Abstract
Histotripsy is an experimental focused ultrasound technology that utilizes controlled cavitation (microbubbles) to mechanically homogenize targeted tissues. The bubble cloud produced is easily identifiable on ultrasound images and provides feedback and localization of mechanical ablation. The tissue homogenate is composed of acellular liquefied debris which facilitates drainage and resorption. A sharp treatment boundary is achievable in part due to the nonthermal mechanism of tissue effect. Preclinical studies support the localization of ablative effects and general safety of histotripsy, as well as demonstrate that the neurovascular bundle and urinary sphincter are resistant to structural damage. Analysis of the imaging data of the male human pelvis suggests that a perineal approach affords adequate acoustic aperture for prostate treatment. Histotripsy ablation of implanted tumors is feasible without apparent increased risk of inducing metastasis in initial preclinical studies. Histotripsy is a unique focused ultrasound ablative modality that has significant potential as a focal therapy for prostate cancer.
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References
Xu Z, Ludomirsky A, Eun LY, Hall TL, Tran BC, Fowlkes JB, Cain CA. Controlled ultrasound tissue erosion. IEEE Trans Ultrason Ferroelectr Freq Control. 2004;51:726–36.
Roberts WW, Hall TL, Ives K, Wolf Jr JS, Fowlkes JB, Cain C. Pulsed cavitational ultrasound: a noninvasive technology for controlled tissue ablation (histotripsy) in the rabbit kidney. J Urol. 2006;175:734–8.
Parsons JE, Cain CA, Abrams GD, Fowlkes JB. Pulsed cavitational ultrasound therapy for controlled tissue homogenization. Ultrasound Med Biol. 2006;32:115–29.
Xu Z, Fowlkes JB, Ludomirsky A, Cain CA. Investigation of intensity thresholds for ultrasound tissue erosion. Ultrasound Med Biol. 2005;31:1673–82.
Winterroth F, Xu Z, Wang T, Wilkinson JE, Fowlkes JB, Roberts WW, Cain CA. Examining and analyzing subcellular morphology of renal tissue treated by histotripsy. Ultrasound Med Biol. 2011;37:78–86.
Wu F, Wang Z, Chen W, Bai J, Zhu H, Qiao T. Preliminary experience using high intensity focused ultrasound for the treatment of patients with advanced stage renal malignancy. J Urol. 2003;170:2237–40.
Visioli AG, Rivens IH, ter Haar GR, Horwich A, Huddart RA, Moskovic E, Padhani A, Glees J. Preliminary results of a phase I dose escalation clinical trial using focused ultrasound in the treatment of localized tumours. Eur J Ultrasound. 1999;9:11–8.
Vallencien G, Harouni M, Veillon B, Mombet A, Prapotnich D, Brisset JM, Bougaran J. Focused extracorporeal pyrotherapy: feasibility study in man. J Endourol. 1992;6:173–81.
Kennedy JE, terHaar GR, Cranston D. High intensity focused ultrasound: surgery of the future? Br J Radiol. 2003;76:590–9.
Fry FJ, Kossoff G, Eggleton RC, Dunn F. Threshold ultrasonic dosages for structural changes in the mammalian brain. J Acoust Soc Am. 1970;6:1413–7.
Tran BC, Seo J, Hall TL, Fowlkes JB, Cain CA. Microbubble-enhanced cavitation for noninvasive ultrasound surgery. IEEE Trans Ultrason Ferroelectr Freq Control. 2003;50:1296–304.
Xu Z, Fowlkes JB, Rothman ED, Levin AM, Cain CA. Controlled ultrasound tissue erosion: the role of dynamic interaction between insonation and microbubble activity. J Acoust Soc Am. 2005;117:424–35.
Leighton TG. The forced bubble. In: The acoustic bubble. San Diego, CA: Academic Press; 1994. p. 308–12.
Bataille N, Vallancien G, Chopin D. Antitumoral local effect and metastatic risk of focused extracorporeal pyrotherapy on dunning R-3327 tumors. Eur Urol. 1996;29:72–7.
Kohrmann KU, Michel MS, Gaa J, Marlinghaus E, Alken P. High intensity focused ultrasound as noninvasive therapy for multilocal renal cell carcinoma: case study and review of the literature. J Urol. 2002;167:2397–403.
Marberger M, Schatzl G, Cranston D, Kennedy JE. Extracorporeal ablation of renal tumours with high-intensity focused ultrasound. BJU Int. 2005;95 suppl 2:52–5.
Clarke RL, Ter Haar GR. Temperature rise recorded during lesion formation by high-intensity focused ultrasound. Ultrasound Med Biol. 1997;23:299–306.
Kieran K, Hall TL, Parsons JE, Wolf Jr JS, Fowlkes JB, Cain CA, Roberts WW. Refining histotripsy: defining the parameter space for the creation of non-thermal lesions with high intensity pulsed ultrasound in the in vitro kidney. J Urol. 2007;178:672–6.
Xu Z, Hall TL, Fowlkes JB, Cain CA. Effects of acoustic parameters on bubble cloud dynamics in ultrasound tissue erosion (histotripsy). J Acoust Soc Am. 2007;122:229–36.
Xu Z, Raghavan M, Hall TL, Chang C, Mycek M, Fowlkes JB, Cain CA. High speed imaging of bubble clouds generated in pulsed ultrasound cavitational therapy-histotripsy. IEEE Trans Ultrason Ferroelectr Freq Control. 2007;54:2091–101.
Xu Z, Hall TL, Fowlkes JB, Cain CA. Optical and acoustic monitoring of bubble cloud dynamics at a tissue-fluid interface in ultrasound tissue erosion. J Acoust Soc Am. 2007;121:2421–30.
Xu Z, Raghavan M, Hall TL, Chang C, Mycek M, Fowlkes JB, Cain CA. Evolution of bubble clouds induced by pulsed cavitational ultrasound therapy – histotripsy. IEEE Trans Ultrason Ferroelectr Freq Control. 2008;55:1122–32.
Lake AM, Hall TL, Kieran K, Fowlkes JB, Cain CA. Histotripsy: minimally invasive technology for prostatic tissue ablation in an in vivo canine model. Urology. 2008;72:682–6.
Hall TL, Fowlkes JB, Cain CA. A real-time measure of cavitation induced tissue disruption by ultrasound imaging backscatter reduction. IEEE Trans Ultrason Ferroelectr Freq Control. 2007;54:569–75.
Parsons JE, Cain CE, Fowlkes JB. Spatial variability in acoustic backscatter as an indicator of tissue homogenate production in pulsed cavitational ultrasound therapy. IEEE Trans Ultrason Ferroelectr Freq Control. 2007;54:576–90.
Wang T, Xu Z, Winterroth F, Hall TL, Fowlkes JB, Rothman ED, Roberts WW, Cain CA. Quantitative ultrasound backscatter for pulsed cavitational ultrasound therapy – histotripsy. IEEE Trans Ultrason Ferroelectr Freq Control. 2009;56:995–1005.
Hall TL, Kieran K, Ives K, Fowlkes JB, Cain CA, Roberts WW. Histotripsy of rabbit renal tissue in vivo: temporal histologic trends. J Endourol. 2007;21:1159–66.
Hegarty NJ, Gill IS, Desai MM, Remer EM, O’Malley CM, Kaouk JH. Probe-ablative nephron-sparing surgery: cryoablation versus radiofrequency ablation. Urology. 2006; 68(suppl 1A):7–13.
Hempel CR, Hall TL, Cain CA, Fowlkes JB, Xu Z, Roberts WW. Histotripsy fractionation of prostate tissue: local effects and systemic response in a canine model. J Urol. 2011;185:1484–9.
Hall TL, Hempel CR, Wojno K, Xu Z, Cain CA, Roberts WW. Histotripsy of the prostate: dose effects in a chronic canine model. Urology. 2009;74:932–7.
Firth AM, Haldane SL. Development of a scale to evaluate postoperative pain in dogs. J Am Vet Med Assoc. 1999;214:651–9.
Wheat JC, Hall TL, Hempel CR, Cain CA, Xu Z, Roberts WW. Prostate histotripsy in an anticoagulated model. Urology. 2010;75:207–11.
Lake AM, Xu Z, Cain CA, Wilkinson E, Roberts WW. Renal ablation by histotripsy: does it spare collecting system? J Urol. 2008;179:1150–4.
Styn N, Hall TL, Fowlkes JB, Cain CA, Roberts WW. Histotripsy homogenization of the prostate: thresholds for cavitation damage of periprostatic structures. J Endourol. 2011;25:1531–5.
Wang T, Xu Z, Hall TL, Fowlkes JB, Roberts WW, Cain CA. Active focal zone sharpening for high-precision treatment using histotripsy. IEEE Trans Ultrason Ferroelectr Freq Control. 2011;58:305–15.
Hacker A, Kohrmann KU, Back W, Kraut O, Marlinghaus E, Alken P, Michel MS. Extracorporeal application of high-intensity focused ultrasound for prostatic tissue ablation. BJU Int. 2005;96:71–6.
Hall TL, Hempel CR, Sabb BJ, Roberts WW. Acoustic access to the prostate for extracorporeal ultrasound ablation. J Endourol. 2010;24:1875–81.
Oosterhof GO, Cornel EB, Smits GA, Debruyne FM, Schalken JA. Influence of high-intensity focused ultrasound on the development of metastases. Eur Urol. 1997;32:91–5.
Wu F, Wang Z, Jin C, Zhang J, Chen W, Bai J, Zou J, Zhu H. Circulating tumor cells in patients with solid malignancy treated with high-intensity focused ultrasound. Ultrasound Med Biol. 2004;30:511–7.
Miller DL, Dou C. Contrast-aided diagnostic ultrasound does not enhance lung metastasis in a mouse melanoma tumor model. J Ultrasound Med. 2005;24:349–54.
Miller DL, Dou C. The potential for enhancement of mouse melanoma metastasis by diagnostic and high-amplitude ultrasound. Ultrasound Med Biol. 2006;32:1097–101.
Hancock H, Dreher MR, Crawford N, Pollock CB, Shih J, Wood BJ, Hunter K, Frenkel V. Evaluation of pulsed high intensity focused ultrasound exposures on metastasis in a murine model. Clin Exp Metastasis. 2009;26:729–38.
Zhou L, Yinglu Y. In vivo effect of high energy shock waves on growth and metastasis of the heterografted tumors of nude mice. Chin Med J. 1996;109:157–61.
Gamarra F, Spelsberg F, Dellian M, Goetz AE. Complete local tumor remission after therapy with extra-corporeally applied high-energy shock waves (HESW). Int J Cancer. 1993;55:153–6.
Hoshi S, Orikasa S, Kuwahara A, Suzuki K, Yoshikawa K, Saitoh S, Ohyama C, Satoh M, Kawamura S, Nose M. High energy underwater shock wave treatment on implanted urinary bladder cancer in rabbits. J Urol. 1991;146:439–43.
Geldof AA, DeVoogt HJ, Rao BR. High energy shock waves do not affect either primary tumor growth or metastasis of prostate carcinoma, R3327-MatLyLu. Urol Res. 1989;17:9–12.
Oosterhof GON, Cornel EB, Smits GAHJ, Debruyne FMJ, Schalken JA. The influence of high-energy shock waves on the development of metastases. Ultrasound Med Biol. 1996;22:339–44.
Miller DL, Dou C, Song J. Lithotripter shockwave-induced enhancement of mouse melanoma lung metastasis: dependence on cavitation nucleation. J Endourol. 2004;18:925–9.
Xing Y, Lu X, Pua EC, Zhong P. The effect of high intensity focused ultrasound treatment on metastases in a murine melanoma model. Biochem Biophys Res Commun. 2008;31:645–50.
Hu Z, Yang XY, Liu Y, Sankin GN, Pua EC, Morse MA, Lyerly HK, Clay TM, Zhong P. Investigation of HIFU-induced anti-tumor immunity in a murine tumor model. J Transl Med. 2007;5:34.
Styn NR, Hall TL, Fowlkes JB, Cain CA, Roberts WW. Histotripsy of renal implanted VX-2 tumor in a rabbit model: Investigation of metastases. Urology. 2012;80:724–9.
Huber PE, Debus J. Tumor cytotoxicity in vivo and radical formation in vitro depend on the shock wave-induced cavitation dose. Radiat Res. 2001;156:301–9.
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Roberts, W.W. (2013). Histotripsy. In: Polascik, T. (eds) Imaging and Focal Therapy of Early Prostate Cancer. Current Clinical Urology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-182-0_24
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DOI: https://doi.org/10.1007/978-1-62703-182-0_24
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