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Pseudo-progression after stereotactic radiotherapy of brain metastases: lesion analysis using MRI cine-loops

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Abstract

Stereotactic radiotherapy (SRT) of brain metastasis can lead to lesion growth caused by radiation toxicity. The pathophysiology of this so-called pseudo-progression is poorly understood. The purpose of this study was to evaluate the use of MRI cine-loops for describing the consecutive events in this radiation induced lesion growth. Ten patients were selected from our department’s database that had received SRT of brain metastases and had lesion growth caused by pseudo-progression as well as at least five follow-up MRI scans. Pre- and post SRT MRI scans were co-registered and cine-loops were made using post-gadolinium 3D T1 axial slices. The ten cine loops were discussed in a joint meeting of the authors. The use of cine-loops was superior to evaluation of separate MRI scans for interpretation of events after SRT. There was a typical lesion evolution pattern in all patients with varying time course. Initially regression of the metastases was observed, followed by an enlarging area of new contrast enhancement in the surrounding brain tissue. Analysis of consecutive MRI’s using cine-loops may improve understanding of pseudo-progression. It probably represents a radiation effect in brain tissue surrounding the irradiated metastasis and not enlargement of the metastasis itself.

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References

  1. Macdonald DR, Cascino TL, Schold SC Jr, Cairncross JG (1990) Response criteria for phase II studies of supratentorial malignant glioma. J Clin Oncol 8:1277–1280

    CAS  PubMed  Google Scholar 

  2. 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  CAS  PubMed  Google Scholar 

  3. Miller AB, Hoogstraten B, Staquet M, Winkler A (1981) Reporting results of cancer treatment. Cancer 47:207–214

    Article  CAS  PubMed  Google Scholar 

  4. Brandsma D, Stalpers L, Taal W, Sminia P, van den Bent MJ (2008) Clinical features, mechanisms, and management of pseudoprogression in malignant gliomas. Lancet Oncol 9:453–461

    Article  PubMed  Google Scholar 

  5. Wen PY, Macdonald DR, Reardon DA et al (2010) Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol 28:1963–1972

    Article  PubMed  Google Scholar 

  6. Ruzevick J, Kleinberg L, Rigamonti D (2014) Imaging changes following stereotactic radiosurgery for metastatic intracranial tumors: differentiating pseudoprogression from tumor progression and its effect on clinical practice. Neurosurg Rev 37:193–201

  7. Wiggenraad R, Verbeek-de KA, Mast M et al (2012) Local progression and pseudo progression after single fraction or fractionated stereotactic radiotherapy for large brain metastases. A single centre study. Strahlenther Onkol 188:696–701

    Article  CAS  PubMed  Google Scholar 

  8. Lin NU, Lee EQ, Aoyama H et al (2013) Challenges relating to solid tumour brain metastases in clinical trials, part 1: patient population, response, and progression. A report from the RANO group. Lancet Oncol 14:e396–e406

    Article  PubMed  Google Scholar 

  9. Lawrence YR, Li XA, El Naqa I et al (2010) Radiation dose-volume effects in the brain. Int J Radiat Oncol Biol Phys 76(3):S20–S27

    Article  PubMed Central  PubMed  Google Scholar 

  10. Minniti G, Clarke E, Lanzetta G et al (2011) Stereotactic radiosurgery for brain metastases: analysis of outcome and risk of brain radionecrosis. Radiat Oncol 6:48

    Article  PubMed Central  PubMed  Google Scholar 

  11. Jagannathan J, Petit JH, Balsara K, Hudes R, Chin LS (2004) Long-term survival after gamma knife radiosurgery for primary and metastatic brain tumors. Am J Clin Oncol 27:441–444

    Article  PubMed  Google Scholar 

  12. Kocher M, Soffietti R, Abacioglu U et al (2011) Adjuvant whole-brain radiotherapy versus observation after radiosurgery or surgical resection of one to three cerebral metastases: results of the EORTC 22952-26001 study. J Clin Oncol 29:134–141

    Article  PubMed Central  PubMed  Google Scholar 

  13. Wiggenraad R, Verbeek-de KA, Kal HB et al (2011) Dose-effect relation in stereotactic radiotherapy for brain metastases. A systematic review. Radiother Oncol 98:292–297

    Article  PubMed  Google Scholar 

  14. Patel TR, McHugh BJ, Bi WL et al (2011) A comprehensive review of MR imaging changes following radiosurgery to 500 brain metastases. AJNR Am J Neuroradiol 32:1885–1892

    Article  CAS  PubMed  Google Scholar 

  15. Molenaar R, Wiggenraad R, Verbeek-de KA, Walchenbach R, Vecht C (2009) Relationship between volume, dose and local control in stereotactic radiosurgery of brain metastasis. Br J Neurosurg 23:170–178

    Article  PubMed  Google Scholar 

  16. Hoefnagels FW, Lagerwaard FJ, Sanchez E et al (2009) Radiological progression of cerebral metastases after radiosurgery: assessment of perfusion MRI for differentiating between necrosis and recurrence. J Neurol 256:878–887

    Article  PubMed Central  PubMed  Google Scholar 

  17. Dinkel J, Hintze C, Tetzlaff R et al (2009) 4D-MRI analysis of lung tumor motion in patients with hemidiaphragmatic paralysis. Radiother Oncol 91:449–454

    Article  PubMed  Google Scholar 

  18. Sonke JJ, Belderbos J (2010) Adaptive radiotherapy for lung cancer. Semin Radiat Oncol 20:94–106

    Article  PubMed  Google Scholar 

  19. Barretto RP, Ko TH, Jung JC et al (2011) Time-lapse imaging of disease progression in deep brain areas using fluorescence microendoscopy. Nat Med 17:223–228

    Article  CAS  PubMed  Google Scholar 

  20. Fink J, Born D, Chamberlain MC (2012) Radiation necrosis: relevance with respect to treatment of primary and secondary brain tumors. Curr Neurol Neurosci Rep 12:276–285

    Article  PubMed  Google Scholar 

  21. Giglio P, Gilbert MR (2003) Cerebral radiation necrosis. Neurologist 9:180–188

    Article  PubMed  Google Scholar 

  22. Nonoguchi N, Miyatake S, Fukumoto M et al (2011) The distribution of vascular endothelial growth factor-producing cells in clinical radiation necrosis of the brain: pathological consideration of their potential roles. J Neurooncol 105:423–431

    Article  CAS  PubMed  Google Scholar 

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Conflict of interest

R. Wiggenraad has received speakers fee from Brainlab.

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Correspondence to Ruud Wiggenraad.

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Wiggenraad, R., Bos, P., Verbeek-de Kanter, A. et al. Pseudo-progression after stereotactic radiotherapy of brain metastases: lesion analysis using MRI cine-loops. J Neurooncol 119, 437–443 (2014). https://doi.org/10.1007/s11060-014-1519-x

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  • DOI: https://doi.org/10.1007/s11060-014-1519-x

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