RecruitingNot ApplicableNCT05754203

Efficacy and Safety of Super-hyperfractionation Pulse Radiotherapy Combined With ICIs for Advanced NSCLC

Efficacy and Safety of Super-hyperfractionation Pulse Radiotherapy Combined With Immune Checkpoint Inhibitor for Advanced Non-small Cell Lung Cancer.


Sponsor

Xinqiao Hospital of Chongqing

Enrollment

40 participants

Start Date

Aug 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Investigators intend to combine low-dose hypersensitivity with high-dose immunopotentiation effect, and use super-hyperfractionation pulse radiotherapy, which is expected to achieve the effect of in situ vaccine that can enhance tumor killing, protect normal tissues, reduce immune cell damage and enhance tumor immunogenicity at the same time, and play a stronger immunopotentiation effect in combined immunotherapy. Thereby inducing a stronger abscopal effect of radiotherapy.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of ultra-precise, high-dose radiation (SBRT) with immune checkpoint inhibitor drugs in patients with advanced non-small cell lung cancer (NSCLC) that has not responded to standard treatment, to see if combining these approaches improves outcomes. **You may be eligible if...** - You are 18 or older (and under the study's upper age limit) - You have been diagnosed with stage IIIB or higher non-small cell lung cancer confirmed by biopsy - Your tumor is small enough (under 5 cm) to be suitable for SBRT radiation - You are eligible for immune checkpoint inhibitor therapy - You have given informed consent **You may NOT be eligible if...** - Your lung cancer is small cell or another type not covered by the study - Your tumor is too large for the required radiation technique - You have conditions that prevent safe use of immunotherapy 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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Interventions

RADIATIONSuper-hyperfractionation Pulse Radiotherapy

Radiotherapy design: a single dose of 0.5Gy, 16 consecutive pulses with an interval of 3 minutes (0.5Gy \* 16F), total dose DT: 8Gy; Immunotherapy: PD-1/PD-L1 monoclonal antibodies conforming to CSCO guidelines for lung cancer indications, including Carrilizumab, Tirelizumab, Teripril, Paborizumab, etc., conventional therapeutic dose, Q3W, until progression or the investigator judges that there is no longer clinical benefit or intolerable side effects.


Locations(2)

the second affiliated hospital of Army medical university

Chongqing, Chongqing Municipality, China

Jianguo Sun

Chongqing, China

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NCT05754203


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