Skip to main content
Log in

Analysis of the layering pattern of the apparent diffusion coefficient (ADC) for differentiation of radiation necrosis from tumour progression

  • Neuro
  • Published:
European Radiology Aims and scope Submit manuscript

Abstract

Objectives

To evaluate the added value of diffusion-weighted imaging (DWI) to perfusion-weighted imaging (PWI) for differentiating tumour progression from radiation necrosis.

Methods

Sixteen consecutive patients who underwent removal of a metastatic brain tumour that increased in size after stereotactic radiosurgery were retrospectively reviewed. The layering of the ADC was categorised into three patterns. ADC values were measured on each layer, and the maximum rCBV was measured. rCBV and the layering pattern of the ADC of radiation necrosis and tumour progression were compared.

Results

Nine cases of radiation necrosis and seven cases of tumour progression were pathologically confirmed. Radiation necrosis (88.9 % vs. 14.3 %) showed a three-layer pattern of ADC with a middle layer of minimum ADC more frequently. If rCBV larger than 2.6 was used to differentiate radiation necrosis and tumour progression, the sensitivity was 100 % but specificity was 56 %. If the lesions with the three-layer pattern of ADC with moderately increased rCBV (2.6–4.1) were excluded from tumour progression, the sensitivity and specificity increased to 100 %.

Conclusions

The three-layer pattern of ADC shows high specificity in diagnosing radiation necrosis; therefore, combined analysis of the ADC pattern with rCBV may have added value in the correct differentiation of tumour progression from radiation necrosis.

Key Points

•MRI follow-up often reveals increasing size of enhancing lesions after stereotactic radiosurgery

•Inflammation around tumour necrosis increases regional cerebral blood volume (rCBV), mimicking progression

•A three-layer apparent diffusion coefficient (ADC) pattern on diffusion-weighted MRI suggests radiation necrosis.

•The combined use of rCBV and DW MRI enables accurate differentiation.

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
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Huber PE, Hawighorst H, Fuss M, van Kaick G, Wannenmacher MF, Debus J (2001) Transient enlargement of contrast uptake on MRI after linear accelerator (LINAC) stereotactic radiosurgery for brain metastases. Int J Radiat Oncol Biol Phys 49:1339–1349

    Article  PubMed  CAS  Google Scholar 

  2. Da Silva AN, Nagayama K, Schlesinger D, Sheehan JP (2009) Early brain tumor metastasis reduction following Gamma Knife surgery. J Neurosurg 110:547–552

    Article  PubMed  Google Scholar 

  3. Patel TR, McHugh BJ, Bi WL, Minja FJ, Knisely JP, Chiang VL (2011) A comprehensive review of MR imaging changes following radiosurgery to 500 brain metastases. AJNR Am J Neuroradiol 32:1885–1892

    Article  PubMed  CAS  Google Scholar 

  4. Eisenhauer EA, Therasse P, Bogaerts J et al (2009) New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 45:228–247

    Article  PubMed  CAS  Google Scholar 

  5. Vannucci L (2010) To suppress to rescue? Changing the approach for recalling anticancer immune responses. Front Biosci (Schol Ed) 2:1189–1197

    Article  Google Scholar 

  6. Hamai A, Benlalam H, Meslin F et al (2010) Immune surveillance of human cancer: if the cytotoxic T-lymphocytes play the music, does the tumoral system call the tune? Tissue Antigens 75:1–8

    Article  PubMed  CAS  Google Scholar 

  7. Rabin BM, Meyer JR, Berlin JW, Marymount MH, Palka PS, Russell EJ (1996) Radiation-induced changes in the central nervous system and head and neck. Radiographics 16:1055–1072

    PubMed  CAS  Google Scholar 

  8. Gourmelon P, Marquette C, Agay D, Mathieu J, Clarencon D (2005) Involvement of the central nervous system in radiation-induced multi-organ dysfunction and/or failure. BJR Suppl/BIR 27:62–68

    Article  CAS  Google Scholar 

  9. Chiang CS, Hong JH, Stalder A, Sun JR, Withers HR, McBride WH (1997) Delayed molecular responses to brain irradiation. Int J Radiat Biol 72:45–53

    Article  PubMed  CAS  Google Scholar 

  10. Yoshii Y (2008) Pathological review of late cerebral radionecrosis. Brain Tumor Pathol 25:51–58

    Article  PubMed  Google Scholar 

  11. Asao C, Korogi Y, Kitajima M et al (2005) Diffusion-weighted imaging of radiation-induced brain injury for differentiation from tumor recurrence. AJNR Am J Neuroradiol 26:1455–1460

    PubMed  Google Scholar 

  12. Tung GA, Evangelista P, Rogg JM, Duncan JA 3rd (2001) Diffusion-weighted MR imaging of rim-enhancing brain masses: is markedly decreased water diffusion specific for brain abscess? AJR. Am J Roentgenol 177:709–712

    CAS  Google Scholar 

  13. Ostergaard L, Weisskoff RM, Chesler DA, Gyldensted C, Rosen BR (1996) High resolution measurement of cerebral blood flow using intravascular tracer bolus passages. Part I: Mathematical approach and statistical analysis. Magn Reson Med: Off J Soc Magn Reson Med/Soc Magn Reson Med 36:715–725

    Article  CAS  Google Scholar 

  14. Boxerman JL, Schmainda KM, Weisskoff RM (2006) Relative cerebral blood volume maps corrected for contrast agent extravasation significantly correlate with glioma tumor grade, whereas uncorrected maps do not. AJNR Am J Neuroradiol 27:859–867

    PubMed  CAS  Google Scholar 

  15. Pan HC, Sheehan J, Stroila M, Steiner M, Steiner L (2005) Gamma knife surgery for brain metastases from lung cancer. J Neurosurg 102:128–133

    Article  PubMed  Google Scholar 

  16. Desprechins B, Stadnik T, Koerts G, Shabana W, Breucq C, Osteaux M (1999) Use of diffusion-weighted MR imaging in differential diagnosis between intracerebral necrotic tumors and cerebral abscesses. AJNR Am J Neuroradiol 20:1252–1257

    PubMed  CAS  Google Scholar 

  17. Jagannathan J, Bourne TD, Schlesinger D et al (2010) Clinical and pathological characteristics of brain metastasis resected after failed radiosurgery. Neurosurgery 66:208–217

    Article  PubMed  Google Scholar 

  18. Oh BC, Pagnini PG, Wang MY et al (2007) Stereotactic radiosurgery: adjacent tissue injury and response after high-dose single fraction radiation: Part I—Histology, imaging, and molecular events. Neurosurgery 60:31–44, discussion 44–35

    PubMed  Google Scholar 

  19. Monabati A, Kumar PV, Kamkarpour A (2000) Intraoperative cytodiagnosis of metastatic brain tumors confused clinically with brain abscess. A report of three cases. Acta Cytol 44:437–441

    Article  PubMed  CAS  Google Scholar 

  20. Holtas S, Geijer B, Stromblad LG, Maly-Sundgren P, Burtscher IM (2000) A ring-enhancing metastasis with central high signal on diffusion-weighted imaging and low apparent diffusion coefficients. Neuroradiology 42:824–827

    Article  PubMed  CAS  Google Scholar 

  21. Biousse V, Newman NJ, Hunter SB, Hudgins PA (2003) Diffusion weighted imaging in radiation necrosis. J Neurol Neurosurg Psychiatry 74:382–384

    Article  PubMed  CAS  Google Scholar 

  22. Kang TW, Kim ST, Byun HS et al (2009) Morphological and functional MRI, MRS, perfusion and diffusion changes after radiosurgery of brain metastasis. Eur J Radiol 72:370–380

    Article  PubMed  Google Scholar 

  23. Toh CH, Wei KC, Ng SH, Wan YL, Lin CP, Castillo M (2011) Differentiation of brain abscesses from necrotic glioblastomas and cystic metastatic brain tumors with diffusion tensor imaging. AJNR Am J Neuroradiol 32:1646–1651

    Article  PubMed  CAS  Google Scholar 

  24. Cha S (2006) Update on brain tumor imaging: from anatomy to physiology. AJNR Am J Neuroradiol 27:475–487

    PubMed  CAS  Google Scholar 

  25. Wong JC, Provenzale JM, Petrella JR (2000) Perfusion MR imaging of brain neoplasms. AJR Am J Roentgenol 174:1147–1157

    PubMed  CAS  Google Scholar 

  26. Essig M, Waschkies M, Wenz F, Debus J, Hentrich HR, Knopp MV (2003) Assessment of brain metastases with dynamic susceptibility-weighted contrast-enhanced MR imaging: initial results. Radiology 228:193–199

    Article  PubMed  Google Scholar 

  27. Mitsuya K, Nakasu Y, Horiguchi S et al (2010) Perfusion weighted magnetic resonance imaging to distinguish the recurrence of metastatic brain tumors from radiation necrosis after stereotactic radiosurgery. J Neurooncol 99:81–88

    Article  PubMed  Google Scholar 

  28. Jain R, Narang J, Schultz L et al (2011) Permeability estimates in histopathology-proved treatment-induced necrosis using perfusion CT: can these add to other perfusion parameters in differentiating from recurrent/progressive tumors? AJNR Am J Neuroradiol 32:658–663

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sung Tae Kim.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cha, J., Kim, S.T., Kim, HJ. et al. Analysis of the layering pattern of the apparent diffusion coefficient (ADC) for differentiation of radiation necrosis from tumour progression. Eur Radiol 23, 879–886 (2013). https://doi.org/10.1007/s00330-012-2638-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00330-012-2638-4

Keywords

Navigation