Cargando…
Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development
The failure rate for phase III trials in oncology is high; quantitative predictive approaches are needed. We developed a model‐based meta‐analysis (MBMA) framework to predict progression‐free survival (PFS) from overall response rates (ORR) in relapsed/refractory multiple myeloma (RRMM), using data...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867027/ https://www.ncbi.nlm.nih.gov/pubmed/29168990 http://dx.doi.org/10.1111/cts.12524 |
_version_ | 1783308912958636032 |
---|---|
author | Teng, Zhaoyang Gupta, Neeraj Hua, Zhaowei Liu, Guohui Samnotra, Vivek Venkatakrishnan, Karthik Labotka, Richard |
author_facet | Teng, Zhaoyang Gupta, Neeraj Hua, Zhaowei Liu, Guohui Samnotra, Vivek Venkatakrishnan, Karthik Labotka, Richard |
author_sort | Teng, Zhaoyang |
collection | PubMed |
description | The failure rate for phase III trials in oncology is high; quantitative predictive approaches are needed. We developed a model‐based meta‐analysis (MBMA) framework to predict progression‐free survival (PFS) from overall response rates (ORR) in relapsed/refractory multiple myeloma (RRMM), using data from seven phase III trials. A Bayesian analysis was used to predict the probability of technical success (PTS) for achieving desired phase III PFS targets based on phase II ORR data. The model demonstrated a strongly correlated (R(2) = 0.84) linear relationship between ORR and median PFS. As a representative application of the framework, MBMA predicted that an ORR of ∼66% would be needed in a phase II study of 50 patients to achieve a target median PFS of 13.5 months in a phase III study. This model can be used to help estimate PTS to achieve gold‐standard targets in a target product profile, thereby enabling objectively informed decision‐making. |
format | Online Article Text |
id | pubmed-5867027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58670272018-03-28 Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development Teng, Zhaoyang Gupta, Neeraj Hua, Zhaowei Liu, Guohui Samnotra, Vivek Venkatakrishnan, Karthik Labotka, Richard Clin Transl Sci Research The failure rate for phase III trials in oncology is high; quantitative predictive approaches are needed. We developed a model‐based meta‐analysis (MBMA) framework to predict progression‐free survival (PFS) from overall response rates (ORR) in relapsed/refractory multiple myeloma (RRMM), using data from seven phase III trials. A Bayesian analysis was used to predict the probability of technical success (PTS) for achieving desired phase III PFS targets based on phase II ORR data. The model demonstrated a strongly correlated (R(2) = 0.84) linear relationship between ORR and median PFS. As a representative application of the framework, MBMA predicted that an ORR of ∼66% would be needed in a phase II study of 50 patients to achieve a target median PFS of 13.5 months in a phase III study. This model can be used to help estimate PTS to achieve gold‐standard targets in a target product profile, thereby enabling objectively informed decision‐making. John Wiley and Sons Inc. 2017-11-23 2018-03 /pmc/articles/PMC5867027/ /pubmed/29168990 http://dx.doi.org/10.1111/cts.12524 Text en © 2017 The Authors. Clinical and Translational Science published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Teng, Zhaoyang Gupta, Neeraj Hua, Zhaowei Liu, Guohui Samnotra, Vivek Venkatakrishnan, Karthik Labotka, Richard Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development |
title | Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development |
title_full | Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development |
title_fullStr | Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development |
title_full_unstemmed | Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development |
title_short | Model‐Based Meta‐Analysis for Multiple Myeloma: A Quantitative Drug‐Independent Framework for Efficient Decisions in Oncology Drug Development |
title_sort | model‐based meta‐analysis for multiple myeloma: a quantitative drug‐independent framework for efficient decisions in oncology drug development |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867027/ https://www.ncbi.nlm.nih.gov/pubmed/29168990 http://dx.doi.org/10.1111/cts.12524 |
work_keys_str_mv | AT tengzhaoyang modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment AT guptaneeraj modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment AT huazhaowei modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment AT liuguohui modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment AT samnotravivek modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment AT venkatakrishnankarthik modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment AT labotkarichard modelbasedmetaanalysisformultiplemyelomaaquantitativedrugindependentframeworkforefficientdecisionsinoncologydrugdevelopment |