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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2024-00288 | Registry Identifier | CTRP (Clinical Trial Reporting Program) | |
| 23-007468 | Other Identifier | Mayo Clinic Institutional Review Board |
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Lack of funding
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This study evaluates the relationship between alterations in the GI microbiome and GI inflammation on symptom burden in women with breast cancer receiving chemotherapy.
PRIMARY OBJECTIVES:
I. To describe changes in GI inflammation and the GI microbiome profile in women with breast cancer throughout chemotherapy.
II. To examine how GI inflammation and GI microbiome changes influence symptom experience is used above in women with breast cancer receiving chemotherapy.
III. To examine associations between microbial composition functional profiles at T1 and T2, T3 as well as T4 in patients who report symptom severity in neuropsychological and GI symptoms at the last three timepoints.
IV. To evaluate for differentially abundant metabolites and perturbed metabolic pathways associated with microbiome diversity in patients who do and do not report neuropsychological and GI symptom occurrence at T2, T3 and T4.
OUTLINE: This is an observational study.
Patients undergo stool and blood sample collection, complete questionnaires, and have their medical records reviewed on study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Observational | Patients undergo stool and blood sample collection, complete questionnaires, and have their medical records reviewed on study. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Non-Interventional Study | Other | Non-interventional study |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in GI microbiome profile | To examine longitudinal change in the GI microbiome, the coefficient of variation (CV) of alpha-diversity values will be calculated for stool samples. The CV represents the ratio of the standard deviation to the mean. A low CV indicates that an individual has relatively stable microbial diversity over time and a high CV indicates that an individual has higher microbial diversity over time. | Up to 1 month after chemotherapy treatment completion |
| Change in GI inflammation | GI Inflammation will be quantified through measures of fecal calprotectin to indicate low, medium and high concentrations of bowel inflammation. | Up to 1 month after chemotherapy treatment completion |
| Symptom burden - MSAS | Symptom burden will be measured with a modified version of the Memorial Symptom Assessment Scale (MSAS). The modified MSAS includes 41 symptom items, including 19 GI symptoms. Participants are asked to review the list of symptoms and indicate which had been present in the last week. For each symptom present, participants are asked to rate its duration, severity, and distress. | Up to 1 month after chemotherapy treatment completion |
| Symptom burden - MASCC-MAT | Symptom burden will be measured with the Multinational Association of Supportive Care in Cancer-Antiemesis Tool (MASCC-MAT). The MASCC-MAT assesses acute (i.e., within 24 hours post-chemotherapy) and delayed (i.e., after 24 hours and up to 7 days post-chemotherapy) occurrence of chemotherapy-induced nausea (CIN). | Up to 1 month after chemotherapy treatment completion |
| Symptom burden - LFS | Symptom burden will be measured with the Lee Fatigue Scale (LFS). The LFS consists of 18 items related to fatigue and energy. Scores range from 0-180 with higher scores indicating higher levels of fatigue. |
| Measure | Description | Time Frame |
|---|---|---|
| Associations between microbial composition functional profiles and symptom severity | In patients who report symptom severity in neuropsychological and GI symptoms for at least three timepoints, stool samples will be tested to find distinct diversity and abundance changes between timepoints that are associated with symptom occurrence. | Up to 1 month after chemotherapy treatment completion |
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Inclusion Criteria:
Exclusion Criteria:
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Women with newly diagnosed stage I-III breast cancer recruited from the outpatient breast cancer clinic at University of Iowa Hospital and Clinics and at Mayo Clinic in Rochester and Mayo Clinic in Arizona.
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| Name | Affiliation | Role |
|---|---|---|
| Komal P. Singh, PhD, RN | Mayo Clinic | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic in Arizona | Scottsdale | Arizona | 85259 | United States | ||
| Mayo Clinic in Rochester |
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| Label | URL |
|---|---|
| Mayo Clinic Clinical Trials | View source |
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| Up to 1 month after chemotherapy treatment completion |
| Change in metabolite abundance | In patients who do and do not report neuropsychological and GI symptom occurrence for at least three timepoints, stool samples and blood samples will be evaluated using liquid chromatography-tandem mass spectrometry (LC-MS/MS) to evaluate for change in metabolite abundance and associations between bacterial composition and metabolic profiles. | Up to 1 month after chemotherapy treatment completion |
| Rochester |
| Minnesota |
| 55905 |
| United States |