Fecal Microbiota Transplantation for Preventing Gastrointestinal Symptoms in Extrapulmonary Neuroendocrine Neoplasms: A Real-World Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Fecal Microbiota Transplant (FMT), Standard Therapy.
- Who it may be relevant to
- Registry conditions: Treatment-related Gastrointestinal Toxicity (Including Diarrhea, Constipation, Nausea, and Vomiting), Extrapulmonary Neuroendocrine Neoplasms. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Procedure 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. - Other Standard Therapy
Standard Therapy Alone
Primary outcome measures
- Improvement in treatment-related gastrointestinal symptoms [Time frame: Assessed every two cycles (6 weeks)]
Secondary outcome measures (3)
- Chemotherapy cycle delay rate [Time frame: Assessed every two cycles (6 weeks)]
- Quality of Life (QoL) assessment [Time frame: Assessed every two cycles (6 weeks)]
- Gut microbiota colonization [Time frame: Assessed every two cycles (6 weeks)]
Eligibility criteria
Inclusion criteria
- Age ≥18 years, regardless of gender;
- Anticipated survival period ≥3 months;
- Pathologically confirmed diagnosis of extrapulmonary neuroendocrine neoplasms;
- Development of gastrointestinal adverse reactions (including but not limited to diarrhea, constipation, vomiting, nausea, etc.) within three cycles of standard treatment;
- Patients are capable and willing to sign an informed consent form and complete follow-up;
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) score of 1-3;
- No use of oral/intravenous broad-spectrum antibiotics within 3 days prior to enrollment;
- Ability to swallow capsules without chewing;
- Adequate organ function confirmed by screening laboratory tests.
Exclusion criteria
- Patients with major organ dysfunction or failure, including but not limited to cardiac insufficiency/heart failure, renal insufficiency/failure, or hepatic insufficiency/failure;
- Uncontrolled or severe infection;
- Known history of psychotropic drug abuse, alcoholism, or substance abuse;
- Severe infection accompanied by sepsis or septicemia;
- History of severe allergic reactions or known allergy to components of the liquid live bacterial enteric-coated capsules;
- 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);
- Patients with gastrointestinal perforation and/or fistula;
- Other conditions deemed unsuitable for enrollment by the investigator.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
China · 1 center
- Second Affiliated Hospital, School of Medicine, Zhejiang University — Hangzhou
Identifiers
NCT: NCT06924645 · 2025-0198