Effect of Cabozantinib S-Malate or Lenvatinib Mesylate on Weight and Body Composition in Patients With Metastatic Endocrine Cancer

Thyroid Gland Medullary Carcinoma Clinical Trial

Official title:

Effects of Tyrosine Kinase Inhibitors on Body Composition in Endocrine Tumors -- A Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02592356
• Other study ID #: 2014-0864
• Secondary ID: NCI-2015-0205820
• Status: Completed
• Phase: N/A
• Start date: November 16, 2015
• Est. completion date: March 1, 2024

Study information

• Verified date: March 2024
• Source: M.D. Anderson Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 23
• Est. completion date: March 1, 2024
• Est. primary completion date: March 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age >/= 18 years
• Initiating cabozantinib for progressive DTC, MTC, malignant PH or PGs or lenvatinib for progressive DTC or MTC as determined by patient's endocrinologist
• ECOG performance status 0-2
• Able to communicate in English or Spanish
• Able to provide informed consent

Exclusion Criteria:

• Active participation in any weight reduction program including use of drugs used for weight loss
• Inability to ambulate without assistance (e.g. cane, walker)
• Multiple Endocrine Neoplasia (MEN) 2B (due to differences in body habitus)
• Patients unwilling or unable to comply with the protocol.
• Use of chronic (>3 months consecutively) non-physiological (15 mg/m² hydrocortisone equivalent) doses of glucocorticoids
• Non-English speaking PH and PG patients

Related Conditions & MeSH terms

• Carcinoma
• Differentiated Thyroid Gland Carcinoma
• Malignant Adrenal Gland Pheochromocytoma
• Malignant Paraganglioma
• Paraganglioma
• Pheochromocytoma
• Thyroid Diseases
• Thyroid Gland Medullary Carcinoma
• Thyroid Neoplasms

Intervention

Procedure:
• Computed Tomography
Correlative studies
• Dual X-ray Absorptiometry
Correlative studies
• Physical Examination
Correlative studies

Other:
• Quality-of-Life Assessment
Ancillary studies
• Questionnaire Administration
Ancillary studies

Drug:
• Cabozantinib

• Lenvatinib

Locations

Country	Name	City	State
United States	M D Anderson Cancer Center	Houston	Texas

Sponsors (2)

Lead Sponsor	Collaborator
M.D. Anderson Cancer Center	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Tumor response	Summary descriptive statistics, including proportions, medians, means, 95% confidence intervals, and other simple statistics will be provided for demographics, tumor response rates and blood markers. 95% CI will be reported for the accuracy of DXA compared to CT. The correlation between change of weight/body composition and tumor response will be investigated by logistic regression.	Up to 12 months
Other	Quality of life change	Summary descriptive statistics, including proportions, medians, means, 95% confidence intervals, and other simple statistics will be provided for demographics, tumor response rates and blood markers. 95% CI will be reported for the accuracy of DXA compared to CT. The correlation between change of weight/body composition and tumor response will be investigated by logistic regression.	Baseline to up to 12 months
Primary	Change in weight among patients who have no gastrointestinal (GI) adverse events (AEs) or have =< grade 1 symptoms and those with grade 2 or above AEs, according to the National Cancer Institute Common Toxicity Criteria version 4.0	2-sided paired t-test will be used to measure weight change after successful intervention of diarrhea and anorexia. Linear mixed-effects model will be used to explore the longitudinal weight changes. Summary descriptive statistics, including proportions, medians, means, 95% confidence intervals, and other simple statistics will be provided for demographics, gastrointestinal adverse events, body composition changes and blood markers. 95% confidence intervals (CI) will be reported for the accuracy of DXA compared to computed tomography CT. The correlation between change of weight/body composition and tumor response will be investigated by logistic regression.	Baseline to up to 6 months
Secondary	Change in weight in patients with metastatic endocrine tumors during active intervention to control diarrhea and anorexia	Summary descriptive statistics, including proportions, medians, means, 95% confidence intervals, and other simple statistics will be provided for demographics, body composition changes and blood markers. 95% CI will be reported for the accuracy of DXA compared to CT. The correlation between change of weight/body composition and tumor response will be investigated by logistic regression.	Baseline to up to 12 months
Secondary	Change in adipose tissue in patients with metastatic endocrine tumors during active intervention to control diarrhea and anorexia	Summary descriptive statistics, including proportions, medians, means, 95% confidence intervals, and other simple statistics will be provided for demographics, body composition changes and blood markers. 95% CI will be reported for the accuracy of DXA compared to CT. The correlation between change of weight/body composition and tumor response will be investigated by logistic regression.	Baseline to up to 12 months
Secondary	Change in skeletal muscle in patients with metastatic endocrine tumors during active intervention to control diarrhea and anorexia	Summary descriptive statistics, including proportions, medians, means, 95% confidence intervals, and other simple statistics will be provided for demographics, body composition changes and blood markers. 95% CI will be reported for the accuracy of DXA compared to CT. The correlation between change of weight/body composition and tumor response will be investigated by logistic regression.	Baseline to up to 12 months

External Links

•   University of Texas MD Anderson Cancer Center Website