Study reveals why immunotherapy works differently in liver, lung, and brain tumors
NCT ID NCT07631611
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at medical records of 938 adults with solid tumors who received immunotherapy. Researchers compared how well the treatment worked when cancer had spread to different organs like the liver, brain, lung, or bone. The goal is to understand why some metastatic sites respond better than others, which could help personalize cancer treatment in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- immune checkpoint inhibitors (ICB therapy)
- What this could lead to
- If successful, this could help doctors choose better immunotherapy strategies based on where a patient's cancer has spread.
- What could go wrong
- This is a retrospective study that looks back at medical records, so it cannot prove cause and effect. Results may not apply to all patients or treatments.
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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938 people
The number who actually took part.
- Started
-
Jan 2016
- Finished
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May 2026
- 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
This study includes adults with solid tumors who developed metastatic cancer in the brain, liver, lung, or bone. All participants received first-line or second-line immune checkpoint inhibitor (ICB) therapy and completed at least three treatment cycles with available imaging follow-up. The study population represents real-world patients treated at Sun Yat-sen Memorial Hospital, the Third Affiliated Hospital of Sun Yat-sen University, and the First Affiliated Hospital of Chongqing Medical University, with complete clinical and survival data that allow evaluation of organ-specific treatment response and progression. Individuals with unclear metastatic sites, incomplete treatment information, or major data gaps were not included.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Age ≥18 years. * Pathologically confirmed solid tumor with a documented primary tumor site. * At least one metastatic site in the brain, liver, lung, or bone confirmed by imaging or pathology (single or multiple lesions allowed). * Received first-line or second-line immune checkpoint inhibitor (ICB) therapy, including PD-1, PD-L1, or CTLA-4 inhibitors, either alone or in combination. * Completed at least 3 cycles of ICB therapy. * At least one evaluable imaging follow-up after initiation of immunotherapy. * Available clinical and follow-up data, including treatment initiation date, response assessment, progression status, and survival status. * Meets institutional ethics requirements for retrospective studies. Exclusion Criteria: * Unclear or undocumented metastatic site, or lack of imaging/pathologic evidence supporting metastasis. * ICB treatment regimen cannot be clearly determined (e.g., unclear combination therapy components). * Missing more than 20% of key clinical variables or incomplete follow-up data (e.g., missing PFS or OS information). * Received fewer than 3 cycles of ICB therapy. * Major treatment interruption or poor treatment adherence. * Concurrent active malignancy that may interfere with outcome assessment. * Severe immune-related disease (e.g., systemic lupus erythematosus) or organ transplantation requiring long-term immunosuppression. * Participation in another interventional clinical trial that may affect treatment evaluation. * Data errors or logical inconsistencies that cannot be resolved after review.
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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.
Contacts and locations
Locations
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Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China
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