SB8, an approved bevacizumab biosimilar based on totality of evidence: scientific justification of extrapolation

Future Oncol. 2023 Feb;19(6):427-450. doi: 10.2217/fon-2022-1273. Epub 2023 Mar 8.

Abstract

SB8 is a biosimilar of bevacizumab based on its similarity demonstrated by physicochemical, functional, non-clinical and clinical studies. Supported by the concept of extrapolation, SB8 was authorized and is used in a similar manner across all types of tumors as reference bevacizumab. Furthermore, SB8 offers convenience with prolonged stability compared with reference bevacizumab in diluted form. Although a biosimilar must demonstrate biosimilarity to a reference product with the 'totality of evidence' in a stringent regulatory process for marketing authorization, some concerns remain among healthcare practitioners, particularly about extrapolation. This review summarizes the concepts of the totality of evidence and extrapolation in biosimilar development and the role of bevacizumab biosimilars in the management of metastatic colorectal cancer as an extrapolated indication.

Keywords: SB8; VEGF inhibitor; bevacizumab; biosimilar; extrapolation; metastatic colorectal cancer; monoclonal antibody; non-small-cell lung cancer; real-world evidence; totality of evidence.

Publication types

  • Review

MeSH terms

  • Bevacizumab / therapeutic use
  • Biosimilar Pharmaceuticals* / therapeutic use
  • Colonic Neoplasms*
  • Drug Approval
  • Humans
  • Rectal Neoplasms*

Substances

  • Bevacizumab
  • Biosimilar Pharmaceuticals

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