Treatment of cancer with dihydropyrazino-pyrazines
US-9505764-B2 · Nov 29, 2016 · US
US10183019B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10183019-B2 |
| Application number | US-201715459111-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 15, 2017 |
| Priority date | Apr 17, 2013 |
| Publication date | Jan 22, 2019 |
| Grant date | Jan 22, 2019 |
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Provided herein are methods for treating or preventing glioblastoma multiforme (GBM) characterized by O6-methylguanine-DNA methyltransferase (MGMT) expression and/or promoter methylation status, comprising administering an effective amount of a Dihydropyrazino-Pyrazine Compound to a patient having glioblastoma multiforme (GBM) characterized by O6-methylguanine-DNA methyltransferase (MGMT) expression and/or promoter methylation status.
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What is claimed is: 1. A method for achieving a Response Assessment for Neuro-Oncology (RANO) Working Group for glioblastoma multiforme of complete response, partial response or stable disease in a patient having glioblastoma multiforme characterized by MGMT protein expression or promoter hypomethylation status, comprising administering an effective amount of 1-ethyl-7-(2-methyl-6-(1H-1,2,4-triazol-3-yl)pyridin-3-yl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one or a pharmaceutically acceptable salt, stereoisomer or tautomer thereof to said patient. 2. The method of claim 1 , wherein the glioblastoma multiforme is that in which the PI3K/mTOR pathway is activated. 3. The method of claim 2 , wherein the glioblastoma multiforme is that in which the PI3K/mTOR pathway is activated due to ERBB2 mutation, PTEN mutation or loss, NF1 mutation or loss, PIK3Ca mutation, EGFR mutation or overexpression, Met amplification, PDGFRa activation or amplification, AKT amplification or a combination thereof. 4. The method of claim 1 , wherein the glioblastoma multiforme is characterized by MGMT protein expression. 5. The method of claim 1 , wherein the glioblastoma multiforme is characterized by MGMT promoter hypomethylation.
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