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DOI 10.1038/s41416-020-0853-3

Медицинская библиотека · British journal of cancer · 2020

Effects of effective stereotactic radiosurgery for brain metastases on the adjacent brain parenchyma.

Wagner Sabine, Lanfermann Heinrich, Wohlgemuth Walter Alexander, Gufler Hubert

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Аннотация

BACKGROUND

To evaluate whether functional and metabolic MRI can detect radiation-induced alterations in the adjacent areas after effective stereotactic radiosurgery (SRS) for brain metastases. If confirmed, these techniques may be suited for monitoring the timely stratification of patients for neuroprotective treatments after irradiation.

METHODS

Inclusion criteria were complete response, partial response, or stable disease on routine follow-up MR-scans. Multiparametric 3T-MRI was performed with diffusion-weighted imaging, dynamic susceptibility perfusion-weighted imaging, and two-dimensional proton MR-spectroscopy. Parameters were measured in the SRS-treated target and in the adjacent parenchyma up to both 0.75 cm and 1.5 cm from the target border.

RESULTS

Nineteen lesions in sixteen consecutive patients met the inclusion criteria. The median follow-up time was 39 months (range, 10-142) with 41 multiparametric MR-examinations in total. We found low values of N-acetyl-aspartate up to 1.5 cm from the target borders of SRS (P = 0.043) associated with high values of choline (P = 0.004) at the end of the observation period. Lactate levels in the adjacent tissue declined over time, whereas continuously high apparent-diffusion-coefficient values were noted (P < 0.001).

CONCLUSION

Multiparametric MRI can depict radiobiological effects and their time course at a distance from the effectively treated site after SRS for brain metastases, even if conventional MRI findings are inconspicuous.

Для цитирования: Wagner Sabine, Lanfermann Heinrich, Wohlgemuth Walter Alexander, Gufler Hubert. Effects of effective stereotactic radiosurgery for brain metastases on the adjacent brain parenchyma.. British journal of cancer. 2020. DOI: 10.1038/s41416-020-0853-3.

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