Skip to main content

Advertisement

Log in

Pathologic Diagnosis and Genetic Analysis of Sequential Biopsy Following Coaxial Low-Power Microwave Thermal Coagulation For Pulmonary Ground-Glass Opacity Nodules

  • Clinical Investigation
  • Non-Vascular Interventions
  • Published:
CardioVascular and Interventional Radiology Aims and scope Submit manuscript

Abstract

Purpose

To evaluate the feasibility, safety, and diagnostic performance of sequential core-needle biopsy (CNB) technique following coaxial low-power microwave thermal coagulation (MTC) for ground-glass opacity (GGO) nodules.

Materials and Methods

From December 2017 to July 2019, a total of 32 GGOs (with diameter of 12 ± 4 mm) in 31 patients received two times of CNBs, both prior to and immediately after MTC at a power of 20 watts. The frequency and type of complications associated with CNBs were examined. The pathologic diagnosis and genetic analysis were performed for specimens obtained from the two types of biopsy.

Results

The technical success rates of pre- and post-MTC CNBs were 94% and 100%, respectively. The complication rate was significantly lower with post-MTC CNB as compared to pre-MTC CNB (42% versus 97%, p < 0.001). Larger amount of specimens could be obtained by post-MTC CNB. The pathological diagnosis rate of post-MTC CNB was significantly higher than that of pre-MTC CNB (100% versus 75%, p = 0.008), whereas the success rates of genetic analysis were comparable between the two groups (100% versus 84%, p = 0.063). Regular ablation could be further performed after post-MTC CNB to achieve local tumor control.

Conclusion

Sequential biopsy following coaxial low-power MTC can reduce the risk of complications and provide high-quality specimens for pulmonary GGOs. Combining this technique with standard ablation allows for simultaneous diagnosis and treatment within a single procedure.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Hansell DM, Bankier AA, MacMahon H, McLoud TC, Muller NL, Remy J. Fleischner Society: glossary of terms for thoracic imaging. Radiology. 2008;246(3):697–722. https://doi.org/10.1148/radiol.2462070712.

    Article  PubMed  Google Scholar 

  2. Scholten ET, Jong PA, Hoop B, Klaveren R, Amelsvoortorst S, Oudkerk M, et al. Towards a close computed tomography monitoring approach for screen detected subsolid pulmonary nodules. Eur Respir J. 2015;45(3):765–73.

    Article  Google Scholar 

  3. Van Haren RM, Correa AM, Sepesi B, Rice DC, Hofstetter WL, Mehran RJ, et al. Ground Glass Lesions on Chest Imaging: Evaluation of Reported Incidence in Cancer Patients Using Natural Language Processing. Ann Thorac Surg. 2019;107(3):936–40. https://doi.org/10.1016/j.athoracsur.2018.09.016.

    Article  PubMed  Google Scholar 

  4. Park JH, Lee KS, Kim JH, Shim YM, Kim J, Choi YS, et al. Malignant pure pulmonary ground-glass opacity nodules: prognostic implications. Korean J Radiol. 2009;10(1):12–20. https://doi.org/10.3348/kjr.2009.10.1.12.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Kim HY, Shim YM, Lee KS, Han J, Yi CA, Kim YK. Persistent pulmonary nodular ground-glass opacity at thin-section CT: histopathologic comparisons. Radiology. 2007;245(1):267–75. https://doi.org/10.1148/radiol.2451061682.

    Article  PubMed  Google Scholar 

  6. Kodama H, Yamakado K, Hasegawa T, Takao M, Taguchi O, Fukai I, et al. Radiofrequency ablation for ground-glass opacity-dominant lung adenocarcinoma. J Vas Intervent Radiol JVIR. 2014;25(3):333–9. https://doi.org/10.1016/j.jvir.2013.11.035.

    Article  Google Scholar 

  7. Yang X, Ye X, Lin Z, Jin Y, Zhang K, Dong Y, et al. Computed tomography-guided percutaneous microwave ablation for treatment of peripheral ground-glass opacity-Lung adenocarcinoma: a pilot study. J Cancer Res Therapeut. 2018;14(4):764–71. https://doi.org/10.4103/jcrt.JCRT_269_18.

    Article  Google Scholar 

  8. Iguchi T, Hiraki T, Gobara H, Fujiwara H, Matsui Y, Soh J, et al. Percutaneous radiofrequency ablation of lung cancer presenting as ground-glass opacity. Cardiovasc Intervent Radiol. 2015;38(2):409–15. https://doi.org/10.1007/s00270-014-0926-x.

    Article  PubMed  Google Scholar 

  9. Hertzanu Y, Ye X. Computed tomography-guided percutaneous microwave ablation: a new weapon to treat ground-glass opacity-lung adenocarcinoma. J Cancer Res Therapeut. 2019;15(2):265–6. https://doi.org/10.4103/jcrt.JCRT_65_19.

    Article  Google Scholar 

  10. Kerr KM, Bubendorf L, Edelman MJ, Marchetti A, Mok T, Novello S, et al. Second ESMO consensus conference on lung cancer: pathology and molecular biomarkers for non-small-cell lung cancer. Ann Oncol Official J Euro Soc Med Oncol. 2014;25(9):1681–90. https://doi.org/10.1093/annonc/mdu145.

    Article  CAS  Google Scholar 

  11. Hsu TH, Fidler ME, Gill IS. Radiofrequency ablation of the kidney: acute and chronic histology in porcine model. Urology. 2000;56(5):872–5. https://doi.org/10.1016/s0090-4295(00)00737-8.

    Article  CAS  PubMed  Google Scholar 

  12. Clasen S, Krober SM, Kosan B, Aebert H, Fend F, Bomches A, et al. Pathomorphologic evaluation of pulmonary radiofrequency ablation: proof of cell death is characterized by DNA fragmentation and apoptotic bodies. Cancer. 2008;113(11):3121–9. https://doi.org/10.1002/cncr.23882.

    Article  PubMed  Google Scholar 

  13. Schneider T, Reuss D, Warth A, Schnabel PA, von Deimling A, Herth FJ, et al. The efficacy of bipolar and multipolar radiofrequency ablation of lung neoplasms—aresults of an ablate and resect study. Eur J Cardiothorac Surg. 2011;39(6):968–73. https://doi.org/10.1016/j.ejcts.2010.08.055.

    Article  PubMed  Google Scholar 

  14. Nguyen CL, Scott WJ, Young NA, Rader T, Giles LR, Goldberg M. Radiofrequency ablation of primary lung cancer: results from an ablate and resect pilot study. Chest. 2005;128(5):3507–11. https://doi.org/10.1378/chest.128.5.3507.

    Article  PubMed  Google Scholar 

  15. Wang Q, Huang J, Ma K, Li T, Chen M, Wang S, et al. Evaluation of ghost cell survival in the area of radiofrequency ablation. PLoS ONE. 2012;7(12):e53158. https://doi.org/10.1371/journal.pone.0053158.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Hasegawa T, Kondo C, Sato Y, Inaba Y, Yamaura H, Kato M, et al. Pathologic Diagnosis and Genetic Analysis of a Lung Tumor Needle Biopsy Specimen Obtained Immediately After Radiofrequency Ablation. Cardiovasc Intervent Radiol. 2018;41(4):594–602. https://doi.org/10.1007/s00270-017-1845-4.

    Article  PubMed  Google Scholar 

  17. Tselikas L, de Baere T, Deschamps F, Hakime A, Besse B, Teriitehau C, et al. Diagnostic yield of a biopsy performed immediately after lung radiofrequency ablation. Eur Radiol. 2017;27(3):1211–7. https://doi.org/10.1007/s00330-016-4447-7.

    Article  PubMed  Google Scholar 

  18. Hasegawa T, Kondo C, Sato Y, Inaba Y, Yamaura H, Kato M, et al. Diagnostic Ability of Percutaneous Needle Biopsy Immediately After Radiofrequency Ablation for Malignant Lung Tumors: An Initial Experience. Cardiovasc Intervent Radiol. 2016;39(8):1187–92. https://doi.org/10.1007/s00270-016-1324-3.

    Article  PubMed  Google Scholar 

  19. Guo Z, Shi H, Li W, Lin D, Wang C, Liu C, et al. Chinese multidisciplinary expert consensus: Guidelines on percutaneous transthoracic needle biopsy. Thoracic cancer. 2018;9(11):1530–43. https://doi.org/10.1111/1759-7714.12849.

    Article  PubMed  PubMed Central  Google Scholar 

  20. National Institutes of Health NCI, U.S. Department of Health and Human Services. Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. https://www.ctepcancergov/protocolDevelopment/electronic_applications/docs/CTCAE_v5_Quick_Reference_85x11pdf accessed June 20, 2020.

  21. Freund MC, Petersen J, Goder KC, Bunse T, Wiedermann F, Glodny B. Systemic air embolism during percutaneous core needle biopsy of the lung: frequency and risk factors. BMC Pulmon Med. 2012;12:2. https://doi.org/10.1186/1471-2466-12-2.

    Article  Google Scholar 

  22. Yeow KM, Su IH, Pan KT, Tsay PK, Lui KW, Cheung YC, et al. Risk factors of pneumothorax and bleeding: multivariate analysis of 660 CT-guided coaxial cutting needle lung biopsies. Chest. 2004;126(3):748–54. https://doi.org/10.1378/chest.126.3.748.

    Article  PubMed  Google Scholar 

  23. Tai R, Dunne RM, Trotman-Dickenson B, Jacobson FL, Madan R, Kumamaru KK, et al. Frequency and Severity of Pulmonary Hemorrhage in Patients Undergoing Percutaneous CT-guided Transthoracic Lung Biopsy: single-Institution Experience of 1175 Cases. Radiology. 2016;279(1):287–96. https://doi.org/10.1148/radiol.2015150381.

    Article  PubMed  Google Scholar 

  24. Lu CH, Hsiao CH, Chang YC, Lee JM, Shih JY, Wu LA, et al. Percutaneous computed tomography-guided coaxial core biopsy for small pulmonary lesions with ground-glass attenuation. J Thorac Oncol. 2012;7(1):143–50. https://doi.org/10.1097/JTO.0b013e318233d7dd.

    Article  PubMed  Google Scholar 

  25. Inoue D, Gobara H, Hiraki T, Mimura H, Kato K, Shibamoto K, et al. CT fluoroscopy-guided cutting needle biopsy of focal pure ground-glass opacity lung lesions: diagnostic yield in 83 lesions. Eur J Radiol. 2012;81(2):354–9. https://doi.org/10.1016/j.ejrad.2010.11.025.

    Article  PubMed  Google Scholar 

  26. Tomiyama N, Yasuhara Y, Nakajima Y, Adachi S, Arai Y, Kusumoto M, et al. CT-guided needle biopsy of lung lesions: a survey of severe complication based on 9783 biopsies in Japan. Eur J Radiol. 2006;59(1):60–4. https://doi.org/10.1016/j.ejrad.2006.02.001.

    Article  PubMed  Google Scholar 

  27. Yang JS, Liu YM, Mao YM, Yuan JH, Yu WQ, Cheng RD, et al. Meta-analysis of CT-guided transthoracic needle biopsy for the evaluation of the ground-glass opacity pulmonary lesions. British J Radiol. 2014;87(1042):20140276. https://doi.org/10.1259/bjr.20140276.

    Article  Google Scholar 

  28. Wang J, Ni Y, Yang X, Huang G, Wei Z, Li W, et al. Diagnostic ability of percutaneous core biopsy immediately after microwave ablation for lung ground-glass opacity. J Cancer Res Therapeut. 2019;15(4):755–9. https://doi.org/10.4103/jcrt.JCRT_399_19.

    Article  Google Scholar 

Download references

Acknowledgements

This is a retrospective analysis of prospectively collected data. This study was approved by the institutional review board of our hospital (No. [2017]036) and was compliant with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all participants included in this study. Jiachang Chi and Min Ding collected the data of the patients, designed the pipeline of the analysis and drafted the manuscript. Bo Zhai conceived and coordinated the overall study and revised the manuscript. All authors read and approved the final manuscript.

Funding

This study was funded by the Innovation Funding of Renji Hospital (No. PY2018-III-11).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Bo Zhai.

Ethics declarations

Conflict of Interest

The authors declare that they have no conflict of interest.

Ethical Approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. For this type of study formal consent is not required.

Consent for Publication

Consent for publication was obtained for every individual person’s data included in the study.

Informed Consent

Informed consent was obtained from all individual participants included in the study.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chi, J., Ding, M., Wang, Z. et al. Pathologic Diagnosis and Genetic Analysis of Sequential Biopsy Following Coaxial Low-Power Microwave Thermal Coagulation For Pulmonary Ground-Glass Opacity Nodules. Cardiovasc Intervent Radiol 44, 1204–1213 (2021). https://doi.org/10.1007/s00270-021-02782-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00270-021-02782-9

Keywords

Navigation