Switching Between Reference Biologics and Biosimilars for the Treatment of Rheumatology, Gastroenterology, and Dermatology Inflammatory Conditions: Considerations for the Clinician

Curr Rheumatol Rep. 2017 Jun;19(6):37. doi: 10.1007/s11926-017-0658-4.

Abstract

Purpose of review: Biosimilars of the reference biologic therapeutics infliximab, etanercept, adalimumab, and rituximab are entering the market. Clinical and real-world data on the effects of reference → biosimilar switching are limited. This review was carried out to assess the current body of switching data.

Recent findings: Fifty-three switching studies were identified. Infliximab publications covered CT-P13 (25 studies), SB2 (1), infliximab NK (1), and unspecified infliximab biosimilars (2). Etanercept publications covered SB4 (2) and GP2015 (2). Adalimumab publications covered ABP 501 (2) and SB5 (1). Rituximab publications covered CT-P10 (1). Efficacy and safety data generally showed no differences between patients who switched treatments versus those who did not. No differences were seen pre- and post-switch. Immunogenicity data were presented in 19/37 (51%) studies. Additional data from switching studies of these therapies are still required, as is continuing pharma-covigilance. Switching should remain a case-by-case clinical decision made by the physician and patient on an individual basis supported by scientific evidence.

Keywords: Biologics; Biosimilars; Clinical trials; Real world data; Switching.

Publication types

  • Review

MeSH terms

  • Antirheumatic Agents / therapeutic use*
  • Biological Products / therapeutic use*
  • Biosimilar Pharmaceuticals / therapeutic use*
  • Dermatologic Agents / therapeutic use*
  • Drug Substitution
  • Gastrointestinal Agents / therapeutic use*
  • Gastrointestinal Diseases / drug therapy
  • Humans
  • Rheumatic Diseases / drug therapy
  • Skin Diseases / drug therapy
  • Treatment Outcome

Substances

  • Antirheumatic Agents
  • Biological Products
  • Biosimilar Pharmaceuticals
  • Dermatologic Agents
  • Gastrointestinal Agents