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A retrospective, multicenter, real-world study on thermal ablation for the treatment of patients with EGFR-sensitive mutant non-small cell lung cancer (NSCLC) (RAC-NSCLC)

A retrospective, multicenter, real-world study on thermal ablation for the treatment of patients with EGFR-sensitive mutant non-small cell lung cancer (NSCLC) (RAC-NSCLC)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111145
Enrollment
Unknown
Registered
2025-10-27
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

EGFR-sensitive mutated non-small cell lung cancer

Interventions

Observation group:None

Sponsors

Shanghai Pudong Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with stage I-III non-squamous NSCLC confirmed by histology or cytology (according to the 9th edition of the AJCC lung Cancer staging criteria). 2. Tumor tissue samples or blood samples have been confirmed by local laboratory tests to have EGFR-sensitive mutations (including EGFR19del/ 21L858R, which can exist alone or coexist with other EGFR site mutations). If the tumor tissue is inaccessible or the patient does not undergo tissue biopsy, a blood sample can be sent for testing. 3. Have received local ablation treatment and completed at least one imaging follow-up after treatment

Exclusion criteria

Exclusion criteria: In addition to NSCLC, another malignant disease has been diagnosed within the past five years (excluding completely resected basal cell carcinoma, carcinoma in situ of the bladder, and carcinoma in situ of the cervix). 2. There are contraindications for ablation (including but not limited to) a. Individuals with severe bleeding tendencies and coagulation disorders that cannot be corrected in the short term (prothrombin time >18 seconds, prothrombin activity 38.5 ?; d. Those with severe anemia, dehydration and serious disorders of nutritional metabolism that cannot be corrected or improved in the short term; e. Anticoagulant therapy and/or antiplatelet drugs (except for new oral anticoagulant drugs such as dabigatran and rivaroxaban) were discontinued for no more than 5 to 7 days before ablation; f. Patients with implanted cardiac pacemakers. 3. Those who are deemed unsuitable for inclusion by the doctor.

Design outcomes

Primary

MeasureTime frame
3-year event-free survival rate;

Secondary

MeasureTime frame
Local Control Rate, LCR;

Countries

China

Contacts

Public ContactLi Maoquan

Shanghai Pudong Hospital

cjr.limaoquan@vip.163.com+86 139 0170 2180

Outcome results

None listed

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