Abstract
Laser ablation (LA) is a percutaneous tumor ablation technique that utilizes laser light delivered interstitially into the biological tissue to provoke a local hyperthermia according to a planned action. The laser light is coherent and monochromatic, it can be very collimated and focused and delivered though optical fibers with little loss of energy from the source to the target. The nature of the effects of the interaction of the laser light with the tissues depends on many factors, among which the most relevant are the laser wavelength, laser power, exposure time, pulse duration and repetition frequency in case of pulsed emission, the beam characteristics, the optical characteristics of the applicator, and physical properties of the tissue. Inside the biological tissue, light can be reflected, transmitted, scattered and absorbed. Only absorbed energy can produce biological effects while the other above-mentioned phenomena could affect the shape, the extension and the position of the warmed up volume. During the ablation process, coagulation becomes appreciable in the range of temperatures between 54 and 60 °C, depending on the heating rate. Above 60 °C, both the denaturation of larger structural proteins and cellular components accelerate, leading to widespread coagulation and rapid cell death in a duration of less than one second. Currently, most LA procedures use Nd:YAG (λ = 1064 nm) or semiconductor diode lasers (λ = 800–980 nm) operating in the range of 2–40 W. Laser fibers can be multiple and placed into the tissue and can be activated simultaneously to rapidly treat a large volume of tissue if the laser equipment has several laser sources inside. The cooled catheters are now a new technology, a progress for ablative techniques. These cooled systems allow avoiding a too rapid dehydration, reducing carbonization and then sublimation of the tissue which is a limiting factor in the efficiency of the ablation process in terms of the transfer of energy to the tissue itself. The most used guidance systems for positioning the applicator in the portion of tissue to be ablated is ultrasonic imaging; the least used is the systems using CT imaging, while the systems using Magnetic Resonance imaging are very interesting, but also they are very expensive, cumbersome and not so comfortable for the patient. They, however, allow to control in real-time of all the ablation phases from planning to final assessment of the ablative process.
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Notes
- 1.
The Pennes equation was developed around 1948 [11] and, in the years to follow, it has been deeply analyzed and reinterpreted also at the mathematical level. Pennes conducted a study on a mathematical model based on the energy balance of an arbitrary volume of tissue. In this model the energy transfer is due to the phenomenon of conduction, metabolism and movement of blood or convection. In more detail, it takes into account many parameters including the thermal conductivity of the tissue—the capacity of the tissue to conduct heat, the rate of perfusion and the specific heat capacity of the blood, the specific heat and the mass density of the tissue, the density of the absorbed power—the external heat input to the tissue or the energy released from the outside, and again the heat generated by tissue metabolism (generally negligible compared to other heat inputs), the tissue and arterial blood temperatures over time—the kinetics of heat transfer caused, respectively, by thermal conduction (fats and proteins) and convection (blood flow). Alternative theoretical models have been studied to describe the characteristics of heat transfer of tumors more accurately, considering the “thermally significant” blood vessels, but the bioheat transfer (BHTE) serves as a good starting point. The balance equations are linear and, therefore, the tissue studies can be solved by various methods. For this last reason, the Pennes equation is universally recognized as the equation of human warmth (“bioheat equation”).
References
Townes CH. Optical masers and their possible applications to biology. Biophys J. 1962;2(2 Pt 2):325–9.
Maiman TH. Biomedical lasers evolve toward clinical applications. Hosp Manage. 1966;101(4):39–41.
Solon LR, Aronson R, Gould G. Physiological implications of laser beams. Science. 1961;134(3489):1506–8.
Bown SG. Phototherapy in tumors. World J Surg. 1983;7(6):700–9.
Muller GJ, Roggan A. Laser-induced interstitial thermotherapy. Bellingham, WA: SPIE-The International Society for Optical Engineering; 1995.
Jacques SL. Laser-tissue interactions. Photochemical, photothermal, and photomechanical. Surg Clin North Am. 1992;72(3):531–58.
Jacques SL. Optical properties of biological tissues: a review. Phys Med Biol. 2013;58(11):R37–61.
Schena E, Saccomandi P, Fong Y. Laser ablation for cancer: past, present and future. J Funct Biomater. 2017;8(2):E19.
Nikfarjam M, Christophi C. Interstitial laser thermotherapy for liver tumours. Br J Surg. 2003;90(9):1033–47.
Saccomandi P, Schena E, Caponero MA, Di Matteo FM, Martino M, Pandolfi M, et al. Theoretical analysis and experimental evaluation of laser-induced interstitial thermotherapy in ex vivo porcine pancreas. IEEE Trans Biomed Eng. 2012;59(10):2958–64.
Pennes HH. Analysis of tissue and arterial blood temperatures in the resting human forearm. J Appl Physiol. 1948;1(2):93–122.
Stafford RJ, Shetty A, Elliott AM, Klumpp SA, McNichols RJ, Gowda A, et al. Magnetic resonance guided, focal laser induced interstitial thermal therapy in a canine prostate model. J Urol. 2010;184(4):1514–20.
Dewhirst MW, Viglianti BL, Lora-Michiels M, Hanson M, Hoopes PJ. Basic principles of thermal dosimetry and thermal thresholds for tissue damage from hyperthermia. Int J Hyperth. 2003;19(3):267–94.
Dewey WC. Arrhenius relationships from the molecule and cell to the clinic. Int J Hyperth. 2009;25(1):3–20.
Stafford RJ, Fuentes D, Elliott AA, Weinberg JS, Ahrar K. Laser-induced thermal therapy for tumor ablation. Crit Rev Biomed Eng. 2010;38(1):79–100.
Schwarzmaier H-J, Goldbach T, Ulrich F, Schober R, Kahn T, Kaufmann R, et al. Improved laser applicators for interstitial thermotherapy of brain structures. In: Cerullo LJ, Heiferman KS, Liu H, Podbielska H, Wist AO, Zamorano LJ, editors. Proceedings of the clinical applications of modern imaging technology II, Los Angeles, CA, USA, 23 Jan 1994. Orlando, FL: International Society for Optics and Photonics; 1994. p. 4–12.
Amin Z, Donald JJ, Masters A, Kant R, Steger AC, Bown SG, et al. Hepatic metastases: interstitial laser photocoagulation with real-time US monitoring and dynamic CT evaluation of treatment. Radiology. 1993;187(2):339–47.
Schroder T, Castren-Persons M, Lehtinen A, Taavitsainen M. Percutaneous interstitial laser hyperthermia in clinical use. Ann Chir Gynaecol. 1994;83(4):286–90.
Matthewson K, Coleridge-Smith P, O’Sullivan JP, Northfield TC, Bown SG. Biological effects of intrahepatic neodymium:yttrium-aluminum-garnet laser photocoagulation in rats. Gastroenterology. 1987;93(3):550–7.
Matsumoto R, Selig AM, Colucci VM, Jolesz FA. Interstitial Nd:YAG laser ablation in normal rabbit liver: trial to maximize the size of laser-induced lesions. Lasers Surg Med. 1992;12(6):650–8.
Pacella CM, Bizzarri G, Ferrari FS, Anelli V, Valle D, Bianchini A, et al. [Interstitial photocoagulation with laser in the treatment of liver metastasis]. Radiol Med. 1996;92(4):438–47.
Pacella CM, Bizzarri G, Francica G, Bianchini A, De Nuntis S, Pacella S, et al. Percutaneous laser ablation in the treatment of hepatocellular carcinoma with small tumors: analysis of factors affecting the achievement of tumor necrosis. J Vasc Interv Radiol. 2005;16(11):1447–57.
Pacella CM, Francica G, Di Lascio FM, Arienti V, Antico E, Caspani B, et al. Long-term outcome of cirrhotic patients with early hepatocellular carcinoma treated with ultrasound-guided percutaneous laser ablation: a retrospective analysis. J Clin Oncol. 2009;27(16):2615–21.
Huang GT, Wang TH, Sheu JC, Daikuzono N, Sung JL, Wu MZ, et al. Low-power laserthermia for the treatment of small hepatocellular carcinoma. Eur J Cancer. 1991;27(12):1622–7.
Nolsoe CP, Torp-Pedersen S, Burcharth F, Horn T, Pedersen S, Christensen NE, et al. Interstitial hyperthermia of colorectal liver metastases with a US-guided Nd-YAG laser with a diffuser tip: a pilot clinical study. Radiology. 1993;187(2):333–7.
Vogl TJ, Mack MG, Straub R, Roggan A, Felix R. Magnetic resonance imaging-guided abdominal interventional radiology: laser-induced thermotherapy of liver metastases. Endoscopy. 1997;29(6):577–83.
van Hillegersberg R, van Staveren HJ, Kort WJ, Zondervan PE, Terpstra OT. Interstitial Nd:YAG laser coagulation with a cylindrical diffusing fiber tip in experimental liver metastases. Lasers Surg Med. 1994;14(2):124–38.
Moller PH, Lindberg L, Henriksson PH, Persson BR, Tranberg KG. Temperature control and light penetration in a feedback interstitial laser thermotherapy system. Int J Hyperth. 1996;12(1):49–63.
Heisterkamp J, van Hillegersberg R, Sinofsky E, Ijzermans JN. Heat-resistant cylindrical diffuser for interstitial laser coagulation: comparison with the bare-tip fiber in a porcine liver model. Lasers Surg Med. 1997;20(3):304–9.
Sturesson C. Interstitial laser-induced thermotherapy: influence of carbonization on lesion size. Lasers Surg Med. 1998;22(1):51–7.
Mensel B, Weigel C, Hosten N. Laser-induced thermotherapy. Recent Results Cancer Res. 2006;167:69–75.
Möller PH, Lindberg L, Henriksson PH, Persson BRR, Tranberg K-G. Interstitial laser thermotherapy: comparison between bare fibre and sapphire probe. Lasers Med Sci. 1995;10:193–200.
Heisterkamp J, van Hillegersberg R, Ijzermans JN. Critical temperature and heating time for coagulation damage: implications for interstitial laser coagulation (ILC) of tumors. Lasers Surg Med. 1999;25(3):257–62.
Muralidharan V, Christophi C. Interstitial laser thermotherapy in the treatment of colorectal liver metastases. J Surg Oncol. 2001;76(1):73–81.
Steger AC, Lees WR, Shorvon P, Walmsley K, Bown SG. Multiple-fibre low-power interstitial laser hyperthermia: studies in the normal liver. Br J Surg. 1992;79(2):139–45.
Germer CT, Albrecht D, Roggan A, Buhr HJ. Technology for in situ ablation by laparoscopic and image-guided interstitial laser hyperthermia. Semin Laparosc Surg. 1998;5(3):195–203.
Germer CT, Albrecht D, Isbert C, Ritz J, Roggan A, Buhr HJ. Diffusing fibre tip for the minimally invasive treatment of liver tumours by interstitial laser coagulation (ILC): an experimental ex vivo study. Lasers Med Sci. 1999;14(1):32–9.
Heisterkamp J, Van Hillegersberg R, Sinofsky EL, Ijzermans JNM. Interstitial laser photocoagulation with four cylindrical diffusing fibre tips: importance of mutual fibre distance. Lasers Med Sci. 1999;14:216–20.
Heisterkamp J, van Hillegersberg R, Ijzermans JN. Interstitial laser coagulation for hepatic tumours. Br J Surg. 1999;86(3):293–304.
Saccomandi P, Schena E, Giurazza F, Del Vescovo R, Caponero MA, Mortato L, et al. Temperature monitoring and lesion volume estimation during double-applicator laser-induced thermotherapy in ex vivo swine pancreas: a preliminary study. Lasers Med Sci. 2014;29(2):607–14.
Vogl TJ, Muller PK, Hammerstingl R, Weinhold N, Mack MG, Philipp C, et al. Malignant liver tumors treated with MR imaging-guided laser-induced thermotherapy: technique and prospective results. Radiology. 1995;196(1):257–65.
Vogl TJ, Mack MG, Roggan A, Straub R, Eichler KC, Muller PK, et al. Internally cooled power laser for MR-guided interstitial laser-induced thermotherapy of liver lesions: initial clinical results. Radiology. 1998;209(2):381–5.
Vogl TJ, Eichler K, Straub R, Engelmann K, Zangos S, Woitaschek D, et al. Laser-induced thermotherapy of malignant liver tumors: general principals, equipment(s), procedure(s)—side effects, complications and results. Eur J Ultrasound. 2001;13(2):117–27.
de Jode MG, Lamb GM, Thomas HC, Taylor-Robinson SD, Gedroyc WM. MRI guidance of infra-red laser liver tumour ablations, utilising an open MRI configuration system: technique and early progress. J Hepatol. 1999;31(2):347–53.
Rieke V, Butts Pauly K. MR thermometry. J Magn Reson Imaging. 2008;27(2):376–90.
Diederich CJ, Nau WH, Kinsey A, Ross T, Wootton J, Juang T, et al. Catheter-based ultrasound devices and MR thermal monitoring for conformal prostate thermal therapy. Conf Proc IEEE Eng Med Biol Soc. 2008;2008:3664–8.
Ahrar K, Gowda A, Javadi S, Borne A, Fox M, McNichols R, et al. Preclinical assessment of a 980-nm diode laser ablation system in a large animal tumor model. J Vasc Interv Radiol. 2010;21(4):555–61.
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Pacella, C.M., Breschi, L., Bottacci, D., Masotti, L. (2020). Physical Principles of Laser Ablation. In: Pacella, C., Jiang, T., Mauri, G. (eds) Image-guided Laser Ablation. Springer, Cham. https://doi.org/10.1007/978-3-030-21748-8_2
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