Literature DB >> 28727871

Biosimilars in Oncology in the United States: A Review.

Chadi Nabhan1, Sandeep Parsad2, Anthony R Mato3, Bruce A Feinberg1.   

Abstract

IMPORTANCE: Biosimilars are biological medicines that contain a highly similar version of the active substance of an already approved biologic reference product. The availability of biosimilars might provide an opportunity to lower health care expenditures as a result of the inherent price competition with their reference product. Understanding how biosimilar cancer drugs are regulated, approved, and paid for, as well as their impact in a value-based care environment, is essential for physicians and other stakeholders in oncology. OBSERVATIONS: Important structural and regulatory differences exist between biosimilar and generic medications. Minor differences in clinically inactive components with no clinically meaningful differences between biosimilars and their reference biologic are allowed. A biosimilar uses the same mechanism of action as the reference biologic, and its condition of use is the same as the approved indication, although extrapolation is permitted across indications under regulatory guidance. A biosimilar has to have a similar route of administration, dosage, and strength as the reference biologic. As patent expiration of multiple cancer biologics will occur in the next few years, more biosimilars might enter the market. Whether the approval and use of biosmilars as replacements for these heavily prescribed reference biologics will ultimately lead to cost savings is unknown and requires longer follow-up. Two biosimilars with an oncology supportive care indication are currently approved in the United States; both are myeloid growth factors. CONCLUSIONS AND RELEVANCE: The financial impact of generic drug competition can be dramatic, but significant differences in regulatory and development processes between generics and biosimilars limit such comparisons and likely present significant challenges for biosimilar approval and adoption in the US market. However, a value-based care environment and their cost-savings potential make biosimilars an attractive option for the therapeutic arsenal. Oncologists' understanding of biosimilars is critical to moving forward.

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Year:  2018        PMID: 28727871     DOI: 10.1001/jamaoncol.2017.2004

Source DB:  PubMed          Journal:  JAMA Oncol        ISSN: 2374-2437            Impact factor:   31.777


  9 in total

1.  Early Adoption of Biosimilar Growth Factors in Supportive Cancer Care.

Authors:  Xiaoxue Chen; Abiy Agiro; John Barron; David Debono; Michael Fisch
Journal:  JAMA Oncol       Date:  2018-12-01       Impact factor: 31.777

Review 2.  A Developer's Perspective on Clinical Evidence and Benefits for Rituximab Biosimilar Uptake, with a Focus on CT-P10.

Authors:  Dasom Choi; Soohyun Lee; Seungmin Kim; Sangwook Yoon
Journal:  Clin Drug Investig       Date:  2022-03-24       Impact factor: 2.859

Review 3.  Opportunities and Challenges in Drug Development for Pediatric Cancers.

Authors:  Theodore W Laetsch; Steven G DuBois; Julia Glade Bender; Margaret E Macy; Lucas Moreno
Journal:  Cancer Discov       Date:  2020-12-04       Impact factor: 38.272

4.  Characteristics of Clinical Trials Evaluating Biosimilars in the Treatment of Cancer: A Systematic Review and Meta-analysis.

Authors:  Doni Bloomfield; Elvira D'Andrea; Sarosh Nagar; Aaron Kesselheim
Journal:  JAMA Oncol       Date:  2022-04-01       Impact factor: 33.006

5.  A bibliometric analysis of the global research on biosimilars.

Authors:  Akram Hernández-Vásquez; Christoper A Alarcon-Ruiz; Guido Bendezu-Quispe; Daniel Comandé; Diego Rosselli
Journal:  J Pharm Policy Pract       Date:  2018-03-27

6.  Did the Introduction of Biosimilars Influence Their Prices and Utilization? The Case of Biologic Disease Modifying Antirheumatic Drugs (bDMARD) in Bulgaria.

Authors:  Konstantin Tachkov; Zornitsa Mitkova; Vladimira Boyadzieva; Guenka Petrova
Journal:  Pharmaceuticals (Basel)       Date:  2021-01-14

7.  Barriers to Oncology Biosimilars Uptake in the United States.

Authors:  Chadi Nabhan; Amy Valley; Bruce A Feinberg
Journal:  Oncologist       Date:  2018-07-26

8.  Academic oncology clinicians' understanding of biosimilars and information needed before prescribing.

Authors:  John W Cook; Megan K McGrath; Margie D Dixon; Jeffrey M Switchenko; R Donald Harvey; Rebecca D Pentz
Journal:  Ther Adv Med Oncol       Date:  2019-01-06       Impact factor: 8.168

9.  Biologicals and Biosimilars in Hematology: The Case of Rituximab.

Authors:  Arnold G Vulto
Journal:  Hemasphere       Date:  2019-11-19
  9 in total

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