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A study to evaluate the safety and effectiveness of PCV chemotherapy in patients with recurrent high-grade glioma with IDH1/2 mutation

A study to evaluate the safety and effectiveness of PCV chemotherapy in patients with recurrent high-grade glioma with IDH1/2 mutation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15005759
Enrollment
Unknown
Registered
2014-12-31
Start date
2015-02-02
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Recurrent High-grade Glioma

Interventions

Case series:PCV Chemotherapy (Lomustine/vincristine/c kappa hydrazine)

Sponsors

Tiantan Hospital,Capital Medical University; Heibei Yanda Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. A diagnosis of high-grade glioma was established by pathological method,and the recurrency of the disease is ongoing; 2. the report of the pathological diagnosis contained the status of IDH gene, and showed that IDH1/2 mutation existed; 3. the age of the patient is between 18 years old and 70 years old; 4. the condition of the patient permits the procedure of chemotherapy using PCV schema; 5. the patient is informed consent, and willing to join in this research.

Exclusion criteria

Exclusion criteria: 1. The diagnosis is not recurrent high-grade glioma; 2. the diagnosis of high-grade glioma was not established by pathological method; 3. no molecular neuropathological report is available, or the report showed that IDH1/2 mutation did not exist; 4. the age of the patient does not meet the requirement of this research; 5. the condition of the patient does not permit the procedure of chemotherapy using PCV schema; 6. there are other conditions that the clinicans believe that the PCV chemotherapy is not appropriate for the patient; 7. the patient is not willing to join in this research.

Design outcomes

Primary

MeasureTime frame
progression free survival;6-month progression-free survival rate;12-month progression-free survival rate;6-month survival rate;12-month survival rate;6-month life quality;12-month life quality;

Countries

China

Contacts

Public ContactJi Nan
cnpsycho@163.com+86 13910713896

Outcome results

None listed

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