Clinical trial · Interventional
Study on the Optimal Combination Pattern of the Combined Treatment of Radiotherapy and Immunotherapy for the Abscopal Effect in Non-Small Cell Lung Cancer (NSCLC) With Multiple Metastases
An Umbrella Trial of Combining Different Radiotherapy Fractionation Patterns With Immunotherapy for Multiple Metastases of Non-Small Cell Lung Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to conduct a prospective, multicenter, umbrella clinical study to compare the abscopal effects of different radiotherapy fractionation patterns combined with Benmelstobart, and to explore an efficient and low-toxic treatment strategy for non-small cell lung cancer (NSCLC) with multiple metastases. The main objective is to explore and compare the control rates of abscopal lesions in NSCLC patients with multiple metastases when different radiotherapy fractionation patterns are combined with Benmelstobart.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| NSCLC Stage IV Without EGFR/ALK Mutation | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Benmelstobart combined with Bevacizumab and chemotherapy | Drug | — | UNRESOLVED |
| Benmelstobart combined with chemotherapy | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (6)
- type
- EXPERIMENTAL
- label
- Group A
- interventionNames
- Drug: Benmelstobart combined with chemotherapy
- type
- EXPERIMENTAL
- label
- Group B
- interventionNames
- Drug: Benmelstobart combined with chemotherapy
- type
- EXPERIMENTAL
- label
- Group C
- interventionNames
- Drug: Benmelstobart combined with chemotherapy
- type
- EXPERIMENTAL
- label
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Patient must meet all of the following inclusion criteria to be enrolled in this study: 1. Non-small cell lung cancer confirmed by pathological histology. 2. More than 3 metastatic lesions. 3. No brain metastases or stable lesions. 4. Negative for driver genes (including EGFR, ALK, ROS, BRAF, MET, RET). 5. Performance status (PS) score of 0-1, with an expected survival period of more than 3 months. 6. Age between 18 and 75 years old. 7. Assessment by PET-CT (including FDG and FMISO, not mandatory). 8. No contraindications to immunotherapy and radiotherapy. 9. Signed the informed consent form. Exclusion Criteria: * Patients with any of the following criteria are not eligible for enrollment in this study: 1. Those with severe dysfunction of important vital organs (heart, liver, kidney). 2. Those accompanied by other malignant tumors. 3. Uncontrolled heart diseases or myocardial infarction within the past 6 months. 4. Those with a history of mental illness. 5. Other situations in which the researcher deems it inappropriate for the subject to participate in the study.
References
Publications (0)
Data not yet available