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This is a combination therapy consisting of stereotactic body radiotherapy (SBRT), nimotuzumab, and tislelizumab. - **SBRT** is a form of highly precise external radiation therapy that delivers high doses of radiation to tumors in a small number of fractions, minimizing exposure to surrounding healthy tissue. It is used primarily for localized solid tumors. - **Nimotuzumab** is a humanized monoclonal antibody targeting the epidermal growth factor receptor (EGFR). By binding EGFR, it inhibits downstream signaling pathways involved in tumor cell proliferation and survival. - **Tislelizumab** is an anti-programmed death receptor 1 (PD-1) monoclonal antibody developed by BeiGene. It blocks PD-1 interaction with its ligands PD-L1/PD-L2 on tumor cells, thereby restoring T-cell function and enhancing immune-mediated antitumor activity[1][2][4]. Tislelizumab has been approved for several indications including esophageal squamous cell carcinoma, gastric/gastroesophageal junction adenocarcinoma, non-small cell lung cancer, urothelial carcinoma, hepatocellular carcinoma, Hodgkin lymphoma[6][8][10]. This combination aims to leverage the local control provided by SBRT with the systemic antitumor effects of EGFR inhibition (nimotuzumab) and immune checkpoint blockade (tislelizumab).
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