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Whole-Brain Radiotherapy plus Sequential or Simultaneous Integrated Boost in the Treatment of Limited Number of Brain Metastases in Non-Small Cell lung Cancer

Whole-Brain Radiotherapy plus Sequential or Simultaneous Integrated Boost in the Treatment of Limited Number of Brain Metastases in Non-Small Cell lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018582
Enrollment
Unknown
Registered
2018-09-25
Start date
2018-10-01
Completion date
Unknown
Last updated
2018-10-01

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

Conditions

non small cell lung cancer with brain metastasis

Interventions

Two groups:whole-brain radiotherapy plus sequential versus simultaneous integrated boost

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Pathologically diagnosed patients with non-small cell lung cancer; 2. Signing radiotherapy consent before treatment, no contraindications for radiotherapy; 3. Imaging CT or MRI or PET-CT confirmed intracranial metastases lesions =10; 4. Aged 18-80 years old, ECOG 0-2 points or Kanofsky score >60 points, expected to survive more than 1 month; 5. The maximum diameter of intracranial metastatic lesions less than 5 cm; 6. Extracranial lesions receive systemic treatment as planned; 7. Can cooperate with the completion of the MMSE questionnaire content.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women, women of childbearing age are not contraceptive; 2. Patients with a history of other active malignancies other than non small cell lung cancer brain metastases before enrollment; 3. Being undergoing other clinical trials; 4. Patients with severe co-morbidity, including myocardial infarction, severe arrhythmia, severe cerebrovascular disease, mental illness, etc.; 5. No condition of regular follow-up and poor compliance; 6. Use targeted drugs; 7. Cannot accept MRI or CT examin; 8. Allergic to contrast agents; 9. Cannot meet prescription dose requirements; 10. with leptomeningeal involvement.

Design outcomes

Primary

MeasureTime frame
Mini-mental State Examination;

Countries

China

Contacts

Public ContactDaiyuan MA

Affiliated Hospital of North Sichuan Medical College

mdylx@163.com+86 13990889661

Outcome results

None listed

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