NSCLC Clinical Trial
This protocol is a phase II multi-center randomized controlled trial (RCT) evaluating the efficacy of SBRT in multi-metastatic NSCLC patients who are pan-negative for driver mutations.
Lung cancer is the leading cause of cancer death. Forty percent of patients are diagnosed as
metastatic lung cancer, and about 50% of them are pan-negative for driver mutations. The
median overall survival(OS) for these patients is 11 months, and maintenance therapy can
only prolong 2 months of OS. The NCCN guidelines recommend 4-6 cycles of chemotherapy with
or without maintenance chemotherapy.
Published data showed that radiotherapy modulates tumor phenotypes, enhances antigen
presentation and tumor immunogenicity. The regression of out-field lesions was termed as
"abscopal effect". The combination of radiotherapy with immunotherapeutic agents may promote
the host anti-tumor immune response and increase the rate of abscopal effect.Published data
showed that abscopal effect appeared in 20%-30% patients with metastatic malignant tumors
who were treated with the combination of SBRT and GM-CSF.
The investigators evaluate the efficacy of the combination of SBRT and GM-CSF in the
multi-metastatic NSCLC participants who are pan-negative for driver mutations. Patients
enrolled will be randomized into two groups. The control group will receive the standard
regimen as NCCN recommends. The experimental group will receive both the standard
chemotherapy and the extra SBRT to primary lesions or metastatic lesions combined with
GM-CSF. The investigators compare progress free survival(PFS) of the two groups.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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