Literature DB >> 29249839

A Calibrated Power Prior Approach to Borrow Information from Historical Data with Application to Biosimilar Clinical Trials.

Haitao Pan1, Ying Yuan2, Jielai Xia3.   

Abstract

A biosimilar refers to a follow-on biologic intended to be approved for marketing based on biosimilarity to an existing patented biological product (i.e., the reference product). To develop a biosimilar product, it is essential to demonstrate biosimilarity between the follow-on biologic and the reference product, typically through two-arm randomization trials. We propose a Bayesian adaptive design for trials to evaluate biosimilar products. To take advantage of the abundant historical data on the efficacy of the reference product that is typically available at the time a biosimilar product is developed, we propose the calibrated power prior, which allows our design to adaptively borrow information from the historical data according to the congruence between the historical data and the new data collected from the current trial. We propose a new measure, the Bayesian biosimilarity index, to measure the similarity between the biosimilar and the reference product. During the trial, we evaluate the Bayesian biosimilarity index in a group sequential fashion based on the accumulating interim data, and stop the trial early once there is enough information to conclude or reject the similarity. Extensive simulation studies show that the proposed design has higher power than traditional designs. We applied the proposed design to a biosimilar trial for treating rheumatoid arthritis.

Entities:  

Keywords:  Bayesian adaptive design; Biosimilarity index; Biosimilars; Borrow information; Calibrated power prior; Follow-up biologics; Historical data

Year:  2016        PMID: 29249839      PMCID: PMC5726611          DOI: 10.1111/rssc.12204

Source DB:  PubMed          Journal:  J R Stat Soc Ser C Appl Stat        ISSN: 0035-9254            Impact factor:   1.864


  13 in total

1.  A note on the power prior.

Authors:  Beat Neuenschwander; Michael Branson; David J Spiegelhalter
Journal:  Stat Med       Date:  2009-12-10       Impact factor: 2.373

2.  Scientific considerations for assessing biosimilar products.

Authors:  Shein-Chung Chow; Jun Wang; Laszlo Endrenyi; Peter A Lachenbruch
Journal:  Stat Med       Date:  2012-08-30       Impact factor: 2.373

3.  An adapted F-test for homogeneity of variability in follow-on biological products.

Authors:  Jun Yang; Nan Zhang; Shein-Chung Chow; Eric Chi
Journal:  Stat Med       Date:  2012-08-30       Impact factor: 2.373

4.  Impact of variability on the choice of biosimilarity limits in assessing follow-on biologics.

Authors:  Nan Zhang; Jun Yang; Shein-Chung Chow; Laszlo Endrenyi; Eric Chi
Journal:  Stat Med       Date:  2012-08-30       Impact factor: 2.373

5.  Statistical assessment of biosimilarity based on relative distance between follow-on biologics.

Authors:  Seung-Ho Kang; Shein-Chung Chow
Journal:  Stat Med       Date:  2012-09-02       Impact factor: 2.373

6.  On the interchangeability of biologic drug products.

Authors:  Laszlo Endrenyi; Chiann Chang; Shein-Chung Chow; Laszlo Tothfalusi
Journal:  Stat Med       Date:  2012-08-22       Impact factor: 2.373

7.  Comparability of critical quality attributes for establishing biosimilarity.

Authors:  Jason J Z Liao; Patrick F Darken
Journal:  Stat Med       Date:  2012-08-17       Impact factor: 2.373

8.  Comments on the FDA draft guidance on biosimilar products.

Authors:  Shein-Chung Chow; Laszlo Endrenyi; Peter A Lachenbruch
Journal:  Stat Med       Date:  2012-08-18       Impact factor: 2.373

9.  Statistical Considerations in the Design of Biosimilar Cancer Clinical Trials.

Authors:  Chul Ahn; Seung-Chun Lee
Journal:  Ungyong Tonggye Yongu       Date:  2011-06-01

10.  Radiographic, clinical, and functional outcomes of treatment with adalimumab (a human anti-tumor necrosis factor monoclonal antibody) in patients with active rheumatoid arthritis receiving concomitant methotrexate therapy: a randomized, placebo-controlled, 52-week trial.

Authors:  Edward C Keystone; Arthur F Kavanaugh; John T Sharp; Hyman Tannenbaum; Ye Hua; Leah S Teoh; Steven A Fischkoff; Elliot K Chartash
Journal:  Arthritis Rheum       Date:  2004-05
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  6 in total

1.  Bayesian clinical trial design using historical data that inform the treatment effect.

Authors:  Matthew A Psioda; Joseph G Ibrahim
Journal:  Biostatistics       Date:  2019-07-01       Impact factor: 5.899

2.  A Bayesian group sequential design for randomized biosimilar clinical trials with adaptive information borrowing from historical data.

Authors:  Wen Zhang; Zhiying Pan; Ying Yuan
Journal:  J Biopharm Stat       Date:  2022-06-09       Impact factor: 1.503

Review 3.  Novel clinical trial design and analytic methods to tackle challenges in therapeutic development in rare diseases.

Authors:  Yimei Li; Rima Izem
Journal:  Ann Transl Med       Date:  2022-09

4.  An adaptive power prior for sequential clinical trials - Application to bridging studies.

Authors:  Adrien Ollier; Satoshi Morita; Moreno Ursino; Sarah Zohar
Journal:  Stat Methods Med Res       Date:  2019-11-15       Impact factor: 3.021

Review 5.  Comparative Study of Bayesian Information Borrowing Methods in Oncology Clinical Trials.

Authors:  Liwen Su; Xin Chen; Jingyi Zhang; Fangrong Yan
Journal:  JCO Precis Oncol       Date:  2022-03

6.  Bayesian adaptive design for pediatric clinical trials incorporating a community of prior beliefs.

Authors:  Yu Wang; James Travis; Byron Gajewski
Journal:  BMC Med Res Methodol       Date:  2022-04-21       Impact factor: 4.612

  6 in total

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