Laser interstitial thermal therapy for treatment of cerebral radiation necrosis

References

• Sheline GE, Wara WM, Smith V. Therapeutic irradiation and brain injury. Int J Radiat Oncol Biol Phys. 1980;6(9):1215–1228.
   PubMed Web of Science ®Google Scholar
• Ali FS, Arevalo O, Zorofchian S, et al. Cerebral radiation necrosis: incidence, pathogenesis, diagnostic challenges, and future opportunities. Curr Oncol Rep. 2019;21(8):66.
   PubMed Web of Science ®Google Scholar
• Rahmathulla G, Marko NF, Weil RJ. Cerebral radiation necrosis: a review of the pathobiology, diagnosis and management considerations. J Clin Neurosci. 2013;20(4):485–502.
   PubMed Web of Science ®Google Scholar
• Akanda ZZ, Hong W, Nahavandi S, et al. Post-operative stereotactic radiosurgery following excision of brain metastases: a systematic review and meta-analysis. Radiother Oncol. 2019;142:27–35.
   PubMed Web of Science ®Google Scholar
• Pollock BE, Link MJ, Branda ME, et al. Incidence and management of late adverse radiation effects after arteriovenous malformation radiosurgery. Neurosurgery. 2017;81(6):928–934. Dec 1
   PubMed Web of Science ®Google Scholar
• Novotny J, Jr., Kollova A, Liscak R. Prediction of intracranial edema after radiosurgery of meningiomas. J Neurosurg. 2006;105:120–126.
   PubMed Web of Science ®Google Scholar
• Conti A, Pontoriero A, Siddi F, et al. Post-treatment edema after meningioma radiosurgery is a predictable complication. Cureus. 2016;8(5):e605.
   PubMed Web of Science ®Google Scholar
• Shaw E, Arusell R, Scheithauer B, et al. Prospective randomized trial of low- versus high-dose radiation therapy in adults with supratentorial low-grade glioma: initial report of a North Central Cancer Treatment Group/Radiation Therapy Oncology Group/Eastern Cooperative Oncology Group study. JCO. 2002;20(9):2267–2276.
   PubMed Web of Science ®Google Scholar
• Corn BW, Yousem DM, Scott CB, et al. White matter changes are correlated significantly with radiation dose. Observations from a randomized dose-escalation trial for malignant glioma (Radiation Therapy Oncology Group 83-02). Cancer. 1994;74(10):2828–2835.
   PubMed Web of Science ®Google Scholar
• Sneed PK, Mendez J, Vemer-van den Hoek JG, et al. Adverse radiation effect after stereotactic radiosurgery for brain metastases: incidence, time course, and risk factors. JNS. 2015;123(2):373–386.
   PubMed Web of Science ®Google Scholar
• Colaco RJ, Martin P, Kluger HM, et al. Does immunotherapy increase the rate of radiation necrosis after radiosurgical treatment of brain metastases? JNS. 2016;125(1):17–23.
   PubMed Web of Science ®Google Scholar
• Remler MP, Marcussen WH, Tiller-Borsich J. The late effects of radiation on the blood brain barrier. Int J Radiat Oncol Biol Phys. 1986;12(11):1965–1969.
   PubMed Web of Science ®Google Scholar
• Nordal RA, Nagy A, Pintilie M, et al. Hypoxia and hypoxia-inducible factor-1 target genes in central nervous system radiation injury: a role for vascular endothelial growth factor. Clin Cancer Res. 2004;10(10):3342–3353.
   PubMed Web of Science ®Google Scholar
• Fajardo LF, Berthrong M. Vascular lesions following radiation. Pathol Annu. 1988;23 Pt (1):297–330.
   PubMedGoogle Scholar
• Woodworth GF, Garzon-Muvdi T, Ye X, et al. Histopathological correlates with survival in reoperated glioblastomas. J Neurooncol. 2013;113(3):485–493.
   PubMed Web of Science ®Google Scholar
• Tihan T, Barletta J, Parney I, et al. Prognostic value of detecting recurrent glioblastoma multiforme in surgical specimens from patients after radiotherapy: should pathology evaluation alter treatment decisions? Hum Pathol. 2006;37(3):272–282.
   PubMed Web of Science ®Google Scholar
• Mitsuya K, Nakasu Y, Horiguchi S, et al. Perfusion weighted magnetic resonance imaging to distinguish the recurrence of metastatic brain tumors from radiation necrosis after stereotactic radiosurgery. J Neurooncol. 2010;99(1):81–88.
   PubMed Web of Science ®Google Scholar
• Kim YH, Oh SW, Lim YJ, et al. Differentiating radiation necrosis from tumor recurrence in high-grade gliomas: assessing the efficacy of 18F-FDG PET, 11C-methionine PET and perfusion MRI. Clin Neurol Neurosurg. 2010;112(9):758–765.
   PubMed Web of Science ®Google Scholar
• Chuang MT, Liu YS, Tsai YS, et al. Differentiating radiation-induced necrosis from recurrent brain tumor using MR perfusion and spectroscopy: a meta-analysis. PloS One. 2016;11(1):e0141438.
   PubMed Web of Science ®Google Scholar
• Vellayappan B, Tan CL, Yong C, et al. Diagnosis and management of radiation necrosis in patients with brain metastases. Front Oncol. 2018;8:395.
   PubMed Web of Science ®Google Scholar
• Narloch JL, Farber SH, Sammons S, et al. Biopsy of enlarging lesions after stereotactic radiosurgery for brain metastases frequently reveals radiation necrosis. Neuro Oncol. 2017;19(10):1391–1397.
   PubMed Web of Science ®Google Scholar
• Glass JP, Hwang TL, Leavens ME, et al. Cerebral radiation necrosis following treatment of extracranial malignancies. Cancer. 1984;54(9):1966–1972.
   PubMed Web of Science ®Google Scholar
• Giglio P, Gilbert MR. Cerebral radiation necrosis. Neurologist. 2003;9(4):180–188.
   PubMed Web of Science ®Google Scholar
• Levin VA, Bidaut L, Hou P, et al. Randomized double-blind placebo-controlled trial of bevacizumab therapy for radiation necrosis of the central nervous system. Int J Radiat Oncol Biol Phys. 2011;79(5):1487–1495.
   PubMed Web of Science ®Google Scholar
• Furuse M, Nonoguchi N, Kuroiwa T, et al. A prospective, multicentre, single-arm clinical trial of bevacizumab for patients with surgically untreatable, symptomatic brain radiation necrosis(dagger). Neurooncol Pract. 2016;3(4):272–280.
   PubMed Web of Science ®Google Scholar
• Woo E, Lam K, Yu YL, et al. Cerebral radionecrosis: is surgery necessary? J Neurol Neurosurg Psychiatry. 1987;50(11):1407–1414.
   PubMed Web of Science ®Google Scholar
• Williamson R, Kondziolka D, Kanaan H, et al. Adverse radiation effects after radiosurgery may benefit from oral vitamin E and pentoxifylline therapy: a pilot study. Stereotact Funct Neurosurg. 2008;86(6):359–366.
   PubMed Web of Science ®Google Scholar
• Glantz MJ, Burger PC, Friedman AH, et al. Treatment of radiation-induced nervous system injury with heparin and warfarin. Neurology. 1994;44(11):2020–2027.
   PubMed Web of Science ®Google Scholar
• Hong CS, Deng D, Vera A, et al. Laser-interstitial thermal therapy compared to craniotomy for treatment of radiation necrosis or recurrent tumor in brain metastases failing radiosurgery. J Neurooncol. 2019;142(2):309–317.
   PubMed Web of Science ®Google Scholar
• Torres-Reveron J, Tomasiewicz HC, Shetty A, et al. Stereotactic laser induced thermotherapy (LITT): a novel treatment for brain lesions regrowing after radiosurgery. J Neurooncol. 2013;113(3):495–503.
   PubMed Web of Science ®Google Scholar
• Carpentier A, McNichols RJ, Stafford RJ, et al. Real-time magnetic resonance-guided laser thermal therapy for focal metastatic brain tumors. Neurosurgery. 2008;63(suppl_1):ONS21–28; discussion ONS28-29.
   PubMed Web of Science ®Google Scholar
• Carpentier A, McNichols RJ, Stafford RJ, et al. Laser thermal therapy: real-time MRI-guided and computer-controlled procedures for metastatic brain tumors. Lasers Surg Med. 2011;43(10):943–950.
   PubMed Web of Science ®Google Scholar
• Rahmathulla G, Recinos PF, Valerio JE, et al. Laser interstitial thermal therapy for focal cerebral radiation necrosis: a case report and literature review. Stereotact Funct Neurosurg. 2012;90(3):192–200.
   PubMed Web of Science ®Google Scholar
• Smith CJ, Myers CS, Chapple KM, et al. Long-term follow-up of 25 cases of biopsy-proven radiation necrosis or post-radiation treatment effect treated with magnetic resonance-guided laser interstitial thermal therapy. Neurosurgery. 2016;79(suppl_1):S59–S72.
   PubMed Web of Science ®Google Scholar
• Rammo R, Asmaro K, Schultz L, et al. The safety of magnetic resonance imaging-guided laser interstitial thermal therapy for cerebral radiation necrosis. J Neurooncol. 2018;138(3):609–617.
   PubMed Web of Science ®Google Scholar
• Chaunzwa TL, Deng D, Leuthardt EC, et al. Laser thermal ablation for metastases failing radiosurgery: a multicentered retrospective study. Neurosurgery. 2018;82(1):56–63.
   PubMed Web of Science ®Google Scholar
• Ahluwalia M, Barnett GH, Deng D, et al. Laser ablation after stereotactic radiosurgery: a multicenter prospective study in patients with metastatic brain tumors and radiation necrosis. J Neurosurg. 2019;130(3):804–811.
   Web of Science ®Google Scholar
• Bastos DCA, Rao G, Oliva ICG, et al. Predictors of local control of brain metastasis treated with laser interstitial thermal therapy. Neurosurgery. 2019. DOI:10.1093/neuros/nyz357
   Web of Science ®Google Scholar
• Hong CS, Cord BJ, Kundishora AJ, et al. MRI-guided laser interstitial thermal therapy for radiation necrosis in previously irradiated brain arteriovenous malformations. Pract Radiat Oncol. 2020. DOI:10.1016/j.prro.2020.02.003
   Web of Science ®Google Scholar
• Hong CS, Beckta JM, Kundishora AJ, et al. Laser Interstitial Thermotherapy for Treatment of Symptomatic Peritumoral Edema After Radiosurgery for Meningioma. World Neurosurg. 2020;136:295–300.
   PubMed Web of Science ®Google Scholar
• Torcuator RG, Hulou MM, Chavakula V, et al. Intraoperative real-time MRI-guided stereotactic biopsy followed by laser thermal ablation for progressive brain metastases after radiosurgery. J Clin Neurosci. Feb 2016;24:68–73.
   PubMed Web of Science ®Google Scholar
• Hernandez RN, Carminucci A, Patel P, et al. Magnetic resonance-guided laser-induced thermal therapy for the treatment of progressive enhancing inflammatory reactions following stereotactic radiosurgery, or PEIRs, for metastatic brain disease. Neurosurgery. 2019;85(1):84–90.
   PubMed Web of Science ®Google Scholar
• Chao ST, Ahluwalia MS, Barnett GH, et al. Challenges with the diagnosis and treatment of cerebral radiation necrosis. Int J Radiat Oncol Biol Phys. 2013;87(3):449–457.
   PubMed Web of Science ®Google Scholar
• Strauss SB, Meng A, Ebani EJ, et al. Imaging glioblastoma posttreatment: progression, pseudoprogression, pseudoresponse, radiation necrosis. Radiol Clin North Am. 2019;57(6):1199–1216.
   PubMed Web of Science ®Google Scholar
• Ellingson BM, Chung C, Pope WB, et al. Pseudoprogression, radionecrosis, inflammation or true tumor progression? Challenges associated with glioblastoma response assessment in an evolving therapeutic landscape. J Neurooncol. 2017;134(3):495–504.
   PubMed Web of Science ®Google Scholar
• Delgado-Lopez PD, Rinones-Mena E, Corrales-Garcia EM. Treatment-related changes in glioblastoma: a review on the controversies in response assessment criteria and the concepts of true progression, pseudoprogression, pseudoresponse and radionecrosis. Clin Transl Oncol. 2018;20(8):939–953.
   PubMed Web of Science ®Google Scholar
• Kano H, Flickinger JC, Tonetti D, et al. Estimating the risks of adverse radiation effects after Gamma knife radiosurgery for arteriovenous malformations. Stroke. 2017;48(1):84–90.
   PubMed Web of Science ®Google Scholar
• Cohen-Inbar O, Starke RM, Paisan G, et al. Early versus late arteriovenous malformation responders after stereotactic radiosurgery: an international multicenter study. J Neurosurg. 2017;127(3):503–511.
   PubMed Web of Science ®Google Scholar