Second chance: can a different immunotherapy drug be safely retried after lung inflammation?
NCT ID NCT07775820
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study looks at whether people with lung cancer who developed lung inflammation (pneumonitis) from immunotherapy can safely restart treatment with a different type of immunotherapy drug. Researchers will compare outcomes in patients who restart with a PD-L1 inhibitor, those who restart with a PD-1 inhibitor, and those who do not restart immunotherapy at all. The main focus is on whether the lung inflammation comes back, and the study also tracks other side effects and how well the cancer responds. This is an observational study, meaning doctors choose the treatment as part of routine care, and about 150 adults across multiple centers in China will take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Restarting immunotherapy with a PD-L1 inhibitor or a PD-1 inhibitor after checkpoint inhibitor pneumonitis has resolved.
- What this could lead to
- If successful, this could help guide doctors on whether and how to safely resume immunotherapy in lung cancer patients who have experienced checkpoint inhibitor pneumonitis, potentially improving cancer control without unacceptable risks.
- What could go wrong
- This is an observational study, not a randomized trial, so results may be influenced by patient selection. Rechallenging with immunotherapy carries a risk of pneumonitis recurrence or other immune-related side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of adults with histologically confirmed lung cancer who were treated with immune checkpoint inhibitor and subsequently developed checkpoint inhibitor pneumonitis. Eligible participants will be identified from participating centers in China and classified according to subsequent routine clinical management: PD-L1 inhibitor rechallenge, PD-1 inhibitor rechallenge, or no immune checkpoint inhibitor rechallenge. Both retrospective clinical records and prospective follow-up information will be collected.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 18 years or older. 2. Histologically confirmed lung cancer. 3. Development of checkpoint inhibitor pneumonitis after treatment with immune checkpoint inhibitor. 4. Eastern Cooperative Oncology Group performance status of 0, 1, or 2. 5. Provision of written informed consent. Exclusion Criteria: 1. Incomplete clinical information required for the study analyses. 2. Considered unsuitable for participation by the investigator.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
5 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Nanfang Hospital, Southern Medical University
RECRUITINGGuangzhou, Guangdong, 510400, China
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Shenzhen People's Hospital
RECRUITINGShenzhen, Guangdong, 518020, China
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The First Affiliated Hospital of Guangzhou Medical University
RECRUITINGGuangzhou, Guangdong, 510030, China
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The First Affiliated Hospital of Wenzhou Medical University
RECRUITINGWenzhou, Zhejiang, 325088, China
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The Second Affiliated Hospital of Nanchang University
RECRUITINGNanchang, Jiangxi, 330200, China
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