647
Views
74
CrossRef citations to date
0
Altmetric
Reviews

Laser interstitial thermal therapy in the management of brain metastasis and radiation necrosis after radiosurgery: An overview

, , , &
Pages 223-232 | Received 11 Nov 2015, Published online: 08 Feb 2016

References

  • Papers of special note have been highlighted as:
  • • of interest
  • •• of considerable interest
  • Anzai Y, Lufkin R, DeSalles A, et al. Preliminary experience with MR-guided thermal ablation of brain tumors. AJNR Am J Neuroradiol. 1995;16(1):39–48. discussion 9–52.
  • Ascher PW, Justich E, Schrottner O. Interstitial thermotherapy of central brain tumors with the Nd:YAG laser under real-time monitoring by MRI. J Clin Laser Med Surg. 1991;9(1):79–83.
  • Sakai T, Fujishima I, Sugiyama K, et al. Interstitial laserthermia in neurosurgery. J Clin Laser Med Surg. 1992;10(1):37–40.
  • Bown SG. Phototherapy in tumors. World J Surg. 1983;7(6):700–709.
  • Sugiyama K, Sakai T, Fujishima I, et al. Stereotactic interstitial laser-hyperthermia using Nd-YAG laser. Stereotact Funct Neurosurg. 1990;54–55:501–505.
  • Banerjee C, Snelling B, Berger MH, et al. The role of magnetic resonance-guided laser ablation in neurooncology. Br J Neurosurg. 2015;29(2):192–196.
  • Carpentier A, Chauvet D, Reina V, et al. MR-guided laser-induced thermal therapy (LITT) for recurrent glioblastomas. Lasers Surg Med. 2012;44(5):361–368.
  • 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.

•• Long-term results of first phase 1 study investigating the efficacy of Laser interstitial thermal therapy (LITT) in patients with metastatic tumors.

• Recent review summarizing all the current indications of LITT in neurosurgical conditions.

  • Mohammadi AM, Schroeder JL. Laser interstitial thermal therapy in treatment of brain tumors–the NeuroBlate System. Expert Rev Med Devices. 2014;11(2):109–119.
  • Rahmathulla G, Recinos PF, Kamian K, et al. MRI-guided laser interstitial thermal therapy in neuro-oncology: a review of its current clinical applications. Oncology. 2014;87(2):67–82.
  • Chen L, Wansapura JP, Heit G, et al. Study of laser ablation in the in vivo rabbit brain with MR thermometry. J Magn Reson Imaging. 2002;16(2):147–152.
  • Cheng MK, McKean J, Boisvert D, et al. Effects of photoradiation therapy on normal rat brain. Neurosurgery. 1984;15(6):804–810.
  • Tracz RA, Wyman DR, Little PB, et al. Comparison of magnetic resonance images and the histopathological findings of lesions induced by interstitial laser photocoagulation in the brain. Lasers Surg Med. 1993;13(1):45–54.
  • Wyman DR, Whelan WM, Wilson BC. Interstitial laser photocoagulation: Nd:YAG 1064 nm optical fiber source compared to point heat source. Lasers Surg Med. 1992;12(6):659–664.
  • Elias Z, Powers SK, Atstupenas E, et al. Hyperthermia from interstitial laser irradiation in normal rat brain. Lasers Surg Med. 1987;7(4):370–375.
  • McDannold N. Quantitative MRI-based temperature mapping based on the proton resonant frequency shift: review of validation studies. Int J Hyperthermia, North American Hyperthermia Group. 2005;21(6):533–546.
  • el-Ouahabi A, Guttmann CR, Hushek SG, et al. MRI guided interstitial laser therapy in a rat malignant glioma model. Lasers Surg Med. 1993;13(5):503–510.
  • Leonardi MA, Lumenta CB. Stereotactic guided laser-induced interstitial thermotherapy (SLITT) in gliomas with intraoperative morphologic monitoring in an open MR: clinical expierence. Minim Invasive Neurosurg. 2002;45(4):201–207.
  • Kahn T, Bettag M, Ulrich F, et al. MRI-guided laser-induced interstitial thermotherapy of cerebral neoplasms. J Comput Assist Tomogr. 1994;18(4):519–532.
  • Reimer P, Bremer C, Horch C, et al. MR-monitored LITT as a palliative concept in patients with high grade gliomas: preliminary clinical experience. J Magn Reson Imaging. 1998;8(1):240–244.
  • Schwarzmaier HJ, Eickmeyer F, Von Tempelhoff W, et al. MR-guided laser-induced interstitial thermotherapy of recurrent glioblastoma multiforme: preliminary results in 16 patients. Eur J Radiol. 2006;59(2):208–215.
  • Fabiano AJ, Qiu J. Delayed failure of laser-induced interstitial thermotherapy for postradiosurgery brain metastases. World Neurosurg. 2014;82(34):e559–e563.

•• Reported the utility of LITT in managing refractory cerebral edema following radiosurgery for metastasis.

  • Tovar-Spinoza Z, Carter D, Ferrone D, et al. The use of MRI-guided laser-induced thermal ablation for epilepsy. Childs Nerv Syst. 2013;29(11):2089–2094.
  • Hawasli AH, Bagade S, Shimony JS, et al. Magnetic resonance imaging-guided focused laser interstitial thermal therapy for intracranial lesions: single-institution series. Neurosurgery. 2013;73(6):1007–1017.
  • 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

•• First reported case of utility of LITT in a patient with RN following treatment for brain metastasis.

  • Fabiano AJ, Alberico RA. Laser-interstitial thermal therapy for refractory cerebral edema from post-radiosurgery metastasis. World Neurosurg. 2014;81(34):652.e1–e4.
  • Flickinger JC, Kondziolka D, Lunsford LD, et al. A multi-institutional experience with stereotactic radiosurgery for solitary brain metastasis. Int J Radiat Oncol Biol Phys. 1994;28(4):797–802.
  • Kondziolka D, Patel A, Lunsford LD, et al. Stereotactic radiosurgery plus whole brain radiotherapy versus radiotherapy alone for patients with multiple brain metastases. Int J Radiat Oncol Biol Phys. 1999;45(2):427–434.
  • Yamamoto M, Hara M, Ide M, et al. Radiation-related adverse effects observed on neuro-imaging several years after radiosurgery for cerebral arteriovenous malformations. Surg Neurol. 1998;49(4):385–397. discussion 97–8.
  • Chin LS, Ma L, DiBiase S. Radiation necrosis following gamma knife surgery: a case-controlled comparison of treatment parameters and long-term clinical follow up. J Neurosurg. 2001;94(6):899–904.
  • Ganz JC, Reda WA, Abdelkarim K. Adverse radiation effects after Gamma Knife Surgery in relation to dose and volume. Acta Neurochirurgica. 2009;151(1):9–19.
  • 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. J Neurosurg. 2015;123(2):373–386.
  • Minniti G, Clarke E, Lanzetta G, et al. Stereotactic radiosurgery for brain metastases: analysis of outcome and risk of brain radionecrosis. Radiat Oncol. 2011;6:48.
  • Jagannathan J, Petit JH, Balsara K, et al. Long-term survival after gamma knife radiosurgery for primary and metastatic brain tumors. Am J Clin Oncol. 2004;27(5):441–444.
  • Kano H, Shuto T, Iwai Y, et al. Stereotactic radiosurgery for intracranial hemangioblastomas: a retrospective international outcome study. J Neurosurg. 2015;122(6):1469–1478.
  • Nayak L, Lee EQ, Wen PY. Epidemiology of brain metastases. Curr Oncol Rep. 2012;14(1):48–54.
  • Lin X, DeAngelis LM. Treatment of Brain Metastases. J Clinical Oncology. 2015;33:3475–3484.
  • Barnholtz-Sloan JS, Sloan AE, Davis FG, et al. Incidence proportions of brain metastases in patients diagnosed (1973 to 2001) in the Metropolitan Detroit Cancer Surveillance System. J Clinical Oncology. 2004;22(14):2865–2872.
  • Winter A, Laing J, Paglione R, et al. Microwave hyperthermia for brain tumors. Neurosurgery. 1985;17(3):387–399.
  • Britt RH, Pounds DW, Lyons BE. Feasibility of treating malignant brain tumors with focused ultrasound. Prog Exp Tumor Res. 1984;28:232–245.
  • Roberts DW, Coughlin CT, Wong TZ, et al. Interstitial hyperthermia and iridium brachytherapy in treatment of malignant glioma. A phase I clinical trial. J Neurosurg. 1986;64(4):581–587.
  • Svaasand LO, Ellingsen R. Optical penetration in human intracranial tumors. Photochem Photobiol. 1985;41(1):73–76.
  • Schulze PC, Vitzthum HE, Goldammer A, et al. Laser-induced thermotherapy of neoplastic lesions in the brain–underlying tissue alterations, MRI-monitoring and clinical applicability. Acta Neurochirurgica. 2004;146(8):803–812.
  • Takizawa T. The carbon dioxide laser surgical unit as an instrument for surgery of brain tumours–its advantages and disadvantages. Neurosurg Rev. 1984;7(2–3):135–144.
  • Jaunich M, Raje S, Kim K, et al. Bio-heat transfer analysis during short pulse laser irradiation of tissues. Int J Heat Mass Transf. 2008;51(23–24):5511–5521.
  • Goldberg SN, Gazelle GS, Mueller PR. Thermal ablation therapy for focal malignancy: a unified approach to underlying principles, techniques, and diagnostic imaging guidance. AJR Am J Roentgenol. 2000;174(2):323–331.
  • Seegenschmiedt MH, Brady LW, Sauer R. Interstitial thermoradiotherapy: review on technical and clinical aspects. Am J Clin Oncol. 1990;13(4):352–363.
  • Larson TR, Bostwick DG, Corica A. Temperature-correlated histopathologic changes following microwave thermoablation of obstructive tissue in patients with benign prostatic hyperplasia. Urology. 1996;47(4):463–469.
  • Goldberg SN, Gazelle GS, Halpern EF, et al. Radiofrequency tissue ablation: importance of local temperature along the electrode tip exposure in determining lesion shape and size. Acad Radiol. 1996;3(3):212–218.
  • Thomsen S. Pathologic analysis of photothermal and photomechanical effects of laser-tissue interactions. Photochem Photobiol. 1991;53(6):825–835.
  • Laidler KJ. The development of the Arrhenius equation. J Chem Educ. 1984;61(6):494.
  • Schober R, Bettag M, Sabel M, et al. Fine structure of zonal changes in experimental Nd:YAG laser-induced interstitial hyperthermia. Lasers Surg Med. 1993;13(2):234–241.
  • Schulze PC, Adams V, Busert C, et al. Effects of laser-induced thermotherapy (LITT) on proliferation and apoptosis of glioma cells in rat brain transplantation tumors. Lasers Surg Med. 2002;30(3):227–232.
  • Sloan AE, Ahluwalia MS, Valerio-Pascua J, et al. Results of the NeuroBlate System first-in-humans Phase I clinical trial for recurrent glioblastoma: clinical article. J Neurosurg. 2013;118(6):1202–1219.
  • Hawasli AH, Ray WZ, Murphy RK, et al. Magnetic resonance imaging-guided focused laser interstitial thermal therapy for subinsular metastatic adenocarcinoma: technical case report. Neurosurgery. 2012;70(2 Suppl Operative):332–337. discussion 8.
  • Murovic JA, Chang SD. The pathophysiology of cerebral radiation necrosis and the role of laser interstitial thermal therapy. World Neurosurg. 2015;83(1):23–26.
  • McNichols RJ, Gowda A, Kangasniemi M, et al. MR thermometry-based feedback control of laser interstitial thermal therapy at 980 nm. Lasers Surg Med. 2004;34(1):48–55.
  • Mohammadi AM, Hawasli AH, Rodriguez A, et al. The role of laser interstitial thermal therapy in enhancing progression-free survival of difficult-to-access high-grade gliomas: a multicenter study. Cancer Med. 2014;3(4):971–979.

• One of the initial studies showing the efficacy of LITT therapy in patients with difficult to access high-grade gliomas in terms of progression-free survival.

  • Xiang-Pan L, Yuxin C, Xiao-Fei W, et al. Bevacizumab alleviates radiation-induced brain necrosis: a report of four cases. J Cancer Res Ther. 2015;11(2):485–487.
  • Kureshi SA, Hofman FM, Schneider JH, et al. Cytokine expression in radiation-induced delayed cerebral injury. Neurosurgery. 1994;35(5):822–829. discussion 9–30.
  • 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.
  • Kim JH, Brown SL, Jenrow KA, et al. Mechanisms of radiation-induced brain toxicity and implications for future clinical trials. J Neurooncol. 2008;87(3):279–286.
  • Nonoguchi N, Miyatake S, Fukumoto M, et al. The distribution of vascular endothelial growth factor-producing cells in clinical radiation necrosis of the brain: pathological consideration of their potential roles. J Neurooncol. 2011;105(2):423–431.
  • Kim JH, Chung YG, Kim CY, et al. Upregulation of VEGF and FGF2 in normal rat brain after experimental intraoperative radiation therapy. J Korean Med Sci. 2004;19(6):879–886.
  • Pena LA, Fuks Z, Kolesnick RN. Radiation-induced apoptosis of endothelial cells in the murine central nervous system: protection by fibroblast growth factor and sphingomyelinase deficiency. Cancer Res. 2000;60(2):321–327.
  • Hallahan DE, Spriggs DR, Beckett MA, et al. Increased tumor necrosis factor alpha mRNA after cellular exposure to ionizing radiation. Proc Natl Acad Sci U S A. 1989;86(24):10104–10107.
  • Cheng KM, Chan CM, Fu YT, et al. Acute hemorrhage in late radiation necrosis of the temporal lobe: report of five cases and review of the literature. J Neurooncol. 2001;51(2):143–150.
  • Shaw PJ, Bates D. Conservative treatment of delayed cerebral radiation necrosis. J Neurol Neurosurg Psychiatry. 1984;47(12):1338–1341.
  • Kohshi K, Imada H, Nomoto S, et al. Successful treatment of radiation-induced brain necrosis by hyperbaric oxygen therapy. J Neurol Sci. 2003;209(1–2):115–117.
  • 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.
  • Wong ET, Huberman M, Lu X-Q, et al. Bevacizumab reverses cerebral radiation necrosis. J Clinical Oncology. 2008;26(34):5649–5650.
  • Gonzalez J, Kumar AJ, Conrad CA, et al. Effect of bevacizumab on radiation necrosis of the brain. Int J Radiat Oncol Biol Phys. 2007;67(2):323–326.
  • Liu AK, Macy ME, Foreman NK. Bevacizumab as therapy for radiation necrosis in four children with pontine gliomas. Int J Radiat Oncol Biol Phys. 2009;75(4):1148–1154.
  • Matuschek C, Bolke E, Nawatny J, et al. Bevacizumab as a treatment option for radiation-induced cerebral necrosis. Strahlentherapie Und Onkologie Organ der Deutschen Rontgengesellschaft [et al]. 2011;187(2):135–139.
  • Deibert CP, Ahluwalia MS, Sheehan JP, et al. Bevacizumab for refractory adverse radiation effects after stereotactic radiosurgery. J Neurooncol. 2013;115(2):217–223.
  • 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.
  • 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.

•• One of the initial studies showing the efficacy of LITT therapy in six patients with radiation necrosis.

  • Rao MS, Hargreaves EL, Khan AJ, et al. Magnetic resonance-guided laser ablation improves local control for postradiosurgery recurrence and/or radiation necrosis. Neurosurgery. 2014;74(6):658–667. discussion 67.
  • Tobler WD, Sawaya R, Tew JM Jr. Successful laser-assisted excision of a metastatic midbrain tumor. Neurosurgery. 1986;18(6):795–797.
  • Roux FX, Merienne L, Fallet-Bianco C, et al. Stereotaxic laser interstitial thermotherapy. A new alternative in the therapeutic management of some brain tumors. Neurochirurgie. 1992;38(4):238–244.
  • Jethwa PR, Barrese JC, Gowda A, et al. Magnetic resonance thermometry-guided laser-induced thermal therapy for intracranial neoplasms: initial experience. Neurosurgery. 2012;71(1 Suppl Operative):133–144; 144–145.
  • Carpentier A, McNichols RJ, Stafford RJ, et al. Real-time magnetic resonance-guided laser thermal therapy for focal metastatic brain tumors. Neurosurgery. 2008;63(1 Suppl 1):ONS21–ONS28. discussion ONS8–ONS9.

•• First phase 1 study investigating the safety and utility of LITT in patients with metastatic tumors.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.