| Literature DB >> 30167887 |
Dietmar Tamandl1, Ahmed Ba-Ssalamah2, Gernot Böhm3, Klaus Emmanuel4, Rosemarie Forstner5, Reinhold Függer6, Benjamin Henninger7, Oliver Koch4, Claus Kölblinger8, Hans-Jörg Mischinger9, Wolfgang Schima10, Helmut Schöllnast11, Stefan Stättner12, Klaus Kaczirek13.
Abstract
Rapid advances in imaging technology have improved the detection, characterization and staging of colorectal liver metastases, hepatocellular carcinoma and cholangiocarcinoma. A variety of imaging modalities are available and play a pivotal role in the work-up of patients, particularly as imaging findings determine resectability. Surgery often represents the only measure that can render long-term survival possible. Imaging is also indispensable for the assessment of responses to neoadjuvant treatment and for the detection of recurrence. At a consensus meeting held in June 2017 in Vienna, Austria, Austrian experts in the fields of surgery and radiology discussed imaging requirements prior to and after hepatic surgery for malignant liver lesions. This consensus was refined by online voting on a total of 47 items. Generally, the degree of consensus was high. The recommendations relate to the type of preferred preoperative imaging modalities, technical settings with respect to computed tomography and magnetic resonance imaging, use of contrast agents, reporting, postoperative follow-up, and long-term follow-up. Taking local resources into account, these consensus recommendations can be implemented in daily clinical practice at specialized centers as well as outpatient diagnostic institutes in Austria.Entities:
Keywords: Cholangiocarcinoma; Colorectal liver metastases; Hepatic surgery; Hepatocellular carcinoma; Imaging
Mesh:
Year: 2018 PMID: 30167887 PMCID: PMC6244807 DOI: 10.1007/s00508-018-1387-z
Source DB: PubMed Journal: Wien Klin Wochenschr ISSN: 0043-5325 Impact factor: 1.704
Recommendations and degree of consensus, part 1
| Item no. | Statement | Consensus level, % |
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| 1CLM | CT of the chest and abdomen should be performed as basic examinations. Negative results preclude further assessment. Contrast-enhanced MRI is only indicated in (potentially) resectable lesions | 100 |
| 1CLMi | If CT reveals visible steatosis, which implicates the risk of false negative findings, additional MRI should be considered, even if CT is negative | 88 |
| 1CLMii | In lean patients, sonography is optional as an additional assessment | 65 |
| 1HCC | Lesions of uncertain malignancy suspected in patients at risk for HCC: CT serves as the basic examination with the purpose of characterizing the lesions. If locoregional techniques are feasible: | 100 |
| 1CCC | CT is the basic examination; further characterization calls for contrast-enhanced MRI plus MRCP sequences. It is strongly recommended to perform MRCP sequences prior to stenting | 93 |
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| 2 | In all three entities, CT of the chest and abdomen is mandatory | 98 |
| 2HCCi | An exception is the patient at risk who presents with a hepatic lesion (suspected HCC in liver cirrhosis, chronic viral hepatitis, or steatohepatitis). Here, CT assessment of the entire abdomen and chest should only be performed if a lesion suggesting HCC is present | 100 |
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| 3CLM | For the initial assessment, we strongly recommend arterial and portal venous phases. Additional unenhanced series prior to the application of contrast agents are optional | 97 |
| 3HCC | 3-phasic or 4‑phasic with arterial/portal venous/equilibrium phases, with the unenhanced phase being optional | 97 |
| 3CCC | 3-phasic or 4‑phasic with arterial/portal venous/equilibrium phases, with the unenhanced phase being optional | 95 |
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| 4 | The maximum slice thickness should not exceed 3 mm in all entities | 98 |
| 4i | For the assessment of arterial vessels, a maximum slice thickness of 1 mm is optional in case of specific surgical issues or in patients with Klatskin tumors | 88 |
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| 5 | Coronal reconstruction for portal venous and arterial phases, with a slice thickness of 3 mm. Sagittal reconstructions for spine assessment | 95 |
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| 6 | An iodine dose of 0.6 g/kg body weight (i. e. 2 ml/kg for an agent with an iodine content of 300 mg/ml) should be used for the standard 64 slice system. Reductions might be possible when using modern generation scanners | 95 |
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| 7CLM | 3–5 ml/s | 88 |
| 7HCC | 4 ml/s | 82 |
| 7HCCi | Imaging of the arterial phase should focus at the late arterial phase, i. e. using bolus tracking with a delay of 15–18 s. Definition of the late arterial phase: enhancement of the hepatic artery and portal vein | 98 |
| 7CCC | 3–5 ml/s | 87 |
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| 8 | Soft-tissue kernel according to the recommendations of the manufacturer | 92 |
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| 9 | No role in the routine preoperative staging. PET-CT is a problem-solving tool in high-risk patients and should be used to investigate uncertain extrahepatic findings | 97 |
Minimum voting score, 13; maximum voting score, 65, numbers are given as percentage of maximum voting score. Item no. refers to consecutive numbers of statements as discussed during the expert panel meeting. If a statement was made for one specific entity, this was specified with subscripts (CLM, HCC or CCC)
PET-CT positron emission tomography-computed tomography, CT computed tomography, MRI magnetic resonance imaging, PET positron emission tomography, MRCP magnetic resonance cholangiopancreatography, CLM colorectal liver metastases, HCC hepatic cellular carcinoma, CCC cholangiocellular carcinoma, ADC apparent diffusion coefficient, Gd gadolinium, RECIST Response Evaluation Criteria in Solid Tumors, SOS sinusoidal obstruction syndrome
Recommendations and degree of consensus, part 2
| Item no. | Statement | Consensus Level, % |
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| 10 | At least 1.5 T | 100 |
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| 11 | Axial T2w single-shot TSE, T2w-TSE (at least one T2w sequence with fat suppression), 2D/3D-T1w GRE with chemical shift imaging (in-phase and opposed-phase), dynamic 3D-T1w GRE with fat saturation dynamically after application of contrast agent (late arterial, portal venous, equilibrium phases; when using hepatocyte-specific contrast agents, hepatobiliary phase after 20 min or 60–120 min, depending on the contrast agent) | 97 |
| 12 | Diffusion-weighted sequences with low, intermediate and high b values of e. g. 50, 400, 800. ADC map | 95 |
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| 13 | T2w-weighted sequences and DWI can be performed after the application of a contrast agent and T2w MRCP prior to the application of a contrast agent | 92 |
| 14 | In patients with significant ascites, paracentesis prior to imaging might be considered to improve image quality | 82 |
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| 15 | A maximum of 5 mm for 2D sequences, a maximum of 3 mm for 3D sequences | 100 |
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| 16 | Dosing of contrast agents: 0.1 mmol/kg body weight for non-specific Gd chelate and 0.025 mmol/kg body weight for gadoxetic acid | 100 |
| 17 | Flow rate: contrast agents should be applied manually or by means of a contrast agent injector at a dose of 1 ml/s, followed by a sodium chloride flush | 95 |
| 18 | Bolus triggering for the arterial phase | 97 |
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| 19CLM | Gadoxetic acid for all patients | 93 |
| 19HCC | Gd-containing contrast agent | 82 |
| 19CCC | Peripheral CCC: gadoxetic acid; Klatskin tumor: Gd-containing contrast agent | 85 |
| 19CLM-CCCi | Imaging studies for purposes of comparison should always be conducted using identical parameters. An exception to this rule is the arterial phase during follow-up of CLM, which can be dispensable | 98 |
| 19CLMii | In the setting of neoadjuvant chemotherapy of CLM, it is strongly recommended to conduct MRI before and after treatment or prior to surgery | 92 |
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| 20CLMi | Detailed description of metastatic lesions. Minimum requirements include the number of lesions, size (in mm) of the largest metastases and description of segmental distribution. Importantly, unaffected segments should be mentioned, as this allows for surgery to be considered or precluded in the first place. The term “multiple” should not be rashly used when lesions are countable. Differentiation from lesions that are reliably benign | 100 |
| 20CLMii | Proximity of lesions to vital structures (e. g., blood vessels, bile ducts). Presumed preservability of inflow/outflow | 100 |
| 20CLMiii | Anatomical description, description of relevant normal variations | 100 |
| 20CLMiv | If applicable, description of the quality of the parenchyma (e. g., cirrhosis, steatosis, etc.) | 100 |
| 20CLMv | Description of extrahepatic lesions | 100 |
| 20HCC | Number of unequivocal HCC lesions. The recommendations given for 20CLMi to v apply here as well, with a particular focus on portal vein thrombosis, if applicable | 100 |
| 21CLMi | Response to prior neoadjuvant therapy and size of lesion(s; not necessarily according to RECIST) | 100 |
| 21CLMii | Metastatic lesions that have disappeared during neoadjuvant treatment should be mentioned | 100 |
| 21CLMiii | Signs of chemotherapy-induced liver injury (e. g., steatosis, SOS) | 100 |
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| 22 | Postoperative CT using the arterial and portal venous phases is strongly recommended. For suspected bleeding, an unenhanced CT phase should also be performed | 100 |
| 23 | MR, MRCP in case of biliary complications | 100 |
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| 24 | 3–6 month intervals according to local preference | 97 |
| 25 | PET/CT should not be performed routinely, only in cases of unclear findings | 97 |
Minimum voting score, 13; maximum voting score, 65, numbers are given as percentage of maximum voting score. Item no. refers to consecutive numbers of statements as discussed during the expert panel meeting. If a statement was made for one specific entity, this was specified with subscripts (CLM, HCC or CCC)
CT computed tomography, MRI magnetic resonance imaging, PET positron emission tomography, MRCP magnetic resonance cholangiopancreatography, CLM colorectal liver metastases, HCC hepatic cellular carcinoma, CCC cholangiocellular carcinoma, ADC apparent diffusion coefficient, Gd gadolinium, RECIST response evaluation criteria in solid tumors, SOS sinusoidal obstruction syndrome