Fecal Microbiota Transplantation for Preventing Gastrointestinal Symptoms in Extrapulmonary Neuroendocrine Neoplasms: A Real-World Study

NCT ID: NCT06924645

Last Updated: 2025-04-11

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-05-01
• Study Completion Date: 2028-12-31

Brief Summary

Existing studies have demonstrated that patients with different types of tumors exhibit significant increases in Enterobacter and Staphylococcus genera, along with marked decreases in Lactobacillus, Bacteroides, Bifidobacterium, and Enterococcus genera in their feces following chemotherapy. Research reports indicate a significant decline in bacterial diversity in rectal cancer patients post-chemotherapy, particularly showing reduced abundances of Porphyromonas, Peptostreptococcus, and Veillonella. Motoori et al. found that esophageal cancer patients undergoing combined chemotherapy with 5-FU, cisplatin, and docetaxel experienced significant reductions in intestinal Lactobacillus, alongside notable increases in Clostridium difficile and Enterococcus. Iida et al. confirmed that gut microbiota enhances the therapeutic efficacy of platinum-based agents and CpG oligonucleotides in cancer treatment. Concurrent studies suggest that probiotic supplementation during chemotherapy alleviates chemotherapy-related gastrointestinal reactions. Fecal microbiota transplantation (FMT), which involves transferring functional microbiota from healthy donors to patients' gastrointestinal tracts to reconstruct gut microbiota and improve microbial homeostasis, has emerged as a key clinical approach for regulating gut dysbiosis. It is currently recognized as the most effective established therapy for recurrent Clostridioides difficile infection (CDI). Previous studies have indicated FMT as a relatively safe, effective, and recommended treatment modality, while providing theoretical and experimental foundations for elucidating its efficacy and safety in preventing/reducing gastrointestinal symptoms associated with digestive tract cancer therapies.

This study aims to evaluate the improvement of treatment-related gastrointestinal symptoms and safety profile of FMT in extrapulmonary neuroendocrine tumor patients.

Conditions

Treatment-related Gastrointestinal Toxicity (Including Diarrhea, Constipation, Nausea, and Vomiting); Extrapulmonary Neuroendocrine Neoplasms

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Fecal microbiota transplantation

Fecal Microbiota Transplantation (FMT) is delivered as a single dose of oral microbiota capsules within 72 hours before starting standard therapy.

Group Type: EXPERIMENTAL

Fecal Microbiota Transplant (FMT)

Intervention Type: PROCEDURE

Fecal Microbiota Transplantation (FMT) is delivered as a single dose of oral microbiota capsules within 72 hours before starting standard therapy.

Control

Standard Therapy Alone

Group Type: ACTIVE_COMPARATOR

Standard Therapy

Intervention Type: OTHER

Standard Therapy Alone

Interventions

Fecal Microbiota Transplant (FMT)

Fecal Microbiota Transplantation (FMT) is delivered as a single dose of oral microbiota capsules within 72 hours before starting standard therapy.

Intervention Type: PROCEDURE

Standard Therapy

Standard Therapy Alone

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Age ≥18 years, regardless of gender;

2. Anticipated survival period ≥3 months;

3. Pathologically confirmed diagnosis of extrapulmonary neuroendocrine neoplasms;

4. Development of gastrointestinal adverse reactions (including but not limited to diarrhea, constipation, vomiting, nausea, etc.) within three cycles of standard treatment;

5. Patients are capable and willing to sign an informed consent form and complete follow-up;

6. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) score of 1-3;

7. No use of oral/intravenous broad-spectrum antibiotics within 3 days prior to enrollment;

8. Ability to swallow capsules without chewing;

9. Adequate organ function confirmed by screening laboratory tests.

Exclusion Criteria

1. Patients with major organ dysfunction or failure, including but not limited to cardiac insufficiency/heart failure, renal insufficiency/failure, or hepatic insufficiency/failure;

2. Uncontrolled or severe infection;

3. Known history of psychotropic drug abuse, alcoholism, or substance abuse;

4. Severe infection accompanied by sepsis or septicemia;

5. History of severe allergic reactions or known allergy to components of the liquid live bacterial enteric-coated capsules;

6. Female subjects with a positive pregnancy test, lactating women, or women of childbearing potential who refuse to use contraceptive measures during the observation period (15 weeks);

7. Patients with gastrointestinal perforation and/or fistula;

8. Other conditions deemed unsuitable for enrollment by the investigator.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

Sponsor Role: lead

Responsible Party

caiwen

Chief Physician

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Second Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, Zhejiang, China

Countries

China

Facility Contacts

Wen Cai

Role: primary

Other Identifiers

2025-0198

Identifier Type: -

Identifier Source: org_study_id