Difference between revisions of "Tislelizumab (Baizean)"

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**[[Non-small cell lung cancer, squamous]]
 
**[[Non-small cell lung cancer, squamous]]
 
*[[Urothelial carcinoma]]
 
*[[Urothelial carcinoma]]
*[[MSI-H or dMMR|MSI-H or dMMR solid tumors (tissue-agnostic)]]
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*[[Malignant solid neoplasm, MSI-H or dMMR|MSI-H or dMMR solid tumors (tissue-agnostic)]]
  
 
==History of changes in NMPA indication==
 
==History of changes in NMPA indication==
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[[Category:Hepatocellular carcinoma medications]]
 
[[Category:Hepatocellular carcinoma medications]]
 
[[Category:Classical Hodgkin lymphoma medications]]
 
[[Category:Classical Hodgkin lymphoma medications]]
[[Category:MSI-H or dMMR medications]]
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[[Category:Malignant solid neoplasm, MSI-H or dMMR medications]]
 
[[Category:Nasopharyngeal carcinoma medications]]
 
[[Category:Nasopharyngeal carcinoma medications]]
 
[[Category:Non-small cell lung cancer medications]]
 
[[Category:Non-small cell lung cancer medications]]

Revision as of 23:25, 21 September 2023

Mechanism of action

From the NCI Drug Dictionary: A monoclonal antibody directed against the negative immunoregulatory human cell surface receptor programmed cell death 1 (PD-1), with potential immune checkpoint inhibitory and antineoplastic activities. Upon administration, tislelizumab binds to PD-1 and inhibits the binding of PD-1 to the PD-1 ligands programmed cell death-1 ligand 1 (PD-L1), and PD-1 ligand 2 (PD-L2). This prevents the activation of PD-1 and its downstream signaling pathways. This may restore immune function through the activation of both T cells and T-cell-mediated immune responses against tumor cells.

Diseases for which it is used

History of changes in NMPA indication

  • 2019-12-26: Initial approval
  • Uncertain date: Full approval for first-line treatment of patients with advanced squamous non-small cell lung cancer (NSCLC) in combination with chemotherapy.
  • Uncertain date: Full approval for first-line treatment of patients with advanced non-squamous NSCLC in combination with chemotherapy.
  • Uncertain date: Full approval for second- or third-line treatment of patients with locally advanced or metastatic NSCLC who progressed on prior platinum-based chemotherapy.
  • Uncertain date: Conditional approval for the treatment of patients with classical Hodgkin’s lymphoma (cHL) who received at least two prior therapies
  • Uncertain date: Conditional approval for the treatment of patients with locally advanced or metastatic urothelial carcinoma (UC) with PD-L1 high expression whose disease progressed during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy
  • Uncertain date: Conditional approval for the treatment of patients with hepatocellular carcinoma (HCC) who have received at least one systemic therapy
  • Uncertain date: Conditional approval for the treatment of patients with advanced unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) solid tumors.

Also known as

  • Code name: BGB-A317
  • Generic name: tilelizumab
  • Brand name: Baizean