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Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience
PURPOSE: We sought to develop placental growth factor as a predictive pharmacodynamic biomarker for motesanib efficacy as first-line therapy in patients with advanced nonsquamous non–small-cell lung cancer. EXPERIMENTAL DESIGN: Placental growth factor was evaluated at baseline and study week 4 (afte...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196848/ https://www.ncbi.nlm.nih.gov/pubmed/25314641 http://dx.doi.org/10.1371/journal.pone.0108048 |
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author | Bass, Michael B. Yao, Bin Hei, Yong-Jiang Ye, Yining Davis, Gerard J. Davis, Michael T. Kaesdorf, Barbara A. Chan, Sabrina S. Patterson, Scott D. |
author_facet | Bass, Michael B. Yao, Bin Hei, Yong-Jiang Ye, Yining Davis, Gerard J. Davis, Michael T. Kaesdorf, Barbara A. Chan, Sabrina S. Patterson, Scott D. |
author_sort | Bass, Michael B. |
collection | PubMed |
description | PURPOSE: We sought to develop placental growth factor as a predictive pharmacodynamic biomarker for motesanib efficacy as first-line therapy in patients with advanced nonsquamous non–small-cell lung cancer. EXPERIMENTAL DESIGN: Placental growth factor was evaluated at baseline and study week 4 (after 3 weeks treatment) in an exploratory analysis of data from a randomized phase 2 study of motesanib 125 mg once daily plus carboplatin/paclitaxel and in a prespecified analysis of data from a randomized, double-blind phase 3 study of motesanib 125 mg once daily plus carboplatin/paclitaxel vs placebo plus carboplatin/paclitaxel (MONET1). Associations between fold-change from baseline in placental growth factor and overall survival were evaluated using Cox proportional hazards models. RESULTS: In the phase 2 study, serum placental growth factor increased from baseline a mean 2.8-fold at study week 4. Patients with ≥2.2-fold change from baseline in placental growth factor (n = 18) had significantly longer overall survival than those with <2.2-fold change (n = 19; 22.9 vs 7.9 months; hazard ratio, 0.30; 95% CI, 0.12–0.74; P = 0.009). Consequently, placental growth factor was investigated as a pharmacodynamic biomarker in the phase 3 MONET1 study. There was no association between log-transformed placental growth factor fold-change from baseline to week 4 (continuous variable) and overall survival (hazard ratio, 0.98; 95% CI, 0.79–1.22; P = 0.868). MONET1 did not meet its primary endpoint of overall survival. Likewise, median overall survival was similar among patients with ≥2.0-fold change in placental growth factor (n = 229) compared with <2.0-fold change (n = 127; 14.8 vs 13.8 months; hazard ratio, 0.88; 95% CI, 0.67–1.15, P = 0.340). CONCLUSIONS: Our results illustrate the challenges of successfully translating phase 2 biomarker results into phase 3 studies. TRIAL REGISTRATION: ClinicalTrials.gov NCT00460317, NCT00369070 |
format | Online Article Text |
id | pubmed-4196848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41968482014-10-16 Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience Bass, Michael B. Yao, Bin Hei, Yong-Jiang Ye, Yining Davis, Gerard J. Davis, Michael T. Kaesdorf, Barbara A. Chan, Sabrina S. Patterson, Scott D. PLoS One Research Article PURPOSE: We sought to develop placental growth factor as a predictive pharmacodynamic biomarker for motesanib efficacy as first-line therapy in patients with advanced nonsquamous non–small-cell lung cancer. EXPERIMENTAL DESIGN: Placental growth factor was evaluated at baseline and study week 4 (after 3 weeks treatment) in an exploratory analysis of data from a randomized phase 2 study of motesanib 125 mg once daily plus carboplatin/paclitaxel and in a prespecified analysis of data from a randomized, double-blind phase 3 study of motesanib 125 mg once daily plus carboplatin/paclitaxel vs placebo plus carboplatin/paclitaxel (MONET1). Associations between fold-change from baseline in placental growth factor and overall survival were evaluated using Cox proportional hazards models. RESULTS: In the phase 2 study, serum placental growth factor increased from baseline a mean 2.8-fold at study week 4. Patients with ≥2.2-fold change from baseline in placental growth factor (n = 18) had significantly longer overall survival than those with <2.2-fold change (n = 19; 22.9 vs 7.9 months; hazard ratio, 0.30; 95% CI, 0.12–0.74; P = 0.009). Consequently, placental growth factor was investigated as a pharmacodynamic biomarker in the phase 3 MONET1 study. There was no association between log-transformed placental growth factor fold-change from baseline to week 4 (continuous variable) and overall survival (hazard ratio, 0.98; 95% CI, 0.79–1.22; P = 0.868). MONET1 did not meet its primary endpoint of overall survival. Likewise, median overall survival was similar among patients with ≥2.0-fold change in placental growth factor (n = 229) compared with <2.0-fold change (n = 127; 14.8 vs 13.8 months; hazard ratio, 0.88; 95% CI, 0.67–1.15, P = 0.340). CONCLUSIONS: Our results illustrate the challenges of successfully translating phase 2 biomarker results into phase 3 studies. TRIAL REGISTRATION: ClinicalTrials.gov NCT00460317, NCT00369070 Public Library of Science 2014-10-14 /pmc/articles/PMC4196848/ /pubmed/25314641 http://dx.doi.org/10.1371/journal.pone.0108048 Text en © 2014 Bass et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bass, Michael B. Yao, Bin Hei, Yong-Jiang Ye, Yining Davis, Gerard J. Davis, Michael T. Kaesdorf, Barbara A. Chan, Sabrina S. Patterson, Scott D. Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience |
title | Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience |
title_full | Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience |
title_fullStr | Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience |
title_full_unstemmed | Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience |
title_short | Challenges in Developing a Validated Biomarker for Angiogenesis Inhibitors: The Motesanib Experience |
title_sort | challenges in developing a validated biomarker for angiogenesis inhibitors: the motesanib experience |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196848/ https://www.ncbi.nlm.nih.gov/pubmed/25314641 http://dx.doi.org/10.1371/journal.pone.0108048 |
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