Evaluating cancer immunotherapy effectiveness in lung and esophageal cancer patients
Official title: Investigating the Biomarkers in Tumor Microenvironment and Peripheral Blood Microenvironment to Evaluate the Efficacy of Cancer Immunotherapy in Chest Cancer Patients
Run by The First Affiliated Hospital of Soochow University · NCT06790797 · Data updated 2026-11-12
This study is testing how well immunotherapy works for people with lung and esophageal cancer by looking at changes in their immune cells before and after treatment.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | The First Affiliated Hospital of Soochow University Academic / other |
| Drugs / interventions | immunotherapy |
| Locations | 1 site (Suzhou, Jiangsu) |
| Status | Recruiting |
| Started | February 12, 2023 |
| Main results expected | July 30, 2027 |
| Study ends | July 30, 2027 |
| Registry record updated | January 24, 2025 |
| Trial ID | NCT06790797 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 to 80 with a confirmed diagnosis of lung or esophageal cancer who are set to receive PD-1/PD-L1 antibody immunotherapy.
✕Probably not a fit
Patients with hematogenic infectious diseases, immediate treatment needs, or severe mental illnesses may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study investigates the impact of immunotherapy on the immune status of patients with lung and esophageal cancer. Researchers will collect tumor tissue and peripheral blood samples before and after treatment to analyze changes in cancer-specific T-cell populations. Techniques such as single-cell RNA sequencing, multiplex immunohistochemistry, and flow cytometry will be employed to identify potential biomarkers that predict the efficacy of immunotherapy. The goal is to understand how these biomarkers correlate with treatment responses and improve patient outcomes.
Why it matters
Potential benefit: If successful, this study could lead to better prediction of immunotherapy responses, allowing for more personalized treatment plans for cancer patients.
How similar studies have gone: Other studies have shown promise in identifying biomarkers for immunotherapy efficacy, suggesting that this approach may yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with a pathological diagnosis of lung cancer or esophageal cancer who have agreed to receive PD-1/PD-L1 antibody immunotherapy; * Age between 18 and 80 years old; * ECOG PS score of 0 or 1; * Adequate organ and bone marrow function; * Anticipated survival time of at least 12 weeks; * Willing and able to provide written informed consent. Exclusion Criteria: * Patients with hematogenic infectious diseases, such as HIV, hepatitis B or hepatitis C. * Patients with tumor emergencies that require immediate treatment. * Poor vascular conditions. * Abnormal coagulation function or receiving anticoagulant or thrombolytic therapy. * Patients with hematogenic infectious diseases, such as HBV. * Patients with psychiatric disorders or severe mental illnesses. * Patients who have difficulty communicating or are unable to be followed up for a long time. * Other situations that are not suitable for inclusion in the study.
Where it's running
-
The first affiliated hospital of soochow university
Suzhou, Jiangsu, China Recruiting
Study contacts
- Study coordinator: Mi Liu
- Email: mi.liu831116@icoud.com
- Phone: 86-0512-67972216
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Heart-friendly medicines to protect chest-area cancer patients from radiation damage
This Phase 2 trial tests whether taking atorvastatin and lisinopril can reduce heart damage in adults with chest-area cancers who receive radiation therapy.
-
CEA-targeted CAR-T for advanced CEA-positive solid tumors
This trial will try CEA-targeted CAR-T cell infusions in adults with advanced CEA-positive cancers (such as colorectal, gastric, esophageal, lung, or pancreatic cancer) to see if the treatment is safe and helps control the disease.
-
Virtual exercise program to preserve function and prevent disability during chemotherapy
This trial tests whether supervised resistance sessions by video plus short home aerobic workouts help adults 18–64 maintain strength and stay active while receiving curative-intent chemotherapy.
-
IDOV-Immune for advanced solid tumors
This trial will try a single IV infusion of an engineered oncolytic vaccinia virus called IDOV-Immune in adults with advanced solid tumors that no longer respond to standard treatments.
-
Using brodalumab to treat immune-related side effects from cancer therapy
This study is testing if brodalumab can help cancer patients who are having immune-related side effects from their immunotherapy treatment feel better.
-
Evaluating BL-M07D1 for HER2 Expressing Solid Tumors
This study is testing a new treatment called BL-M07D1 to see if it is safe and effective for people with advanced solid tumors that have a specific protein called HER2 after they have tried other treatments.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.