Skip to content

Cancelled by the investigator. A Perfusion MRI-based Spatiotemporal Heterogeneity Quantification Nomogram Model for Predicting Antiangiogenic Therapy Failure in Recurrent Glioblastoma

A Perfusion MRI-based Spatiotemporal Heterogeneity Quantification Nomogram Model for Predicting Antiangiogenic Therapy Failure in Recurrent Glioblastoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103199
Enrollment
Unknown
Registered
2025-05-26
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastoma

Interventions

Observation group:None

Sponsors

Chongqing Huatan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) patients diagnosed with the first recurrence of glioblastoma via clinicoradiological confirmation following the Stupp standard treatment protocol [1]; (2) patients received bevacizumab (Avastin; Roche) at 10 mg/kg, either alone or alongside other drugs such as temozolomide, irinotecan, oxaliplatin, or 5-fluorouracil, with differing dosage schedules; (3) availability of baseline MRI examinations including T2WI, T2-FLAIR, CE-T1WI, and conventional DSC perfusion prior to antiangiogenic therapy; (4) between the initiation of antiangiogenic therapy and tumor progression, at least three consecutive MRI scans (using the same protocol as baseline) were performed, with each scan separated by a minimum interval of one month; (5) serum VEGF was measured once before antiangiogenic therapy and three consecutive times after the initiation of treatment, with at least a two-week interval between each measurement.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: (1) patients with less than 3 follow-up MRI examinations after the initiation of antiangiogenic therapy; (2) patients who underwent additional therapeutic interventions including reoperation, re-irradiation, or other immunotherapies; (3) patients who exhibited tumor progression during the first three consecutive MRI scans after the initiation of treatment.

Design outcomes

Primary

MeasureTime frame
Cerebral Blood Volume (CBV);Time to progression, TTP;

Secondary

MeasureTime frame
Progression mode;

Countries

China

Contacts

Public ContactHuiyu Ruan

Chongqing Huatan Hospital

jianzhong210@163.com+86 191 1215 6748

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026