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The rise of oncology biosimilars: from process to promise
biologic biosimilar breast cancer SB3 trastuzumab

The rise of oncology biosimilars: from process to promise


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Summary

  • Biosimilars are biologic products that are highly similar to the approved originator molecule, with no clinically meaningful differences.
  • They are expected to play a key role in cancer treatment by reducing costs and improving access.
  • Regulatory bodies use robust mechanisms for approval, involving comprehensive analytical and nonclinical comparisons with the originator.
  • Important product attributes, such as post-translational modifications, must be similar between biosimilars and originators.
  • A robust clinical development program is essential to assess pharmacokinetics, pharmacodynamics, efficacy, safety, and immunogenicity.
  • Approval in one indication may allow for extrapolation across all indications of the originator biologic.
  • The approval of several trastuzumab biosimilars illustrates the practical benefits for patients, clinicians, and payers.

Biologics are an increasingly central element of the cancer treatment armamentarium. Unlike traditional pharmaceuticals, which are usually small molecules, biologics are large compounds derived from living organisms, or recombinant proteins produced by cells transformed with the genetic information encoding the corresponding protein. Typically, they are protein based, with inherently complex sequences and 3D structures. Unlike small-molecule drugs, they cannot be manufactured chemically. Instead, living host systems are required, which are typically human or animal cells; the process is inevitably harder to control than the process of chemical synthesis.

The importance of biologics in oncology is exemplified by the fact that the three biggest selling cancer drugs of 2015 were all monoclonal antibody-based biologics: rituximab, bevacizumab and trastuzumab. At that time, all three remained under patent protection. However, since then, the patent protection for these biologic agents has expired and biosimilar forms of each drug are now available. This represents the beginning of a new era in oncology.

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biologic, biosimilar, breast cancer, SB3, trastuzumab

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