General information

Class/mechanism: PD-L1 blocking antibody. PD-L1 (programmed death-1 ligand 1) expressed on tumor cells and tumor-infiltrating immune cells can result in inhibition of anti-tumor immune responses. Avelumab binds to PD-1 and B7.1 receptors on T-cells and antigen presenting cells and prevents PD-L1's inhibitory effects on the immune system. As a result, avelumab stimulates immune responses, including anti-tumor immune effects.[1][2][3]
Route: IV
Extravasation: no information

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias or the prescribing information.[1]

Toxicity management

Diseases for which it is established

Patient drug information

History of changes in FDA indication

Merkel cell carcinoma

Renal cell carcinoma

Urothelial carcinoma

History of changes in EMA indication

  • 2017-09-18: Initial marketing authorization as Bavencio. Bavencio is indicated as monotherapy for the treatment of adult patients with metastatic Merkel cell carcinoma (MCC). (Based on JAVELIN Merkel 200)
  • 2019-10-24: Extension of indication to include first-line combination treatment with avelumab and axitinib in adult patients with advanced renal cell carcinoma (aRCC).
  • 2021-01-21: Extension of indication to include a new indication for Bavencio in the treatment as monotherapy for the first-line maintenance treatment of adult patients with locally advanced or metastatic urothelial carcinoma (UC) who are progression-free following platinum based chemotherapy.

History of changes in Health Canada indication

  • 2017-12-18: Initial notice of compliance with conditions for the treatment of metastatic Merkel Cell Carcinoma (MCC) in previously treated adults.
  • 2018-05-04: Notice of compliance with conditions for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-based chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-based chemotherapy.
    • 2019-05-14: Conditions were met for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-based chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-based chemotherapy.
  • 2019-11-06: New indication for the treatment of adult patients with metastatic Merkel cell carcinoma (MCC)
  • 2020-12-10: New indication for the maintenance treatment of patients with unresectable locally advanced or metastatic urothelial carcinoma (UC) whose disease has not progressed following first-line platinum-based chemotherapy.

History of changes in PMDA indication

  • 2017-09-27: New approval for the treatment of unresectable Merkel cell carcinoma.
  • 2019-12-20: New indication and a new dosage for the treatment of unresectable or metastatic renal cell carcinoma.
  • 2021-02-24: New indication for the maintenance therapy of unresectable urothelial carcinoma in patients who have received chemotherapy.

Also known as

  • Code name: MSB-0010718C
  • Brand name: Bavencio

References