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OncoMatch/Clinical Trials/NCT05502913

Fecal Microbiota Transplantation With Immune Checkpoint Inhibitors in Lung Cancer

Is NCT05502913 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Antibiotics for metastatic lung cancer.

Phase 2RecruitingSoroka University Medical CenterNCT05502913Data as of May 2026

Treatment: AntibioticsImmunotherapy has recently become a main-stream treatment option in cancer care, with improved clinical outcomes in many malignancies, especially that of lung cancer. The long-term benefits of this treatment however are limited. There is therefore a critical need to distinguish predictive biomarkers of response from those of resistance, and to develop synergistic strategies for improved therapeutic response. Strong emerging evidence indicates that the gut microbiome has the ability to influence response to immunotherapy. Unlike tumor genomics, the gut microbiome is modifiable, and thus its modulation to enhance response to immunotherapy is an attractive therapeutic strategy. Working hypothesis: Fecal Microbiota Transplant (FMT) treatment in conjunction with standard (chemo-)immunotherapy as a first-line treatment for metastatic lung cancer enhances disease control rate. The main objective of this study is to evaluate the safety and efficacy of Fecal Microbiota Transplant (FMT) in altering response to immunotherapy in patients with metastatic lung cancer. The overall goal is to determine microbiome compositional and gene-content changes in patients who respond more efficiently to immunotherapy subsequent to FMT. This understanding may lead to future microbiome-based treatments in combination with immunotherapy to significantly increase lung cancer treatment efficacy. In this prospective clinical and molecular study, we will perform an in-depth analysis of the potential role of FMT in the context of immunotherapy.

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Disease stage

Metastatic disease required

Metastatic Lung Cancer

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Cannot have received: pre- or probiotics

Treatment with pre- or probiotics in the four weeks prior to randomization.

Cannot have received: systemic chemotherapy

Exception: allowed if >30 days from baseline

Systemic chemotherapy <30 days from baseline

Cannot have received: corticosteroids (prednisone)

Exception: allowed if ≤60mg daily or ≤30 days, and not within 8 weeks of randomization

Prolonged treatment with corticosteroids (equivalent to prednisone >60mg daily for >30 days) within 8 weeks of randomization

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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