Patients enrollment
This study was approved by the institutional ethics committee of our hospital, patients diagnosed with pulmonary metastases contiguous with the mediastinum who underwent RFA were retrospectively investigated at our hospital from August 2014 to May 2018. The target lesions of all cases were confirmed clinically or pathologically as hepatocellular carcinoma (HCC). “Contiguous with mediastinum” was defined as the distance between metastatic lesion and mediastinum was less than 3 mm on CT or MR images.
The inclusion criteria for this study were: I) a single metastatic lesion contiguous with mediastinum in the unilateral lobe of lung; II) lesion size less than 3 cm in diameter; III) orthotopic HCC shown to be inactive without recurrence and intrahepatic metastasis as indicated by enhance imaging after surgical and (or) interventional therapy; IV) no increase in numbers of pulmonary lesions after 1-2 months of observation; V) patients refuse to accept surgical resection; and VI) Karnofsky performance status (KPS) greater than 70%.
The exclusion criteria were: I) patients with severe coagulation dysfunction including thrombocyte number < 30×109/L, international normalized ratio (INR) > 3.0, prothrombin time > 30 s, or prothrombin activity (PTA) < 40%; II) acute infection or chronic infection in acute phase; III) severe pulmonary hypertension defined as mean pulmonary artery pressure (mPAP) > 35 mmHg measured by cardiac catheterization and (or) Doppler echocardiogram; IV) severe pulmonary insufficiency defined as PaO2 < 60 mmHg, with and without PaCO2 > 50 mmHg; and V) implantation of cardiac pacemaker.
Artificial pneumothorax adjuvant RFA procedure
All patients underwent contrast enhanced CT (CECT) of the chest prior to RFA in order to evaluate the anatomic relationship between lesions and peripheral cardiovascular structures. CECT was performed using the SOMATOM Force CT system (Siemens, Munich, Germany) with intravenous administration of Omnipaque (GE Medical, USA) as a contrast agent. Before the procedure, patients in a supine position received continuous electrocardiogram (ECG) monitoring and were hypodermically injected with 1% lidocaine. Then, the puncture point and needle track were determined by CT scan (MIYABI, Siemens, Munich, Germany). Subsequently, the biopsy needle was penetrated into the target in a direction away from the heart and vessels. When the procedure was accomplished, the biopsy needle was removed.
Thereafter, the artificial pneumothorax technique was performed using a 22-G puncture needle (NPAS-100, COOK, USA) with a blunt tip. The needle was inserted along the well-designed puncture proposal, which specifies insertion route, depth and angle. When the needle tip reached the edge of the pleura, the needle core was pulled out, 1-2 ml of saline was injected locally to form a water capsule using T-stopcock and tubes. Then, saline in the tube flowed into the cavity, and the water capsule disappeared gradually as the needle tip continued to be inserted and reached into the pleura cavity. Then, 100-500 ml of CO2 gas was frequently administered to separate the lung parenchyma. CT scanning was performed individually after injection of 100, 200, 300, 400, and 500 ml CO2 until the tumor was separated from the mediastinum and a feasible puncture path was established.
After the RF electrode was successfully inserted into the tumor based on the CT scanning assessment, percutaneous RFA (Model 1500, RITA Medical System, Mountain View, CA, USA) was performed at 60-70 W for 5-12 min at a rating temperature of 90℃. During the process, an 18-G unipolar electrode (Uniblate) was chosen (the length of the needle was 15 cm and the maximum ablation range of a single electrode was 3×3 cm2). The ablation procedure was terminated when the ablation zone completely overlapped the target tumor and an ablative margin of 5-10 mm beyond the tumor boarder was achieved. Then, the RF electrode was withdrawn for coagulation of the needle track to avoid needle implantation and bleeding. During the procedure, 5-10 mg of morphine was intravenously injected for analgesia and sedation based on pain degree of patients. The ablation zone was defined as the pulmonary texture around the tumor that showed a circular exudation shadow with ground-glass appearance on CT imaging. After RFA, CO2 in the pleura cavity was aspirated with a 50-ml syringe and expelled through the T-stopcock until no additional gas could be aspirated.
Follow up
CECT was performed to evaluate the therapeutic response of tumors at 1, 3, 6, and 12 months post ablation and at 6-month intervals thereafter. If incomplete tumor ablation was detected by CECT, secondary RFA was performed. According to the reporting criteria of image-guided tumor ablation 12,13, technical success was defined as a tumor that was treated according to the initial protocol and was covered completely by the ablation zone. Local tumor progression (LTP) was defined as the appearance of new tumor foci at the ablative margin. Intrapulmonary distant recurrence (IDR) was defined as any occurrence of a new tumor foci in the lung.
During follow-up, adverse events (AEs) after ablation, local tumor progression free survival (LTPFS), and overall survival (OS) were recorded for each patient. AEs were classified in this study according to AE classification of the Society of Interventional Radiology 14. The definition of major complication included moderate AE, severe AE, life-threatening or disabling event, patient death or unexpected pregnancy abortion. Mild AE was defined as minor complication. To assess the post-ablative pain, a visual analogue scale (VAS, a numerical rating scale: 0–10) was used based on previous publications: score 1–3 corresponding to slight pain, score 4–6 corresponding to moderate pain and score 7–10 corresponding to severe pain 5,15.
Statistical analysis
Statistical analysis was performed using SPSS software (version 22.0; SPSS Inc, Chicago, IL, USA). Categorical variables were described as numbers (percentages). Continuous variables were described as mean ± standard deviation (SD) or medians (range) according to the normality results using the Kolmogorov–Smirnov test. Survival was calculated by Kaplan-Meier survival analysis.