercially available for the treatment of excessive sleepiness. Bupropion is FDA approved and commercially available for the treatment of depression. Minocycline is FDA approved and commercially available for the treatment of bacterial infection. The different possible combinations of these drugs being used in this study are investigational.
Up to 32 patients will take part in this study. All will be enrolled at MD Anderson.
研究类型
注册 (实际的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习地点
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Texas
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Houston、Texas、美国、77030
- UT MD Anderson Cancer Center
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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:
- Patients with a pathologically proven diagnosis of epithelial carcinoma of the oropharynx, nasopharynx, hypopharynx, larynx, or oral cavity being treated at MDACC.
- Patients >/= 18 years old and </= 65 years old.
- Patients with the above cancers scheduled to receive definitive concurrent chemoradiation over 6 - 7 weeks.
- Patients who speak English (due to the novel research and its complexity, we are only accruing English speaking patients to the protocol)
- Patients must agree to discontinue any current herbal supplement use, and refrain from taking any herbal supplement while on protocol.
- Patients must be willing and able to review, understand, and provide written consent.
- Women of childbearing potential (women who are not postmenopausal for at least one year and are not surgically sterile) must have negative urine pregnancy test..
- Sexually active males and females must agree to use birth control or abstinence for the duration of the trial.
Exclusion Criteria:
- Patients who are taking medications or have conditions that potentially preclude use of any study medications or interventions as determined by the treating physician
- Patients taking CHANTIX (smoking cessation medication)
- Patients who are enrolled in other symptom management trial or receiving active therapy as part of a treatment clinical trial.
- Bile duct obstruction or cholelithiasis
- History of clinically significant cutaneous drug reaction, or a history of clinically significant hypersensitivity reaction, including multiple allergies or drug reaction
- Pre-existing psychosis or bipolar disorder. Patients with major depressive disorder or severe depression (a score of 13 or greater on the BDI Fast Screen (BDI-FS) will be excluded. If this is the case, we will notify their treating physician for appropriate management or referral.
- Pre-existing renal impairment: The screening cut off for serum creatinine > the upper limit of normal, will be done by the oncologist to qualify for chemoradiation.
- Pre-existing hepatic impairment: The screening for total bilirubin > 1.5 times the upper limit of normal will be done by the oncologist to qualify for chemoradiation. The screening for >2 times the upper limit of normal hepatotoxicity: Alkaline phosphatase (ALP) and Alanine aminotransferase (ALT) will be done by the oncologist to qualify for chemoradiation.The screening results for Aspartate aminotransferase (AST) must be < 2 times the upper limit of normal if available in the medical records.
- Pre-existing Tourette's syndrome
- Seizure disorder
- Anorexia/bulimia in past two months
- Use of monoamine oxidase (MAO inhibitors) within 14 days
- Patients undergoing abrupt discontinuation of ethanol or sedatives (including benzodiazepines)
- Patients currently taking any of the study drugs
- Hypersensitivity to any tetracyclines
- Patients on anticoagulants (ie warfarin/heparin)
- Patients with INR > 1.5.
- Patients being treated with concurrent cetuximab chemotherapy with radiation therapy.
- Patients currently receiving any tetracycline family antibiotic or within the previous past 14 days before chemoradiation.
- Previous radiation therapy for a cancer in the head and neck region.
- Patients with a history of cardiac disease, including angina and cardiac ischemia, left ventricular hypertrophy, myocardial infarction, and mitral valve prolapse.
- Patients taking antifungals, antiretrovirals, and macrolides that are strong CYP3A4 strong inhibitors including indinavir, nelfinavir, ritonavir, clarithromycin, itraconazole, ketoconazole, and nefazodone.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
---|---|
安慰剂比较:Placebo
Placebo by mouth 2 times every day.
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1 by mouth twice a day.
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实验性的:Armodafinil
Armodafinil 150 mg by mouth once a day.
|
150 mg by mouth once a day.
其他名称:
|
实验性的:Minocycline
Minocycline 100 mg by muth two times a day.
|
100 mg by mouth twice a day.
其他名称:
|
实验性的:Bupropion
Bupropion 100 mg by mouth two times a day.
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100 mg by mouth twice a day.
其他名称:
|
实验性的:Armodafinil + Minocycline
Armodafinil 150 mg by mouth once a day. Minocycline 100 mg by mouth two times a day. |
150 mg by mouth once a day.
其他名称:
100 mg by mouth twice a day.
其他名称:
|
实验性的:Armodafinil + Bupropion
Armodafinil 150 mg by mouth once a day. Bupropion 100 mg by mouth two times a day. |
150 mg by mouth once a day.
其他名称:
100 mg by mouth twice a day.
其他名称:
|
实验性的:Minocycline + Bupropion
Minocycline 100 mg by muth two times a day. Bupropion 100 mg by mouth two times a day. |
100 mg by mouth twice a day.
其他名称:
100 mg by mouth twice a day.
其他名称:
|
实验性的:Armodafinil + Minocycline + Bupropion
Armodafinil 150 mg by mouth once a day. Minocycline 100 mg by muth two times a day. Bupropion 100 mg by mouth two times a day. |
150 mg by mouth once a day.
其他名称:
100 mg by mouth twice a day.
其他名称:
100 mg by mouth twice a day.
其他名称:
|
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 |
---|---|---|
Treatment Effects on 5 Selected Symptoms (Average MDASI-HNC Scores)
大体时间:10 weeks
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Treatments ability to reduce values of 5 symptoms comprised of MD Anderson Symptom Inventory (MDASI)-Head and Neck Cancer (HNC) scores for fatigue, difficulty swallowing, sleep disturbance, pain, and lack of appetite collected during the 10 weeks of chemoradiation treatment.
symptoms that are caused by their disease or by their treatment.
Symptom severity score is comprised of average of the five above MDASI core items (fatigue, difficulty swallowing, sleep disturbance, pain, and lack of appetite).
Participants were asked to rate severity of each symptom at their worst in last 24 hours; each item rated from 0 to 10, with 0 = symptom not present and 10 = as bad as you can imagine.
Total average score range: 0 to 10. Lower scores indicated better outcome.
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10 weeks
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合作者和调查者
调查人员
- 首席研究员:David I. Rosenthal, MD, MA, BA、UT MD Anderson Cancer Center
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
关键字
其他相关的 MeSH 术语
其他研究编号
- 2009-0517
- R01 026582-26 (其他赠款/资助编号:National Cancer Institute)
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.
Placebo的临床试验
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City of Hope Medical CenterNational Cancer Institute (NCI)主动,不招人造血和淋巴细胞肿瘤 | 骨髓纤维化 | 慢性淋巴细胞白血病 | 缓解期成人急性髓性白血病 | 骨髓增生异常综合症 | 缓解期成人急性淋巴细胞白血病 | 骨髓增殖性肿瘤 | 慢性期慢性粒细胞白血病,BCR-ABL1 阳性 | 成人淋巴母细胞淋巴瘤 | 加速期慢性粒细胞白血病,BCR-ABL1 阳性 | HLA-A*0201 阳性细胞存在 | 巨细胞病毒感染 | 成人霍奇金淋巴瘤 | 成人非霍奇金淋巴瘤美国
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Mila (bMotion Technologies)完全的
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Universidad Autonoma de MadridCentro Universitario La Salle完全的