Skip to content

Survival analysis of patients with stage III unresectable non-small cell lung cancer without combination radiotherapy: a real-world observational study exploring the cornerstone status of radiotherapy in the immune era

Survival analysis of patients with stage III unresectable non-small cell lung cancer without combination radiotherapy: a real-world observational study exploring the cornerstone status of radiotherapy in the immune era

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118155
Enrollment
Unknown
Registered
2026-02-02
Start date
2026-02-06
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

lung cancer

Interventions

Observation group:NA

Sponsors

Affiliated Hospital of Guilin Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>=18 years old; 2. Histopathological diagnosis of locally advanced NSCLC (AJCC 8th edition); 3. Judgment that it cannot be surgically resected (based on chest CT, PET-CT and mediastinoscopy evaluation); 4. Receiving >= 2 cycles of platinum-containing chemotherapy (cisplatin/carboplatin/nidaplatin + pemetrexed/paclitaxel/gemcitabine, etc.) combined with PD-1/PD-L1 inhibitors (tislelizumab, pembrolizumab, sintilimab, etc.); 5. The interval from diagnosis to the first chemotherapy =8 weeks apart) can be evaluated; 8. Survival status can be confirmed by hospital system or telephone follow-up.

Exclusion criteria

Exclusion criteria: 1. Driver gene positive: EGFR-sensitive mutation (Ex19del/L858R), ALK/ROS1/RET/MET fusion, etc.; 2. Previous neoadjuvant chemotherapy, immunotherapy or other systemic anti-cancer therapy; 3. Active autoimmune disease (requiring immunosuppressant therapy), interstitial lung disease (CTCAE=grade 2), etc.

Design outcomes

Primary

MeasureTime frame
Median progression-free survival;

Secondary

MeasureTime frame
Median overall survival time;Disease Control Rate;Objective Response Rate;12-month survival rate;12-month progression-free survival;Adverse events;

Countries

China

Contacts

Public ContactZhu Lin

Affiliated Hospital of Guilin Medical College

doctor_zl0301@163.com+86 773 288 2906

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026