Rofo 2022; 194(05): 515-520
DOI: 10.1055/a-1669-9342
Interventional Radiology

Detectability of Target Lesion During CT-Guided Tumor Ablations: Impact on Ablation Outcome

Nachweisbarkeit der Zielläsion bei CT-gesteuerten Tumorablationen: Auswirkungen auf das Ablationsergebnis
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
,
Niveditha Senthilvel
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
,
Philipp Bruners
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
,
Sebastian Keil
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
,
Georg Lurje
2   Department of Surgery and Transplantation, University Hospital RWTH Aachen, Germany
,
Markus Zimmermann
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
,
Christiane K Kuhl
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
,
Peter Isfort
1   Department of Diagnostic and Interventional Radiology, University Hospital RWTH Aachen, Germany
› Author Affiliations

Abstract

Purpose Small hepatic malignancies scheduled for CT-guided percutaneous ablation may have been identified in the hepatobiliary phase of liver MRI or in a specific phase of multi-phase CT but may be occult on unenhanced CT used to guide the ablation. We investigated whether the detectability of the target lesion would impact the efficacy of CT-guided hepatic tumor ablations.

Materials and Methods We included 69 patients with 99 malignant liver lesions (25 primary, 44 metastases) who underwent IRE (n = 35), RFA (n = 41), or MWA (n = 23) between 01/2015 and 06/2018. All procedures were performed under CT guidance. Lesions not detectable on CT (NDL) were targeted through identification of anatomical landmarks on preinterventional contrast-enhanced CT or MRI. Rates of incomplete ablation, size of ablation zone, local tumor recurrence, intrahepatic progression-free survival (ihPFS), and adverse event rates were compared for detectable lesions (DL) vs. NDL.

Results 40 lesions were NDL, and 59 lesions were DL on unenhanced CT. The mean follow-up was 16.2 months (14.8 for DL and 18.2 for NDL). The mean diameter of NDL and DL was similar (12.9 mm vs. 14.9 mm). The mean ablation zone size was similar (37.1 mm vs. 38.8 mm). Incomplete ablation did not differ between NDL vs. DL (5.0 % [2/40; 0.6–16.9 %] vs. 3.4 % [2/59; 0.4–11.7 %]), nor did local tumor recurrence (15.4 % [6/39; 5.7 %–30.5 %] vs. 16.9 % [10/59; 8.4–29.0 %]), or median ihPFS (15.5 months vs. 14.3 months).

Conclusion Target lesion detectability on interventional CT does not have a significant impact on outcome after percutaneous liver ablation when anatomical landmarks are used to guide needle placement.

Key Points:

  • Liver tumors can be successfully ablated even if they are not detectable on the navigational CT scan.

  • Anatomical landmarks should be used and compared to preinterventional imaging.

Citation Format

  • Barzakova E, Senthilvel N, Bruners P et al. Detectability of Target Lesion During CT-Guided Tumor Ablations: Impact on Ablation Outcome . Fortschr Röntgenstr 2022; 194: 515 – 520

Zusammenfassung

Ziel Intrahepatische maligne Läsionen, geplant für CT-gesteuerte perkutane Ablation, können MR-tomographisch oder CT-graphisch in einer bestimmten Kontrastmittelphase abgrenzbar sein, jedoch okkult in der nativen CT-Untersuchung, genutzt zur Planung der Ablation. Ziel dieser Studie ist zu untersuchen, ob die Abgrenzbarkeit der Zielläsion in der Planungsuntersuchung einen Einfluss auf das kurz- und mittelfristige Ablationsergebnis hat.

Material und Methoden Es wurden 69 Patienten mit insgesamt 99 malignen Leberläsionen (25 Primärtumoren, 44 Metastasen) eingeschlossen, die zwischen 01/2015 und 06/2018 irreversibler Elektroporation (n = 35), Radiofrequenzablation (n = 41) oder Mikrowellenablation (n = 23) unterzogen wurden. Alle Verfahren wurden unter CT-Führung durchgeführt. Läsionen, die in der Planungs-CT nicht nachweisbar waren (NDL), wurden durch die Korrelation zu anatomischen Landmarken in der kontrastverstärkten CT oder MRT-Voruntersuchung lokalisiert. Es wurden die Raten unvollständiger Ablation, lokalen Tumorrezidivs, die Größe der Ablationszone, das intrahepatische progressfreie Überleben (ihPFS) und die Komplikationsraten für nachweisbare Läsionen (DL) gegenüber NDL verglichen.

Ergebnisse 40 Läsionen waren NDL, 59 Läsionen waren DL auf die native Planungs-CT. Die mittlere Beobachtungsdauer war 16,2 Monate (14,8 für DL und 18,2 für NDL). Die mittleren Durchmesser von NDL und DL waren ähnlich (12,9 mm vs. 14,9 mm). Die mittleren Ablationszonengrößen waren ähnlich (37,1 mm vs. 38,8 mm). Es zeigten sich keine wesentlichen Unterschiede zwischen NDL und DL bezüglich der Häufigkeit unvollständiger Ablationen (5,0 % [2/40; 0,6 %–16,9 %] gegenüber 3,4 % [2/59; 0,4 %–11,7]), des Auftretens eines lokalen Tumorrezidivs (15,4 % [6/39; 5,7 %–30,5 %] gegenüber 16,9 % [10/59; 8,4 %–29,0]) oder des medianen ihPFS (15,5 Monate gegenüber 14,3 Monate).

Schlussfolgerung Die Nachweisbarkeit der Zielläsion in dem periinterventionellen Planungs-CT hat keinen signifikanten Einfluss auf das Ergebnis nach perkutanen Leberablationen, wenn anatomische Landmarken zur Nadelplatzierung genutzt werden.

Kernaussagen:

  • Lebertumoren können erfolgreich abladiert werden, auch wenn sie in dem nativen Planungs-CT nicht nachweisbar sind.

  • Anatomische Landmarken sollten verwendet und mit der präinterventionellen Bildgebung verglichen werden.



Publication History

Received: 18 April 2021

Accepted: 07 October 2021

Article published online:
18 November 2021

© 2021. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Mahnken A, Pereira P, de Baère T. Interventional oncologic approaches to liver metastases. Radiology 2013; 266: 407-430
  • 2 Kulaylat M, Gibbs J. Thermoablation of colorectal liver metastasis. J Surg Oncol 2010; 101: 699-705
  • 3 Meloni M, Chiang J, Laeseke P. et al. Microwave ablation in primary and secondary liver tumours: technical and clinical approaches. Int J Hyperthermia 2017; 33: 15-24
  • 4 Guenette J, Dupuy D. Radiofrequency ablation of colorectal hepatic metastases. J Surg Oncol 2010; 102: 978-987
  • 5 Lencioni R. Loco-regional treatment of hepatocellular carcinoma. Hepatology 2010; 52: 762-773
  • 6 Scheffer H, Vroomen L, Nielsen K. et al. Colorectal liver metastatic disease: efficacy of irreversible electroporation--a single-arm phase II clinical trial (COLDFIRE-2 trial). BMC Cancer 2015; 15: 772
  • 7 Crocetti L, de Baere T, Lencioni R. Quality improvement guidelines for radiofrequency ablation of liver tumours. Cardiovasc Intervent Radiol 2010; 33: 11-17
  • 8 Ahmed M, Solbiati L, Brace C. et al. Image-guided tumor ablation: standardization of terminology and reporting criteria – a 10-year update. Radiology 2014; 273: 241-260
  • 9 Wells S, Hinshaw J, Lubner M. et al. Liver Ablation: Best Practice. Radiol Clin North Am 2015; 53: 933-971
  • 10 Pua B, Sofocleous C. Imaging to optimize liver tumor ablation. Imaging Med 2010; 2: 433-443
  • 11 Wood B, Kruecker J, Abi-Jaoudeh N. et al. Navigation systems for ablation. J Vasc Interv Radiol 2010; 21: 257-263
  • 12 van Tilborg A, Scheffer H, Nielsen K. et al. Transcatheter CT arterial portography and CT hepatic arteriography for liver tumor visualization during percutaneous ablation. J Vasc Interv Radiol 2014; 25: 1101-1111
  • 13 Luu H, Klink C, Niessen W. et al. Non-Rigid Registration of Liver CT Images for CT-Guided Ablation of Liver Tumors. PLoS One 2016; 11: e0161600
  • 14 Abi-Jaoudeh N, Kruecker J, Kadoury S. et al. Multimodality image fusion-guided procedures: technique, accuracy, and applications. Cardiovasc Intervent Radiol 2012; 35: 986-998
  • 15 Appelbaum L, Mahgerefteh S, Sosna J. et al. Image-guided fusion and navigation: applications in tumor ablation. Tech Vasc Interv Radiol 2013; 16: 287-295
  • 16 Varga E, Pattynama P, Freudenthal A. Manipulation of mental models of anatomy in interventional radiology and its consequences for design of human–computer interaction. Cogn Tech Work 2013; 15: 457-473
  • 17 Filippiadis D, Binkert C, Pellerin O. et al. Cirse Quality Assurance Document and Standards for Classification of Complications: The Cirse Classification System. Cardiovasc Intervent Radiol 2017; 40: 1141-1146
  • 18 Van Tilborg A, Meijerink M, Sietses C. et al. Long-term results of radiofrequency ablation for unresectable colorectal liver metastases: a potentially curative intervention. Br J Radiol 2011; 84: 556-565
  • 19 Kurowecki D, Kielar A, Shabana W. et al. Incidence of local recurrence 1 year following radiofrequency ablation for hepatocellular carcinoma: a single center experience. J Vasc Interv Radiol 2016; 27: 124
  • 20 Solbiati L, Ahmed M, Cova L. et al. Small liver colorectal metastases treated with percutaneous radiofrequency ablation: local response rate and long-term survival with up to 10-year follow-up. Radiology 2012; 265: 958-968
  • 21 Livraghi T, Solbiati L, Meloni F. et al. Percutaneous radiofrequency ablation of liver metastases in potential candidates for resection: the “test-of-time approach”. Cancer 2003; 97: 3027-3035
  • 22 Niessen C, Beyer L, Pregler B. et al. Percutaneous Ablation of Hepatic Tumors Using Irreversible Electroporation: A Prospective Safety and Midterm Efficacy Study in 34 Patients. J Vasc Interv Radiol 2016; 27: 480-486
  • 23 Hori T, Nagata K, Hasuike S. et al. Risk factors for the local recurrence of hepatocellular carcinoma after a single session of percutaneous radiofrequency ablation. J Gastroenterol 2003; 38: 977-981
  • 24 Wiggermann P, Puls R, Vasilj A. et al. Thermal ablation of unresectable liver tumors: factors associated with partial ablation and the impact on long-term survival. Med Sci Monit 2012; 18: 88-92
  • 25 Kim Y, Rhim H, Cho O. et al. Intrahepatic recurrence after percutaneous radiofrequency ablation of hepatocellular carcinoma: analysis of the pattern and risk factors. Eur J Radiol 2006; 59: 432-441
  • 26 Wang X, Sofocleous C, Erinjeri J. et al. Margin size is an independent predictor of local tumor progression after ablation of colon cancer liver metastases. Cardiovasc Intervent Radiol 2013; 36: 166-175
  • 27 Boulkhrif H, Luu H, van Walsum T. et al. Accuracy of semi-automated versus manual localisation of liver tumours in CT-guided ablation procedures. Eur Radiol 2018; 28: 4978-4984
  • 28 Takaki H, Yamakado K, Nakatsuka A. et al. Computed tomography fluoroscopy-guided radiofrequency ablation following intra-arterial iodized-oil injection for hepatocellular carcinomas invisible on ultrasonographic images. Int J Clin Oncol 2013; 18: 46-53