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Clinical Trial of Stereotactic Body Radiation Therapy with Third-Line Tyrosine Kinase Inhibitor in Patients with EGFRm Oligometastatic Non-Small-Cell Lung Cancer

Clinical Trial of Stereotactic Body Radiation Therapy with Third-Line Tyrosine Kinase Inhibitor in Patients with EGFRm Oligometastatic Non-Small-Cell Lung Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054857
Enrollment
Unknown
Registered
2021-12-28
Start date
2021-12-28
Completion date
Unknown
Last updated
2022-12-12

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

Interventions

Aggressive local stereotactic radiotherapy with third-line TKI vs. TKI only:No

Sponsors

Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 and <= 80 years; 2. Eligible participants had pathologically confirmed adenocarcinoma, gene sequencing confirmed EGFRm, stage IIIB-IV, receive either third-line tyrosine kinase inhibitor (TKI) treatment alone or with stereotactic radiotherapy; 3. According to RECIST 1.1, there is at least one measurable lesion; 4. Eastern Cooperative Oncology Group performance status score of <= 2; 5. No more than 5 metastases in total; 6. From 2018 to 2021, received medical treatment in Sichuan Provincial People's Hospital; 7. Informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Used imilar drugs in clinical trials; 3. Patients deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
ORR (Objective Response Rate);PFS (Progress-Free Survival);

Secondary

MeasureTime frame
OS (Overall Survival);

Countries

China

Contacts

Public ContactWang Xiaoshan

Sichuan Provincial People's Hospital

xiaoshanwangxue@163.com+86 13880626968

Outcome results

None listed

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