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Houston, Texas 77030


Purpose:

The goal of this clinical research study is to learn about possible weight, muscle, and/or fat loss in patients receiving cabozantinib or lenvatinib.


Study summary:

Baseline Visit: If you agree to take part in this study, you will have the following tests and procedures at a baseline visit within 10 days after starting either cabozantinib or lenvatinib: - Your height, weight, waist, and hips will be measured. - You will have basic tests of your physical strength and balance. Your hand grip strength will be measured, you will be asked to rise from a chair without using your arms to push off, and you will complete a 6-minute walk test. - You will have a full-body dual-energy x-ray absorptiometry (DXA) scan to measure the amount of fat and muscle in your body. Images from a standard computed tomography (CT) scan will also be collected and reviewed for this purpose. If you are scheduled only for a chest CT scan as part of your regular care, your abdomen will also be scanned at the same time for research purposes. - You will meet with a dietician to talk about your current and past eating habits. - You will fill out questionnaires about any pain or other symptoms you may have had; about any gastrointestinal (GI) side effects you may be having before you start chemotherapy; about the amount of physical exercise and activity you get; and about your food intake over the last 24 hours. Together the questionnaires should take about 20-25 minutes to complete. You will be receiving cabozantinib or lenvatinib as part of your standard of care. Study Visits: After the baseline visit, you will have study visits on the following schedule. Some of these visits will be at the same time as your scheduled clinic visits with your regular doctor. However, some assessments will be done in between clinic visits online or by phone. Month 1 and 2: One (1) time every 2 weeks (+/- 1 week) during Months 1 and 2, you will fill out 3 questionnaires at home: - You will be asked about any gastrointestinal (GI) and other side effects you may be having. This will be done by phone and should take about 5-10 minutes. - You will fill out an online questionnaire at home about your eating habits over the last 24 hours. If you do not have internet access, you will complete the questionnaire over the phone with a member of the study staff. This should take about 10 minutes. - You will complete a questionnaire about any symptoms you may be having online or by phone. This should take about 5-8 minutes. At Months 3, 6, and 12 (± 4 weeks) you will come to the clinic: - Your height, weight, waist, and hips will be measured. - You will have the same tests of your physical strength and balance that you had at the baseline visit. - You will complete the same questionnaires you completed at the baseline visit. These will be done on paper or on a computer or tablet. - You will have a DXA scan to measure the amount of fat and muscle in your body. - If you are having certain GI side effects (such as diarrhea, nausea, vomiting, mouth sores, and so on), the study doctor will talk with you about receiving standard drugs to help with those side effects. You may ask the study staff for information about how the drugs are given and their risks. You may also meet with a dietician, who may recommend ways to help improve some side effects. Between clinic visits: °Two (2) times per month (+/- 1 week) between Months 3 and 6, and once a month (+/- 1 week) between Months 6 and 12, you will complete 3 questionnaires at home about your food intake over the past 24 hours; any symptoms you may be having; and any GI or other side effects you may be having. The questionnaires may be completed online or by phone and together should take about 20 minutes. Length of Study Participation: Your participation in this study will be over after the Month 12 visit. This is an investigational study. Up to 25 patients will take part in this study. All will be enrolled at MD Anderson.


Criteria:

Inclusion Criteria: 1. Age >/= 18 years 2. Initiating cabozantinib for progressive DTC, MTC, malignant PH or PGs or lenvatinib for progressive DTC or MTC as determined by patient's endocrinologist 3. ECOG performance status 0-2 4. Able to communicate in English or Spanish 5. Able to provide informed consent Exclusion Criteria: 1. Active participation in any weight reduction program including use of drugs used for weight loss 2. Inability to ambulate without assistance (e.g. cane, walker) 3. Multiple Endocrine Neoplasia (MEN) 2B (due to differences in body habitus) 4. Patients unwilling or unable to comply with the protocol. 5. Use of chronic (>3 months consecutively) non-physiological (15 mg/m² hydrocortisone equivalent) doses of glucocorticoids 6. Non-English speaking PH and PG patients


NCT ID:

NCT02592356


Primary Contact:

Principal Investigator
Naifa L. Busaidy, MD
M.D. Anderson Cancer Center


Backup Contact:

N/A


Location Contact:

Houston, Texas 77030
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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