About this trial
This study will gather data from new and existing patients with patient medical records, and patient/family/caregiver reported information to establish a clear natural history of disease suitable to serve as an external, contemporary or historical control arm for future therapeutic development programs of drugs, devices, or biologic interventions in DMG or DIPG.
Eligibility criteria
Qualifiers
Diagnosis of diffuse midline glioma according to the WHO 2021 Classification of Tumors of the Central Nervous System diagnostic criteria including diffuse intrinsic pontine glioma (DIPG). In the absence of a pathologically confirmed diagnosis, a grade IV glioma involving the thalamus, hypothalamus, brainstem, cerebellum, midbrain, or spinal cord, or with a pontine epicenter and diffuse involvement of the pons.
Patients with any performance status, comorbidity or disease severity are eligible
Patients or their legally-authorized representative must be willing and able to provide electronic, informed consent (and assent, if applicable)
Informed consent obtained for the XCELSIOR longitudinal outcomes registry (NCT03793088).
Disqualifiers
Patient or legally-authorized representative is unable to provide informed consent.
Patient or caregiver is unable to complete the PRO and ClinRO by an electronic platform.
Trial design
Treatments tested in this trial
- Not listed