Abstract
Aim
To assess the efficacy and toxicity profile of protocol-based interstitial pulsed-dose-rate (PDR) brachytherapy for penile carcinoma.
Patients and methods
From August 2002 to February 2014, 13 men with penile cancer were treated by interstitial brachytherapy. The tumor stage was T1 for eight patients, T2 for four patients, and T3 for one patient. The tumor grade was well differentiated for five patients and moderately differentiated for seven patients, while it was unknown for one patient. Lymph node staging was positive for three of 13 patients. All patients were treated using interstitial PDR brachytherapy with dose specifications according to the Paris system. For data collection of erectile dysfunction, the International Index of Erectile Function questionnaire was used, supplemented by the follow-up data.
Results
The median follow-up was 54.0 months (range, 13–155 months). Only one patient (1/13, 7.7 %) with local failure was documented. At 5 and 10 years, the local cumulative recurrence rate, disease-free survival, and the cancer-specific survival rates were 12.5 % (95 % CI, 80.4–119.6), 80.8 % (95 % CI, 75.2–124.8), and 77.9 % (95 % CI, 74.3–125.7), respectively. At the time of analysis, nine of 13 men were alive; two of 13 men died of distant metastases from the tumor and two for other reasons with no sign of cancer disease. Serious late side effects such as soft tissue necrosis occurred in four of 13 patients (30 %) and all were successfully treated with medication. Mutilating salvage surgery was not necessary in any of the cases. Urethral stenosis was documented for two of 13 (15.4 %) and dysuria occurred in four of 13 patients (30.8 %). Eight of 11 men (72.7 %) never or only sometimes had erectile dysfunction.
Conclusion
In selected patients, interstitial PDR brachytherapy of penile cancer is effective as an organ-sparing treatment. It yields satisfactory results for the conservation of sexual function.
Zusammenfassung
Ziel
Analyse der Ergebnisse von 13 Patienten mit Plattenepithelkarzinom des Penis, die mittels protokollbasierter interstitieller „Pulsed-dose-rate“-(PDR)-Brachytherapie behandelt wurden.
Patienten und Methoden
Von August 2002 bis Februar 2014 wurden 13 Männer mit Peniskarzinom mittels Brachytherapie behandelt. Das Tumorstadium war bei 8 Patienten T1, bei 4 Patienten T2 und bei einem Patienten T3. Der Differenzierungsgrad war bei 5 Patienten gut, bei 7 Patienten moderat und in einem Fall unbekannt. Bei 3/13 Patienten war der Lymphknotenstatus positiv. In allen Fällen wurde eine interstitielle PDR-Brachytherapie mit Dosisspezifikation gemäß dem Paris-System angewandt. Für die Datenerhebung von erektiler Dysfunktion wurde der IIEF-Fragebogen (International Index of Erectile Function) verwendet und durch die Nachsorgedaten ergänzt.
Ergebnisse
Das mediane Follow-up betrug 54,0 Monate (Spanne 13–155 Monate). Nur bei einem Patienten (1/13, 7,7 %) wurde ein Lokalrezidiv diagnostiziert. Die 5‑ und 10-jährige kumulative Lokalrezidivrate, das krankheitsfreie sowie das tumorspezifische Überleben lagen bei jeweils 12,5 % (95 %-Konfidenzintervall [95%-KI] 80,4–119,6), 80,8 % (95 %-KI 75,2–124,9) und 77,9 % (95 %-KI 74,3–125,7). Aktuell waren 9/13 Männern am Leben. Es verstarben 2/13 Männer am Tumor durch Fernmetastasen und 2 krankheitsfrei aus anderen Gründen. Ernsthafte späte Nebenwirkungen wie Weichteilnekrosen traten in 4/13 Fällen (30,8 %) auf und wurden alle erfolgreich medikamentös behandelt. Ein entstellender chirurgischer Eingriff war in keinem Fall notwendig. Urethrastenosen wurden bei 2 Patienten diagnostiziert und Miktionsbeschwerden traten bei 4 Patienten auf. Insgesamt 8/13 Männern (61,5 %) hatten niemals oder nur manchmal eine erektile Dysfunktion.
Schlussfolgerung
Bei ausgewählten Patienten ist die interstitielle PDR-Brachytherapie bei Peniskarzinom eine effektive, organschonende Behandlung. Sie kann zufriedenstellende Resultate in der Erhaltung der Sexualfunktion erzielen.
Similar content being viewed by others
References
Backes DM, Kurman RJ, Pimenta JM et al (2009) Systematic review of human papillomavirus prevalence in invasive penile cancer. Cancer Causes Control 20:449–457
Chaudhary AJ, Ghosh S, Bhalavat RL et al (1999) Interstitial brachytherapy in carcinoma of the penis. Strahlenther Onkol 175:17–20
Chaux A, Netto GJ, Rodriguez IM et al (2013) Epidemiologic profile, sexual history, pathologic features, and human papillomavirus status of 103 patients with penile carcinoma. World J Urol 31:861–867
Crook J, Ma C, Grimard L (2009) Radiation therapy in the management of the primary penile tumor: an update. World J Urol 27:189–196
Crook JM, Jezioranski J, Grimard L et al (2005) Penile brachytherapy: results for 49 patients. Int J Radiat Oncol Biol Phys 62:460–467
Crook JM, Haie-Meder C, Demanes DJ et al (2013) American Brachytherapy Society - Groupe Europeen de Curietherapie - European Society of Therapeutic Radiation Oncology (ABS-GEC-ESTRO) consensus statement for penile brachytherapy. Brachytherapy 12:191–198
Crevoisier R de, Slimane K, Sanfilippo N et al (2009) Long-term results of brachytherapy for carcinoma of the penis confined to the glans (N- or NX). Int J Radiat Oncol Biol Phys 74:1150–1156
Delannes M, Malavaud B, Douchez J et al (1992) Iridium-192 interstitial therapy for squamous cell carcinoma of the penis. Int J Radiat Oncol Biol Phys 24:479–483
Delaunay B, Soh PN, Delannes M et al (2014) Brachytherapy for penile cancer: efficacy and impact on sexual function. Brachytherapy 13:380–387
Ficarra V, Righetti R, D’Amico A et al (2000) General state of health and psychological well-being in patients after surgery for urological malignant neoplasms. Urol Int 65:130–134
Hakenberg OW, Comperat EM, Minhas S et al (2015) EAU guidelines on penile cancer: 2014 update. Eur Urol 67:142–150
Hasan S, Francis A, Hagenauer A et al (2015) The role of brachytherapy in organ preservation for penile cancer: A meta-analysis and review of the literature. Brachytherapy 14:517–524
Heideman DA, Waterboer T, Pawlita M et al (2007) Human papillomavirus-16 is the predominant type etiologically involved in penile squamous cell carcinoma. J Clin Oncol 25:4550–4556
Kamsu-Kom L, Bidault F, Mazeron R et al (2015) Clinical experience with pulse dose rate brachytherapy for conservative treatment of penile carcinoma and comparison with historical data of low dose rate brachytherapy. Clin Oncol (R Coll Radiol) 27:387–393
Kiltie AE, Elwell C, Close HJ et al (2000) Iridium-192 implantation for node-negative carcinoma of the penis: the Cookridge Hospital experience. Clin Oncol (R Coll Radiol) 12:25–31
Krengli M, Masini L, Comoli AM et al (2014) Interstitial brachytherapy for eyelid carcinoma. Outcome analysis in 60 patients. Strahlenther Onkol 190:245–249
Langsenlehner T, Mayer R, Quehenberger F et al (2008) The role of radiation therapy after incomplete resection of penile cancer. Strahlenther Onkol 184:359–363
Lestrade L, Bari B De, Pommier P et al (2014) Role of brachytherapy in the treatment of cancers of the anal canal. Long-term follow-up and multivariate analysis of a large monocentric retrospective series. Strahlenther Onkol 190:546–554
Lont AP, Kroon BK, Horenblas S et al (2006) Presence of high-risk human papillomavirus DNA in penile carcinoma predicts favorable outcome in survival. Int J Cancer 119:1078–1081
Mosconi AM, Roila F, Gatta G et al (2005) Cancer of the penis. Crit Rev Oncol Hematol 53:165–177
Pimenta A, Gutierrez C, Mosquera D et al (2015) Penile brachytherapy-Retrospective review of a single institution. Brachytherapy 14:525–530
Romero FR, Romero KR, Mattos MA et al (2005) Sexual function after partial penectomy for penile cancer. Urology 66:1292–1295
Rozan R, Albuisson E, Giraud B et al (1995) Interstitial brachytherapy for penile carcinoma: a multicentric survey (259 patients). Radiother Oncol 36:83–93
Soh PN, Delaunay B, Nasr EB et al (2014) Evaluation of sexual functions and sexual behaviors after penile brachytherapy in men treated for penile carcinoma. Basic Clin Androl 24:13
Yoshida K, Yamazaki H, Takenaka T et al (2014) High-dose-rate interstitial brachytherapy in combination with androgen deprivation therapy for prostate cancer: are high-risk patients good candidates? Strahlenther Onkol 190:1015–1020
Acknowledgments
The present publication was performed in fulfillment of the requirements for obtaining the degree “Dr. med. dent.” at the Friedrich-Alexander-University Erlangen-Nürnberg (FAU).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
J. Seibold, V. Strnad, and R. Fietkau state that there are no conflicts of interest.
Rights and permissions
About this article
Cite this article
Seibold, J., Strnad, V. & Fietkau, R. Organ-sparing treatment of penile cancer with interstitial pulsed-dose-rate brachytherapy. Strahlenther Onkol 192, 467–472 (2016). https://doi.org/10.1007/s00066-016-0968-x
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00066-016-0968-x