RecruitingNCT04680377

Using Microbiome to Predict Durvalumab Toxicity in Post- Concurrent Chemoradiation Therapy (CCRT) NSCLC Patients

Using Microbiome to Predict Durvalumab Toxicity in Post-CCRT NSCLC Patients (Microdurva)


Sponsor

Jun Zhang, MD, PhD

Enrollment

44 participants

Start Date

Apr 12, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

This phase IV study is hoping to determine if examining the microbiome in non-small cell lung cancer participants who will receive durvalumab can predict treatment toxicity.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is exploring whether the mix of bacteria living in your gut (your microbiome) can predict which lung cancer patients will have serious side effects from a drug called durvalumab — an immunotherapy given after chemotherapy and radiation for non-small cell lung cancer (NSCLC). **You may be eligible if...** - You are 18 or older - You have non-small cell lung cancer treated with at least two cycles of platinum-based chemotherapy plus radiation (54–66 Gy) - You have a life expectancy of at least 12 weeks - You are in good physical condition (ECOG 0 or 1) - You are able to follow study visits and procedures **You may NOT be eligible if...** - You have not had the required prior chemotherapy and radiation - Your overall health does not meet the study's organ function requirements - You are unable or unwilling to consent and comply with the study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(2)

The University of Kansas Cancer Center, Westwood Campus

Kansas City, Kansas, United States

Rhode Island Hospital, Brown University

Providence, Rhode Island, United States

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NCT04680377


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