2021
DOI: 10.1093/noajnl/vdab169
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Preclinical and clinical evaluation of German-sourced ONC201 for the treatment of H3K27M-mutant diffuse intrinsic pontine glioma

Abstract: Background Diffuse intrinsic pontine glioma (DIPG) is a fatal childhood brainstem tumor for which radiation is the only treatment. Case studies report a clinical response to ONC201 for patients with H3K27M-mutant gliomas. Oncoceutics (ONC201) is only available in the United States and Japan; however, in Germany, DIPG patients can be prescribed and dispensed a locally produced compound—ONC201 German-sourced ONC201 (GsONC201). Pediatric oncologists face the dilemma of supporting the administrat… Show more

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Cited by 19 publications
(12 citation statements)
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References 45 publications
(67 reference statements)
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“…ONC201 is an immunostimulatory small molecule antagonist dopamine receptors (DRD2/3) that has been reported in a range of malignancies including H3 K27M -mutant DIPG/DMG [ 103 ]. In preclinical murine models, this has been shown to double the OS [ 104 ]. Currently, there is an ongoing phase 2 clinical trial that looks to assess its efficacy further in pediatric H3 K27M -mutant gliomas.…”
Section: Ongoing Investigations and Future Considerationsmentioning
confidence: 99%
“…ONC201 is an immunostimulatory small molecule antagonist dopamine receptors (DRD2/3) that has been reported in a range of malignancies including H3 K27M -mutant DIPG/DMG [ 103 ]. In preclinical murine models, this has been shown to double the OS [ 104 ]. Currently, there is an ongoing phase 2 clinical trial that looks to assess its efficacy further in pediatric H3 K27M -mutant gliomas.…”
Section: Ongoing Investigations and Future Considerationsmentioning
confidence: 99%
“…Furthermore, ACTs targeting the ganglioside GD2 as well as HER2 show promising preclinical results (discussed below). 69,70 Benefits-ACT success stories.…”
Section: Adoptive Cell Transfer Strategiesmentioning
confidence: 99%
“…This is underpinned by sophisticated improvements to protocol-driven clinical trials that utilize combinations of chemotherapies that attempt to address the somatic and epigenetic heterogeneity of these cancers. However, for some of the most aggressive types of childhood malignancies, there remains no effective pharmacologic intervention and children succumb to their disease within a short timeframe (39,(43)(44)(45). As 35% to 40% of children's malignancies originate in cells of the lymphoid linage where BCL6 plays a critical role in their maturation, there is a potential for targeting BCL6 in combination with therapies focused on the recurring somatic alterations responsible for disease initiation and progression.…”
Section: Bcl6 In Pediatric Cancersmentioning
confidence: 99%
“…DMG. DMGs, including DIPG, are pediatric CNS tumors recognized as the most lethal of all children's cancers (44,45). Palliative radiotherapy is the only approved treatment, with median survival just 9 to 11 months postdiagnosis (79).…”
Section: Pediatric Hggmentioning
confidence: 99%