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A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma
PURPOSE: To estimate the maximum tolerated dose (MTD) and/or identify the recommended Phase II dose (RP2D) for combined INC280 and buparlisib in patients with recurrent glioblastoma with homozygous phosphatase and tensin homolog (PTEN) deletion, mutation or protein loss. METHODS: This multicenter, o...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938467/ https://www.ncbi.nlm.nih.gov/pubmed/31776899 http://dx.doi.org/10.1007/s11060-019-03337-2 |
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author | van den Bent, Martin Azaro, Analia De Vos, Filip Sepulveda, Juan Yung, W. K. Alfred Wen, Patrick Y. Lassman, Andrew B. Joerger, Markus Tabatabai, Ghazaleh Rodon, Jordi Tiedt, Ralph Zhao, Sylvia Kirsilae, Tiina Cheng, Yi Vicente, Sergio Balbin, O. Alejandro Zhang, Hefei Wick, Wolfgang |
author_facet | van den Bent, Martin Azaro, Analia De Vos, Filip Sepulveda, Juan Yung, W. K. Alfred Wen, Patrick Y. Lassman, Andrew B. Joerger, Markus Tabatabai, Ghazaleh Rodon, Jordi Tiedt, Ralph Zhao, Sylvia Kirsilae, Tiina Cheng, Yi Vicente, Sergio Balbin, O. Alejandro Zhang, Hefei Wick, Wolfgang |
author_sort | van den Bent, Martin |
collection | PubMed |
description | PURPOSE: To estimate the maximum tolerated dose (MTD) and/or identify the recommended Phase II dose (RP2D) for combined INC280 and buparlisib in patients with recurrent glioblastoma with homozygous phosphatase and tensin homolog (PTEN) deletion, mutation or protein loss. METHODS: This multicenter, open-label, Phase Ib/II study included adult patients with glioblastoma with mesenchymal-epithelial transcription factor (c-Met) amplification. In Phase Ib, patients received INC280 as capsules or tablets in combination with buparlisib. In Phase II, patients received INC280 only. Response was assessed centrally using Response Assessment in Neuro-Oncology response criteria for high-grade gliomas. All adverse events (AEs) were recorded and graded. RESULTS: 33 patients entered Phase Ib, 32 with altered PTEN. RP2D was not declared due to potential drug–drug interactions, which may have resulted in lack of efficacy; thus, Phase II, including 10 patients, was continued with INC280 monotherapy only. Best response was stable disease in 30% of patients. In the selected patient population, enrollment was halted due to limited activity with INC280 monotherapy. In Phase Ib, the most common treatment-related AEs were fatigue (36.4%), nausea (30.3%) and increased alanine aminotransferase (30.3%). MTD was identified at INC280 Tab 300 mg twice daily + buparlisib 80 mg once daily. In Phase II, the most common AEs were headache (40.0%), constipation (30.0%), fatigue (30.0%) and increased lipase (30.0%). CONCLUSION: The combination of INC280/buparlisib resulted in no clear activity in patients with recurrent PTEN-deficient glioblastoma. More stringent molecular selection strategies might produce better outcomes. Trial registration: NCT01870726. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11060-019-03337-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6938467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-69384672020-01-14 A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma van den Bent, Martin Azaro, Analia De Vos, Filip Sepulveda, Juan Yung, W. K. Alfred Wen, Patrick Y. Lassman, Andrew B. Joerger, Markus Tabatabai, Ghazaleh Rodon, Jordi Tiedt, Ralph Zhao, Sylvia Kirsilae, Tiina Cheng, Yi Vicente, Sergio Balbin, O. Alejandro Zhang, Hefei Wick, Wolfgang J Neurooncol Clinical Study PURPOSE: To estimate the maximum tolerated dose (MTD) and/or identify the recommended Phase II dose (RP2D) for combined INC280 and buparlisib in patients with recurrent glioblastoma with homozygous phosphatase and tensin homolog (PTEN) deletion, mutation or protein loss. METHODS: This multicenter, open-label, Phase Ib/II study included adult patients with glioblastoma with mesenchymal-epithelial transcription factor (c-Met) amplification. In Phase Ib, patients received INC280 as capsules or tablets in combination with buparlisib. In Phase II, patients received INC280 only. Response was assessed centrally using Response Assessment in Neuro-Oncology response criteria for high-grade gliomas. All adverse events (AEs) were recorded and graded. RESULTS: 33 patients entered Phase Ib, 32 with altered PTEN. RP2D was not declared due to potential drug–drug interactions, which may have resulted in lack of efficacy; thus, Phase II, including 10 patients, was continued with INC280 monotherapy only. Best response was stable disease in 30% of patients. In the selected patient population, enrollment was halted due to limited activity with INC280 monotherapy. In Phase Ib, the most common treatment-related AEs were fatigue (36.4%), nausea (30.3%) and increased alanine aminotransferase (30.3%). MTD was identified at INC280 Tab 300 mg twice daily + buparlisib 80 mg once daily. In Phase II, the most common AEs were headache (40.0%), constipation (30.0%), fatigue (30.0%) and increased lipase (30.0%). CONCLUSION: The combination of INC280/buparlisib resulted in no clear activity in patients with recurrent PTEN-deficient glioblastoma. More stringent molecular selection strategies might produce better outcomes. Trial registration: NCT01870726. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11060-019-03337-2) contains supplementary material, which is available to authorized users. Springer US 2019-11-27 2020 /pmc/articles/PMC6938467/ /pubmed/31776899 http://dx.doi.org/10.1007/s11060-019-03337-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Clinical Study van den Bent, Martin Azaro, Analia De Vos, Filip Sepulveda, Juan Yung, W. K. Alfred Wen, Patrick Y. Lassman, Andrew B. Joerger, Markus Tabatabai, Ghazaleh Rodon, Jordi Tiedt, Ralph Zhao, Sylvia Kirsilae, Tiina Cheng, Yi Vicente, Sergio Balbin, O. Alejandro Zhang, Hefei Wick, Wolfgang A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma |
title | A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma |
title_full | A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma |
title_fullStr | A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma |
title_full_unstemmed | A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma |
title_short | A Phase Ib/II, open-label, multicenter study of INC280 (capmatinib) alone and in combination with buparlisib (BKM120) in adult patients with recurrent glioblastoma |
title_sort | phase ib/ii, open-label, multicenter study of inc280 (capmatinib) alone and in combination with buparlisib (bkm120) in adult patients with recurrent glioblastoma |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938467/ https://www.ncbi.nlm.nih.gov/pubmed/31776899 http://dx.doi.org/10.1007/s11060-019-03337-2 |
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