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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)
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 2
Contacten en locaties
Studiecontact
- Naam: Chao Family Comprehensive Cancer Center University of California, Irvine
- Telefoonnummer: 1-877-827-8839
- E-mail: ucstudy@uci.edu
Studie Contact Back-up
- Naam: University of California Irvine Medical
Studie Locaties
-
-
California
-
Orange, California, Verenigde Staten, 92868
- Chao Family Comprehensive Cancer Center, University of California, Irvine
-
Contact:
- Carlen Yuen, MD
- Telefoonnummer: 877-827-8839
- E-mail: ucstudy@uci.edu
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Newly Diagnosed Elderly or Frail Glioblastoma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andere namen:
|
|
Experimenteel: Recurrent Elderly or Frail Glioblastoma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andere namen:
|
|
Experimenteel: Newly Diagnosed Frail (Non-GBM) Malignant Glioma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andere namen:
|
|
Experimenteel: Recurrent Frail (Non-GBM) Malignant Glioma
GammaTile®
|
GammaTile is a bioabsorbable collagen tile embedded with cesium-131 radioactive seeds.
Andere namen:
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Percentage of Participants who were able to receive the GammaTile Implant
Tijdsspanne: 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
Tijdsspanne: 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
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Progression-Free Survival (PFS)
Tijdsspanne: 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)
Tijdsspanne: 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
|
Medewerkers en onderzoekers
Sponsor
Medewerkers
Onderzoekers
- Hoofdonderzoeker: Carlen Yuen, MD, Chao Family Comprehensive Cancer Center
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- STUDY00001050
- UCI-25-151 (Andere identificatie: UCI CFCCC)
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
product vervaardigd in en geëxporteerd uit de V.S.
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