Focal partial salvage low-dose-rate brachytherapy for local recurrent prostate cancer after permanent prostate brachytherapy with a review of the literature.

PURPOSE: To investigate the treatment results for focal partial salvage re-implantation against local recurrence after permanent prostate brachytherapy.
MATERIAL AND METHODS: Between January 2010 and September 2015, 12 patients were treated with focal partial salvage re-implantation for local recurrence after low-dose-rate brachytherapy using (125)I seeds. The focal clinical target volume (F-CTV) was delineated on positive biopsy areas in a mapping biopsy, combining the cold spots on the post-implant dosimetry for initial brachytherapy. The F-CTV was expanded by 3 mm to create the planning target volume (PTV) as a margin to compensate for uncertainties in image registration and treatment delivery. The prescribed dose to the PTV was 145 Gy. The characteristics and biochemical disease-free survival (BdFS) rates were analyzed. Genitourinary (GU) and gastrointestinal (GI) toxicities were evaluated using the Common Terminology Criteria for Adverse Events version 4.
RESULTS: The median prostate-specific antigen (PSA) level at re-implantation was 4.09 ng/ml (range: 2.91-8.24 ng/ml). The median follow-up time was 56 months (range: 6-74 months). The median RD2cc and UD10 were 63 Gy and 159 Gy, respectively. The 4-year BdFS rate was 78%, which included non-responders. Biochemical recurrence occurred in two patients after 7 and 31 months, respectively. The former was treated with hormonal therapy after biochemical failure, and the latter underwent watchful waiting (PSA at the last follow-up of 53 months: 7.3 ng/ml) at the patient's request. No patients had grade 3 GU/GI toxicities or died after salvage re-implantation.
CONCLUSIONS: The partial salvage low-dose-rate brachytherapy used to treat local recurrence after permanent prostate brachytherapy is well-tolerated, with high biochemical response rates. This treatment can be not only a method to delay chemical castration but also a curative treatment option in cases of local recurrence of prostate carcinoma after seed implantation.

Purpose

Permanent prostate brachytherapy using 125I for patients with low- or intermediate-risk prostate cancer is an effective treatment option, and can achieve high biochemical progression-free survival [1, 2]. However, there are some cases of locoregional recurrence. Currently, there are few recommendations for a relapse of prostate cancer, except for palliative androgen deprivation therapy (ADT). Despite its antineoplastic activity on prostate cancer, the duration of its effectiveness is limited. In retrospective studies, ADT was found to be associated with cardiac sequelae, including coronary heart disease, myocardial infarction (MI), and sudden cardiac death [3]. Considering the site of recurrence in cases of subsequent biochemical relapse, the development of new therapeutic approaches (salvage re-irradiation) will be necessary. Salvage re-irradiation using brachytherapy for local recurrence will be a curative treatment. There are few reports on salvage re-irradiation using 125I permanent prostate brachytherapy for local recurrence after seed implantation.

The purpose of this study was to evaluate the effectiveness of partial salvage re-implantation to develop an effective treatment option for local recurrence after permanent prostate brachytherapy.

Material and methods

Patients and decision criteria for salvage re-implantation

Between January 2010 and September 2015, 12 patients were treated with partial salvage 125I brachytherapy for local recurrence after permanent prostate brachytherapy. The 12 patients underwent initial permanent prostatic implantation (monotherapy) using 125I radioactive seeds for low- or intermediate-risk prostate carcinoma at our institution between September 2004 and October 2008. Eligibility criteria for focal partial salvage re-implantation were as follows: 1) biochemical failure was defined using the Phoenix criteria (prostate-specific antigen [PSA]-nadir + 2.0 ng/ml); 2) a systematic bilateral template-guided prostate/seminal vesicle trans-perineal mapping biopsy with a 5 mm sampling frame (more than 20 biopsies) was performed for patients with biochemical failure, and locoregional clinical failure was diagnosed by a positive template biopsy; 3) pre-retreatment PSA < 10 ng/ml; 4) no lymph node or distant metastases on computed tomography (CT) or bone scan. A systematic bilateral mapping biopsy was performed according to the procedures described by Bott et al. [4]. If a biopsy needle placed at the apex could not obtain an adequate sample from the base of the prostate gland, or a cold spot in initial brachytherapy was located in only the apex or base side of the prostate, we divided the biopsy areas into two parts (apex and base sides) and detected the presence of malignancy in each part. As the re-implantation is not considered a standard procedure, locoregional clinical failure and PSA < 10 ng/ml warranted salvage re-implantation. One patient with a negative biopsy (patient #1 in Table 1) had a large cold spot (initial V100: 58%) and long PSA doubling time (15 months), and thus had suspected local recurrent disease, based on reports by Zagars et al. [5] that patients with a PSA doubling time (PSA-DT) exceeding 8 months had only a 7% metastatic rate and by Zelefsky et al. [6] that the 3-year incidence of distant metastasis for patients with PSA-DT of more than 12 months was 7%. Written informed consent for treatment was obtained from all patients prior to initial seed implantation and salvage re-implantation. They were also informed about the use of their clinical data. This retrospective study was approved by the ethics board of our institution, and the committee waived the need for re-informed consent.

Table 1

Patients and treatment characteristics

Patient	Age before salvage	D90 for initial PID (Gy)	V100 for initial PID (%)	RD2cc for initial PID (Gy)	UD10 for initial PID (Gy)	Elapsed time from initial to salvage (months)	initial PSA before initial BT (ng/ml)	Nadir PSA after initial BT (ng/ml)	Biopsy cores no. before salvage	Biopsy Gleason score before salvage	PSA before biopsy (ng/ml)	PSA before salvage (ng/ml)	Hormonal therapy before salvage (months)	Follow-up after salvage (months)	No. of seeds in initial BT	No. of seeds in salvage	Nadir PSA after salvage (ng/ml)	Time to biochemical failure after salvage (months)
1	65	85	58	75	104	51	10.8	0.6	20	NA	4.7	4.7	NA	74	70	45	0.18	NA
2	75	110	74	80	112	40	11.8	1.35	24	3 + 3	7.01	7.01	NA	64	65	55	0.08	NA
3	61	107	74	89	120	55	6.7	0.84	27	3 + 3	2.88	3.42	NA	62	70	55	0.21	NA
4	67	98	65	88	125	70	7.2	0.37	26	4 + 4	1.91	2.91	NA	60	85	50	< 0.05	NA
5	76	84	68	134	98	34	9.38	0.77	27	3 + 4	5.61	5.61	NA	59	67	61	< 0.05	NA
6	70	70	64	112	127	36	8.39	1.24	31	3 + 3	5.09	4.97	NA	58	59	43	< 0.05	NA
7	69	96	69	65	110	55	6.3	0.88	35	4 + 3	4.13	5.25	NA	53	60	38	0.11	31
8	65	146	91	79	110	42	10.74	1.17	29	3 + 4	6.55	8.24	NA	48	57	40	4.47	9
9	78	35	32	76	101	105	11.1	1.15	34	4 + 4	3.32	3.55	NA	33	64	50	0.16	NA
10	67	113	80	86	152	93	5.03	0.39	36	4 + 3	4.86	0.87	5(Zoladex)	8	56	28	0.29	NA
11	70	138	88	78	224	83	5.74	0.4	30	3 + 3	4.173	0.95	3(Leuplin)	6	49	30	< 0.05	NA
12	67	87	72	89	168	86	10.81	0.76	32	3 + 3	5.104	1.58	1(Leuplin)	6	49	40	0.94	NA

BT – brachytherapy, D90 – minimum dose received by 90% of the volume expressed as a percentage of the prescription dose, NA – not available, PID – post-implant dosimetry, PSA – prostate specific antigen, RD2cc – minimum dose received by 2 cc of the rectum, UD10 – minimum doses received by 10% of the urethral volume, V100 – percentage of the prostate volume covered by 100% of the prescription dose

Focal partial salvage re-implantation planning and procedure

The focal partial clinical target volume (F-CTV) was delineated on positive biopsy areas in a mapping biopsy, combining the cold spots on the post-implant CT-based dosimetric analysis for initial permanent prostate brachytherapy taking into account microscopic carcinoma in the cold spot with a negative biopsy. Although multi-parametric magnetic resonance imaging (MRI) was performed in 5 of 12 patients before re-implantation, it was impossible to identify the recurrent localization. The F-CTV was expanded by 3 mm to create the planning target volume (PTV) as a margin to compensate for uncertainties in image registration and treatment delivery, such as movement, and PTV contour was restricted to organs at risk (OARs), such as the rectum and bladder. The dose prescribed to the PTV during intra-operative planning was 145 Gy. Variseed ver. 8.0 software (Varian Medical Systems Inc., Palo Alto, CA, USA) was used for treatment planning (Figure 1). The rectum and urethra were also delineated as OARs on real-time transrectal ultrasonography. Planning criteria for the OAR were according to the following ESTRO/EAU/EORTC recommendations for primary brachytherapy: rectum D2cc value (RD2cc; i.e., the minimum dose in the maximum irradiated 2 cc of the rectum) < the reference prescription dose, and prostatic urethra D10 value (UD10; i.e., minimum doses received by 10% of the urethral volume) < 150% of the reference prescription dose [7]. To estimate the doses for the entire prostate, the whole prostate was also contoured.

Fig. 1

Example of the dose distribution in intra-operative planning on a representative patient. On the trans-rectal ultrasound image, the focal clinical target volume (dark brown), planning target volume (cyan), prostate (red), urethra (green), and rectum (blue) images are contoured. The dose distributions are shown in light green (100% = 145 Gy) and purple (150% = 217.5 Gy). The focal clinical target volume received a dose of approximately 150%, and the planning target volume received a dose of approximately 100%. Rectum sparing in the dose distribution is apparent

Patient follow-up (PSA value and toxicity)

Prostate-specific antigen measurements were performed 1 and 6 months post-operatively and subsequently every 3 months. Biochemical failure was defined according to the Phoenix definition [8]. Genitourinary (GU) and gastrointestinal (GI) toxicities were evaluated using the Common Terminology Criteria for Adverse Events version 4.0 (CTCAE-4) [9]. Toxicity was evaluated at baseline, 1, and 6 months post-operatively, and every 6 months thereafter. It was impossible to evaluate erectile dysfunction (ED) for all 12 patients because of incomplete ED status at the time of salvage brachytherapy, although sexual toxicity is often evaluated after radiation therapy [10], and such evaluation is important for re-irradiation studies.

Statistics

Statistical analyses were performed using SPSS ver. 18 (SPSS Inc., Chicago, IL, USA). Biochemical disease-free survival (BdFS) was estimated according to Kaplan-Meier analysis. P-values less than 0.05 were considered to indicate statistical significance.

Results

Baseline characteristics

Tables 1 and 2 show the characteristics and summary of each patient. The median PSA nadir after initial permanent prostate brachytherapy was 0.81 ng/ml (range: 0.37-1.35 ng/ml). The median PSA at re-implantation was 4.09 ng/ml (range: 2.91-8.24 ng/ml). The median elapsed time from the initial treatment to salvage treatment was 55 months (range: 34-105 months). The median number of systematic bilateral mapping biopsies per patient was 29.5 (range: 20-36). Three (25%) patients received neoadjuvant hormonal therapy ranging from 1 to 5 months just before salvage treatment, and no patient received adjuvant hormonal therapy. The median number of seeds per patient in salvage re-implantation was 44 (range: 28-61). The mean activity per seed in salvage re-implantation was 0.410 U (range: 0.368-0.444 U). The activity per seed in accordance with the size of the PTV was adequately selected. The median follow-up time was 56 months (range 6-74 months).

Table 2

Summary of data for patients at the first treatment

Factor	Value (range)
PSA at treatment (median)	8.89 ng/ml (5.03-11.8)
PSA at nadir (median)	0.81 ng/ml (0.37-1.35)
D90 (median)	97 Gy (35-146)
V100 (median)	71% (32-91)
RD2 (median)	83 Gy (65-134)
UD10 (median)	116% (98-224)

D90 – minimum dose received by 90% of the volume expressed as a percentage of the prescription dose, PSA – prostate specific antigen, RD2 – minimum dose received by 2 cc of the rectum, UD10 – minimum doses received by 10% of the urethral volume, V100 – percentage of the volume covered by 100% of the prescription dose

Intra-operative dosimetric parameters for F-CTV, PTV, rectum, urethra, and prostate in focal partial re-implantation

The median D90 (the minimum dose received by 90% of the volume expressed as a percentage of the prescription dose) values for F-CTV and PTV were 200 Gy (range: 145-236) and 165 Gy (range: 129-206), respectively. The median RD2cc and UD10 were 63 Gy (range: 28-89) and 159 Gy (range: 125-198), respectively. The median D90 and V100 (percentage of the volume covered by 100% of the prescription dose) values for the prostate were 142 Gy (range: 76-206) and 86% (range 64-100), respectively.

Biochemical outcomes and survival

Including non-responders, the Kaplan-Meier 4-year BdFS estimates were 78% (Figure 2). One patient with a negative biopsy had declined PSA after re-implantation (from 4.7 to 0.23 ng/ml), reflecting the implanted coverage of the cold spot areas on post-implant dosimetry for initial brachytherapy. Biochemical failure occurred in two patients (17%) after 7 months (nadir 4.47 ng/ml) and 31 months (nadir 0.11 ng/ml). The former was treated with ADT after the failure, the latter got a watchful waiting (PSA at the last follow-up of 53 months: 7.3 ng/ml) at the patient's request. No patient died after salvage treatment.

Fig. 2

BdFS estimates for focal partial salvage permanent prostate brachytherapy

Toxicity

Table 3 summarizes the GU and GI toxicities. The most frequent GU toxicity was grade 1 urinary frequency, often present before salvage re-implantation. Four patients (33%) experienced urinary frequency that was managed with medication (grade 2) until the time of the last follow-up. No patient had grade 3 urinary retention. One patient (8%) had grade 1 urinary incontinence caused by re-irradiation. No patient experienced grade 2 or more severe urinary incontinence after salvage treatment. One (8%) experienced radiation cystitis (grade 2), which improved by itself immediately. No patient experienced grade 3 radiation cystitis. No patient had grade 1 radiation proctitis before salvage treatment. After re-implantation, one patient (8%) had radiation proctitis (grade 2) due to aspirin usage, which improved with no use of aspirin and without laser therapy. No patient experienced grade 3 or higher radiation proctitis.

Table 3

Frequencies of GU and GI toxicities

	Pre-treatment	12 months post-treatment	24 months post-treatment	36 months post-treatment	48 months post-treatment
No. of patients	12	9	9	8	7
GU toxicity
Grade 2	0	4	4	4	3
Grade 3	0	0	0	0	0
GI toxicity
Grade 2	0	0	1	0	0
Grade 3	0	0	0	0	0

GI – gastrointestinal, GU – genitourinary

Discussion

In this study, focal partial salvage re-implantation against local recurrence of prostate cancer after permanent prostate brachytherapy provided durable local control. The 4-year BdFS rate after partial salvage re-implantation was 78%. There are few reports with a small number of patients evaluating the effectiveness of partial salvage re-implantation for local recurrence after permanent prostate brachytherapy [11, 12, 13] (Table 4). Compared with other reports, we illustrated improved tolerability of the treatment with a high PSA control rate at a longer median follow-up time (median: 56 months). Sasaki et al. demonstrated that seven patients underwent salvage partial low dose rate brachytherapy for biopsy-proven, localized prostate cancer recurrence with no significant genitourinary or gastrointestinal toxicity, and the PSA levels remained under control in five patients at a median follow-up of 27 months [11]. In the study, the 2-year BdFS rate after focal salvage re-implantation was not determined but would have been 58% according to our calculation. Although Peters et al. [12] reported focal salvage permanent prostate brachytherapy in 20 patients, the initial treatments in 13 of these cases were external-beam radiation therapy (EBRT) or intensity-modulated radiation therapy (IMRT). Therefore, the latter finding was fundamentally different from that in our study. Seven prostate cancer cases matched subjects in our study. They demonstrated that the biochemical response and quality of life were acceptable at a median follow-up time of 36 months in 20 patients. However, they did not show the BdFS rates for focal salvage re-implantation alone. Hsu et al. [13] reported that 15 patients underwent MRI-guided focal partial salvage permanent prostate implantation for biopsy-proven localized recurrent prostate cancer after initial low dose rate brachytherapy as definitive monotherapy (13 patients) or combined modality therapy (2 patients). The 3-year BdFS rate after focal partial salvage re-implantation was 71% in 15 patients at a median follow-up of 23.3 months. However, they did not demonstrate the BdFS rate of re-implantation for local recurrence after initial permanent prostate implant as monotherapy.

Table 4

Clinical results of partial salvage re-implantation for local recurrence after permanent prostate brachytherapy

Study	Year	No. of patients	Previously irradiated method	Salvage LDR dose (Gy)	Median follow-up after salvage (months)	Biochemical disease free survival rate (%)	Grade 3 GU complication (patients)	Grade 3 GI complication (patients)	Grade 4 GU complication (patients)	Grade 4 GI complication (patients)
Hsu et al. [13]	2013			144 (for I) or 125 (for Pd) or 108 (for I) + EBRT (40Gy)	23.3	100% (2-years), 71% (3-years)	0 (0%)	0 (0%)	0 (0%)	0 (0%)
		13	LDR
		2	LDR + EBRT (45 Gy)
Sasaki et al. [11]	2014				27	58% (2-years)	0 (0%)	0 (0%)	0 (0%)	0 (0%)
		6	LDR	145
		1	LDR + EBRT (45 Gy)	145
Peters et al. [12]	2014				36	60% (3-years)	1 (5%)	0 (0%)	0 (0%)	0 (0%)
		7	LDR	144
		7	EBRT (70 Gy)	144
		6	IMRT (76 Gy)	144
Present study					56	78% (4-years)	0 (0%)	0 (0%)	0 (0%)	0 (0%)
		12	LDR	145

EBRT – external-beam radiation therapy, GI – gastrointestinal, GU – genitourinary, IMRT – intensity-modulated radiation therapy, LDR – low dose rate brachytherapy

The study presented here highlights the possibility to perform re-implantation therapy targeting only the recurrent localized lesion (partial salvage re-implantation) after seed implantation, not only to prevent or postpone the use of ADT but also to cure prostate carcinomas. Androgen deprivation therapy is the mainstay of treatment for a relapse of prostate cancer after seed implantation. The impact of immediate ADT on specific survival for prostate cancer in PSA relapse is unclear except in patients with rapidly progressing disease [14]. Some retrospective reports with a small number of patients have shown the feasibility of salvage local irradiation for localized persistent prostate cancer (LDR brachytherapy after EBRT [15]/radical prostatectomy [16], and stereotactic radiotherapy after LDR brachytherapy [17]).

Permanent prostate brachytherapy sometimes causes insufficient dose coverage due to the technique. Immediate re-implantation as a salvage treatment is recommended in such cases [18]. We did not re-implant immediately for the under-dosed area and carefully observed the PSA values. Indeed, in 11 of 12 patients in our study, the D90 for the entire prostate could not sufficiently ensure the prescription dose (145 Gy). However, the median initial PSA before initial brachytherapy and the median nadir PSA after initial brachytherapy were 8.9 and 0.8 ng/ml, respectively (maximum nadir PSA: 1.35 ng/ml). The largest tumor focus within the prostate (called the index lesion) [19] seemed to be irradiated. Consequently, there was no need to re-implant right after the initial implantation.

The Gleason score was increased at recurrence in 6 of 12 patients (50%) compared with that at the initial brachytherapy in this study. The high score indicates that it is difficult to achieve durable disease control after salvage treatment. However, we did demonstrate a high durable disease control rate (4-year BdFS rate: 78%). Due to histological changes after radiation therapy, it may not always be accurate for recurrent prostate carcinoma to be evaluated for malignancy using the Gleason system according to recommendations of both the College of American Pathologists and World Health Organization [20].

Salvage re-irradiation using high-dose-rate brachytherapy can also be a treatment option. Chen et al. [21] reported that the 5-year biochemical control was 51% at a median follow-up time of 59.6 months after salvage high dose rate brachytherapy, and late grade 3 GU/GI and late grade 2 GU/GI toxicities were observed in 2%, 0%, 54%, and 4%, respectively. It is difficult to say which brachytherapy is superior to others at this time.

Seed migration may be critical for partial salvage LDR brachytherapy. Wang et al. reported that it had no impact on the implant quality of initial whole prostate LDR brachytherapy [22]. However, in focal partial re-implantation, it is necessary to avoid seed migration to maintain implant quality.

The optimized tumor control dose to the target is undetermined at present. In this study, the dose prescribed to the PTV during intra-operative planning was 145 Gy. Sasaki et al. designed salvage partial low dose rate brachytherapy delivering 144 Gy to positive biopsy sites, corresponding to cold spot areas at the initial low dose rate brachytherapy [11]. Peters et al. reported that a dose of > 144 Gy was prescribed to the target area and was delineated on MRI combining biopsy results [12]. Hsu et al. reported that the prescription dose for implants was 144 Gy for 125I, 125 Gy for 103Pd, and 108 Gy for 125I with IMRT (40 Gy) [13]. Future investigations for prescription dose recommendations are required to estimate salvage re-implantation as a curable treatment.

The recommended CTV delineation and PTV margin size is also unclear at present. Langley et al. [23] reported that the F-CTV is delineated as the gross visible or clinically demonstrable location and the extent of the targeted cancer plus clinically insignificant disease; it was expanded to create the focal PTV to compensate for uncertainties in image registration and treatment delivery, such as movement, and the focal PTV contours would be restricted to OAR contours such as those of the urethra and rectum. Groenendaal et al. [24] reported that the application of a margin of 2 voxels (voxel size 2.5 × 2.5 × 2.5 mm3; 5 mm margin) to an MR-based tumor delineation in five patients with biopsy-proven prostate cancer (PSA: 14-29 ng/ml; pathological Gleason: 6-8; pathological T stage: T2a-T3a) enables the coverage of approximately 85-100% of the tumor. Sasaki et al. [11] reported that the clinical target volume (CTV) was manually delineated as a region of local recurrence with biopsy positivity and initial under-dosage according to MRI/initial CT dosimetry, and the PTV included the CTV plus a 5 mm margin (5 mm posterior margin). Peters et al. [12] reported that the treatment margins were expanded up to half of the prostate to account for uncertainties in the definition and delineation of the gross tumor volume (based on T2-weighted magnetic resonance imaging [T2W-MRI]), combining biopsy results and multi-parametric MRI and the uncertainty in matching of the MRI and ultrasound images. Hsu et al. [13] demonstrated MRI-guided focal partial salvage permanent prostate implantation for local recurrent prostate cancer after initial implantation, and they defined the CTV as defined as an area of local recurrence with initial under-dosage. In the current study, F-CTV was not delineated on imaging modalities such as MRI but rather on positive biopsy areas in a 5 mm mapping biopsy, combining the cold spots on post-implant dosimetry and taking into account microscopic carcinoma in the cold spot with a negative biopsy. We performed MRI in 5 of 12 cases to delineate the recurrent gross tumor; however, it was impossible to identify the location of the tumor in 5 cases. If the needle biopsy did not sufficiently cover the apex to the base of the prostate gland or the cold spot in initial brachytherapy located in only the apex or base side of the prostate, we divided the biopsy areas into two parts (apex and base sides) and detected the presence of malignancy in each part. The F-CTV will not necessarily include the cold spot with a negative biopsy, thus, it is difficult to conclude that our F-CTV is adequate. Regarding the PTV margin size, the F-CTV was expanded by 3 mm to create the PTV as a margin to compensate for uncertainties in image registration and treatment delivery. In the re-implantation study, a 3 mm margin to both the positive biopsy areas and cold spots may also be a practical first step. Without a systematic comparison of margin distances, we cannot conclude that 3 mm is an adequate distance.

More accurate diagnostic imaging can improve the treatment effect for better disease control. Biochemical progression is due to either local recurrence or distant metastasis, and the PSA doubling time was identified as a predictive factor of distant metastases [5, 6, 25]. Peter et al. and Sasaki et al. demonstrated that, due to less time to biochemical recurrence/a shorter PSA doubling time, some patients failed to reflect probable (micro) metastatic disease at the time of focal salvage [11, 12]. In the present study, one patient who had a shorter PSA doubling time at the time point of partial salvage had PSA progression after salvage treatment. A shorter PSA doubling time may imply the existence of regional or distant recurrence, even if locoregional clinical failure was diagnosed by a positive biopsy, and no lymph node or distant metastases were diagnosed on pelvic-CT or bone scan.

This study analyzed only a small number of patients retrospectively. Partial salvage re-implantation for patients with biochemical failure after permanent brachytherapy was effective and safe. However, it is difficult to draw a conclusive result from such a population. A large clinical trial regarding such a treatment may be warranted. In that case, careful follow-up after re-irradiation is important, including prevention of constipation-reducing rectal toxicity [26], because a previous prospective phase II study on whole prostate salvage LDR brachytherapy after EBRT or brachytherapy reported 30% grade 3-4 GI toxicities and 13% grade 3-4 GU toxicities [27].

Conclusions

Partial salvage low dose rate brachytherapy for local recurrence after permanent prostate brachytherapy is well tolerated, with high biochemical response rates. This treatment can be not only a method to delay chemical castration but also a curative treatment option in cases of local recurrence of prostate carcinoma after seed implantation.