- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07821112
Phase II Elderly/Frail Pts With Newly Diagnosed or Recurrent Malignant Glioma Tx Treated With Cesium-131 GammaTile® (ENDURANCE)
A Phase II Study of Elderly and Frail Patients With Newly Diagnosed or Recurrent Malignant Glioma Treated With Cesium-131 GammaTile® (ENDURANCE Trial)
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Fase
- Fase 2
Kontakter og plasseringer
Studiekontakt
- Navn: Chao Family Comprehensive Cancer Center University of California, Irvine
- Telefonnummer: 1-877-827-8839
- E-post: ucstudy@uci.edu
Studer Kontakt Backup
- Navn: University of California Irvine Medical
Studiesteder
-
-
California
-
Orange, California, Forente stater, 92868
- Chao Family Comprehensive Cancer Center, University of California, Irvine
-
Ta kontakt med:
- Carlen Yuen, MD
- Telefonnummer: 877-827-8839
- E-post: ucstudy@uci.edu
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Supratentorial
- A bi-dimensionally measurable lesion of at least 10 mm, visible on two or more axial slices 5 mm apart.
- The pre-operative tumor planned for resection is ≤ 7 cm in maximal dimension.
- Tumor, which in the opinion of the enrolling neurosurgeon, is amenable to attempted gross total resection (GTR) or near total resection (NTR).
- Anticipated GT placement (i.e., closest aspect of post resection tumor bed anticipated to receive GT placement) that is > 15mm from the optic chiasm or brainstem.
- If multifocal, must be fully resectable in one operative bed. Surgical protocol will follow current institutional standards.
- Able to receive 5-aminolevulinic acid (5-ALA, Gleolan) or other institutionally standard immunofluorescent-guidance such as fluorescein, prior to surgery to optimize GTR or NTR of enhancing tumor.
Karnofsky Performance Scale (KPS)
- Elderly GBM: baseline KPS score of ≥ 60.
- Frail GBM: baseline (pre-GBM diagnosis) is <70 and surgical management is expected to improve KPS to ≥ 60.
Exclusion Criteria:
- Staged surgery planned (prior biopsy allowed).
- Bilateral tumors, or multi-focal tumors that cannot be encompassed in one operative field.
- Spinal tumors are excluded.
- Enhancing extension into brainstem or thalamus, or significant invasion into the corpus callosum that would preclude a high likelihood of GTR or NTR.
- Leptomeningeal disease not expected to be encompassed by the surgical resection.
- Evidence of diffuse leptomeningeal disease that requires whole brain irradiation are excluded from this trial.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Newly Diagnosed Elderly or Frail Glioblastoma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andre navn:
|
|
Eksperimentell: Recurrent Elderly or Frail Glioblastoma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andre navn:
|
|
Eksperimentell: Newly Diagnosed Frail (Non-GBM) Malignant Glioma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andre navn:
|
|
Eksperimentell: Recurrent Frail (Non-GBM) Malignant Glioma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of Participants who were able to receive the GammaTile Implant
Tidsramme: 28 days
|
Feasibility is defined by proportion of participants who were able to be treated with GammaTile
|
28 days
|
|
Number of Participants with Treatment-related Adverse Events
Tidsramme: 24 months
|
Safety and tolerability will be determined by the proportion, nature, and severity of treatment-related adverse events in accordance with the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 5.0. Adverse events (AEs) are reported based on clinical laboratory tests, vital sign and weight measurements, physical examinations, performance status evaluations, magnetic resonance imaging, and any other medically indicated assessments. |
24 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Progression-Free Survival (PFS)
Tidsramme: 24 months
|
Progression-Free Survival (PFS) as measured by Response Assessment in Neuro-Oncology (RANO) 2.0 on brain MRI with and without contrast.
|
24 months
|
|
Overall Survival (OS)
Tidsramme: 24 months
|
Overall Survival (OS) as measured by time from registration to death of any cause as documented dates of registration and death within the electronic medical system.
|
24 months
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Carlen Yuen, MD, Chao Family Comprehensive Cancer Center
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- STUDY00001050
- UCI-25-151 (Annen identifikator: UCI CFCCC)
Legemiddel- og utstyrsinformasjon, studiedokumenter
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