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Open Access 01.12.2015 | Interventional

Thermal ablation of colorectal liver metastases: a position paper by an international panel of ablation experts, the interventional oncology sans frontières meeting 2013

verfasst von: Alice Gillams, Nahum Goldberg, Muneeb Ahmed, Reto Bale, David Breen, Matthew Callstrom, Min Hua Chen, Byung Ihn Choi, Thierry de Baere, Damian Dupuy, Afshin Gangi, Debra Gervais, Thomas Helmberger, Ernst-Michael Jung, Fred Lee, Riccardo Lencioni, Ping Liang, Tito Livraghi, David Lu, Franca Meloni, Philippe Pereira, Fabio Piscaglia, Hyunchul Rhim, Riad Salem, Constantinos Sofocleous, Stephen B. Solomon, Michael Soulen, Masatoshi Tanaka, Thomas Vogl, Brad Wood, Luigi Solbiati

Erschienen in: European Radiology | Ausgabe 12/2015

Abstract

Objectives

Previous attempts at meta-analysis and systematic review have not provided clear recommendations for the clinical application of thermal ablation in metastatic colorectal cancer. Many authors believe that the probability of gathering randomised controlled trial (RCT) data is low. Our aim is to provide a consensus document making recommendations on the appropriate application of thermal ablation in patients with colorectal liver metastases.

Methods

This consensus paper was discussed by an expert panel at The Interventional Oncology Sans Frontières 2013. A literature review was presented. Tumour characteristics, ablation technique and different clinical applications were considered and the level of consensus was documented.

Results

Specific recommendations are made with regard to metastasis size, number, and location and ablation technique. Mean 31 % 5-year survival post-ablation in selected patients has resulted in acceptance of this therapy for those with technically inoperable but limited liver disease and those with limited liver reserve or co-morbidities that render them inoperable.

Conclusions

In the absence of RCT data, it is our aim that this consensus document will facilitate judicious selection of the patients most likely to benefit from thermal ablation and provide a unified interventional oncological perspective for the use of this technology.

Key Points

• Best results require due consideration of tumour size, number, volume and location.

• Ablation technology, imaging guidance and intra-procedural imaging assessment must be optimised.

• Accepted applications include inoperable disease due to tumour distribution or inadequate liver reserve.

• Other current indications include concurrent co-morbidity, patient choice and the test-of-time approach.

• Future applications may include resectable disease, e.g. for small solitary tumours.

Introduction

Colorectal cancer is the second most common cause of cancer death in developed countries and the third most common malignancy worldwide [1]. Fifty percent of patients develop liver metastases yet only a minority (10–15 %) can undergo hepatic resection. Five-year survival following liver resection ranges between 31 % and 58 % in carefully selected patients [2, 3]. The remainder are usually offered chemotherapy and/or local tumour ablation. Median survival following systemic treatment is now of the order of 20–22 months in patients who receive biological agents and multiple sequential chemotherapy regimes, 5-year survival remains close to 0 %. Five-year survival following ablation varies between 17 % and 51 % (Table 1). Our aim is to present a consensus paper with recommendations on how radiofrequency and other types of thermal ablation should be built into the overall management plan of patients with colorectal liver metastases. The need for robust long-term follow-up data meant that this paper concentrated on radiofrequency (RF) ablation, the only thermal ablation source at present with substantial follow-up literature. RF ablation was first performed in the early 1990s and in the first few years there were a number of significant changes in technology which resulted in improved ablation efficacy [8, 9]. By the late 1990s and early 2000s ablation was becoming accepted in the interventional radiology community but was still viewed with some scepticism by the oncology and surgical communities. The first few surgical papers from the early 2000s reflect this, but more recently there has been genuine enthusiasm for a technique that can deliver effective focal therapy to many more patients than could be treated with resection alone [10‐12]. The effectiveness and the limitations of RF ablation are now well understood. The question of where ablation fits in the overall management of patients with metastatic colorectal cancer is still being debated. In the last few years there have been numerous reviews of the ablation literature [13‐26]. All of these have concluded that there is insufficient data, in particular randomised controlled trial (RCT) data, and as a result have had difficulty providing recommendations on the role of ablation. Attempts at RCT have not been successful due to difficulties in randomisation, cross-over between treatment arms, changes in chemotherapy regimes and expense. However, many ablation practitioners and early pioneers feel that the field has sufficiently matured for initial recommendations to be made. The following consensus document was discussed at a meeting of ablation experts which included more than 25 interventional oncologists, from around the world, all of whom had substantial personal experience in liver ablation.

Table 1

Survival following ablation of colorectal liver metastases. Papers were included if: Only patients with colorectal liver metastases were included. A minimum of 50 patients were treated with ablation. More than 3 year survival was provided. Where multiple papers were published by the same group over several years, the most complete/recent paper was used

Author	No of pts	Patient population:-no of patients with resectable disease (RD) vs. unresectable disease (UD)	Approach to ablation:	Mean/Median no of tumours	Mean/ Median diameter (cm)	Extra-hepatic disease (EHD) %	3 yr survival	4 yr survival	5 yr survival	7, 8 & 10 yr survival	Comment
Abdalla et al. (2004) [4]	418	Mixed RD and UD RF in 57 UD	Open	RF 1 (1-8)	RF 2.5	0	RF 37 %	RF 22 %			Unfavourable comparison of ablation to resection, similar results in ablation + resection vs. ablation alone. Favourable comparison to chemotherapy in liver only disease patients but different patient populations.
Agcaoglu et al. (2013) [5]	395	Mixed RD and UD RF in 295 UD	Laparoscopic	RF 3 (1-11)	RF 3.4	RF 22			RF 17 %		Used laparoscopic RF ablation to extend therapeutic envelope in patients with UD
Bale et al.(2012) [6]	63	37 UD 26 RD	Percutaneous	2 (1-14)	2 (0.5-13)	0	44 %		27 %		Significantly different outcome between RD and UD
Gillams and Lees (2009) [7]	123	UD	Percutaneous	2.1 (1-5)	2.9 (0.9-5)	0	49 %		24 %		A subpopulation of 69 patients with < 3 tumours, < 3.5 cm diameter (actual number 1.7, mean size 2.2 cm) had 5 yr survival of 33 %
Hamada et al. (2012) [29]	84	UD	Percutaneous	1.7	2.3 (0.5-9)	27	45 %		21 %		On multivariate analysis tumour size > 3 cm, multiple tumours, prior chemotherapy and uncontrolled EHD were significant
Hammill et al.(2011) [30]	101	Mixed but all Rx with RF RD 64 UD 37	Laparoscopic	1.6 RD 3.5 UD	3 RD 4 UD	0			49 % RD 18 % UD		RF can provide similar results to resection in selected patients
Jakobs et al.(2006) [31]	68	UD	Percutaneous	2.7	2.3 (0.5 – 5)	0	68 %
Kim et al. (2011) [32]	505	Mixed RD and UD RF 177 in UD due to comorbidity, > 4 scattered tumours, difficult site for resection	Open and Percutaneous	RF 1.6	RF 2.1 (0.5-6.2)	0			Single tumours < 3 cm RF 51 %		Same % overall (51, 51) and disease free survival (34, 32) for patients with single tumours < 3 cm treated with RF ablation/resection.
Machi et al.(2006) [33]	100	UD	Percutaneous 61 Laparoscopic 23 Open 62	3.5 all, Percutaneous 2.3, Laparoscopic 2.7, open 4.9	3.0 all, Percutaneous 3.5, Laparoscopic 2.3 Open 2.8	20 all Percutaneous 30, Laparoscopic 0, Open 18	42 %		31 %		Median survival of 30 months in patients with no EHD vs. 20 months in those with EHD Type of approach ceased to be significant on MV analysis Median survival of 48 months in those with RF ablation prior to chemotherapy vs. 22 months in those with RF ablation after chemotherapy
Reuter et al. (2009) [34]	192	Mixed RD and UD RF in 66 UD	Open	RF 2.8	RF 3.2	RF 15			RF 21 %		Poorer PFS for RF ablation as compared with resection but the same overall survival. 5 yr survival 23 % after resection vs. 21 % for RF. Note resection was used in larger tumours, mean 5.3 cm vs. 3.2 cm for RF ablation
Sofocleous et al. (2011) [35]	56	UD (Post resection)	Percutaneous	1.3 (1-4)	1.9 (0.5 – 5.7)	30	41 %				RF ablation as salvage in poor risk patients
Solbiati et al. (2012) [36]	99	UD (60) RD (39)	Percutaneous	2	2.2 (0.8-4 )	7	69 %		48 %	7 yr 25 % 10 yr 18 %
Sorensen et al. (2007) [37]	102	UD(100) RD (2, patient choice)	Percutaneous 153 Open 25	3.3 (1-17)	2.2 (0.5-6.5)	0	46 %	26 %
Van Tilborg et al. (2011) [38]	100	UD	Open 221 Percutaneous 16	2.4	2.4 (0.2-8.3)	Limited and treatable by resection, RT or RF	77 %		36 %	8 yr 24 %	Size and no. were significant Percutaneous approach chosen for recurrence, small superficial tumours, co-morbid and elderly patients
Veltri et al.(2008) [39]	122	UD	Percutaneous 108 Open 14	1.6	2.9 (0.5-8)	21	38 %		22 %		Tumour size impacted survival <3 cm 36 months vs. > 3 cm 23 months survival

Materials and methods

An initial draft was prepared for discussion and circulated prior to The International Oncology Sans Frontières Congress 2013. This document was then discussed and specific recommendations were made. Each recommendation, such as tumour size, was put to a vote, by an open show of hands. The document was then modified and disseminated electronically for comment. Feedback on subsequent versions was received from all authors. Each recommendation is accompanied with a description of the level of consensus achieved. Where there was consensus among all or nearly all (>95 %) members, the consensus level is described as strong. Where the majority (>80 % of experts) but not all agreed, the level of consensus is described as moderate. Only recommendations where >80 % consensus was achieved are included.

These guidelines are based on experience with radiofrequency ablation as the need for long-term follow-up data meant that there was insufficient data for some of the newer technologies, such as microwave (MW) and irreversible electroporation (IRE). Cryoablation and laser ablation are not widely implemented in colorectal liver metastases and again the data is limited. When more data, for example from high power MW, becomes available a revision of the current recommendations will be considered.

Literature review

A PubMed search of the literature from 1998 to March 2013 using the search terms: colorectal and ablation; treatment and colorectal liver metastases; radiofrequency ablation and liver metastases; ablation and liver metastases, produced in excess of 5000 results. These were further refined by only including papers specifically related to colorectal liver metastases and radiofrequency ablation technology with a defined minimum length of follow-up and minimum numbers of patients. The rationale for this was that all new techniques and procedures have an intrinsic learning curve. This was well studied at the time of introduction of laparoscopic cholecystectomy and again for laparoscopic-assisted colectomy and has also been shown to be true of ablation [27, 28]. Mulier estimated that treatment of at least 100 liver tumours was required for the mastery of RF ablation [28]. Accordingly, in most series the mean number of tumours treated per patient is two, and therefore series with a minimum of 50 patients (i.e. approximately 100 tumours in total) with colorectal liver metastases treated with RF and 3-year follow-up were included in the survival analysis (Table 1) [4‐7, 29‐39]. Furthermore, papers that did not separate the results of ablation with or without resection were not included, as this confounding variable could potentially obscure results. To avoid duplication of reporting, for those centres with multiple publications over many years, the most recent or most comprehensive report was selected. Abstracts were not included as this format does not provide sufficient detail for the study to be analysed.

All authors defined patients as having resectable or unresectable disease and RF ablation was almost without exception applied to patients with unresectable disease; details of the population have been specified. Of the 15 papers, four used both open and percutaneous approaches, two open only, two laparoscopic only, six percutaneous only and one used all three approaches. Four of the papers included resection, ablation and combined resection and ablation data. For our survival analysis we have shown the results from the ablation subgroup.

Survival analysis

The total population of patients who underwent RF ablation from the 15 papers was 1613. Mean tumour number per patient was 2.2 (1–3.5) and mean tumour size 2.6 cm (1.7–4). Eight papers included patients with extra-hepatic disease but one specified that all sites of extrahepatic disease were potentially treatable by resection, radiotherapy or ablation. The mean 3-year survival from the date of first thermal ablation was 50 % (37–77 %) and the mean 5-year survival was 31 % (17–51 %). Nearly all studies used RF ablation in patients with unresectable disease, but when ablation was applied to patients with potentially resectable disease the 5-year survival increased to 50 %. The mean 5-year survival for the percutaneous, laparoscopic and open approaches were 30 %, 28 % and 21 %, respectively.

Table 2 shows a summary of morbidity, mortality and hospital stay for the percutaneous, laparoscopic and open approaches with comparison to resection and combined resection and ablation. Table 3 shows the local recurrence rates according to procedural approach and size of tumour ablated.

Table 2

Mortality, morbidity and hospital stay

Category	Mortality, %	Major complications, %	Hospital stay, mean days (range)
Open resection	1–5 [4, 5]	25–30 [37] 21 [32]	13 (5–55) [40] 13.4 [32] 9.8 [34]
Combined open RF ablation + resection	4.5 [40]	37 [32] 32 [40]	15 [32]
Open RF ablation	2.3 [41] 1.1 [42] 0.0 [34]	32 [41] 10 [34] 9.6 [42]	6.6 [34] 4.2 [32]
Laparoscopic RF ablation	0.3 [5] 0.0 [30]	4.4 [5] 3.1 [30]	3.3 [30]
Percutaneous RF ablation	0.0 [7, 29, 31, 35‐37]	4.7 [7] 4.0 [35] 2.2 [29] 1.3 [36] 1.1 [39] 0.0 [31]	2 (1–9) [40] 1.3 [43] 1.0 [7]

RF radiofrequency

Table 3

Local recurrence (LR) in the immediate vicinity of the treated tumour

Author	Open RF ablation, %	Laparoscopic RF ablation, %	Percutaneous RF ablation, %	Resection^a	Size (cm)	%^b LR and size
Abdalla et al. (2004) [4]	9			2
De Baere et al. (2000) [44] Elias et al. (2004) [45]	6 (mean size 1.3 cm) 7		10 (mean size 2.6 cm)	7-9
Hamada et al. (2012) [29]			28		<3 >3	14 69
Hammill et al. (2011) [30]		5			<3 3–5 >5	3 4 27
Jakobs et al. (2006) [31]			18
Mackay et al. (2009) [41]	60			7
Nielsen et al. (2013) [42]	13				<3 3–5 >5	9 27 45
Reuter et al. (2009) [34]	17
Solbiati et al. (2012) [36]			12		<2 2–3 All < 3 >3	5 19 10 45
Van Duijnhoven et al. (2006) [46]	43		52
Veltri et al. (2008) [39]			26		<3 >3	33 67
Wang et al. (2013) [47]			48		<2.5 ≥2.5	41 70

^aPublished local recurrence rates following resection of colorectal liver metastases from the same authors

^bLocal recurrence rates by tumour diameter, showing better local control in smaller tumours

RF radiofrequency

Recommendations – tumour and technique specific considerations (Table 4)

Table 4

Summary of recommendations. Tumour and technical considerations

Parameter	Preferred	Caveat
Tumour size	<3 cm	Well located tumours <5 cm may be suitable for ablation
Tumour number	1–3 optimal, <5 preferable	6–9 maximum
Tumour location next to major bile ducts	Avoid	Consider high flow biliary cooling via nasobiliary tubes or other non-thermal interventional oncology techniques
Tumours located in contact with blood vessels	Suitable for ablation with careful follow-up and repeat treatment if necessary	Consider more intensive RF ablation to compensate for blood flow cooling, could consider IRE or MW
Tumours located within 1 cm of vulnerable structures, e.g. colon	Require displacement from the ablation zone using adjunctive measures, e.g. percutaneous hydro- or gas-dissection	Laparoscopic approach if adequate separation cannot be achieved percutaneously
Extra-hepatic disease (EHD)	Suitable for liver ablation as long as all sites of EHD disease are radically treated	Palliative liver ablation in patients with more extensive EHD is not recommended
Local recurrence should be minimised by:	1. Achieving >1 cm ablation margins in 3D 2. Maximising operator experience 3. GA should be available as required 4. Optimal definition of the tumour 5. Optimal intra-procedural assessment of the ablation zone	Conscious sedation procedures are an acceptable alternative in unfit patients

Tumour size (maximum longitudinal diameter in the axial plane (cm))

Thermal ablation is particularly effective in treating small- to medium-sized tumours. Many series report attempts at treating tumours larger than 5 cm in diameter, even up to 11 or 12 cm, but the incomplete ablation rate and local recurrence rate for these large tumours is very high and so these patients are better served by other treatment modalities. Analysis of local recurrence rates and survival shows an advantage for small tumours. These are detailed in Table 3 where consistently lower local tumour progression is reported with reducing tumour size. The most common cut-off point is 3 cm [29, 30, 36, 39]. However, tumours up to 5 cm can be completely ablated and permanently eradicated depending on their anatomical position and the treatment protocol used. For example, Hammil et al. [30] reported a 3 % local recurrence rate for <3-cm tumours and a 4 % recurrence rate for 3- to 5-cm tumours. Recurrence rates for >5 cm tumours ranges from 27–45 % and so thermal ablation with curative intent is not generally recommended for metastases >5 cm [30, 42].

The consensus was that smaller, <3 cm, tumours are more straightforward to treat than larger tumours, but that well located tumours <5 cm can be effectively treated depending on their anatomical position and the treatment protocol used. Well located tumours are defined as those with easy access, located such that clear margins can be achieved.

Consensus level: strong.

Tumour number

As ablation is a focal, minimally invasive technique, there is a limit to the number of tumours that can be successfully treated. Most centres will accept patients with five tumours or less. Some centres treat up to nine tumours, if the maximum diameter is <4 cm, and usually at two treatment sessions [48, 49]. As in the resection literature, the best results are achieved in solitary tumours, Gillams et al. [32] reported 3-year survival in excess of 80 % and Kim et al. [50] reported 5-year survival of 51 % in solitary tumours. Additional tumours that develop during follow-up, including new tumours in the post-resection liver remnant or local recurrence, should be considered for ablation based upon anatomical and size criteria.

The consensus was that patients with five or fewer tumours should routinely be considered for ablation and that patients with nine or fewer tumours should be considered in selected cases.

Consensus level: strong.

Overall liver tumour volume

In addition to the size and number of individual tumours, the overall liver tumour volume is also important. For example, in the EORTC 4004 (CLOCC) trial patients with nine or fewer tumours were treated, but the maximum individual tumour diameter allowed was 4 cm [49]. A crude overall liver tumour volume can be calculated from the product of the mean maximum tumour size and mean number. Analysis of the 5-year survival in four papers where patients without extra-hepatic disease were treated shows a direct correlation between crude liver tumour volume and survival with the best results in those with small volume disease (R² 0.7) (Fig. 1) [7, 30, 32, 38]. We would therefore recommend that in addition to size and number of tumours, the total liver tumour volume is taken into consideration.

Consensus level: strong

Relationship to central bile ducts

Ablation to within 1 cm of the major bile ducts (common bile duct, common hepatic, right and left hepatic ducts) runs the risk of bile duct injury [51]. The secondary effects, cholangitis and liver abscesses can be very significant, particularly if the patient requires chemotherapy at some later date. Therefore thermal ablation in this area is not recommended unless the bile ducts can be effectively protected. There is limited data suggesting high-flow bile duct cooling, for example via a nasobiliary tube, is effective in protecting the bile ducts [52]. Alternative techniques such as IRE, stereotactic body radiotherapy or transarterial therapies could be considered [53]. The consensus is that central bile ducts must be effectively protected or alternative technologies sought.

Consensus level: strong

Relationship to blood vessels

Ablation of tumours next to blood vessels is more difficult due to the cooling effect of blood flow. Ablation can be applied to tumours in contact with larger vessels (>3 mm in diameter) accepting an increased risk for tumour recurrence and the need for more than one treatment. This well known phenomenon has not been quantified in detail, but the risk of recurrence varies with the size of the vessel, the ablation technology and the length of vessel contact with the tumour. Strategies to ablate more vigorously next to blood vessels have been successfully adopted by many centres but are not part of standard commercial protocols. These strategies include increased power or duration of ablation next to the vessel or preferential placement of applicators towards the vessel side of the tumour. The patient and referring clinician should be advised as to the possible need for repeat treatment and the necessity of appropriate follow-up to detect and treat early tumour re-growth and so control the liver tumour load. Alternative technologies, for example microwave and IRE, may also have a role [54].

Consensus level: strong

Proximity to vulnerable structures

Ablation in close proximity to vulnerable structures, such as the colon, requires measures to create an acceptable safety margin or an operative approach [40]. Percutaneous hydro/gas dissection is a simple and very effective technique and should be part of the routine armamentarium of any ablation practice [55‐57].

Consensus level: strong

As size, number and location are all important features, there is a strong consensus that these three factors should be considered in concert when evaluating the appropriateness of ablation in any given patient.

Patients with small volume, ablatable liver metastases and extra-hepatic disease

Patients with extra-hepatic disease can be divided into those with limited, treatable extra-hepatic disease, by resection, ablation or radical radiotherapy, and those with more extensive disease for which the only treatment option is chemotherapy. The first group can benefit from ablation in the liver if the primary site and others sites of extra hepatic disease are radically treated, for example ablation of small volume lung metastases [58‐60]. Liver ablation in patients with more extensive extra-hepatic disease is of uncertain value. There is a wide range of survival reported for this group depending on volume of disease, sites involved, chemotherapy regimen and response, but in one paper the 5-year survival for 85 patients who had extra-pulmonic, extra-hepatic disease but limited liver disease treated with liver ablation was only 3 % [7]. The optimal ablation patient, as for resection, has disease limited to the liver.

Consensus level: strong

Maximising local tumour control

Many studies show higher local recurrence rates after ablation than after resection (Table 3). The ease of repeated treatment, particularly by the percutaneous approach, compensates to a degree for the higher local recurrence rate. This was confirmed in a study by Otto et al. [61] where RF ablation was performed as first-line treatment for smaller tumours, median 3 cm (range 1–5 cm), and resection was used for larger tumours, median 5 cm (range 1–14 cm). The estimated 5-year survival was similar: 48 % for ablation and 51 % for resection. The local recurrence rate was higher following ablation but there were more options for repeat intervention (either surgery or ablation) for new or recurrent disease, an important feature as most stage IV cancer patients will have multiple metastatic events. Similarly, Reuter et al. [34] showed different rates of disease-free progression between the resection and ablation group but overall survival was the same. Nevertheless, it is still of major importance to get good local tumour control (i.e. <5 % local tumour progression) and ideally percutaneous ablation would provide both excellent local tumour control and the option for repeated treatments for new metastases.

In addition to the factors already discussed such as tumour size, what else should we do to maximise local tumour control?

a. Obtaining adequate ablative margins is essential (strong consensus)
Colorectal liver metastases are less well perfused than the surrounding liver so it is easier to ablate to the tumour edge than to ablate the normally perfused liver around the metastasis which is required in order to achieve an ablative margin [62]. Applicators need to be positioned specifically to achieve a margin. A minimum 1-cm ablation margin is required in all directions or to the edge of the liver to maximise the likelihood of complete ablation. Greater than 1-cm margins further reduces the likelihood of local tumour progression [47]. Margins are particularly important where tumour definition is poor, for example in downsized tumours following chemotherapy.
b. Excellent definition of the extent of the tumour is required (strong consensus)
Contrast-enhanced imaging is recommended. Several studies show high local tumour recurrence rates where un-enhanced ultrasound (US), un-enhanced computed tomography (CT) or CT fluoroscopy have been used [29, 39, 46, 47].
c. Operator experience (strong consensus)
Experience with performing a minimum of 100 liver tumour ablations has been correlated with decreased recurrence rates. Each ablation technology/device has a different set of properties. Limited experience with multiple different devices is particularly unhelpful as it further dilutes the operator experience.
d. General anaesthesia (GA) (strong consensus)
The use of GA increases the rate of complete ablation [28]. Consequently GA should be freely available to be used at the discretion of the interventional oncologist. In patients who are not fit enough for GA, a moderate conscious sedation procedure is a valid option [63].
e. Pre-procedural assessment scans should be less than 2 weeks old (strong consensus)
The mean volume doubling time of colorectal liver metastases is 100 days therefore recent studies are needed for patient selection. Detailed confirmatory imaging at the time of treatment will facilitate complete ablation.
f. Monitoring ablation results at the time of treatment using contrast-enhanced CT, MRI or US and performing more ablation as needed, with further applicator insertions, higher power or additional treatment duration, at the same session will increase the chances of complete ablation with adequate margins in all dimensions. We therefore strongly recommend contrast-enhanced intra-procedural CT, MRI or US [64] (strong consensus).

Current clinical Indications for thermal ablation (Fig. 2, Table 5)

Table 5

Clinical recommendations

Clinical indication	Rationale	Consensus level
Ablation ± chemotherapy is recommended as the treatment of choice in patients with non-resectable but limited liver disease	RCT data shows significantly better disease free survival when ablation is added to chemotherapy Data from large case series shows a 5-year survival of 30 % (17–51 %) in ablation patients which is substantially different from the near 0 % seen after chemotherapy, albeit in different populations	Strong
Ablation ± chemotherapy is recommended in patients with limited liver disease who could otherwise only undergo resection following portal vein embolisation or staged resection but are suitable for ablation	5-year survival results are the same following ablation as for resection following downsizing with chemotherapy, portal vein embolisation or staged resection without the high morbidity associated with multiple procedures	Strong
Ablation is recommended as the treatment of choice in patients with non-resectable disease due to inadequate liver reserve, including most patients who have had a major liver resection	Risk of liver failure is very low Additional technical considerations include non-standard access, possible concomitant portal hypertension and the relationship of the tumour to major veins or bile ducts that subtend a major portion of the liver remnant	Strong
Ablation is recommended as the treatment of choice in patients with resectable disease who cannot undergo surgery due to medical co-morbidity	Surgical resection remains a major procedure with mortality of <3–5 % and major morbidity 25–30 %. The morbidity can be even higher in the older age group. Percutaneous ablation remains a low morbid, minimally invasive procedure that is well tolerated even by the medically unfit	Strong
Ablation is offered in some centres to patients with resectable disease as part of a ‘test-of-time approach’	Initial ablation does not prevent subsequent resection but does provide time for the tumour biology to declare. Patients with occult non-resectable disease will be spared ineffective surgery	Moderate
Patient choice; patients with ablatable and resectable disease may prefer to undergo ablation	Ablation can be performed as long as the patient has had an opportunity to discuss treatment options with both surgeons and interventional oncologists	Strong
The addition of chemotherapy to ablation is beneficial	Neoadjuvant chemotherapy is advocated in patients with non-ablatable/resectable disease with the goal of downsizing to ablatable/resectable disease. First-line ablation is recommended in small volume disease followed by adjuvant chemotherapy. Ablation should still be performed in patients who cannot undergo/tolerate chemotherapy	Strong
The percutaneous approach is favoured over and above the open approach	The open approach to ablation still carries a mortality and an unnecessarily high morbidity. Unless ablation is being performed as part of a surgical resection procedure, a percutaneous approach should be used	Strong
Ablation of small, <3 cm, solitary tumours is not currently an accepted indication but this may become a future indication	Retrospective comparisons suggest very similar outcomes between resection and ablation in these patients. An RCT would be welcomed by this panel of experts	Strong
Ablation is not recommended as a debulking tool	There is no evidence to support debulking in colorectal liver metastases	Strong
An interventional oncologist should be a standing member of the institutional colorectal liver metastasis tumour board	Access to ablation is still uneven and the advice given to patients does not always originate with an interventional oncologist qualified in percutaneous ablation – this needs to be rectified	Strong

RF radiofrequency, RCT randomised controlled trial, IRE irreversible electroporation, MW microwave

Patients with non-resectable disease due to number and distribution of metastases should receive ablation ± chemotherapy instead of systemic chemotherapy alone

The last 15 years have seen a marked improvement in both response rates and survival following systemic chemotherapy. Median survival is now of the order of 20–22 months in patients who receive biological agents and multiple sequential chemotherapy regimes [65]. Nevertheless, 5-year survival is close to 0 % unless patients can undergo and benefit from surgery. RF ablation has been successfully applied in patients with non-resectable, small-volume liver disease, often in conjunction with chemotherapy, and this has resulted in 3-year survival rates of 37–77 % and 5-year survival rates of 17–51 % (Table 1) [4‐7, 29‐39]. Abdalla compared ablation in unresectable patients with chemotherapy in un-ablatable patients, all with liver-only disease, and showed a significant improvement in survival in the ablation group median survival: 25 months versus 16.5 months (p = 0.005) [4]. Even though in this study RF ablation was applied to a different population than those receiving chemotherapy alone, who may have had more numerous or larger tumours, both groups had liver-only disease at surgical staging, had potentially curable disease on pre-operative staging, and were sufficiently fit to undergo major surgery, thus many consider that this marked improvement in survival in the RF ablation group is likely to reflect a benefit.

There has been one RCT (EORTC 4004, CLOCC trial) which aimed to study the benefit of adding ablation to systemic chemotherapy in patients with initially inoperable metastases. Inevitably there was an element of cross-over, so 5/59 (8.5 %) of those in the non-ablation arm were successfully downsized on chemotherapy, and subsequently underwent surgical resection [49]. This study suffered from slow accrual, was initially a phase III study but was downgraded to a phase II study, and closed early. As a result it was not sufficiently powered to allow assessment of differences in overall survival but did show significant differences in progression-free survival (PFS) at 3 years: 27.6 % in the ablation arm versus 10.6 % in the non-ablation arm (p = 0.025). The overall survival in the non-ablation arm was much higher than expected and there were also significant differences in salvage therapy between the two groups with the non-ablation arm receiving more systemic treatment. Differences in overall survival at 30 months were not significant, but the survival curves continue to separate on follow-up; 47 % versus 36 % at 4 years and 40 % versus 30 % at 5 years.

The most common approach to patients presenting with non-resectable disease is to use downsizing with neoadjuvant chemotherapy followed by resection ± portal vein embolisation and/or staged resection. However, the survival results of resection following portal vein embolisation are only 25 % at 5 years [66]. Furthermore, nearly 40 % of patients undergoing portal vein embolisation never get to resection and many patients planned for staged resection also fail to complete the course of treatment [67, 68]. Some, but not all, of these patients will have ablatable disease with comparable 5-year survival post-ablation but a higher chance of completing radical treatment to all sites of disease. Therefore, ablation should be considered in those with ablatable disease particularly if they fail to develop adequate liver volumes post-portal vein embolisation.

There is now general agreement that RF ablation is a useful adjunct to systemic treatment and it is widely applied in non-resectable but limited liver-only disease. For precise details on the appropriate tumour size, number and tumour location for ablation please see the section on tumour specific parameters.

Consensus level: strong

Patients with non-resectable disease due to inadequate liver reserve either because of prior resection or widely scattered tumours

Ablation is an accepted treatment for patients with small volume disease which cannot be resected due to limited liver reserve including most patients who have had a previous major liver resection [69]. Forty to 70 % of patients will develop new metastases after even a successful resection, with clear margins on pathological analysis, and the majority cannot undergo repeat resection [12, 70, 71]. Ablation is indicated in those inoperable patients who have limited, liver-only disease with or without chemotherapy.

The authors advise that additional factors to be considered are:

access, for example to a high left lobe liver remnant which may require a transthoracic approach
the possibility of post-resection portal hypertension with low platelets and upper abdominal venous collaterals which may affect the chosen electrode trajectory
the relationship of any tumour to a single remaining hepatic vein, portal vein branch or major bile duct that subtends a significant percentage of the remnant liver and could be damaged by ablation.

The risk of transient liver failure post-ablation in metastatic disease with a normal volume and normal functioning background liver parenchyma is very low and has only been described in two patients from a total cohort of 309 (0.6 %); both patients had undergone extended prior resection and at the time of ablation had only one and two remaining liver segments, respectively [4].

Consensus level: strong

The role and approach to ablation in a patient with resectable disease but patient co-morbidity, for example cardiac, renal or respiratory disease, prevents a major procedure

Liver resection remains a major procedure which is not applicable to less fit patients. Liver resection still carries a finite mortality risk although mortality rates in experienced modern surgical practices should be less than 3 % and certainly less than 5 %. Major morbidity is still high at approximately 25–30 %. Morbidity can be even higher, up to 40 %, in the over 70-year age group [72]. Percutaneous RF ablation is much less invasive, mortality is rare and major complication rates below 2.5 % have been reported from several experienced centres [29, 31, 36, 39]. All centres should aim for a major morbidity of <5 % and for the treatment of small volume disease (fewer than three tumours, <3 cm in diameter) <2 %. Both laparoscopic and open RF ablation carry a higher morbidity, require general anaesthesia, entail a longer hospital stay and increased cost, and should be reserved for specific indications. Open RF ablation without resection still carries a small mortality (<2.3 %) and the major complication rate varies between 9.6 % and 32 % (Table 2) [34, 41, 42]. Therefore the percutaneous approach is favoured. In more heavily morbid patients, ablation under moderate sedation may be preferable to GA.

Consensus level: strong

Test-of-time approach

The rationale for this approach is that ablation is often successful in treating small tumours without the need for resection but should ablation be unsuccessful, resection is still feasible. At the same time an interval is built into the patients’ treatment programme so that as undetectable microscopic liver metastases enlarge, they become detectable on imaging. This apparent disease progression often changes the patient’s status from resectable to unresectable. This test of time approach was first described in 2003 [63]. In that paper, of the 88 patients treated, 26 % remained tumour-free, negating the need for resection, 50 % developed more widespread disease progression and became unsuitable for resection, and 24 % underwent resection. A modified test-of-time approach has been used by another group for poor risk patients, i.e. those who had positive margins at liver resection or those recurring within 6 months of liver resection [35]. The test-of-time approach was considered an acceptable application.

Consensus level: moderate

Patient choice

This indication applies to a small percentage of all patients undergoing RF ablation (2–19 %) [36, 37] who opt for ablation despite being suitable for resection. RF ablation can be undertaken with the proviso that patients should have had an opportunity to discuss the probable outcomes with each of the relevant specialties and in this way make a well informed decision.

Consensus level: strong

What is the optimal timing of chemotherapy for patients receiving combined treatment?

Neoadjuvant chemotherapy

Neoadjuvant chemotherapy is advocated in patients who are not suitable for ablation de novo, in the hope that downsizing will permit definitive treatment with resection or ablation. A 5-year survival of 34 % has been reported by one group using RF ablation in a small group of 36 patients following neoadjuvant chemotherapy [73]. A technical limitation to treating patients who have undergone neoadjuvant chemotherapy prior to ablation can be difficulty in visualising treated hepatic tumours for example because of the development of hepatosteatosis ± tumour shrinkage. Additional techniques to define the tumours in the presence of chemotherapy-induced hepatosteatosis and tumour shrinkage,for example MRI with liver specific contrast agents, and larger treatment margins are recommended. Attempts to target and ablate tumours that are no longer visible on imaging using historical data and fusion techniques may be unsuccessful. However, tumours that have “disappeared’ on imaging are still detectable in pathology specimens and as they enlarge are very likely to ‘re-appear’ on follow-up imaging, so there should be a plan in place to treat these tumours when they do re-declare [74, 75].

Adjuvant chemotherapy

There is some evidence that adjuvant chemotherapy after liver resection maybe beneficial. A retrospective study in 235 patients showed a 5-year survival of 53 % in a subgroup of 99 patients who received (mostly 5FU-leucovorin based) adjuvant chemotherapy versus 25 % in those who did not have post-operative chemotherapy [76]. Two randomised studies, also using 5FU-leucovorin chemotherapy, showed a non-significant trend towards a benefit (p = 0.125 and 0.13, respectively). When these studies were pooled the median relapse-free survival in the chemotherapy arm was 28 months versus 19 in the control arm (p = 0.058) and the overall survival was 62 vs. 47 months (p = 0.095) [77, 78]. A randomised phase III trial of perioperative (six cycles prior followed by six cycles after resection) chemotherapy using FOLFOX (5FU and Oxaliplatin) showed a 7.3 % increase in PFS at 3 years in the chemotherapy arm (p = 0.058) [79]. A recently published follow-up report of the same cohort at 8.5 years showed no difference in overall survival, but this regime is still recommended because of the improvement in PFS [80].

Similarly there is early data to support adjuvant chemotherapy after ablation. Machi et al. [33] studied RF ablation as a first-line treatment versus RF ablation following chemotherapy and showed an increased overall survival of 26 months (48 months for first-line RF ablation vs. 22 months for RF ablation after chemotherapy). However, this study was insufficiently powered for statistical analysis. Siperstein et al. [81] showed an overall survival of 28 months versus 19 months for those who received chemotherapy after laparoscopic ablation (p = 0.02) and another paper reported a 10-year survival of 18 % in patients treated with percutaneous ablation and adjuvant chemotherapy using 5FU and Irinotecan [36].

As percutaneous ablation carries a low morbidity, the interval between ablation and adjuvant chemotherapy can be less than after open ablation or resection, with many commencing chemotherapy approximately 2 weeks post-ablation.

Although more evidence needs to be acquired, ablation plus chemotherapy seems to be better than either ablation or chemotherapy alone. This is in line with animal data. In a series of laboratory studies, larger ablations were consistently achieved when a combination of Doxil and ablation was used as compared with thermal ablation alone [82, 83]. For patients with ablatable disease at presentation, adjuvant chemotherapy may be preferred to neoadjuvant chemotherapy. Patients who cannot undergo chemotherapy, for example due to significant co-morbidity, side effects or poor tolerance often tolerate ablation and should be considered for ablation if the size and location of their tumours is appropriate [7].

Consensus level: strong

Can ablation be used to debulk liver metastases followed by chemotherapy?

Surgical debulking is an established part of the management of some tumours, for example metastatic ovarian cancer. There has been some discussion in the surgical community of using resection to debulk colorectal metastases prior to systemic chemotherapy but this is not evidence-based. As a focal minimally invasive technique, ablation is a less effective debulking tool. It is therefore preferable to concentrate resources on performing ablation with curative intent in limited disease.

Consensus level: strong

Choice of approach

Local recurrence

A decrease in local recurrence rates following open ablation compared to other approaches has not been confirmed in all studies. Local recurrence following open ablation varies between 6 % and 60 % and following percutaneous ablation between 10 % and 52 % (Table 3) [44, 46, 84, 85]. All studies report lower rates of local recurrence in smaller tumours.

Need for invasive staging

One often quoted reason for an intra-operative approach is the need for invasive staging. There are several conflicting papers showing both a substantial and a minimal benefit from open or laparoscopic staging [86, 87]. In the current era of excellent preoperative staging with good quality CECT, MRI and PET-CT, the benefit of operative staging is likely to be very small [86].

We further stress the percutaneous approach is the least invasive method for performing ablation. Open ablation carries an increased mortality and morbidity over percutaneous ablation [34, 41, 42] and should be reserved for patients undergoing resection for un-ablatable disease including:

Bulk disease

Resection of multiple clustered tumours in one area with ablation to between one and four tumours in the remnant liver.

Laparoscopic ablation

This technique requires a high level of expertise but has been developed in a few centres who report a reduction in morbidity, cost and hospital stay as compared with open ablation (Table 2) [5, 30]. Tumours that are adherent to vulnerable structures but are otherwise suitable for ablation may be best approached laparoscopically. However, a percutaneous approach should be favoured in tumours that are treatable either laparoscopically or percutaneously in order to minimise expense of hospital stay, morbidity and mortality [7, 30, 32, 40, 43].

Consensus level: strong

Access to Interventional Oncology ablation programmes and expertise

An interventional oncologist qualified in percutaneous ablation should be a standing member of the institutional colorectal cancer liver metastasis tumour board making recommendations on management. We feel that the successful selection of patients suitable for tumour ablation is predicated on purposeful involvement of a qualified interventional oncologist in the decision making process.

Consensus level: strong

Future indications for thermal ablation: can thermal ablation be used in resectable disease, in particular in small, solitary tumours, <3 cm in diameter?

The old mantra that the only chance of cure lies with resection is no longer true. Thermal ablation can and does result in cure in selected patients [42, 88].

Whilst there are several retrospective studies showing better survival following resection than following ablation, the two techniques are nearly always applied selectively with ablation being used in the patient group who are expected to fare less well [5, 85]. More often than not the ablation group has more disease, including extra-hepatic disease, is older and has more co-morbidities, or attempts have been made to ablate larger, >5-cm, tumours which are unlikely to succeed. When ablation has been applied as first-line therapy to patients with resectable disease, the 5-year survival results have been very similar to surgical series [30, 61].

Although there is one study showing comparable local tumour progression between wedge resection, anatomical resection and ablation [45], most surgical series report higher local tumour progression following ablation than after resection [43]. Despite this the overall survival is often similar [34].

There are five retrospective studies that show comparable survival between resection and ablation particularly when ablation is applied to smaller, <3-cm tumours. The results from Kim, Otto and Reuter have already been discussed [32, 34, 61]. Two other, smaller series also showed comparable results. Hur [89] reported on 23 patients who underwent resection compared with 15 who underwent either percutaneous or intraoperative RF ablation for </=3-cm tumours. The 5-year survival was 56 % and 55 %, respectively. Oshowo [90] compared resection and percutaneous ablation in solitary tumours of any size and found a similar 3-year survival. All of these studies are relatively small; more evidence is required. The possibility of a prospective RCT between surgical resection and ablation has been debated for over a decade and would be welcomed by this panel of experts. Likewise we would call for direct comparison to other therapies, for example chemo/radioembolisation or focal radiation therapy.

Consensus level: strong

Future directions

The gold standard RCT data, is very difficult to achieve and expensive. Vested interests, evolving technologies and patient resistance to randomisation are substantial barriers. The only attempted randomised trial of chemotherapy ± ablation (EORTC 40004) failed to accrue and the authors concluded that the chances of a further RCT were minimal. In addition changes in chemotherapy over the time-course of the study and significant differences in salvage therapy meant the initial endpoints and statistical framework proved inadequate.

In the interim, more, clearer and cleaner published data are required. Papers dealing with one tumour type, for example colorectal or breast liver metastases rather than mixed tumour populations, uniform technologies and approaches, larger series, more patient details and more specific patient groups are required to clarify what ablation can offer, and local recurrence rates should be reduced. Patients need better access to ablation programmes and to interventional oncology expertise.

Conclusion

Thermal ablation is widely, but not universally, accepted as part of the management of patients with unresectable colorectal liver metastases. Not all patients who are suitable for ablation have access to good quality ablation expertise. Furthermore, ablation has not yet reached its full potential; more can be done. It is our intention that these recommendations will facilitate the judicious selection of the patients who are most likely to benefit from ablation therapy and provide a unified interventional oncology perspective as we attempt to generate greater consensus from other oncology disciplines for the use of this clearly beneficial technology.

Acknowledgments

The scientific guarantor of this publication is Dr. Gigi Solbiait. The authors of this manuscript declare relationships with the following companies: Angiodynamics, Bayer, Boston Scientific, Bracco, BTG and Biocompatibles, Celon-Olympus, CeloNova, Celsion, Cosman Company, Covidien, Endocare, Esaote, Ethicon, Galil, GE Heathcare Gore, Microsulis, Neuwave Medical, Perfint, Pharmacept, Phillips Healthcare, Samsung, Siemens, Terumo. The authors state that this work has not received any funding. No complex statistical methods were necessary for this paper. Institutional Review Board approval and written informed consent were not required for this study because this is a review of existing published work.

Some study subjects or cohorts have been previously reported in a number of different journals as this is a review of the literature. Methodology: retrospective, not applicable, multicentre study.

Open Access This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Titel: Thermal ablation of colorectal liver metastases: a position paper by an international panel of ablation experts, the interventional oncology sans frontières meeting 2013
verfasst von: Alice Gillams
Nahum Goldberg
Muneeb Ahmed
Reto Bale
David Breen
Matthew Callstrom
Min Hua Chen
Byung Ihn Choi
Thierry de Baere
Damian Dupuy
Afshin Gangi
Debra Gervais
Thomas Helmberger
Ernst-Michael Jung
Fred Lee
Riccardo Lencioni
Ping Liang
Tito Livraghi
David Lu
Franca Meloni
Philippe Pereira
Fabio Piscaglia
Hyunchul Rhim
Riad Salem
Constantinos Sofocleous
Stephen B. Solomon
Michael Soulen
Masatoshi Tanaka
Thomas Vogl
Brad Wood
Luigi Solbiati
Publikationsdatum: 01.12.2015
Verlag: Springer Berlin Heidelberg
Erschienen in: European Radiology / Ausgabe 12/2015
Print ISSN: 0938-7994
Elektronische ISSN: 1432-1084
DOI: https://doi.org/10.1007/s00330-015-3779-z

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Abstract

Objectives

Methods

Results

Conclusions

Key Points

Introduction

Materials and methods

Literature review

Survival analysis

Recommendations – tumour and technique specific considerations (Table 4)

Tumour size (maximum longitudinal diameter in the axial plane (cm))

Tumour number

Overall liver tumour volume

Relationship to central bile ducts

Relationship to blood vessels

Proximity to vulnerable structures

Patients with small volume, ablatable liver metastases and extra-hepatic disease

Maximising local tumour control

Current clinical Indications for thermal ablation (Fig. 2, Table 5)

Patients with non-resectable disease due to number and distribution of metastases should receive ablation ± chemotherapy instead of systemic chemotherapy alone

Patients with non-resectable disease due to inadequate liver reserve either because of prior resection or widely scattered tumours

The role and approach to ablation in a patient with resectable disease but patient co-morbidity, for example cardiac, renal or respiratory disease, prevents a major procedure

Test-of-time approach

Patient choice

What is the optimal timing of chemotherapy for patients receiving combined treatment?

Neoadjuvant chemotherapy

Adjuvant chemotherapy

Can ablation be used to debulk liver metastases followed by chemotherapy?

Choice of approach

Local recurrence

Need for invasive staging

Laparoscopic ablation

Access to Interventional Oncology ablation programmes and expertise

Future indications for thermal ablation: can thermal ablation be used in resectable disease, in particular in small, solitary tumours, <3 cm in diameter?

Future directions

Conclusion

Acknowledgments

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