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A Study on the Safety and Efficacy of Aumolertinib Combined with Consolidative Radiotherapy or Thermal Ablation in the Treatment of Advanced EGFR-Mutated Non-Small Cell Lung Cancer

A Study on the Safety and Efficacy of Aumolertinib Combined with Consolidative Radiotherapy or Thermal Ablation in the Treatment of Advanced EGFR-Mutated Non-Small Cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124574
Enrollment
Unknown
Registered
2026-05-14
Start date
2026-05-18
Completion date
Unknown
Last updated
2026-05-18

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

Interventions

Consolidative Radiotherapy or Thermal Ablation group:Consolidative Radiotherapy or Thermal Ablation

Sponsors

Xiaolan People's Hospital of Zhongshan City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with histologically confirmed advanced NSCLC harboring sensitive EGFR mutations (exon 19 deletion or exon 21 L858R mutation), with no restrictions on the number, location, or size of metastatic lesions (including both oligometastases and multiple metastases). 2.Have not previously received EGFR-TKIs or immune checkpoint inhibitors; 3.No history of interstitial lung disease; 4.Basic functional status of vital organs is essentially normal. 5.Aged >= 18 years; 6.Signed informed consent form;

Exclusion criteria

Exclusion criteria: 1.Patients currently receiving other effective treatments; 2.Refractory nausea and vomiting, chronic gastrointestinal diseases, or inability to swallow medication, which may affect the ingestion, transit, or absorption of the drug. 3.Patients with severe concomitant diseases or any other conditions deemed by the investigator to make the patient unsuitable for participation in this study. 4.Patients who have not undergone regular efficacy and safety assessments.

Design outcomes

Primary

MeasureTime frame
Progression-free survival (PFS);

Secondary

MeasureTime frame
Overall survival;Duration of almonertinib treatment;Treatment-related adverse events;

Countries

China

Contacts

Public ContactXin Li

Xiaolan People's Hospital of Zhongshan City

lixinwp@163.com+86 760 89822346

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026