The Gut Microbiome and Immunotherapy Response in Solid Cancers

Cancer Clinical Trial

Official title:

The Gut Microbiome and Immunotherapy Response in Solid Cancers

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06050733
• Other study ID #: 23-0028
• Status: Recruiting
• Start date: June 30, 2023
• Est. completion date: June 30, 2024

Study information

• Verified date: January 2024
• Source: The University of Texas Medical Branch, Galveston
• Contact: Kristen McGovern, PhD
• Phone: 409-772-8126
• Email: kamcgove[@]utmb.edu
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The aim of this study is characterize the gastrointestinal microbiomes of patient with solid cancer undergoing standard of care treatment with programmed cell death protein 1 (PD-1) /programmed cell death ligand (PD-L1) blockade.

Description:

Frontline treatment for solid cancers such as renal cell carcinoma includes immunotherapies such as immune checkpoint inhibitor (ICI) therapy. Despite an increase in overall survival in cancer patients undergoing ICI therapy, many patients' tumors are unresponsive or eventually progress. Recent studies indicate that the gut microbiome composition is associated with clinical response to ICI treatment. Following the success of preclinical research, two recent studies investigated the efficacy of fecal microbiota transplant (FMT) from cancer patients responsive to programmed cell-death protein 1 (PD-1) blockade, a type of ICI treatment, to patients nonresponsive to treatment. Notably, 30-40% of the FMT recipients in these studies subsequently responded to anti-PD-1 therapy. However, the effectiveness of FMT may vary among donors, there is no clear agreement on the ideal FMT composition, and FMT carries the risk of transmitting infection. An alternative to FMT is identification of specific efficacious commensals for supplementation. While the specific commensals enriched in cancer patients with more favorable outcomes vary from study to study, several are commonly reported, including Akkermansia muciniphila, Bacteroides spp., Bifidobacterium spp., Ruminococcaceae spp., and Faecalibacterium spp. Cancer-related fatigue is experienced by nearly all patients during treatment, and cancer-related cognitive impairment (CRCI), which is a decrease in neurocognitive functioning that can be caused by cancer or its treatment, is present in up to ¾ of patients during treatment. Fatigue and CRCI have both been linked to the composition of the gut microbiome in cancer patients. Specific Aims Specific Aim 1: Characterize the gut microbiome of solid cancer patients that have had disease progression during standard-of-care treatment with PD-1 or programmed cell death ligand 1 (PD-L1) blockade and compare to solid cancer patients that were stable or experienced tumor shrinkage during standard-of-care treatment with PD-1/PD-L1 blockade. Specific Aim 2: Assess neuropsychological measures of cognition and fatigue in solid cancer patients undergoing standard-of-care treatment with PD-1/PD-L1 blockade and determine associations with composition of the gut microbiome.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 16
• Est. completion date: June 30, 2024
• Est. primary completion date: June 30, 2024
• Gender: All
• Age group: 35 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Current diagnosis of malignant solid cancer that is nonresectable or metastatic.

2. Ages 35 to 75 years.

3. Treatment with immunotherapy, specifically programmed cell death protein 1 (PD-1) or programmed cell death ligand 1 (PD-L1) inhibitor, for at least 3 months but less than 24 months (except for previously responsive subjects re-enrolling as non-responsive patients).

4. Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 guidelines.

5. Participant is willing and able to give informed consent for participation in the study

Exclusion Criteria:

1. Significant heart, liver, blood or respiratory disease.

2. Current diagnosis of HIV, Hepatitis B or Hepatitis C.

3. History of heart disease.

4. Uncontrolled diabetes mellitus.

5. Subjects with a history of inflammatory bowel disease, Celiac disease or active diverticular disease.

6. Females who are pregnant or lactating.

7. Treatment with chemotherapy within the past 2 years.

8. Treatment with kinase inhibitors within the past 3 months.

9. Previous radiation therapy for brain metastases.

10. Other medical condition or medication administration deemed exclusionary by the study investigators.

Related Conditions & MeSH terms

• Cancer

Locations

Country	Name	City	State
United States	University of Texas Medical Branch	Galveston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
The University of Texas Medical Branch, Galveston

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Characterization of fecal microbiome using molecular methods	Characterization of the fecal microbiome using a commercially available sampling kit and our lab's patented array for PCR.	baseline
Secondary	Cognitive Function as measured by Montreal Cognitive Assessment	The Montreal Cognitive Assessment (MoCA) will be used to assess cognition.; The Montreal Cognitive Assessment (MoCA) is a rapid assessment of cognition. The MoCA consists of 9 questions with the following subcategories: visuospatial/executive, naming, memory, language, abstraction, delayed recall and orientation. The MoCA has been used extensively to detect cognitive impairment in many conditions, including head trauma. Version 7.1 will be used. Scores range from 0 to 30, higher score being a better outcome.	baseline
Secondary	Fatigue as measured by the Multidimensional Fatigue Symptom Inventory	Multidimensional Fatigue Symptom Inventory Short Form (MFSI-SF) from the Moffitt Cancer Center, University of South Florida The MFSI-SF is a 30 question assessment designed to assess the principal manifestations of fatigue.; There 5 subscales used to calculate a total score. The subscales are: General Fatigue, Physical Fatigue, Emotional Fatigue, Mental Fatigue, and Vigor (an estimate of the patient's energy level). The total score is calculated with the equation: (general + physical + emotional + mental) - vigor = total score.; The range of the total score is -24 to 96, with the higher the number meaning more fatigue.	baseline
Secondary	Fatigue and Cognition as measured by the Fatigue and Altered Cognition Scale	The Fatigue and Altered Cognition Scale (FACS) is a joint project from University of Texas Medical Branch and Texas A&M University. The FACS is a 20 question assessment designed to access perceived fatigue and cognition.; There are 2 subscales used to calculate a total score. The subscales are: Fatigue and Altered Cognition. The total score is calculated by adding the subscales together. The range of the total score is 0-100, with a higher score indicating more fatigue and altered cognition.	baseline
Secondary	Gastrointestinal Health measured by the Gastrointestinal Symptom Rating Scale	The Gastrointestinal Symptom Rating Scale (GSRS) is a specific 15-item questionnaire. Subjects are asked to numerically score their subjective symptoms on a scale of 1-7 (1 = no discomfort at all; 7 = very severe discomfort) . The sum of the scores for all 15 items is regarded as the GSRS total score. Total scores range from 15 (best outcome) to 105 (worst outcome).	baseline