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Almonertinib is a third-generation small molecule EGFR tyrosine kinase inhibitor that targets both EGFR-sensitizing and T790M resistance mutations, primarily developed for the treatment of advanced or metastatic EGFR-mutated non-small cell lung cancer (NSCLC)[8]. SHR-1701, also known as retlirafusp alfa, is a bifunctional recombinant fusion protein composed of an anti-PD-L1 monoclonal antibody fused to the extracellular domain of TGF-beta receptor II. This design enables dual inhibition of PD-L1 and TGF-beta signaling pathways, aiming to enhance antitumor immune responses[5][2][3]. The combination of almonertinib with SHR-1701 is being investigated in clinical trials for relapsed or advanced malignancies, including NSCLC and other solid tumors[1][4].
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