by J Li 2024 Cited by 2The study aimed to provide a complete toxicity profile and toxicity spectrum for anti-PD-1 and anti-PD-L1 drugs.
Drug class: anti-PD-1 and PD-L1 monoclonal antibodies (immune checkpoint inhibitors) drugs, over-the-counter medicines and natural products.
prescribing anti-PD-1 drugs to an increasing number of patients.1 We performed a systematic review and meta-analysis of immune-related adverse eventsof anti-PD-1 and anti-PD-L1 drugs. We included organ specific and other adverse eventspotentially related to inflammation and gathered data from both ClinicalTrials.gov and published literature.
Drugs Targeting the PD-1/PD-L1 Pathway. A small, first-in-human trial of the anti-PD-1 drug nivolumab reported promising results, and
Additionally, several new drugs based on the anti-TIGIT and anti-PD-1/PD-L1 combination, such as AZD2936 and MK-7684 A, and novel combination strategies, such as anti-TIGIT plus anti-PD-1/PD-L1 agents plus chemotherapy or chemoradiotherapy, are being evaluated clinically (Table 1). These advances are expected to expand the benefits of the anti
specific immunotherapy drugs, checkpoint inhibitors (anti-PD-1, anti-PD-L1 The checkpoint inhibitors marketed in France are list I drugs, reserved for
A hypothetical explanation for the improved efficacy of anti‐PD1 drugs compared with anti‐PD‐L1 antibodies could be that anti PD‐1 antibodies are able to inhibit the binding of PD‐1 not only to PD‐L1 but also to PD‐L2, which is an important interaction that also inhibits the activation of T cells. 28 In fact, previous data
The first anti-PD-1 mAbs, nivolumab and pembrolizumab, were approved by the US Food and Drug Administration (FDA) in 2024 and the first anti-PD-
Monoclonal antibody drugs targeting these immune checkpoints are being evaluated in multiple clinical trials, the majority of which are testing their combination with anti-PD-1 or anti-PD-L1
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