Lung Cancer (NSCLC)
Conditions
Keywords
Lung Caner(NSCLC), Pulsed Electric Field Ablation
Brief summary
The goal of this observational study is to evaluate the performances of a percutaneous Pulsed Electrical Field (PEF) ablation to treat patients with primary early-stage lung cancer (NSCLC) or lung oligometastatic Tumors who are unresectable or refusal surgery/Radiotherapy. The main questions the study aims to answer are: The safety and technical feasibility of the PEF ablation. The preliminary efficacy of the PEF ablation for target lesion in lung Patients who meet the inclusion/exclusion criteria will be given percutaneous PEF ablation to the target lesions under general anesthesia. Then follow-up to 12 months to monitor any progression by about 3 months interval. Target Subject： Patients with early-stage primary non-small cell lung cancer(NSCLC) or pulmonary oligometastatic tumors who are not surgical resectable or unsuitable for surgery/radiotherapy
Detailed description
Safety, technical feasibility including procedure operation success and tumor ablation technical success be evaluated. The primary efficacy endpoint is the complete ablation rate of the ablated lesions at month 6. Other efficacy endpoints are local tumor progression-Free Survival(PFS), Overall Survival (OS) and proportion of patients requiring initiation of other anti-tumor interventions through 12 months. Pulmonary function and quality of life (EORTC QLQ-C30, EORTC QLQ-LC13) will be assessed as well.
Interventions
Application of Pulsed Electric Field energy to ablate the lung tumor through percutaneous approach.
Sponsors
Energenx Medical LTD.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
No
Inclusion criteria
1. Age ≥18 years but ≤ 79 years, male or female 2. Pathologically diagnosed primary NSCLC and stage IA, or oligometastatic lung tumors that primary cancer has been controlled. the maximum diameter of the lesion is ≤3cm, (Pathological diagnosis includes conventional pathological examination or ROSE rapid on-site evaluation) 3. For multiple primary lung cancers, the number of lesions is ≤3 and the maximum diameter of the lesion(s) is ≤3cm. For metastatic tumors, the number of lesions in one side of lung is ≤3 (total lesions in both sides \<5), the maximum diameter of the lesion(s) is ≤3cm. 4. ECOG score ≤ 2; 5. Expected survival ≥ 12 months; 6. Clinical assessment as unsuitable for surgical resection or refusing surgery and radiotherapy. 7. Assessed by an anesthesiologist as suitable for general anesthesia; 8. Agree to receive ablation therapy and sign the informed consent form.
Exclusion criteria
1. Received any form of local tumor therapy for the target lung tumor lesion(s) within 6 months. 2. Currently receiving systemic anti-tumor therapy, such as chemotherapy, targeted therapy, immunotherapy etc. (For pulmonary oligometastatic tumors with primary cancer controlled already, if systemic anti-tumor therapy still needs to be continued, it is acceptable. For primary NSCLC patients, according to guideline recommendations, no concurrent systemic anti-tumor therapy is indicated). 3. The distance between tumor lesion edge and important structures such as heart, diaphragm and mediastinum is less than 10mm. 4. With a history of hypersensitivity to medications to be used in general anesthesia or drugs required during the procedure/follow-up (such as contrast-enhanced CT scan). 5. Anemia (Hemoglobin (HGB) \< 9 g/dL), dehydration, and severe metabolic disorders that cannot be improved or well managed in the short term. 6. Coagulation abnormalities (INR \>1.5 or APTT \>1.5 ULN), or platelet count below 90 x 10\^9/L. 7. Uncontrolled lung or systemic infection. Or uncontrolled skin infection at the puncture site or fever \> 38.5°C. 8. Currently using anticoagulant therapy and/or antiplatelet drugs (such as warfarin, dabigatran, rivaroxaban, and other new oral anticoagulants) and have not been discontinued for more than 5 to 7 days prior to ablation therapy. 9. Receiving high-dose immunosuppressive drugs (prednisone exceeding 10mg/day or equivalent). If discontinued for more than 4 weeks, it is acceptable. 10. Subject has comorbidity of severe other lung diseases (including interstitial pneumonia, pulmonary fibrosis, severe emphysema or atelectasis) and unsuitable for enrollment with the judgement of the investigator. 11. Malignant pleural effusion on the treatment side of lung. 12. Severe uncontrolled hypertension, diabetes, severe abnormal liver or kidney function, or heart failure that investigator assessed as unsuitable for enrollment. 13. Acute cardio-cerebrovascular events within 3 months, such as acute hemorrhagic or ischemic stroke, acute coronary syndrome, acute myocardial infarction. 14. Psychiatric disease that not well controlled. 15. With a history of recurrent tachyarrhythmia past 2 years. (Including rapid atrial arrhythmias, any rapid ventricular arrhythmias); or history of type II second-degree or III degree atrioventricular block or sinus bradycardia with heart rate \< 45 beats/min, or sinus tachycardia \> 120 beats/min. 16. Implanted electronic device in the body (such as pacemaker, implantable cardioverter defibrillator, or neurostimulator). (it is acceptable If the implanted electronic device is allowed to be turned off during the procedure) 17. There is metal implants near the lesion to be ablated lesion (distance \< 2-3cm) in the lung. 18. Patient is currently participating in another clinical trial. 19. Pregnant or breastfeeding women, or women planning to become pregnant during the study period. 20. Other situations judged by investigator as unsuitable for enrollment.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The clinical safety of the device and/or procedure in the operation of PEF ablation and entire study follow-up. | Through 12 months | Adverse events rate and severe adverse event rate related to the device and/or procedure during the ablation procedure and thereafter 12 months follow-Up |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The success rate of the ablation procedure | Once the procedure is completed. | The success rate of the procedure is defined as the proportion of ablation procedures in which the PEF treatment catheter is deployed to the target lesion and pulsed electrical field energy is delivered and then the catheter is withdrawn out from lung |
| The technical success rate of the PEF ablation | At 24-hour post the procedure | The technical success rate of the PEF ablation that is defined as the proportion of lesions where the CT imaging-assessed ablation zone (Post-ablation Target Zone, PTZ) is larger than the gross tumor region (GTR) at least 5 mm. |
| Complete ablation rate of the target lesions at 6-month and 12-month post the ablation. | At 6-month and 12-month | Complete ablation of the target lesions is defined as to achieve the following criteria on contrast-enhanced CT images ① Lesion disappears; ② Complete cavity formation; ③ Lesion fibrosis, which may be a scar; ④ Lesion shrinks, remains unchanged, or enlarges, but shows no enhancement on contrast-enhanced CT and/or no metabolic activity on PET/CT; ⑤ Atelectasis, with the lesion within the atelectasis showing no contrast enhancement on CT and/or no metabolic activity on PET/CT. The baseline is defined as CT image of 4-6 weeks post the ablation. |
| Proportion of patients with target tumor progression free survival (PFS) at 6-month and 12-month. | At 12 months | The proportion of subjects without target lesion progression in lung at 6-month and 12-month post the PEF procedure in evaluative subjects. |
| Overall Survival (OS) through 12 months. | At 12 months | The proportion of surviving subjects at 12 months after completion of PEF ablation therapy in those evaluative subjects. |
Countries
China
Contacts
CONTACTShaoyu Yang, Doctor
CONTACTXiao Xu, Head of Administrator
Outcome results
None listed