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Glioblastoma Response Prediction to Apatinib

Study on Predicting Response of Recurrent Glioblastoma to Apatinib

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04814329
Enrollment
18
Registered
2021-03-24
Start date
2021-04-22
Completion date
2023-06-30
Last updated
2023-07-21

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

Conditions

Glioblastoma

Keywords

Vascular Endothelial Growth Factor Receptor 2, Biomarkers, glioblastoma

Brief summary

Anti-angiogenic therapy is an important treatment strategy for recurrent glioblastoma. Our previous study provided evidence for a potential benefit of apatinib, a humanized monoclonal antibody against VEGFR-2, when added to temozolomide chemotherapy in patients with recurrent glioblastoma. Some patients showed durable responses and prolonged survival, with recorded survival times of over 30 months in 6.4% patients. However, a subset of patients progressed in 2 months. There is a strong need to better predict and monitor apatinib treatment response to prevent patients from adverse effects of ineffective therapy. In this study, whole genome sequencing and RNA-sequencing of formalin-fixed, paraffin-embedded tumor materials from the participants who received apatinib and temozolomide treatment will be performed to identify the response biomarkers and patients who may benefit most from apatinib, avoiding unnecessary potential toxicity and cost for those who are unlikely to benefit from the drug.

Interventions

OTHERgenetic characteristic

the underlying genetic characteristics that prodicting response

Sponsors

Beijing Sanbo Brain Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Age 18-70 years old 2. recurrent glioblastoma 3. received apatinib plus temozolomide treatment,response and survival data were available 4. tumor tissues were acquired

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
genetic outcomeup to 2 yearsresponse prodicting biomarker

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026