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

N/ANot Yet RecruitingNCT06924645

Second Affiliated Hospital, School of Medicine, Zhejiang University40 enrolled

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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.

Outcomes

Primary Outcomes

Improvement in treatment-related gastrointestinal symptoms

Hart Diarrhea Score

Time frame: Assessed every two cycles (6 weeks)

Secondary Outcomes

Chemotherapy cycle delay rate

Time frame: Assessed every two cycles (6 weeks)

Quality of Life (QoL) assessment

QOL assessment

Time frame: Assessed every two cycles (6 weeks)

Gut microbiota colonization

Performing 16S rRNA sequencing, metagenomic sequencing on the samples.

Time frame: Assessed every two cycles (6 weeks)

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

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes