Tevimbra (tislelizumab)

Indications for Prior Authorization

Tevimbra (tislelizumab)
  • For diagnosis of Esophageal Squamous Cell Carcinoma
    Indicated for the treatment of adult patients with unresectable or metastatic esophageal squamous cell carcinoma after prior systemic chemotherapy that did not include a PD-(L)1 inhibitor

  • For diagnosis of Gastric or Gastroesophageal Junction Adenocarcinoma
    Indicated for the first-line treatment of adults with unresectable or metastatic HER2- negative gastric or gastroesophageal junction adenocarcinoma (G/GEJ) whose tumors express PD-L1 (≥1)

Criteria

Tevimbra

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)
For diagnosis of Esophageal Squamous Cell Carcinoma

  • Diagnosis of esophageal squamous cell carcinoma
  • AND
  • Disease is one of the following:
    • Unresectable
    • Metastatic
    AND
  • Patient has received prior systemic chemotherapy
  • AND
  • Patient has not previously been treated with a PD-(L)1 inhibitor (e.g., Keytruda, Opdivo)
Tevimbra

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)
For diagnosis of Gastric or gastroesophageal junction adenocarcinoma

  • Diagnosis of gastric or gastroesophageal junction adenocarcinoma
  • AND
  • Disease is one of the following:
    • Unresectable
    • Metastatic
    AND
  • Disease is human epidermal growth factor receptor 2 (HER2)-negative
  • AND
  • Tumor(s) express PD-L1 as detected by an FDA-approved test or a test performed at a facility approved by Clinical Laboratory Improvement Amendments (CLIA)
  • AND
  • Used in combination with platinum (e.g., carboplatin, cisplatin, oxaliplatin) and fluoropyrimidine (e.g., fluorouracil) -based chemotherapy
Tevimbra

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)
For diagnosis of All indications listed above

  • Patient does not show evidence of progressive disease while on therapy
P & T Revisions

2025-02-05, 2024-09-27, 2024-09-26

  1. Tevimbra Prescribing Information. BeiGene USA, Inc. San Mateo, CA. December 2024.

  • 2025-02-05: Added criteria for new indication of gastric or gastroesophageal junction adenocarcinoma
  • 2024-09-27: New Program for Tevimbra
  • 2024-09-26: New Program for Tevimbra