Introduction The majority of patients with perihilar cholangiocarcinoma (PHC) has locally advanced disease or distant lymph node metastases on presentation or exploratory laparotomy, which makes them not eligible for resection. As the prognosis of patients with locally advanced PHC or lymph node metastases in the palliative setting is significantly better compared with patients with organ metastases, ablative therapies may be beneficial. Unfortunately, current ablative options are limited. Photodynamic therapy causes skin phototoxicity and thermal ablative methods, such as stereotactic body radiation therapy and radiofrequency ablation, which are affected by a heat/cold-sink effect when tumours are located close to vascular structures, such as the liver hilum. These limitations may be overcome by irreversible electroporation (IRE), a relatively new ablative method that is currently being studied in several other soft tissue tumours, such as hepatic and pancreatic tumours.
Methods and analysis In this multicentre phase I/II safety and feasibility study, 20 patients with unresectable PHC due to vascular or distant lymph node involvement will undergo IRE. Ten patients who present with unresectable PHC will undergo CT-guided percutaneous IRE, whereas ultrasound-guided IRE will be performed in 10 patients with unresectable tumours detected at exploratory laparotomy. The primary outcome is the total number of clinically relevant complications (Common Terminology Criteria for Adverse Events, score of≥3) within 90 days. Secondary outcomes include quality of life, tumour response, metal stent patency and survival. Follow-up will be 2 years.
Ethics and dissemination The protocol has been approved by the local ethics committees. Data and results will be submitted to a peer-reviewed journal.
Conclusion The Ablation with irreversible eLectroportation in Patients with Advanced perihilar CholangiocarcinomA (ALPACA) study is designed to assess the feasibility of IRE for advanced PHC. The main purpose is to inform whether a follow-up trial to evaluate safety and effectiveness in a larger cohort would be feasible.
- hepatobiliary tumours
- hepatobiliary disease
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Strengths and limitations of this study
Both the open and percutaneous approach of irreversible electroporation for perihilar cholangiocarcinoma are prospectively investigated.
Quality of life of participating patients will be closely observed using validated questionnaires.
Strict eligibility criteria may slow the accrual of study participants.
The feasibility study design with consequent relative small sample size does not allow for accurate survival analysis.
Perihilar cholangiocarcinoma (PHC) is a rare biliary malignancy originating at or near the hepatic duct confluence with an annual incidence of approximately 200 patients in the Netherlands.1 2 The typical location in the liver hilum causes biliary obstruction with concomitant jaundice. Surgical resection of PHC consists of a combined extrahepatic bile duct resection and partial liver resection, and offers the best chance for long-term survival, with a reported median overall survival (OS) of 19–40 months and 5-year survival rates of 13%–40%.3–5 Unfortunately, only a subset of patients are eligible to undergo surgical resection, as almost 50% of patients already present with unresectable disease, and of the patients undergoing exploratory laparotomy approximately 40% are found to have locally advanced or metastasised disease.6 Of all patients with ultimately unresectable disease, approximately 50% of tumours are considered locally advanced because of vascular involvement without the possibility of reconstruction or extensive biliary involvement.6 7
Systemic chemotherapy is the standard treatment for patients who are ineligible for curative resection or liver transplantation. The preferred regimen consists of a combination of gemcitabine and cisplatin and results in a median progression-free survival (PFS) of 8 months and a median OS of 12 months.8 Most patients eventually die of cholangitis, sepsis or liver failure, despite biliary stenting to relieve the cholestasis. Although the overall prognosis of unresectable PHC is poor, the median OS for patients with locally advanced PHC or lymph node metastases beyond the hepatoduodenal ligament is significantly longer (14–16 months) compared with patients with organ metastases (3–5 months).6 Long-term survival of up to 36 months has even been reported in some of these patients. This particular subgroup of patients with PHC may benefit from ablative therapies that counteract tumour growth and potentially improve biliary stent patency and survival.9
Several ablative therapies have been investigated for the treatment of advanced PHC, including stereotactic body radiation therapy (SBRT),10 11 photodynamic therapy (PDT)12 13 and endoscopic biliary radiofrequency ablation (RFA).14 15 These modalities show somewhat promising results but also suffer from major limitations. In PDT, severe skin phototoxicity due to the use of slowly degradable photosensitisers is reported.12 Furthermore, thermal ablative modalities (ie, RFA) are limited by thermal damage to surrounding structures and a so-called heat/cold-sink effect. The latter phenomenon is mediated by blood flow in surrounding vessels, creating an area where optimal temperatures are not reached, leaving viable cancer tissue in situ.16 Due to the typical location of PHC in the liver hilum near the portal vein and hepatic arteries, this is particularly challenging.
Irreversible electroporation (IRE) is an image-guided ablation technique based on creating short-pulsed high-voltage current fields. The electrical pulses permeabilise the lipid bilayer of the cell membrane, hereby disrupting intracellular homeostasis and inducing apoptosis.17–19 Because of the non-thermal mechanism, the effect of IRE is not counteracted by a heat/cold-sink effect and causes less damage to surrounding vital structures. In one clinical study including 101 patients, the effect of IRE on vessel patency in close proximity to the ablation zone was evaluated and showed that 151 of 158 major vessels were patent, whereas only 7 vessels exhibited thrombosis or mild narrowing at follow-up.20 In another study, it was observed that tumours in close proximity to major bile ducts could be safely treated with IRE, as 26 of 28 evaluated bile ducts were patent 1 month after treatment (one occlusion occurred).21 Long-term patency of large hilar bile ducts has also been reported in a porcine model, especially when electrodes were positioned more than 2 mm away from the bile ducts.22
Evidence for the use of IRE in PHC is limited to one case report.23 However, several clinical studies have investigated the safety and effectiveness of IRE in hepatic and pancreatic tumours. IRE was shown to be relatively safe and feasible in locally advanced tumours in proximity of vital structures.24–26 In locally advanced pancreatic cancer, IRE-related complications have been reported in 13% of patients with 2% mortality, whereas IRE-related complications in hepatic tumours occurred in 16%.27 28 Complete response of hepatic tumours has been reported in 67%–100%.28 The percutaneous IRE approach, using CT, has been reported to be safe, thereby making it a minimally invasive alternative to open IRE during surgical exploration.29–31 Although the short-term safety profile of IRE has been extensively documented, long-term results are awaited. Potentially improved survival has been reported in a selected group of patients with locally advanced pancreatic cancer.26 32
Given the lack of evidence on the use of IRE in the treatment of advanced PHC, the current study was designed to gather information regarding the safety and feasibility of IRE in these patients prior to palliative chemotherapy.
Methods and analysis
The Ablation with irreversible eLectroportation in Patients with Advanced perihilar CholangiocarcinomA (ALPACA) study is a multicentre, phase I/II safety and feasibility study of the use of IRE treatment with the NanoKnife system (AngioDynamics, Amsterdam Zuid-Oost, the Netherlands) in 20 patients with advanced PHC. In this study, advanced PHC is defined as PHC with vascular involvement or distant lymph node metastases, precluding a resection. Two groups will be distinguished in the study. Patients who present with advanced PHC or have evidence of advanced disease during preoperative work-up will undergo percutaneous CT-guided IRE. Patients who present with potentially resectable PHC that appears to be locally advanced or metastasised to distant lymph nodes at exploratory laparotomy will undergo ultrasound (US)-guided IRE during the same surgical exploration session. Criteria for advanced PHC are summarised in online supplementary additional file 1. The study is conducted at the Academic Medical Center and VU University Medical Center, which both are tertiary referral centres for patients with PHC in Amsterdam, the Netherlands.
Supplementary file 1
The objective of this study is to assess the safety and feasibility of IRE for the treatment of advanced PHC with vascular or lymph node involvement prior to palliative chemotherapy. The main purpose of this feasibility study is to inform whether a follow-up trial to evaluate safety and effectiveness in a larger cohort would be feasible.
Primary study outcome
The primary outcome is the total number of clinically relevant complications within 90 days post-IRE, defined as complications requiring reintervention, prolonged hospital stay, intensive care admission, readmission or complications leading to mortality. These complications are summarised by a Common Terminology Criteria for Adverse Events (CTCAE, V.4.0) score of 3 or higher. Definitions of specific postprocedural complications are provided in online supplementary additional file 2 .
Supplementary file 2
Secondary study outcomes
Technically successful IRE procedure (ability to correctly place the IRE needles and complete the procedure)
Intraprocedural complications related to IRE (cardiac arrhythmias, perforation of organs or vascular structures)
Duration of hospital stay
Quality of life at baseline (outpatient clinic), 6 weeks, 3 months and 6 months after IRE; assessments consists of the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire 30 (EORTC QLQ-C30), the EORTC QOL module for cholangiocarcinoma and gallbladder cancer (EORTC QLQ-BIL21) and the EuroQol 5D
Tumour response on CT imaging (Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 and criteria in table 1) and blood biomarker response (carbohydrate antigen 19-9 (CA 19-9)) at 6 weeks and 6, 12 and 24 months after IRE
Long-term vascular and biliary complications (thrombosis, bile duct stenosis) as assessed on follow-up CT imaging
Time interval between IRE and start of palliative chemotherapy
Duration of palliative chemotherapy (number of cycles)
Metal stent patency (time between stent insertion and replacement)
Survival (1-year and 2-year PFS and OS). PFS is defined as the number of months between the IRE procedure and the time of first evidence of progressive disease as defined by the RECIST criteria and proposed criteria in table 1. OS is defined as the number of months between the IRE procedure and time of death or last follow-up.
Our primary hypothesis is that IRE will add approximately 20%–25% clinically relevant complications (CTCAE ≥3) to the current 40% complication rate associated with biliary drainage in the palliative management of PHC.33 An incidence of 60% complications within 90 days post-IRE will be considered as the acceptable upper limit. This will be related to the observed impact on survival. Our secondary hypothesis is that the patency rate of metal stents will be prolonged because of local tumour control. Furthermore, we hypothesise that median OS is increased by 3 months in patients undergoing IRE. Both the metal stent patency rate and OS of patients in this study will be compared with patients who were eligible for study participation but preferred standard palliative treatment. When necessary, study data may also be compared with a historical cohort of patients treated in our centre.
The study population consists of 20 adults who are diagnosed with either advanced PHC based on imaging or staging laparoscopy, or potentially resectable PHC but ultimately advanced disease during exploratory laparotomy. Patients will be recruited at the outpatient clinic. In case of a planned exploratory laparotomy, patients will be asked to participate in the study in case they appear to have locally advanced or lymph node metastasised PHC at laparotomy. Patients with intrahepatic or extrahepatic organ metastases are not eligible for study participation. Inclusion and exclusion criteria are listed in table 2.
Supplementary file 4
Patients who are candidates for percutaneous CT-guided IRE or US-guided open IRE will be discussed upfront by the ALPACA expert panel. This dedicated panel consists of three interventional radiologists (KPvL, OMvD, MRM), three gastroenterologists (JEvH, EAJR, FvD) and four surgeons (MGB, ORCB, GK, TMvG) .
The general outline of study procedures is presented in figure 1. Patients with potentially resectable PHC undergo the standard preoperative work-up including laboratory testing, CT or MRI, biliary drainage, liver function tests and portal vein embolisation (when indicated). Patients who present with unresectable tumours will undergo CT imaging, laboratory testing and biliary drainage as part of the work-up for percutaneous IRE.
Preprocedural biliary drainage
Biliary drainage for malignant hilar strictures or masses is a complex procedure requiring considerable skill and experience. In the present study, the exact approach of biliary drainage (ie, endoscopically or percutaneously, specified liver segments, unilateral or bilateral) prior to percutaneous IRE is decided for every patient individually as it depends on biliary anatomy, vascular involvement, lobar atrophy and any cause of previous drainage failure at the referring hospital. Preferably, bilateral stenting is performed to protect the bile ducts during IRE. This decision is made by the ALPACA expert panel. All drainage procedures prior to IRE will be performed using plastic stents. A metal biliary stent (sometimes placed at the referring hospital) is not considered a contraindication for IRE as long as a no-touch technique is pursued (ie, IRE electrodes are not in contact with the metal stent).34 35 IRE will be performed when bilirubin levels have decreased below 50 µmol/L, but this threshold is not an absolute contraindication for IRE, as obtaining adequate drainage may be difficult in some patients (eg, PHC arising from primary sclerosing cholangitis).
Candidates for open IRE who initially present with potentially resectable PHC will undergo preoperative biliary drainage as part of the standard preoperative work-up. The optimal method (endoscopically or percutaneously) is decided at the multidisciplinary team meeting, based on biliary anatomy and the cause of previous drainage failure.36
Antibiotic prophylaxis will be administered according to the local hospital’s protocol within 1 hour prior to biliary drainage or IRE. In the Academic Medical Center, ceftriaxone (2000 mg once intravenously) plus gentamicin (5 mg/kg once intravenously) are given. In the VU University Medical Center, ceftriaxone (2000 mg once intravenously) alone (first choice) or augmentin (1200 mg every 6 hours intravenously) plus gentamicin (5 mg/kg once intravenously) (second choice) is given. The same antibiotics regimens will be used for the treatment of cholangitis.
The IRE procedure will be performed under general anaesthesia and epidural analgesia (or preperitoneal wound catheters in the open IRE group) with complete muscle paralysis and under cardiac gating either in the operating room (US-guided open group) or in the interventional radiology suite (CT-guided percutaneous group). During the procedure, cardiac rhythm will be closely monitored and a defibrillator will be present at all times. All electrodes will be placed by trained interventional radiologists with extensive experience with the procedure in other solid tumours (eg, locally advanced pancreatic cancer).
Prior to percutaneous IRE, a pigtail catheter will be placed in the common hepatic artery in the angiography suite entering from the right common femoral artery, for the administration of small amounts of intra-arterial contrast during IRE. This allows repeated and real-time visualisation of the vessels adjacent to or encasing the tumour and the tumour enhancement pattern, thereby improving the safety and accuracy of electrode placement while reducing the total dose of contrast fluid administered. Next, the patient is transported to the CT scan. Procedures will be performed percutaneously under CT fluoroscopy guidance with transcatheter CT arteriography and/or ultrasonographic guidance. After correct patient positioning, a contrast-enhanced CT scan of the abdomen will be performed to confirm correct staging, exact tumour size measurement and for planning of electrode placement. US-guided open IRE will be performed during exploratory laparotomy when locally advanced PHC or distant lymph node metastases are found.
The NanoKnife IRE system (AngioDynamics) will be used in this study. The IRE is set up to produce 90-microsecond high-voltage (1500–3000 V) direct-current (25–45 A) electrical pulses. Typically, 90 pulses will be delivered in 9 sets of 10 pulses between paired unipolar electrodes, with an exposed tip of 2.0 cm (online supplementary additional file 3). The voltage setting for each electroporation will be determined by the distance between each pair of electrodes and will be aimed at 1500 V/cm, with the intent to generate at least 1000 V between electrodes. The electrodes will be placed in and around the tumour under CT guidance or US guidance according to the manufacturer’s guidelines aiming at macroscopic complete ablation with a 5 mm margin, with interelectrode distances of 10–24 mm and a maximum angulation between electrodes of 15°. The predicted treatment zone will be automatically calculated using the NanoKnife generator software based on the exact position of all electrodes.
Supplementary file 3
The number of probes used for ablation depends on tumour size and shape. For a two-dimensional ablation zone with a size of less than 30×25×10 mm, two probes will be used (one active and one standard probe). When the shape of the ablation zone is more three-dimensional, with a maximum size of 30×25×20.5 mm, three probes will be used (one active and two standard). For the ablation of a larger zone, that is, with a maximum size of 30×25×25 mm, four probes will be used. Five probes will be used for tumours up to 30×40×30 mm, and for larger tumours up to 30×47×32 mm six probes will be used. After satisfactory electrode placement, tumour ablation with the NanoKnife will be performed according to protocol under careful ECG monitoring. All pulses will be administered in the absolute refractory period with use of ECG synchronisation to avoid triggering of ventricular arrhythmias. If the lesion is larger or has a different shape than the area that one set of probes can cover (according to manufacturer’s guidelines), multiple ablations will be performed, until the whole tumour area has been ablated. The generator will be programmed to stop delivery and recharge if the current flow exceeds 50 A. Pull-backs will be performed if the target treatment zone is greater than 2 cm in the direction of needle placement, and treatment will be repeated to cover the entire target zone. The number of probes, number of probe replacements (per probe) due to unsatisfactory placement, number of pulses (for each pair of electrodes), interelectrode distance, pulse voltage (V), achieved pulse current (Ampere), pulse length (µs) and pulse interval (ms) will be carefully recorded.
Patients will be monitored on the recovery (open group) and surgical ward (both groups), according to current medical practice. It may be necessary to perform additional drainage of undrained liver segments the day after open IRE. Patients undergoing percutaneous IRE will be discharged after 2–3 days (in the absence of complications). Endoscopic or percutaneous plastic drains will be exchanged for definitive metal stents (fully, partially or uncovered self-expanding metal stents) in all patients through an endoscopic or percutaneous approach preferably within 5 days after the IRE procedure. Bile ducts in atrophic liver lobes will preferably not be drained.
Patients will be treated with optimal palliative chemotherapy with gemcitabine and cisplatin.8 Palliative chemotherapy is preferably started within 6 weeks after IRE when patients have recovered from definitive metal biliary stent placement. The start of chemotherapy may be postponed in the event of IRE-related or biliary drainage-related complications. Gemcitabine (1000 mg/m2) and cisplatin (25 mg/m2) are administered on days 1 and 8 every 3 weeks with a total of 6–8 cycles. Chemotherapy will be discontinued in the event of tumour progression (based on RECIST 1.1 criteria and proposed criteria in table 1).
Figure 2 presents a flow chart of the study follow-up. Six weeks and 6, 12 and 24 months after treatment with IRE, an abdominal CT scan will be made in order to evaluate the effect of IRE (according to table 1). Blood samples will be drawn to measure tumour marker (CA 19-9) response. A CT scan 6 weeks post-IRE is considered the baseline scan for the start of palliative chemotherapy. When the time interval between this baseline scan and start of chemotherapy is prolonged with more than 4 weeks (ie, because of complications), a new baseline scan will be performed. Treatment response will be evaluated following every three cycles of chemotherapy. CT scans at 12 and 24 months post-IRE will be performed to evaluate the long-term tumour response following IRE.
A blinded adjudication committee will assess the occurrence of the primary and secondary endpoints after the last patient has completed follow-up. The primary endpoint will be expressed as the total number of clinically relevant complications in the entire cohort as well as the treatment subgroups (percutaneous and open IRE). Also, the absolute complication risk will be calculated for the entire cohort and the treatment subgroups. Data will be presented as mean±SD, and in case of non-normal distributions as median and IQR. Patient survival will be determined until 2 years after treatment. Patients still alive after 2 years and patients who are lost to follow-up will be censored. The data on OS and PFS will be presented as median survival in months with a CI of 95%. Data on 1-year and 2-year survival will be presented as percentages.
Considering the study’s pilot design and lack of data on post-IRE complications in this patient group, a formal sample size calculation is not feasible. A cohort of 20 patients is suggested to be a reasonable size to investigate the safety and feasibility of the procedure. A range of 8–12 patients per treatment group is accepted while the total sample size remains 20 patients.
Ethics and dissemination
This study is conducted in accordance with the principles of the Declaration of Helsinki and the Dutch Medical Research Involving Human Subjects Act. The Institutional Review Board (IRB) of the Academic Medical Center in Amsterdam approved the protocol on 19 April 2016. Secondary approval was obtained from the local IRB at VU University Medical Center on 14 July 2016. The study has been registered with the Dutch Central Committee on Research Involving Human Subjects (NL56231.018.15) and The Netherlands National Trial Register (NTR5948, 4 July 2016). Informed consent will be obtained from each participating patient in oral and written form prior to any study procedures.
An independent data safety monitoring board (DSMB), consisting of three independent specialists (surgeon, interventional radiologist, medical oncologist), will examine the safety variables (eg, serious adverse events) in a non-blinded manner after completion of 90-day follow-up of the fifth and tenth study patient. The DSMB also assists and advises the trial steering committee so as to protect the validity and credibility of the study. Furthermore, annual non-blinded safety reports, including all serious adverse events per group, will be provided to the IRB. The study is monitored by the Clinical Research Unit of the Academic Medical Center.
Data will be presented at national and international conferences as soon as the primary endpoint has been reached for the final recruited patient. The results of the primary outcome (safety, complications within 90 days after IRE) will be published in a peer-reviewed journal. After completion of 2-year follow-up, results of the secondary survival outcomes will be presented and published as well. Data will be kept at the study sites for 15 years after trial completion, as in accordance with the Dutch Medical Research Involving Human Subjects Act.
The ALPACA study aims to assess the safety profile and feasibility of IRE for advanced PHC prior to palliative chemotherapy. The eventual results of this study will inform us whether a follow-up trial to evaluate safety and effectiveness in a larger cohort will be feasible. Previous studies in the field of hepato-pancreato-biliary (HPB) malignancies have reported acceptable short-term outcomes with the use of IRE in locally advanced hepatic and pancreatic tumours. IRE may potentially overcome the limitations of other modalities, such as skin phototoxicity in PDT, possible heat/cold-sink effect in RFA and the need for multiple fractions in SBRT. In the present study, IRE will not replace the current standard of treatment in patients with locally advanced PHC. Thus, patients meeting the criteria for liver transplantation will be referred to a transplant centre and all patients will be evaluated for systemic chemotherapy.
IRE may be associated with severe complications given the complex anatomy of the liver hilum and the close proximity of the hepatic duct, portal vein and hepatic arteries. In this study, percutaneous electrode placement will be performed under CT fluoroscopy guidance with transcatheter arteriography to prevent puncture of major vessels or electrode placement too close to vital structures. During intraoperative sessions, inspection of the hilum and the use of US will guide electrode placement. Severe complications associated with the procedure may include bile leakage and portal vein or hepatic artery thrombosis, necessitating careful monitoring and instruction of patients on discharge. Specific attention will be paid to the placement of electrodes close to bile ducts, as it was previously demonstrated that biliary strictures may occur when needles are placed within 2–3 mm of the bile ducts.22 37 IRE will not be applied in the event of complete or partial thrombosis of the main portal vein. Partial portal vein thrombosis is considered an exclusion criterion because of the potential risk of worsening of the thrombus, leading to sudden complete portal vein thrombosis in such patients. To reduce the risk of cardiac arrhythmias, patients with a history of severe cardiac disease are not considered eligible for this study. Also, cardiac synchronisation during IRE ablation (ie, pulses not given during the atrial or ventricular systole periods of the cardiac cycle) will be applied to further lower the risk of arrhythmias.38 39
In the present study, a rate of severe complications of 60% within 90 days after IRE is considered an acceptable upper limit. Complications in the standard palliative treatment of patients with unresectable PHC are mainly caused by biliary stent dysfunctions. Dislocation, migration or clogging of stents causes cholangitis with or without a rise in plasma bilirubin, requiring reintervention. This is often accompanied by sepsis and/or liver abscesses. In a prospective study including 157 patients with malignant hilar biliary obstruction, 23% early (<30 days) and 40% late (>30 days) drainage-related complications were observed.33 It is essential to evaluate complications in the present study in light of the association with the IRE procedure itself. However, the maximum accepted complication rate consists of both IRE-related and IRE-unrelated complications. To limit the number of drainage procedures, an expert panel has been initiated for this study to carefully assess the individual biliary drainage strategy.
Although the ALPACA study is primarily designed to assess the safety and feasibility of IRE, our secondary hypothesis is that IRE will prolong OS for 3 months. Patients may also benefit from longer metal stent patency, as was previously reported after PDT in advanced PHC.9 Despite the higher OS benefit claimed in the treatment of other HPB tumours in current literature, we chose 3 months as this reflects, in our perspective, the least clinically relevant survival benefit for an emerging treatment provided that the complication rate is acceptable. Given the primary study purpose, a control group of patients only receiving standard systemic chemotherapy is not included as a treatment arm. However, long-term outcome in patients undergoing IRE and systemic chemotherapy will be compared with patients who were eligible for study participation but preferred standard palliative treatment. Naturally, a valid comparison between IRE and other local therapies or standard treatment may only be possible in a future well-designed prospective randomised controlled trial.
Contributors RJSC, JAV, LGPHV: trial conception and design, drafting and revising the manuscript. ER, ORCB, OMvD, FvD, JEvH, GK, H-JK, KPvL, EAJR, HMV: trial design, revising the manuscript. MH, HJS, JdV, JWW, BMZ: assisting trial design and revising of the manuscript. MGB: trial conception and design, supervising the drafting and revising of the manuscript. TMvG and MRM: principal investigators, trial conception and design, supervising the drafting and revising of the manuscript. All authors read and approved the final manuscript.
Funding The NanoKnife electrodes that will be used in this study are provided by AngioDynamics (Amsterdam-Zuidoost, the Netherlands). The study protocol has not undergone peer review by a funding body.
Competing interests MRM and KPvL are paid educational consultants for AngioDynamics.
Ethics approval The Institutional Review Board (IRB) of the Academic Medical Center in Amsterdam approved the protocol on 19 April 2016. The study has been registered with the Dutch Central Committee on Research Involving Human Subjects (NL56231.018.15). Secondary approval was provided by the local IRB at VU University Medical Center on 14 July 2016.
Provenance and peer review Not commissioned; externally peer reviewed.
Collaborators Trial steering committee: Department of Surgery: ER, GK, TMvG; Department of Radiology: LGPHV, KPvL, MRM; Department of Gastroenterology: JEvH, FvDt; Department of Medical Oncology: H-JK, HMV. ALPACA expert panel: Department of Surgery: MGB, ORCB, GK, TMvGu; Department of Radiology: KPvL, OMvD, MRM; Department of Gastroenterology: JEvH, EAJR, FvD.