Recruiting
Phase 1

Gut Microbiome

Sponsor:

M.D. Anderson Cancer Center

Code:

NCT03819296

Conditions

Clinical Stage 0 Cutaneous Melanoma AJCC v8

Clinical Stage I Cutaneous Melanoma AJCC v8

Clinical Stage IA Cutaneous Melanoma AJCC v8

Clinical Stage IB Cutaneous Melanoma AJCC v8

Clinical Stage II Cutaneous Melanoma AJCC v8

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Best Practice

Biospecimen Collection

Endoscopic Procedure

Fecal Microbiota Transplantation

Infliximab

Study Details

Brief summary:

This trial studies the role of the gut microbiome and effectiveness of a fecal transplant on medication-induced gastrointestinal (GI) complications in patients with melanoma or genitourinary cancer. The gut microbiome (the bacteria and microorganisms that live in the digestive system) may affect whether or not someone develops colitis (inflammation of the intestines) during cancer treatment with immune-checkpoint inhibitor drugs. Studying samples of stool, blood, and tissue from patients with melanoma or genitourinary cancer may help doctors learn more about the effects of treatment on cells, and help doctors understand how well patients respond to treatment. Treatment with fecal transplantation may help to improve diarrhea and colitis symptoms.

Conditions

Clinical Stage 0 Cutaneous Melanoma AJCC v8

Clinical Stage I Cutaneous Melanoma AJCC v8

Clinical Stage IA Cutaneous Melanoma AJCC v8

Clinical Stage IB Cutaneous Melanoma AJCC v8

Clinical Stage II Cutaneous Melanoma AJCC v8

Study ID

NCT03819296

Start date

Feb 21, 2021

Status verified date

Jul, 2026

Completion date

Oct 31, 2026

Anticipated

Primary completion date

Oct 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Diagnosis of any stage melanoma, Non-Small Cell Lung Cancer or genitourinary (GU) malignancies (Project 1).
2. Diagnosis of any cancer type (Projects 2 and 3)
3. Treatment with any ICPI agent
4. Ability to understand and willingness to sign an informed consent form and rate surveys
5. Life expectancy > 4 months (Project 3)
6. ICPI-related diarrhea and/or colitis of any grade with or without concurrent non- GI toxicity as the toxicity group (project 1)
7. Patients with no organ toxicity as the control group (project 1)
8. ICPI-related colitis and/or diarrhea of grade ≥ 2 as GI toxicity (initial episode or recurrence) receiving standard treatment of immunosuppressive agents (steroid, infliximab, vedolizumab, or ustekinumab) any time during the colitis disease course until sustained resolution of GI toxicity, or one- year time point after enrollment (Project 2)
9. ICPI-related colitis and/or diarrhea of grade ≥ 2 as GI toxicity without involvement of non- GI toxicity within 45 days prior to FMT (Project 3)
10. ICPI-related colitis and/or diarrhea of grade ≥ 2 within 45 days prior to FMT with ANY of the following characteristics (project 3):

(i) refractory to treatment of steroid and two doses of non-steroidal immunosuppressants e.g. infliximab, vedolizumab or ustekinumab,

(ii) contraindication for immunosuppressive treatment,

(iii) recurrence after successful initial treatment,

(iv) recurrent symptoms once steroid is tapered down/off or diarrhea/colitis symptoms are steroid dependent, or

(v) patients with a history of refractory ICPI-related colitis and/or diarrhea to medical treatment, even if they have improved symptoms from supportive care within 45 days prior to FMT
11. No concern for active concomitant GI infection for the ICPI diarrhea/colitis work up at the time of protocol therapy initiation as confirmed by stool tests or as per the treating physician based on clinical presentation (project 3)
12. Patient who has been cleared for enrollment by Infectious Diseases consultant or treating physician if positive infection workup or screening tests (e.g. lifelong positive T-spot due to BCG inoculation, chronic colonization) prior to initiation of diarrhea/colitis treatment (project 3)

Exclusion Criteria:

1. Age younger than 18 years
2. History of inflammatory bowel disease, and/or radiation enteritis or colitis with active disease status at the time of study treatment initiation
3. Pregnant and breastfeeding women
4. Women of child-bearing potential who have positive urine or serum pregnancy test or refuse to do pregnancy test unless last menstrual cycle was > 1 year prior to consent and/ or clear documentation states that patient is peri- or post-menopausal or there was recent supporting objective evidence of 'no pregnancy' status (e.g. blood or imaging) within 30 days prior to date of study treatment
5. Patients who develop concurrent non- GI toxicity at the time of FMT treatment (project 3)
6. Patients with active bacterial or fungal infection (Project 3)
7. Donors at risk for monkeypox infection and/ or exposure as determined by a questionnaire (Project 3)

Withdrawal Criteria

1. Patients may withdraw from the trial at any time
2. Patients who develop GI perforation or toxic colitis that require surgery from ICPI colitis
3. In project 3, if the first 30% of cases fail the fecal transplant treatment, then project 3 will be terminated

Study Design

Enrollment

800 participants

Anticipated

Intervention Model

Single group

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

experimental: Supportive Care (standard of care, sample collection, FMT)

PROJECT 1: Patients receive standard of care and undergo collection of stool and blood samples.

PROJECT 2: Patients receive prednisone, infliximab, or vedolizumab per standard of care and undergo standard of care endoscopy 2 months after treatment. Patients also undergo collection of stool, blood, and tissue samples.

PROJECT 3: Patients undergo FMT.

Interventions

Best Practice

Receive standard of care

Biospecimen Collection

Undergo collection of stool, blood, and tissue samples

Endoscopic Procedure

Undergo endoscopy

Fecal Microbiota Transplantation

Undergo FMT

Infliximab

Given intravenously (IV)

Laboratory Biomarker Analysis

Ancillary studies

Prednisone

Given orally

Vedolizumab

Given IV

Primary outcome measure

  • Difference in stool microbiome pattern [ Time Frame: Up to 1 year ]
  • Incidence of adverse events (AE) of fecal microbiota transplantation (FMT) (Project 3) [ Time Frame: Up to 1 year ]

Central Contacts and Locations

Central contacts

Locations

M D Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Principal Investigator:

Yinghong Wang

More Information

Sponsor

M.D. Anderson Cancer Center

Last update posted

Jul 15, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by M.D. Anderson Cancer Center on 2026-07-15.