Stage IA Lung Cancer
Conditions
Brief summary
The purpose of this study is to investigate the efficacy and safety of RFA through a transthoracic or transbronchial approach in the treatment of early-stage peripheral lung cancer.
Detailed description
This study is designed as a prospective, randomized controlled trial with 110 participants, randomized in a 1:1 ratio to CT-guided RFA and bronchoscopy-guided RFA groups. The primary study endpoint is the complete ablation rate at 6 months post-ablation. Secondary study endpoints are technical success rate, complete ablation rate at 12 months post-ablation, local control rate at 1, 2, and 3 years post-ablation, progression free survival, overall survival, and safety. Demographic data, clinical baseline characteristics, CT follow-up data, and safety data will be collected and recorded.
Interventions
DEVICEThe disposable pulmonary radiofrequency ablation catheter and pulmonary radiofrequency ablation system
Procedure: In combination with guided bronchoscopy and CBCT, the ablation catheter is placed in the target lesion. CBCT confirms the tool in the lesion, adjusts the position of the ablation catheter, and monitors the extent of ablation.
DEVICEThe disposable percutaneous radiofrequency ablation needle and pulmonary radiofrequency ablation system
Procedure: The ablation needle is punctured into the lesion under CT guidance. The extent of the ablation is monitored by CT.
Sponsors
Shanghai Chest Hospital
Hangzhou Broncus Medical Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age greater than 18 years. 2. Primary peripheral lung cancer diagnosed by pathology, and preoperative staging reveals clinical stage T1N0M0, stage IA. 3. The planned ablation lesions are assessed to be amenable to CT-guided and bronchoscopy-guided ablation. 4. Assessed as inoperable or refused surgery, agree to undergo initial ablation therapy, and sign informed consent.
Exclusion criteria
1. Patients with platelet \< 50 × 10 9/L, severe bleeding tendency and coagulation dysfunction that cannot be corrected in a short period of time. 2. Patients with severe pulmonary fibrosis and pulmonary hypertension. 3. Perilesional infection and radiation inflammation, puncture site skin infection is not well controlled, systemic infection, high fever \> 38.5℃. 4. Patients with severe liver, kidney, heart, lung and brain dysfunction, severe anemia, dehydration and severe nutritional metabolism disorders that cannot be corrected or improved in a short period of time. 5. Patients with poorly controlled malignant pleural effusion. 6. Anticoagulation therapy and/or antiplatelet agents (except novel oral anticoagulants such as dabigatran and rivaroxaban) are discontinued for less than 5\ 7 days before ablation. 7. Eastern Cooperative Oncology Group (ECOG) score \> 2. 8. Combined with other tumors with extensive metastasis, expected survival \< 6 months. 9. Patients with episodic psychosis. 10. Patients with implantable electronic devices (such as pacemaker or defibrillator). 11. Pregnant women, or patients who have pregnancy plans during the study. 12. Participation or ongoing participation in another clinical study within the past 30 days. 13. Other situations that the investigator deems inappropriate to participate in this study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Complete ablation rate at 6 months after ablation | 6 months | It is defined as the proportion of lesions with complete ablation to all ablated lesions at 6 months after ablation. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Complete ablation rate 12 months after ablation | 12 months | It is defined as the proportion of lesions with complete ablation to all ablated lesions at 12 months after ablation. |
| Local control rate at 1 year, 2 years and 3 years after ablation | 1 year, 2 years and 3years | It is defined as the proportion of lesions with complete ablation and incomplete ablation to all ablated lesions at 1 year, 2 years, and 3 years after ablation. |
| Technical success rate | Immediately after ablation | It is defined as the proportion of lesions which the ablation needle reached and successfully ablated to all lesions intended for ablation. |
| Overall survival (OS) | 3 years | It is defined as the total time from the ablation to the death of the subject. |
| Safety | 12 months | To assess the incidence of device- or procedure-related (serious) adverse events occurring during the study. |
| Progression free survival (PFS) | 3 years | It is defined as the duration from the ablation to the first occurrence of disease progression or the death of the subject. |
Countries
China
Contacts
Primary ContactJiayuan Sun, MD, PhD
Outcome results
None listed