Abstract
Peyronie’s disease is not a rare disorder, and it can be devastating to the affected man. Although the gold-standard treatment of Peyronie’s disease is surgery in the stable phase, nonoperative management is preferred by some men and is the only treatment option in the acute phase of the disease, when surgery is contraindicated. No oral or topical therapy has been shown to be efficacious when administered alone, but some evidence supports their use as part of a combination therapy regimen. Intralesional therapies, particularly collagenase clostridium histolyticum (CCH), have shown promise. Mechanical therapies can provide benefit when applied for prolonged periods of time, improving penile curvature, indentation, and even restoring length. Regardless of the modality chosen, patient counselling is paramount, as recovery of the penis to its predisease state is highly unlikely. Thus, although many options exist for nonsurgical management of Peyronie’s disease, surgery remains the best option for men who desire the most reliable and rapid pathway to a functionally straight, erect penis. The goal of nonsurgical therapy should be a scientifically feasible, safe approach to prevent the progression of, or reduce, deformity and improve sexual function.
Key points
-
No currently available oral or topical therapy is effective as a monotherapy, but some have shown encouraging results as a part of combination therapy.
-
Intralesional verapamil, interferon-α2b, and collagenase clostridium histolyticum (CCH) have been shown to considerably reduce penile curvature, but they cannot achieve absolute straightness.
-
Mechanical therapy and, in particular, traction therapy, is dependent on duration of use and has consistently been shown to delay the progression of Peyronie’s disease and reduce penile deformity.
-
Surgical therapy remains the gold standard and the therapeutic option with the highest probability of achieving functional straightness.
-
Establishing reasonable patient expectations and joint decision-making between patient and clinician are key to achieving patient satisfaction.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Poliklinische plicatieplastiek bij kromstand van de penis
Tijdschrift voor Urologie Open Access 25 July 2023
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$29.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Rent or buy this article
Prices vary by article type
from$1.95
to$39.95
Prices may be subject to local taxes which are calculated during checkout





References
de la Peyronie, F. G. Sur quelques obstacles qui s’opposent a l’ejaculation naturelle de la semence [French]. Mém. Acad. R. Chir. 1, 425–434 (1743).
Schwarzer, U. et al. The prevalence of Peyronie’s disease: results of a large survey. BJU Int. 88, 727–730 (2001).
Mulhall, J. P. et al. Subjective and objective analysis of the prevalence of Peyronie’s disease in a population of men presenting for prostate cancer screening. J. Urol. 171, 2350–2353 (2004).
Dibenedetti, D. B., Nguyen, D., Zografos, L., Ziemiecki, R. & Zhou, X. A. Population-based study of Peyronie’s disease: prevalence and treatment patterns in the United States. Adv. Urol. 2011, 282503 (2011).
Ralph, D. et al. The management of Peyronie’s disease: evidence-based 2010 guidelines. J. Sex. Med. 7, 2359–2374 (2010).
Mulhall, J. P. Expanding the paradigm for plaque development in Peyronie’s disease. Int. J. Impot. Res. 15 (Suppl. 5), 93–102 (2003).
Pryor, J. P. & Ralph, D. J. Clinical presentations of Peyronie’s disease. Int. J. Impot. Res. 14, 414–417 (2002).
Tefekli, A. et al. Peyronie’s disease in men under age 40: characteristics and outcome. Int. J. Impot. Res. 13, 18–23 (2001).
Nugteren, H. M., Nijman, J. M., de Jong, I. J. & van Driel, M. F. The association between Peyronie’s and Dupuytren’s disease. Int. J. Impot. Res. 23, 142–145 (2011).
Dibenedetti, D. B., Nguyen, D., Zografos, L., Ziemiecki, R. & Zhou, X. Prevalence, incidence, and treatments of Dupuytren’s disease in the United States: results from a population-based study. Hand 6, 149–158 (2011).
Van de Water, L. Mechanisms by which fibrin and fibronectin appear in healing wounds: implications for Peyronie’s disease. J. Urol. 157, 306–310 (1997).
Diegelmann, R. F. Cellular and biochemical aspects of normal and abnormal wound healing: an overview. J. Urol. 157, 298–302 (1997).
Davila, H. H., Ferrini, M. G., Rajfer, J. & Gonzalez-Cadavid, N. F. Fibrin as an inducer of fibrosis in the tunica albuginea of the rat: a new animal model of Peyronie’s disease. BJU Int. 91, 830–838 (2003).
El-Sakka, A. I. et al. An animal model of Peyronie’s-like condition associated with an increase of transforming growth factor beta mRNA and protein expression. J. Urol. 158, 2284–2290 (1997).
Sporn, M. B., Roberts, A. B., Wakefield, L. M. & de Crombrugghe, B. Some recent advances in the chemistry and biology of transforming growth factor-beta. J. Cell Biol. 105, 1039–1045 (1987).
Moreland, R. B. & Nehra, A. Pathophysiology of Peyronie’s disease. Int. J. Impot. Res. 14, 406–410 (2002).
El-Sakka, A. I. et al. Histological and ultrastructural alterations in an animal model of Peyronie’s disease. Br. J. Urol. 81, 445–452 (1998).
Mulhall, J. P., Anderson, M. S., Lubrano, T. & Shankey, T. V. Peyronie’s disease cell culture models: phenotypic, genotypic and functional analyses. Int. J. Impot. Res. 14, 397–405 (2002).
Del Carlo, M., Cole, A. A. & Levine, L. A. Differential calcium independent regulation of matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases by interleukin-1beta and transforming growth factor-beta in Peyronie’s plaque fibroblasts. J. Urol. 179, 2447–2455 (2008).
Ferrini, M. G. et al. Antifibrotic role of inducible nitric oxide synthase. Nitric Oxide 6, 283–294 (2002).
Vernet, D. et al. Effect of nitric oxide on the differentiation of fibroblasts into myofibroblasts in the Peyronie’s fibrotic plaque and in its rat model. Nitric Oxide 7, 262–276 (2002).
Coyne, K. S., Currie, B. M., Thompson, C. L. & Smith, T. M. Responsiveness of the Peyronie’s disease questionnaire (PDQ). J. Sex. Med. 12, 1072–1079 (2015).
Hellstrom, W. J. et al. Bother and distress associated with Peyronie’s disease: validation of the Peyronie’s disease questionnaire. J. Urol. 190, 627–634 (2013).
Mulhall, J. P., Schiff, J. & Guhring, P. An analysis of the natural history of Peyronie’s disease. J. Urol. 175, 2115–2118; discussion 2118 (2006).
Chen, J. Y., Hockenberry, M. S. & Lipshultz, L. I. Objective assessments of Peyronie’s disease. Sex. Med. Rev. 6, 438–445 (2018).
Chung, E., De Young, L. & Brock, G. B. Rat as an animal model for Peyronie’s disease research: a review of current methods and the peer-reviewed literature. Int. J. Impot. Res. 23, 235–241 (2011).
Levine, L. A. & Burnett, A. L. Standard operating procedures for Peyronie’s disease. J. Sex. Med. 10, 230–244 (2013).
Sikka, S. C. & Hellstrom, W. J. Role of oxidative stress and antioxidants in Peyronie’s disease. Int. J. Impot. Res. 14, 353–360 (2002).
Paulis, G. et al. Efficacy of vitamin E in the conservative treatment of Peyronie’s disease: legend or reality? A controlled study of 70 cases. Andrology 1, 120–128 (2013).
Hashimoto, K. et al. Outcome analysis for conservative management of Peyronie’s disease. Int. J. Urol. 13, 244–247 (2006).
Pryor, J. P., & Farrell, C. F. Controlled clinic trial of vitamin E in Peyronie’s disease. Prog. Reprod. Biol. 9, 41–45 (1983).
Safarinejad, M. R., Hosseini, S. Y. & Kolahi, A. A. Comparison of vitamin E and propionyl-L-carnitine, separately or in combination, in patients with early chronic Peyronie’s disease: a double-blind, placebo controlled, randomized study. J. Urol. 178, 1398–1403; discussion 1403 (2007).
Calo, L. A. et al. Antioxidant effect of L-carnitine and its short chain esters: relevance for the protection from oxidative stress related cardiovascular damage. Int. J. Cardiol. 107, 54–60 (2006).
Biagiotti, G. & Cavallini, G. Acetyl-L-carnitine versus tamoxifen in the oral therapy of Peyronie’s disease: a preliminary report. BJU Int. 88, 63–67 (2001).
Valente, E. G. et al. L-arginine and phosphodiesterase (PDE) inhibitors counteract fibrosis in the Peyronie’s fibrotic plaque and related fibroblast cultures. Nitric Oxide 9, 229–244 (2003).
Ciociola, F. & Colpi, G. M. Peyronie’s disease: a “triple oxygenant therapy”. Arch. Ital. Urol. Androl. 85, 36–40 (2013).
Abern, M. R., Larsen, S. & Levine, L. A. Combination of penile traction, intralesional verapamil, and oral therapies for Peyronie’s disease. J. Sex. Med. 9, 288–295 (2012).
Shindel, A. W. et al. Pentoxifylline attenuates transforming growth factor-beta1-stimulated collagen deposition and elastogenesis in human tunica albuginea-derived fibroblasts part 1: impact on extracellular matrix. J. Sex. Med. 7, 2077–2085 (2010).
Schandene, L. et al. Differential effects of pentoxifylline on the production of tumour necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) by monocytes and T cells. Immunology 76, 30–34 (1992).
Raetsch, C. et al. Pentoxifylline downregulates profibrogenic cytokines and procollagen I expression in rat secondary biliary fibrosis. Gut 50, 241–247 (2002).
Smith, J. F. et al. Pentoxifylline treatment and penile calcifications in men with Peyronie’s disease. Asian J. Androl. 13, 322–325 (2011).
Safarinejad, M. R., Asgari, M. A., Hosseini, S. Y. & Dadkhah, F. A double-blind placebo-controlled study of the efficacy and safety of pentoxifylline in early chronic Peyronie’s disease. BJU Int. 106, 240–248 (2010).
Bella, A. J. et al. Peyronie’s disease (CME). J. Sex. Med. 4, 1527–1538 (2007).
Zarafonetis, C. J. & Horrax, T. M. Treatment of Peyronie’s disease with potassium para-aminobenzoate (potaba). J. Urol. 81, 770–772 (1959).
Weidner, W., Hauck, E. W. & Schnitker, J. Potassium paraaminobenzoate (POTABA) in the treatment of Peyronie’s disease: a prospective, placebo-controlled, randomized study. Eur. Urol. 47, 530–535; discussion 535–536 (2005).
El-Sakka, A. I. et al. The effects of colchicine on a Peyronie’s-like condition in an animal model. J. Urol. 161, 1980–1983 (1999).
Anderson, M. S., Shankey, T. V., Lubrano, T. & Mulhall, J. P. Inhibition of Peyronie’s plaque fibroblast proliferation by biologic agents. Int. J. Impot. Res. 12 (Suppl. 3), 25–31 (2000).
Akkus, E. et al. Is colchicine effective in Peyronie’s disease? A pilot study. Urology 44, 291–295 (1994).
Kadioglu, A., Tefekli, A., Koksal, T., Usta, M. & Erol, H. Treatment of Peyronie’s disease with oral colchicine: long-term results and predictive parameters of successful outcome. Int. J. Impot. Res. 12, 169–175 (2000).
Prieto Castro, R. M. et al. Combined treatment with vitamin E and colchicine in the early stages of Peyronie’s disease. BJU Int. 91, 522–524 (2003).
Safarinejad, M. R. Therapeutic effects of colchicine in the management of Peyronie’s disease: a randomized double-blind, placebo-controlled study. Int. J. Impot. Res. 16, 238–243 (2004).
Paulis, G. & Brancato, T. Inflammatory mechanisms and oxidative stress in Peyronie’s disease: therapeutic “rationale” and related emerging treatment strategies. Inflamm. Allergy Drug Targets 11, 48–57 (2012).
Carthy, J. M. et al. Tamoxifen inhibits TGF-β-mediated activation of myofibroblasts by blocking non-Smad signaling through ERK1/2. J. Cell. Physiol. 230, 3084–3092 (2015).
Brandt, A. S., Kamper, L., Kukuk, S., Haage, P. & Roth, S. Tamoxifen monotherapy in the treatment of retroperitoneal fibrosis. Urol. Int. 93, 320–325 (2014).
Ralph, D. J., Brooks, M. D., Bottazzo, G. F. & Pryor, J. P. The treatment of Peyronie’s disease with tamoxifen. Br. J. Urol. 70, 648–651 (1992).
Teloken, C. et al. Tamoxifen versus placebo in the treatment of Peyronie’s disease. J. Urol. 162, 2003–2005 (1999).
Yang, G., Nowsheen, S., Aziz, K. & Georgakilas, A. G. Toxicity and adverse effects of Tamoxifen and other anti-estrogen drugs. Pharmacol. Ther. 139, 392–404 (2013).
Bjekic, M. D., Vlajinac, H. D., Sipetic, S. B. & Marinkovic, J. M. Risk factors for Peyronie’s disease: a case-control study. BJU Int. 97, 570–574 (2006).
Jalkut, M., Gonzalez-Cadavid, N. & Rajfer, J. Peyronie’s fisease: a review. Rev. Urol. 5, 142–148 (2003).
Levine, L. A. & Latchamsetty, K. C. Treatment of erectile dysfunction in patients with Peyronie’s disease using sildenafil citrate. Int. J. Impot. Res. 14, 478–482 (2002).
Gonzalez-Cadavid, N. F. & Rajfer, J. Treatment of Peyronie’s disease with PDE5 inhibitors: an antifibrotic strategy. Nat. Rev. Urol. 7, 215–221 (2010).
Ferrini, M. G., Kovanecz, I., Nolazco, G., Rajfer, J. & Gonzalez-Cadavid, N. F. Effects of long-term vardenafil treatment on the development of fibrotic plaques in a rat model of Peyronie’s disease. BJU Int. 97, 625–633 (2006).
Vignozzi, L. et al. Effect of sildenafil administration on penile hypoxia induced by cavernous neurotomy in the rat. Int. J. Impot. Res. 20, 60–67 (2008).
Iacono, F. et al. Histopathologically proven prevention of post-prostatectomy cavernosal fibrosis with sildenafil. Urol. Int. 80, 249–252 (2008).
Chung, E., Deyoung, L. & Brock, G. B. The role of PDE5 inhibitors in penile septal scar remodeling: assessment of clinical and radiological outcomes. J. Sex. Med. 8, 1472–1477 (2011).
Ozturk, U. et al. Effects of sildenafil treatment on patients with Peyronie’s disease and erectile dysfunction. Ir. J. Med. Sci. 183, 449–453 (2014).
Palmieri, A. et al. Tadalafil once daily and extracorporeal shock wave therapy in the management of patients with Peyronie’s disease and erectile dysfunction: results from a prospective randomized trial. Int. J. Androl. 35, 190–195 (2012).
Martin, D. J., Badwan, K., Parker, M. & Mulhall, J. P. Transdermal application of verapamil gel to the penile shaft fails to infiltrate the tunica albuginea. J. Urol. 168, 2483–2485 (2002).
Lee, R. C. & Ping, J. A. Calcium antagonists retard extracellular matrix production in connective tissue equivalent. J. Surg. Res. 49, 463–466 (1990).
Aggeler, J., Frisch, S. M. & Werb, Z. Changes in cell shape correlate with collagenase gene expression in rabbit synovial fibroblasts. J. Cell Biol. 98, 1662–1671 (1984).
Fitch, W. P. 3rd, Easterling, W. J., Talbert, R. L., Bordovsky, M. J. & Mosier, M. Topical verapamil HCl, topical trifluoperazine, and topical magnesium sulfate for the treatment of Peyronie’s disease — a placebo-controlled pilot study. J. Sex. Med. 4, 477–484 (2007).
Di Stasi, S. M. et al. Electromotive instillation of mitomycin immediately before transurethral resection for patients with primary urothelial non-muscle invasive bladder cancer: a randomised controlled trial. Lancet Oncol. 12, 871–879 (2011).
Levine, L. A., Estrada, C. R., Shou, W. & Cole, A. Tunica albuginea tissue analysis after electromotive drug administration. J. Urol. 169, 1775–1778 (2003).
Di Stasi, S. M. et al. Transdermal electromotive administration of verapamil and dexamethasone for Peyronie’s disease. BJU Int. 91, 825–829 (2003).
Greenfield, J. M., Shah, S. J. & Levine, L. A. Verapamil versus saline in electromotive drug administration for Peyronie’s disease: a double-blind, placebo controlled trial. J. Urol. 177, 972–975 (2007).
Mehrsai, A. R. et al. Comparison of transdermal electromotive administration of verapamil and dexamethasone versus intra-lesional injection for Peyronie’s disease. Andrology 1, 129–132 (2013).
Hellstrom, W. J. et al. Single-blind, multicenter, placebo controlled, parallel study to assess the safety and efficacy of intralesional interferon alpha-2B for minimally invasive treatment for Peyronie’s disease. J. Urol. 176, 394–398 (2006).
Teasley, G. H. Peyronie’s disease: a new approach. J. Urol. 71, 611–614 (1954).
Lamprakopoulos, A., Zorzos, I. & Lykourinas, M. The use of betamethasone and hyaluronidase injections in the treatment of Peyronie’s disease. Scand. J. Urol. Nephrol. 34, 355–360 (2000).
Demey, A., Chevallier, D., Bondil, P., Toubol, J. & Amiel, J. Is intracavernosal corticosteroid infiltration really useless in Peyronie’s disease? [French]. Prog. Urol. 16, 52–57 (2006).
Cipollone, G. et al. Betamethasone versus placebo in Peyronie’s disease [Italian]. Arch. Ital. Urol. Androl. 70, 165–168 (1998).
Nehra, A. et al. Peyronie’s disease: AUA guideline. J. Urol. 194, 745–753 (2015).
Hatzimouratidis, K. et al. EAU guidelines on penile curvature. Eur. Urol. 62, 543–552 (2012).
Chung, E., Garcia, F., Young, L. D., Solomon, M. & Brock, G. B. A comparative study of the efficacy of intralesional verapamil versus normal saline injection in a novel Peyronie disease animal model: assessment of immunohistopathological changes and erectile function outcome. J. Urol. 189, 380–384 (2013).
Levine, L. A., Merrick, P. F. & Lee, R. C. Intralesional verapamil injection for the treatment of Peyronie’s disease. J. Urol. 151, 1522–1524 (1994).
Levine, L. A. Treatment of Peyronie’s disease with intralesional verapamil injection. J. Urol. 158, 1395–1399 (1997).
Levine, L. A., Goldman, K. E. & Greenfield, J. M. Experience with intraplaque injection of verapamil for Peyronie’s disease. J. Urol. 168, 621–625; discussion 625–626 (2002).
Rehman, J., Benet, A. & Melman, A. Use of intralesional verapamil to dissolve Peyronie’s disease plaque: a long-term single-blind study. Urology 51, 620–626 (1998).
Bennett, N. E., Guhring, P. & Mulhall, J. P. Intralesional verapamil prevents the progression of Peyronie’s disease. Urology 69, 1181–1184 (2007).
Shirazi, M., Haghpanah, A. R., Badiee, M., Afrasiabi, M. A. & Haghpanah, S. Effect of intralesional verapamil for treatment of Peyronie’s disease: a randomized single-blind, placebo-controlled study. Int. Urol. Nephrol. 41, 467–471 (2009).
Shindel, A. W., Bullock, T. L. & Brandes, S. Urologist practice patterns in the management of Peyronie’s disease: a nationwide survey. J. Sex. Med. 5, 954–964 (2008).
Cavallini, G., Modenini, F. & Vitali, G. Open preliminary randomized prospective clinical trial of efficacy and safety of three different verapamil dilutions for intraplaque therapy of Peyronie’s disease. Urology 69, 950–954 (2007).
Duncan, M. R., Berman, B. & Nseyo, U. O. Regulation of the proliferation and biosynthetic activities of cultured human Peyronie’s disease fibroblasts by interferons-alpha, -beta and -gamma. Scand. J. Urol. Nephrol. 25, 89–94 (1991).
Al-Attar, A. et al. Keloid pathogenesis and treatment. Plast. Reconstr. Surg. 117, 286–300 (2006).
Trost, L. W., Ates, E., Powers, M., Sikka, S. & Hellstrom, W. J. Outcomes of intralesional interferon-alpha2B for the treatment of Peyronie disease. J. Urol. 190, 2194–2199 (2013).
Stewart, C. A. et al. Intralesional injection of interferon-alpha2b improves penile curvature in men with Peyronie’s disease independent of plaque location. J. Urol. 194, 1704–1707 (2015).
Brazzelli, M. et al. Collagenase clostridium histolyticum for the treatment of Dupuytren’s contracture: systematic review and economic evaluation. Health Technol. Assess. 19, 1–202 (2015).
Jordan, G. H. The use of intralesional clostridial collagenase injection therapy for Peyronie’s disease: a prospective, single-center, non-placebo-controlled study. J. Sex. Med. 5, 180–187 (2008).
Gelbard, M. et al. Clinical efficacy, safety and tolerability of collagenase clostridium histolyticum for the treatment of Peyronie disease in 2 large double-blind, randomized, placebo controlled phase 3 studies. J. Urol. 190, 199–207 (2013).
US Food and Drug Administration. Drug safety information for Xiaflex. FDA https://www.fda.gov/downloads/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/UCM208737.pdf (2013).
Gelbard, M. K., James, K., Riach, P. & Dorey, F. Collagenase versus placebo in the treatment of Peyronie’s disease: a double-blind study. J. Urol. 149, 56–58 (1993).
Levine, L. A. et al. Clinical safety and effectiveness of collagenase clostridium histolyticum injection in patients with Peyronie’s disease: a phase 3 open-label study. J. Sex. Med. 12, 248–258 (2015).
Lipshultz, L. I. et al. Clinical efficacy of collagenase Clostridium histolyticum in the treatment of Peyronie’s disease by subgroup: results from two large, double-blind, randomized, placebo-controlled, phase III studies. BJU Int. 116, 650–656 (2015).
Ziegelmann, M. J. et al. Restoration of penile function and patient satisfaction with intralesional collagenase Clostridium histolyticum injection for Peyronie’s disease. J. Urol. 195, 1051–1056 (2016).
Abdel Raheem, A., Capece, M. & Kalejaiye, O. Safety and effectiveness of collagenase clostridium histolyticum in the treatment of Peyronie’s disease using a new modified shortened protocol. BJU Int. 120, 717–723 (2017).
Levine, L. A. & Lenting, E. L. A surgical algorithm for the treatment of Peyronie’s disease. J. Urol. 158, 2149–2152 (1997).
Papagiannopoulos, D., Yura, E. & Levine, L. Examining postoperative outcomes after employing a surgical algorithm for management of Peyronie’s disease: a single-institution retrospective review. J. Sex. Med. 12, 1474–1480 (2015).
Cordon, B. H. et al. Superior cost effectiveness of penile plication versus intralesional collagenase injection for treatment of Peyronie’s disease deformities. Urol. Pract. 4, 118–125 (2017).
Yafi, F. A., Anaissie, J., Zurawin, J., Sikka, S. C. & Hellstrom, W. J. Results of SMSNA survey regarding complications following intralesional injection therapy with collagenase Clostridium histolyticum for Peyronie’s disease. J. Sex. Med. 13, 684–689 (2016).
Trott, K. R. & Kamprad, F. Radiobiological mechanisms of anti-inflammatory radiotherapy. Radiother. Oncol. 51, 197–203 (1999).
Nolan, M. W. et al. Pudendal nerve and internal pudendal artery damage may contribute to radiation-induced erectile dysfunction. Int. J. Radiat. Oncol. Biol. Phys. 91, 796–806 (2015).
Mulhall, J. P., Hall, M., Broderick, G. A. & Incrocci, L. Radiation therapy in Peyronie’s disease. J. Sex. Med. 9, 1435–1441 (2012).
Palmieri, A. et al. A first prospective, randomized, double-blind, placebo-controlled clinical trial evaluating extracorporeal shock wave therapy for the treatment of Peyronie’s disease. Eur. Urol. 56, 363–369 (2009).
Hauck, E. W. et al. Extracorporeal shock wave therapy for Peyronie’s disease: exploratory meta-analysis of clinical trials. J. Urol. 171, 740–745 (2004).
Hatzichristodoulou, G. et al. Extracorporeal shock wave therapy in Peyronie’s disease: results of a placebo-controlled, prospective, randomized, single-blind study. J. Sex. Med. 10, 2815–2821 (2013).
Chung, E., De Young, L., Solomon, M. & Brock, G. B. Peyronie’s disease and mechanotransduction: an in vitro analysis of the cellular changes to Peyronie’s disease in a cell-culture strain system. J. Sex. Med. 10, 1259–1267 (2013).
Raheem, A. A. et al. The role of vacuum pump therapy to mechanically straighten the penis in Peyronie’s disease. BJU Int. 106, 1178–1180 (2010).
Agee, J. M. & Goss, B. C. The use of skeletal extension torque in reversing Dupuytren contractures of the proximal interphalangeal joint. J. Hand Surg. Am. 37, 1467–1474 (2012).
Bailey, A. J., Tarlton, J. F., Van der Stappen, J., Sims, T. J. & Messina, A. The continuous elongation technique for severe Dupuytren’s disease. A biochemical mechanism. J. Hand Surg. Br. 19, 522–527 (1994).
Levine, L. A., Newell, M. & Taylor, F. L. Penile traction therapy for treatment of Peyronie’s disease: a single-center pilot study. J. Sex. Med. 5, 1468–1473 (2008).
Gontero, P. et al. Use of penile extender device in the treatment of penile curvature as a result of Peyronie’s disease. Results of a phase II prospective study. J. Sex. Med. 6, 558–566 (2009).
Martinez-Salamanca, J. I. et al. Acute phase Peyronie’s disease management with traction device: a nonrandomized prospective controlled trial with ultrasound correlation. J. Sex. Med. 11, 506–515 (2014).
Ralph, D. J., Abdel Raheem, A. & Liu, G. Treatment of Peyronie’s disease with collagenase Clostridium histolyticum and vacuum therapy: a randomized, open-label pilot study. J. Sex. Med. 14, 1430–1437 (2017).
Chamberlain, G., Fox, J., Ashton, B. & Middleton, J. Concise review: mesenchymal stem cells: their phenotype, differentiation capacity, immunological features, and potential for homing. Stem Cells 25, 2739–2749 (2007).
Milenkovic, U., Albersen, M. A. & Castiglione, F. The mechanisms and potential of stem cell therapy for penile fibrosis. Nat. Rev. Urol. https://doi.org/10.1038/s41585-018-0109-7 (2018).
Castiglione, F. et al. Intratunical injection of human adipose tissue-derived stem cells prevents fibrosis and is associated with improved erectile function in a rat model of Peyronie’s disease. Eur. Urol. 63, 551–560 (2013).
US National Library of Medicine. ClinicalTrials.gov http://www.clinicaltrials.gov/ct2/show/NCT02395209 (2015).
US National Library of Medicine. ClinicalTrials.gov http://www.clinicaltrials.gov/ct2/show/NCT02414308 (2015).
Twidwell, J. & Levine, L. Topical treatment for acute phase Peyronie’s disease utilizing a new gel, H-100: a randomized, prospective, placebo-controlled pilot study. Int. J. Impot. Res. 28, 41–45 (2016).
Chung, E. et al. Evidence-based management guidelines on Peyronie’s disease. J. Sex. Med. 13, 905–923 (2016).
Dalbeth, N., Lauterio, T. J. & Wolfe, H. R. Mechanism of action of colchicine in the treatment of gout. Clin. Ther. 36, 1465–1479 (2014).
Acknowledgements
Reviewer information
Nature Reviews Urology thanks T. Bivalacqua and other anonymous reviewer(s) for their help with the peer review of this manuscript.
Author information
Authors and Affiliations
Contributions
Both authors researched data for article, made substantial contributions to discussion of content, wrote the manuscript, and reviewed and edited the manuscript before submission.
Corresponding author
Ethics declarations
Competing interests
L.A.L. declares that he has acted as a consultant for Coloplast Corporation, Boston Scientific, and Hybrid Medical and as a lecturer for Abbvie. P.T. declares no competing interests.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Tsambarlis, P., Levine, L.A. Nonsurgical management of Peyronie’s disease. Nat Rev Urol 16, 172–186 (2019). https://doi.org/10.1038/s41585-018-0117-7
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41585-018-0117-7
This article is cited by
-
Is there a new role for oral therapy to treat peyronie’s disease? Commentary on Daily low-dose tadalafil may reduce the penile curvature progression rate in patients with acute Peyronie’s Disease: a retrospective comparative analysis
International Journal of Impotence Research (2023)
-
Poliklinische plicatieplastiek bij kromstand van de penis
Tijdschrift voor Urologie (2023)
-
The collagenase of the bacterium Clostridium histolyticum does not favor metastasis of breast cancer
Breast Cancer (2022)
-
Long-term patient-reported outcomes in men with Peyronie’s disease undergoing nonsurgical and nonintralesional injection management
International Journal of Impotence Research (2021)
-
Collagenase clostridium histolyticum is no longer available in Europe: what does this mean for our patients with Peyronie’s Disease?
International Journal of Impotence Research (2021)