The addition of the anti-PD-L1 drug atezolizumab to NAB-paclitaxel chemotherapy has been shown to significantly improve PD-L1-positive (PD-L1) metastases and improve overall survival (OS) in patients with advanced TNBC(Schmid et al, 2024).
In consideration of these chemotherapeutic off-target tendencies, appropriate combination of chemotherapy drugs with PD‐1/PD-L1 blockade could augment the efficacy of the anti-PD-1/PD-L1 therapies, particularly in less immunogenic, chemo‐sensitive tumors.
Subsequent studies have indicated that the cell-surface expression of PD-L1 protein is an effective biomarker for predicting the response to these drugs; PD-L1 immunohistochemistry (IHC) is to date the only testing method to guide the administration of anti PD-1/PD-L1 agents in NSCLC patients [1,3-6]. Recently, anti PD-1/PD-L1 agents have
Drug Classeschevron_rightPd 1 Pd L1 Inhibitors. PD-1/PD-L1 Inhibitors drugs in this class divided by the of drugs with a specific indication. It
See NCCN guidelines and drug package inserts for more information. Additional anti-PD-L1/PD-L1 drugs are in various phases of clinical and pre-clinical
Therefore, the study of the combined application of anti TIM-3 and anti PD-1/PD-L1 drugs may ameliorate the resistance of PD-1/PD-L1, save T cell failure, and improve the prognosis of patients
The addition of the anti-PD-L1 drug atezolizumab to NAB-paclitaxel chemotherapy has been shown to significantly improve PD-L1-positive (PD-L1) metastases and improve overall survival (OS) in patients with advanced TNBC(Schmid et al, 2024).
Atezolizumab and durvalumab are humanized anti-programmed ligand 1 (PD-L1) monoclonal antibodies that inhibit the binding between PD-L1 and its
In twenty-three trials, the anti-PD-1/PD-L1 inhibitor alone group was compared with the control group, and in thirteen trials, the anti-PD-1/PD-L1 inhibitors plus other drugs group was compared
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