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Whole Brain Radiotherapy Combined with G-CSF Improves the Efficacy of Immunotherapy in Patients with Brain Metastases from Non-small Cell Lung Cancer: A Clinical Study

Whole Brain Radiotherapy Combined with G-CSF Improves the Efficacy of Immunotherapy in Patients with Brain Metastases from Non-small Cell Lung Cancer: A Clinical Study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063621
Enrollment
Unknown
Registered
2022-09-13
Start date
2022-09-13
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Advanced non-small cell lung cancer with multiple brain metastases

Interventions

1:Combined with whole brain radiotherapy and G-CSF on the basis of immunotherapy

Sponsors

Tongji University Affiliated Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 35 Years

Inclusion criteria

Inclusion criteria: ? agreed to follow the trial treatment plan and visit plan, enrolled voluntarily, signed the informed consent in person, aged =18 years old, of both sexes. ? Patients with histologically or cytologically confirmed stage ? non-small cell lung cancer (according to the International Thoracic Tumor Lung Cancer Staging (IASLC) Research Manual, 8th edition) with multiple brain metastases diagnosed by brain imaging. ? The subjects had not received any treatment for brain metastases. (4) The subjects had received PD-1 inhibitor immunotherapy within 2 weeks or had not received immunotherapy. ? Measurable target lesions as judged by RECIST V1.1. ?ECOG score is 0~1; Life expectancy =12 weeks. ? Subjects must have adequate organ function. ? Fertile men and women of reproductive age were willing to use effective contraception from the time of signing the informed consent until 6 months after the last dose of the trial drug; Women of childbearing age must have a negative pregnancy test within 7 days or less before the first trial drug is administered.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
the uptake rate of COVID-19 booster shot among grandparents;grandparents' intention to get a COVID-19 booster shot;

Secondary

MeasureTime frame
grandparents' attitude towards COVID-19 booster shot;

Countries

China

Contacts

Public ContactXiaomei Gong

Tongji University Affiliated Pulmonary Hospital

gongxiaomei1981@163.com18917918986

Outcome results

None listed

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