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Journal of Contemporary Brachytherapy
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4/2010
vol. 2
 
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Clinical Investigations
Original article
Interstitial brachytherapy for penile cancer: the experience of Oncology Centre in Bydgoszcz

Roman Makarewicz
,
Andrzej Lebioda
,
Joanna Terlikiewicz
,
Renata Kabacińska

J Contemp Brachyther 2010; 2, 4: 157-159
Online publish date: 2011/01/14
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Purpose

Penis cancer represents 0.4-0.6% of all cancers cases in male population. Many epidemiological studies have do­cumented the fact that penile cancer is more frequent in uncircumcised men with poor hygiene, phimosis and human papilloma virus infection. Although trauma and veneral diseases have been associated with penile cancer, no causative relationship has been identified [1]. The traditional surgical approach (partial or total penectomy depending on the extent of the disease) provides excellent local control. Radiotherapy of the primary tumor is an alternative organ preserving approach with good results in selected patients with T1-2 lesions with < 4 cm in diameter [2]. Radiation therapy can be delivered as an external beam radiation therapy (EBRT) or as brachytherapy using mainly Iridium-192 and high-dose-rate (HDR) remote afterloading technique. However, the best results have been obtained using brachytherapy with local control rates, ranging from 70% to 90%. Most patients with local failure after radiation therapy can be salvaged surgically. Because of the lack of randomized trials comparing these different treatment modalities, the treatment decision is mainly based on a center’s experience and international guidelines.

In this paper we report results of interstitial HDR brachytherapy in 33 men with penile squamous cell cancer.

Material and methods

From October 1996 to September 2007, 33 male patients with penile squamous cell cancer were treated using brachytherapy HDR at Oncology Centre in Bydgoszcz. The median age was 62, ranged from 47 to 78. The majority of tumors was found in the glands (28 cases); in 3 patients the tumor was located on prepuce and glands, in 2 cases – on the glands and shaft. There were 23 (69.7%) of T1 tumor cases, 7 (21.2%) of T2 and 3 (9.1%) of T3 tumor cases. In all patients the tumor size ranged from 2 to 4 cm. Thirty patients were clinically node negative. Three patients were diagnosed with palpable inguinal lymph nodes and surgical dissection was applied. In two cases EBRT was used as an adjuvant therapy after excision of lymph nodes. Tumor grade was described as follows: 15 cases (53,6%) with grade 1, 10 with grade 2 (35.7%) and 3 cases with grade 6 (10.7%). In 2 patients the gradation was not determined.

Implantation of needles was performed under general anesthesia. Needle placement required 30-45 minutes in the operating room. Before the procedure, catheterization was performed for all patients. Paris system of dosimetry was used for all implants. The system was usually slightly modified (stepping source was used) because of the fle­xibility in choosing dwell times that permits uniform dose distribution. The median number of needles was 4 ranged from 2 to 6. Plexiglas templates were used to maintain the geometry of an implant. The GTV includes all visible and palpable tumor. The CTV consists of GTV including margin of 8-10 mm surrounding clinically evident tumor. The prescribed dose ranged from 48 to 54 Gy with mean dose of 51 Gy given two times daily using HDR remote afterloading device (Nucletron) or 60 Gy applied for six consecutive days using PDR afterloader (Nucletron). The brachytherapy needles were well tolerated. During therapy that lasted less than 10 days, patients remained cathete­rized, being allowed out of bed since the treatment was applied for a short period of time. At the end of the treatment, the needles were removed after pre-medicating a patient with a narcotic analgesic. The median follow-up period was 60 months, ranged 37-168 months. The primary end point was the time to local failure, secondary endpoints – the time to regional and distant failure, disease free survival and overall survival.

The Kaplan-Meier estimation was used to evaluate the survival control rate and locoregional control rate, and survival was measured from the date of pathologic diagnosis.

Results

In the median period of 60 months we observed 9 patients relapsed: 4 cases of local failure, 2 – locoregio­nal failure, 1 patient with locoregional/distant failure and 1 with a distant failure. Salvage penectomy or partial penectomy was performed in 5 cases with local or locoregional failure. Four (80%) of 5 cases with local or locoregional failures were successfully treated with surgery. In all patients, 5 year overall and disease free survival rates were 84.9% (95% CI) and 75.4% (95% CI), respectively (Fig. 1). The 5 years locoregional control rate was 78.8% (95% CI) (Fig. 2).

The acute reactions after radiation were limited to the implant site and were observed in all patients. Moist des­quamation peaks were observed within 1 to 2 weeks after brachytherapy and healed completely after 2-3 months. Sterile distal urethritis were noticed in 10 patients. In gene­ral, the cosmetic outcome was good to excellent. In 5 cases teleangiectasia was noticed, however its appearance was quite acceptable to the patient. Erectile functionality was usually maintained at the same level as before irradiation. Soft tissue necrosis was observed in 3 patients at 10, 12 and 19 months after brachytherapy.

Discussion

Penile cancer is an uncommon disease in developed countries. More frequent occurrence of this disease is observed in developing nations [1]. The traditional policy management of penile squamous cell cancer is surgery and involves partial or total penectomy. For treatment of the primary tumor, 1-2 cm margin of resection is necessary to avoid an unacceptable rate of local recurrence – it is the standard of care [3]. It is understandable that local failure rate is very low after total or partial penectomy. How­ever, psychosexual morbidity of a patient is also the subject of concern. Many conservative therapies such as laser resection, brachytherapy and EBRT are alternative modali­ties for a surgery and offer good local control with functional organ preservation [4]. A potential advantage of brachytherapy is the ability to avoid penile resection. Reported results for interstitial brachytherapy show 5-years local tumor control rates ranging from 72% to 88% [1-8].

In our series, local failure was observed in seven patients. Only in three cases it was associated with regio­nal or distant metastases. In our present series, the failure was related to the tumor grade and its size. Numerous series present poorer results for tumors greater than 4 cm. In 5 from 2 local failures, the tumor size before treatment were greater than 4 cm. As it was mentioned before, local control rate strongly depends on tumor size. Mazeron et al. showed local failures rate at 11% for tumors smaller than 2 cm, 26% for tumors size 2 to 4 cm and 50% for those greater than 4 cm [9]. Our results confirm this observation. In our study, brachytherapy was well tolerated and only three patients developed soft tissue necrosis. Adverse events occurred in the area receiving a very high total dose. Soft tissue necrosis was earlier reported in 23% of patients and it was more common after brachytherapy [9]. An increased risk of necrosis has been reported for doses over 60 Gy for patients with T3 tumors and higher-volume implants > 30 cm3 [2]. The peak time for this adverse effect was 7-18 months after brachytherapy. Our series had a number of limitations. Firstly, the study group was small and it was lacking a control group for comparison. Secondly, this was a retrospective analysis and certain inherent deviation could occur.

Conclusions

Despite discussed limitations, we concluded that sole brachytherapy seems to be a satisfactory local treatment for T1-3 penile squamous cell cancer smaller than 4 cm in size. Penile preservation can be achieved in more than 80% of patients with no decrease in cancer control rates.

References

1. Pizzocaro G, Algaba F, Horenblas S et al. EAU penile cancer guidelines 2009. Eur Urology 2010; 57: 1002-1012.

2. Crook J, Jezioranski J, Cygler JE. Penile brachytherapy: technical aspects and postimplant issues. Brachytherapy 2010; 9: 151-158.

3. Culkin DJ, Beer TM. Advanced penile carcinoma. J Urol 2003; 170: 359-365.

4. Syed S, Eng TY, Thomas ChR et al. Current issues in the mana­gement of advanced squamous cell carcinoma of the penis. Urol Oncol: Seminars and Original Invest 2003; 21: 431-438.

5. Ozsahin M, Jichlinski P, Weber DC et al. Treatment of penile carcinoma: to cut or not to cut? Int J Radiat Oncol Biol Phys 2006; 66: 674-679.

6. Rozan R, Albuisson E, Giraud B et al. Interstitial brachytherapy for penile carcinoma: a multicentric survey (259 patients). Radioth Oncol 1995; 36: 83-93.

7. Crook JM, Jezioranski J, Math M et al. Penile brachytherapy: results for 49 patients. Int J Radiat Oncol Biol Phys 2005; 62: 460–467.

8. Crook J, Grimard L, Tsihlias J et al. Interstitial brachytherapy for penile cancer: an alternative to amputation. J Urol 2002; 167: 506-511.

9. Mazeron JJ, Lang Lois D, Lobo P. Interstitial radiation therapy for carcinoma of the pens using iridium 192 wires: the Henri Mondor experience (1970-1979). Int J Radiat Oncol Biol Phys 1984; 10: 1891-1890.
Copyright: © 2011 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
 
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