Laser interstitial thermal therapy in gliomas
Section snippets
Origins of laser thermotherapy
The term is an acronym for Light Amplification by Stimulated Emission of Radiation, which first appeared as a term in 1959. Laser thermal therapy was clinically used for tissue ablation in 1966, based on the theory that the energy produced by laser light could achieve a high peak power through a ruby tip and could be absorbed by the surrounding tissue as heat [1]. However, using lasers for destroying neoplasms was still problematic because of the lack of a mechanism to monitor and control the
Scientific evolution of pre-commercial clinical laser therapy in the brain
Before the Visualase system was approved in 2007, more than 20 studies had been reported to use Nd:YAG lasers for cerebral gliomas [2]. During that scientific period, the laser treatment was commonly called LITT, but also named interstitial thermo-therapy (ITT) or hyperthermia (HT) in some publications [4,14]. Sugiyama et al. firstly reported a clinical series of 3 glioma cases mixed with 2 metastatic lesions treated by laser in 1990, in which thermocouples were used for temperature control [3
Commercial era of LITT
Currently, two commercial laser systems are clinically available. One is the Visualase Thermal Therapy System with diode lasers that transmit energy at a wavelength of 980 nm, which was approved by the United States Food and Drug Administration (FDA) in 2007. It was also approved in Europe by the CE (Conformité Européenne) in 2018. The other system is the NeuroBlate method with the Nd:YAG laser at a wavelength of 1064, which gained approval from FDA in 2009. Several studies have detailed these
LITT in gliomas
Theoretically, glioma may not be an optimal indication for LITT treatment because of often irregular shape of the target and the invasive character of the pathology, even if the precise ablation and real-time monitoring are achievable. Fig. 2 shows one case with irregular shape that could not be completely ablated. However, it is reasonable as a minimally invasive choice in the following circumstances: patients too sick for a craniotomy, some gliomas that are deeply seated or involving eloquent
Outlook for LITT
Prospective randomized or case-control trials demonstrating a statistically significant effect of LITT in gliomas remain lacking. However, there is solid rationale for believing that targeted treatment in focal lesions or in combination with immunotherapy could lead to positive results [18]. Several studies are ongoing and registered. Some have been closed but remain unpublished to date. Those ongoing and promising focus on shortening the treatment time by replacing open surgery with LITT and
Future directions
There is still much we do not know about the interaction between catheter-delivered fiberoptic laser therapy and gliomas. Better understanding of the effect of the laser on glioma tissue and the surrounding brain may allow for alterations in the timing and intensity of treatment. It is possible that the effect of heat could be used to provoke an immunological response in gliomas or improve the penetration of chemotherapy, as discussed above, or even increase the sensitivity to radiation.
Conclusion
LITT is currently used as a treatment for some focal recurrent glioma lesions on a personalized basis. Only well-designed randomized trials could lift this ablation treatment to a higher standard. The concepts of superior efficacy of immunotherapy through disruption of the BBB has been proposed, but still lacks proof as well. Overall, a significant benefit of LITT for gliomas might well rely on advances in immunotherapy and other systemic therapies that benefit from BBB disruption might have on
Declaration of competing interest
The authors declare no conflict of interest.
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