Corrigendum: First Experience of Ultrasound-guided Percutaneous Ablation for Recurrent Hepatoblastoma after Liver Resection in Children

Scientific Reports 5: Article number: 16805; published online: 18 November 2015; updated: 16 September 2016.

However, PAT achieves exceptional response in children. We hypothesized that PAT is an alternative treatment for recurrent HB and could serve as an adjunct to the existing treatment modalities for HB. Therefore, the aim of our study was to summarize and report our first experience of PAT for recurrent HB in children.

Patients and Methods
Patients. This retrospective study was performed according to the guidelines of the Helsinki Declaration. It was registered and approved by the ethics committee at The First Affiliated Hospital of Sun Yat-sen University. All patients' parents gave written informed consent before treatment.
From August 2013 to October 2014, postoperative recurrences were detected in a total of 5 children with HB. All patients underwent PAT for their recurrent tumors. We retrospectively reviewed their records. The patient's ages ranged from 23 months to 11 years (mean age, 4 years), andthere were 3 males and 2 females. The initial tumor size in these patients was 7.1 ± 3.0 cm (range, 2.4-12.8 cm). According to the International Society of Pediatric Oncology (SIOPEL) study group, 2 patients were staged as Pre Treatment Extent of Disease (PRETEXT) stage II, 2 were staged as PRETEXT stage III and 1 was staged as PRETEXT stage IV. Before surgery, 3 patients received neoadjuvant chemotherapy and 1 patient received TACE plus neoadjuvant chemotherapy. The diagnosis of suspected HB before chemotherapy was confirmed by biopsy. All patients underwent anatomic liver resections, including left hemihepatectomy in 2 patients, left trisectionectomy 1 patient and segmentectomy in 1 patient. The remaining patient underwent non-anatomic liver resection due to almost the entire tumor protruding the capsule. Moreover, all patients received postoperative chemotherapy. After a follow-up of 2 to 73 months, a total of 8 recurrent tumors were detected in the 5 enrolled patients, including 4 patients with 7 recurrences in the liver and 1 patient with 1 recurrence in the lung. The diagnosis of recurrence was based on the observation of newly emerged tumors on computed tomography (CT) and/or color Doppler ultrasound (US) images and an increase in serum alpha-fetoprotein (AFP). The mean diameter of the recurrent HBs was 1.4 ± 0.8 cm (range, 0.7-3.1 cm). The detailed baseline characteristics of all 5 patients are listed in Table 1, and Table 2 shows the serum AFP levels for these patients at multiple time points.
Percutaneous Ablation Procedures. According to our protocol, RFA was recommended as the first choice for the treatment of favorable tumors, and PEI was performed for unfavorable tumors containing a capsule. Unfavorable tumors were defined as tumors located < 5 mm from important structures, such as the bowel, bile duct, and liver capsule. All ablation procedures were guided and monitored by US. US was performed by X.Y.X., who had 25 years of experience with US. All patients were hospitalized prior to treatment.
Radiofrequency Ablation. RFA was performed under general anesthesia. RFA was performed using a Cool-tip ™ RFA system (Valleylab, Boulder, CO, USA), which consisted of a RF generator with a maximum power of 200 Wand a 17-gauge internally cooled electrode. Using US guidance, the radiofrequency electrode was carefully introduced into the target lesion at the predetermined location. The number of electrodes was dependent on the tumor size, shape, and location. If necessary, after the first application, the needle was pulled out by 1 cm and a second application was started. After the ablation was completed, the needle track was carefully treated with the electrode being retracted by 1 cm increments to prevent bleeding and tumor seeding. A single treatment session consisted of one or two applications. A safety margin of 0.5 cm was employed during the RFA procedure.
Percutaneous Ethanol Injection. After the administration of general anesthesia, an 18-gauge needle (Hakko Co., Ltd, Nagano, Japan) was inserted into the center of the tumor nodule under US guidance, and the tip of the needle was positioned at the inferior aspect of the tumor. Ethanol was injected until the entire tumor appeared hyperechoic upon performing the pullback technique. Two or three cycles of PEI were performed per week, depending on patient's tolerance.
Treatment Outcomes and follow-up. One month after the treatment of recurrent HB, contrast-enhanced CT was performed to evaluate local efficacy. Complete ablation was defined as complete non-enhancement of the treated lesion on contrast-enhanced CT [13][14] . In cases with a viable residual tumor, additional ablation was performed with the aim of complete ablation. If the tumor was still viable after additional ablation, ablation therapy was considered a failure. All patients underwent post-PAT chemotherapy. During the follow-up period, the serum AFP level was measured, and color Doppler US was performed every month. If necessary, additional contrast-enhanced CT was performed. Assessment of response to the treatment was performed with contrast-enhanced CT and AFP level. The definitions used were as follow: complete response = no evidence of disease after complete ablation and normal AFP level; partial response = any tumor size decrease associated with decreased AFP level (>1 log less than the original value); stable disease = no change in tumor size and no change or less than 1 log decrease of AFP level; and progressive disease = unequivocal increase in size of the tumor size and/or new recurrence and/or any unequivocal increase in AFP level 15 . Statistical Analysis. The statistical analyses were performed using SPSS 16.0 statistical software (Chicago, IL, USA). All data are reported as the mean ± standard deviation. Student's t test or the Mann-Whitney test was used to assess the differences between two groups of quantitative variables. The disease-free survival (DFS) and cumulative overall survival (OS) were assessed using the Kaplan-Meier method. The disease-free time was defined as the period from the date of PAT to the development of a new recurrence, death or last follow-up. The survival time after ablation was defined as the period from the completion of PAT to death or last follow-up. The survival time after diagnosis was defined as the period from the diagnosis of HB to death or last follow-up.

Results
Tumor Response. The ablation procedures and outcomes of all 5 enrolled patients are shown in Table 3. RFA was performed in 3 children (No. 1, 4 and 5) with 4 tumors, including 3 tumors in the liver and 1 tumor in the lung. The mean ablation time per tumor was 12.8 min (range, 9-20 min). All tumors were completely ablated as indicated by the contrast-enhanced CT results 1 month after PAT.
PEI was performed in another 2 children (No. 2 and 3) with 4 tumors in the liver that were difficult to ablate using RFA (1 patient with a tumor in the caudate lobe adjacent to the stomach and 3 tumors in segment 6 close to the liver capsule). The mean volume of injected ethanol per tumor was 5.8 mL (range, 3-8 mL). One month later, a residual tumor was detected, and it was treated with an additional injection of 5 mL of ethanol. Finally, complete ablation was achieved after a second session of PAT. The remaining tumors achieved complete ablation after the first ablation (Fig. 1).
Therefore, technical success of PAT for recurrent HB was achieved in all patients (5/5, 100%) (Fig. 2). The complete ablation rate after the first ablation session was 80% (4/5) on a patient-by-patient basis and 87.5% (7/8) on a tumor-by-tumor basis. For the RFA technique, the complete ablation rate after the first session was 100% on both a patient-by-patient basis (3/3) and a tumor-by-tumor basis (4/4). For the PEI technique, the complete ablation rate after the first session was 50% (1/2) on a patient-by-patient basis and 75% (3/4) on a tumor-by-tumor basis.
All patients received chemotherapy after PAT. The following chemotherapeutic regimens were used: irinotecan plus vincristine plus nedaplatin for two patients (No.1 and 2); irinotecan plus vincristine plus temozolomide for two patients (No. 3 and 4); and pirarubicin plus nedaplatin plus cyclophosphamide for 1 patient (No. 5).  Table 3. Ablation procedures and outcomes of all the 5 enrolled patients. PEI: percutaneous ethanol injection; RFA: radiofrequency ablation. CR: complete response, PR: partial response, SD: stable disease, PD: progressive disease.

Follow-up and Survival. After a follow-up of 5-16 months, new distant intrahepatic recurrences,
without extrahepatic recurrences, were detected in two patients (No. 1 and 3). One patient (No. 1) received chemotherapy treatment alone. However, that patient's AFP level did not decrease, and she died due to tumor progression 4 months after ablation. The other patient (No. 3) received 2 sessions of ablation for the new recurrences, and he survived for 9 months after ablation and 82 months after HB diagnosis. One patient (No. 4) was considered to have a partial response because her AFP level decreased but remained abnormal. A complete response was achieved in the remaining 2 patients (No. 2 and 5), and they survived for 7 and 16 months, respectively, after ablation (Table 2). Thus, the overall survival rate was 80% (4/5) at the end of follow-up (Fig. 2). The median DFS time after ablation was 10.4 months, and the DFS rate at 6 months was 60% (Fig. 3). The median cumulative OS time after ablation was 13.8 months, whereas the median cumulative OS time after HB diagnosis was 68.2 months.

Discussion
HB is the most common malignant liver tumor that occurs during childhood 1,2 . Advancements in chemotherapeutic agents and administration protocols as well as innovations in surgical approaches, including the use of vascular exclusion, ultrasonic dissection techniques and liver transplantation, have greatly improved the outcome of children with HB. However, challenges remain in the management of patients with recurrent HB 1 . For example, although liver transplantation is a successful treatment option for children with unresectable HB, with primary transplantation having a 90% survival rate, it has a poor survival rate for patients with recurrent HB after previous liver resection 2,16 . Therefore, further understanding of the optimal treatment is necessary for the management of these cases. Different treatment modalities have been applied for recurrent HB. Chemotherapy is necessary for patients with recurrent HB after surgery. The study of Marsh et al. 17 demonstrated that the combined use of sorafenib and bevacizumab was effective for the treatment of recurrent HB that had previously been extensively treated with multiple chemotherapeutic regimens. In that study, the patient had a progression-free survival of 3 months. However, local ablation helps enable chemotherapy to destroy micrometastases 18 . Considering the age and nutritional state of the child, repeated liver resection was considered difficult, even impossible. Although liver transplantation is an accepted therapy for children with recurrent or refractory HB 2,16 , it is limited by donor availability. If a liver can become tumor free by PAT, it should be considered as a possible alternative treatment. To date, no studies on the efficacy of PAT have been conducted in the particular setting of recurrent HB, although recent case reports have confirmed an acceptable safety profile of PAT in that setting. In 2008, Ye et al. 14 reported a 2-year-old boy with recurrent HB after liver resection treated by percutaneous RFA, and there was no imaging evidence of recurrence after a follow-up of 2 years. Recently, Dunn et al. 19 demonstrated another successful treatment of pulmonary metastasis of HB in a 2-year-old boy using RFA. Both research groups deemed RFA to be a promising technique in children with recurrent HB. Here, we summarized the first experience of US-guided PAT for recurrent HB in children in a tertiary hospital. Three patients were treated by RFA, and 2 patients were treated by PEI, and no patients died due to the ablation treatment. The overall survival rate was 80% at the end of follow-up. Among the 5 enrolled patients, 3 were alive without new recurrence at the end of follow-up. PAT may add a new dimension to the treatment of recurrent HB.
We applied RFA and PEI for the treatment of recurrent tumors. RFA is recommended as the first choice for the majority of tumors, except tumors located < 5 mm from important structures, such as the bowel, bile duct, and liver capsule. For hepatocellular carcinoma in adults, prospective randomized trials 20,21 have revealed that RFA yields higher rates of complete tumor necrosis with fewer treatment sessions and better survival compared with PEI. In our case series, complete ablation was achieved in all patients after the first session of RFA, whereas 1 residual tumor was detected after initial PEI. Although 1 patient developed a fever with a temperature > 39 °C after RFA, no major complications occurred. Further large-scale randomized clinical trials are required to compare RFA with PEI for the treatment of children with recurrent HB.
Four tumors in 2 patients were treated by PEI. Close attention should be paid to the amount of ethanol administered to children during PEI. It is known that for tumors of 3.0 cm or smaller in diameter, the volume of injected ethanol should be calculated as the volume of an oversized sphere, as follows 22 : where V is the volume in milliliters, and D is the largest tumor dimension in centimeters. For tumors that are 3.1-5.0 cm in diameter, the least amount of ethanol that should be administered is equal to the volume of the tumor (V = 4/3π [(D/2) 3 ]), and the upper limit of ethanol volume per session to minimize the toxic effects of ethanol to the adult patient is 60 mL. That is to say, the total amount of ethanol required for the complete destruction of a tumor lesion is approximately 4 mL for a lesion of 1 cm in diameter, 14 mL for a lesion of 2 cm in diameter, and 33 mL for a lesion of 3 cm in diameter 23 . A sufficient dose of ethanol is necessary to achieve necrosis of the entire tumor.
In contrast, a high-dose of ethanol may induce a choking sensation, cough, tachycardia, and even respiratory depression in adults 22 , and the toxic effects of ethanol are greater and more complex in children. Therefore, the dosage protocol used for children required further evaluation to achieve an appropriate balance between local effectiveness and avoidance of complications.
As expected, there is very limited experience of ablation in children. Recently, Gomez et al. 24 searched MEDLINE for papers published between 1995 and 2012 that reported the outcomes of PAT for patients less than 18 years of age. They only found the following numbers of patents reported to have undergone ablation: 3 for liver lesions, 9 for lung metastases, 11 for bone and/or soft tissue lesions and 4 for kidney or pancreatic lesions. Based on the available data, our case series seems to have an acceptable sample size to summarize and evaluate our treatment experience. Furthermore, in addition to recurrent HB, PAT seems to be feasible in children with primary, recurrent or metastatic tumors in various organs. In those children treated by ablation, only 6 (21%) required treatment other than supportive care due to a complication. In the 26 patients whose survival after PAT was reported, the mean overall survival was 22 months (median: 18 months; range: 0.7-96 months).
There are several limitations to the present study. First, only 5 patients with recurrent HB after hepatectomy who underwent PAT were enrolled in this study. However, recurrent HB is rare and it is difficult to accumulate a large sample size of patients with this condition. Secondly, this was a retrospective data analysis from a single institution. Therefore, a properly designed prospective multicenter study is needed to determine if this technique does in fact have efficacy in this setting. Third, this was a single arm PAT treatment study, and there was no direct comparison to other treatment modalities. Randomized controlled clinical trials are needed to provide a comparative evaluation of this technique for the treatment of recurrent HB. Moreover, the follow-up period was short. The long-term results of this treatment are still unclear.
In conclusion, our experience with these 5 cases, although small in number, suggests the feasibility of PAT for recurrent HB. PAT may be a good adjunct to the existing treatment modalities for HB. However, PAT for pediatric tumors is still in its infancy, and further investigation in large-scale randomized clinical trials is necessary to confirm our observations and further determine the role of PAT.