Radical prostatectomy versus brachytherapy for clinically localized prostate cancer on oncological and functional outcomes: a meta-analysis.

BACKGROUND: Prostate cancer (PCa) is a form of malignancy that harms the health status of elderly men worldwide. It is unclear which of radical prostatectomy (RP) or brachytherapy (BT) is the more effective treatment for PCa. This study presents the first highly comprehensive and up-to-date comparative analysis of the overall outcomes of RP versus BT.
METHODS: We conducted a systematic literature search for studies published on PubMed, EMBASE, and the Cochrane Library on the outcomes of RP versus BT in clinically localized PCa. The cumulative analysis was performed using Review Manager Version 5.3 software, and the Chi-square test was employed to test the statistical heterogeneity. The summary odds ratio (OR) and standard mean difference (SMD) was estimated using random effects models at 95% confidence intervals (CIs).
RESULTS: In total, 2 randomized, 2 prospective, and 21 retrospective comparative studies were included. No significant differences in biochemical recurrence rate (BCR) (OR: 1.24; 95% CI: 0.91, 1.68) and prostate cancer-specific mortality (PCSM) (OR: 1.62; 95% CI: 0.86, 3.04) between RP and BT were noted. With erectile dysfunction and urinary incontinence, BT was more protective than RP in both short-term post-operative reports (OR: 2.06; 95% CI: 1.15, 3.70 and OR: 4.62; 95% CI: 2.33, 9.16) and long-term patient outcome reports (SMD: -5.62; 95% CI: -13.81, 2.57 and SMD: -11.52; 95% CI: -18.32, -4.72).
CONCLUSIONS: BT and RP for PCa therapy pose comparable risks of PCSM and BCR, while BT is associated with a lower incidence of erectile dysfunction and urinary incontinence. This study tentatively confirms that BT is an alternative to RP for patients seeking a curative treatment with minimal risks of urinary incontinence and sexual dysfunction. 2020 Translational Andrology and Urology. All rights reserved.

Introduction

Prostate cancer (PCa) accounts for the highest number of newly diagnosed cancer cases among elderly men in developed countries (1). China and other developing countries are also recording annual increases in PCa incidence because of an upsurge in the aging population and changes in dietary patterns. PCa, therefore, represents a significant public global health concern (2). Unlike other forms of cancer, patients with localized PCa (characterized by the absence of an identifiable regional lymph node or distant metastasis) generally have a longer survival period (3). Consequently, the choice of an appropriate therapeutic strategy to reduce the risks of mortality and recurrence while improving the quality of life for PCa patients is of critical importance. According to the American National Academy of Medicine, the comparative efficiency of contemporary treatment options for localized PCa has been a top research priority (4). Currently, most of the patients diagnosed with prostate-specific antigen (PSA)-detected PCa undergo conventional radical treatment encompassing either RP or radiotherapy (5). Prostatectomy (RP) is the standard of surgical treatment of localized PCa and entails the removal of the prostate and seminal vesicles, with or without pelvic lymphadenectomy (6,7). Radiotherapy involves a combination of external-beam radiation therapy (EBRT), androgen deprivation therapy (ADT), and brachytherapy (BT) (8). Nevertheless, BT with implantation of radioisotopes such as iodine-125 or palladium-103 is regarded as the recommended alternative for PCa treatment. BT is given as a single dose and is cost-effective, making it a safe and feasible treatment option for outpatients (9). However, surveillance or active monitoring with deferred radical treatment is the most conservative option and can circumvent the need for an immediate and potentially unnecessary intervention (10). The lack of substantial information on the safety of this option, however, has limited its application. The Scandinavian Prostate Cancer Group 4 trial (SPCG-4) showed that RP decreased the risk of metastases and mortality rates from both PCa and any other cause (11). After an additional 3-year follow-up, the SPCG-4 was more confident that RP reduced the mortality rate of death PCa patients (12). However, the first randomized comparison of active monitoring and radical treatment by the Prostate Testing for Cancer and Treatment (ProtecT) reported that surgery was not effective for patients with PSA-detected cancer (1). Although radical treatment gives patients a survival advantage, it is associated with side-effects such as urinary incontinence and erectile dysfunction, which may have a long-term impact on the quality of life (4,13). To our knowledge, there is currently no sufficient evidence demonstrating the superiority of either RP or BT on both oncologic results and patient-reported outcomes (PRO). This study is thus the first highly comprehensive and up-to-date meta-analysis and systematic review on this subject.

Methods

Literature search

A systematic literature search was performed using reports published in PubMed, EMBASE, and Cochrane Library according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist (PRISMA). The search strategy involved a combination of the following medical subject headings (Mesh) keywords and free words: ((((prostate cancer) OR neoplasia) OR malignancy)) AND (((((((((((Prostatectomies) OR Prostatectomies, Suprapubic) OR Suprapubic Prostatectomies) OR Suprapubic Prostatectomy) OR Prostatectomy, Retropubic) OR Prostatectomies, Retropubic) OR Retropubic Prostatectomies) OR Retropubic Prostatectomy) OR "Prostatectomy" [Mesh])) AND ((((((((((((((((Radioisotope Brachytherapy) OR Curietherapy) OR Brachytherapy, Radioisotope) OR Plaque Therapy, Radioisotope) OR Radioisotope Plaque Therapy) OR Therapy, Radioisotope Plaque) OR Surface Radiotherapy) OR Radiotherapy, Surface) OR Radiotherapy, Intracavity) OR Intracavity Radiotherapy) OR Radiotherapy, Interstitial) OR Interstitial Radiotherapy) OR Radiotherapy, Implant) OR Implant Radiotherapy)) OR "Brachytherapy" [Mesh])). We also hand-searched the articles included in our reference list.

Selection and exclusion criteria

This study comprises publications that met the following criteria: (I) prospective or retrospective studies including full text or meeting abstract; (II) patients with localized PCa in the studies initially with RP or BT as major treatments; (III) studies providing data about the PRO and oncological outcomes of patients after BT or RP; (IV) articles published in English and involving human participants. The exclusion criteria were as follows: (I) reviews, abstracts, or letters; (II) studies with ambiguous results; (III) articles that could not be accessed. If either the timing or sources of the study population overlapped in 2 or more publications by the same authors, our review only included the most recent study or the study with the highest number of participants.

Quality assessment

Two reviewers (P Zhang and B Qian) independently assessed the quality of the study and the risk of bias of the included studies. The criteria detailed in the Cochrane Handbook 5.1.0 was used to evaluate randomized controlled trials (RCT), reporting of blinding, allocation concealment, withdrawals, and loss to follow-up. The nine-star Newcastle-Ottawa scale (NOS) quality assessment scale was used to evaluate the quality of comparative observational studies, for which a higher score indicated a better study quality (14). The quality of the research was estimated from the selection of study groups, comparability of groups, and assessment of outcomes; studies of the highest quality were awarded up to 9 stars. Any disagreements were resolved by consensus.

Data extraction

Data were independently retrieved by 2 investigators, P Zhang, B Qian. Any discrepancies between the 2 investigators’ tallies were settled by incorporating a third investigator, JW Shi. For each study included, we extracted information including the name of the first author, year of publication, study design, country, the number of study participants, the clinical stage of patients, the value of PSA, the number of PCa-specific mortalities (PCSMs), biochemical recurrence, urinary incontinence, sexual dysfunction, and PRO of urinary incontinence post-treatment. Biochemical recurrence (PSA >0.2 ng/mL for PR or PSA > nadir +2 ng/mL for BT) marked the primary endpoint of the study. The secondary endpoint was either urinary incontinence characterized by the need for one or more pads a day or sexual dysfunction defined by patients with postoperative International Index of Erectile Function (IIEF)-5 <17.

Statistical analysis

The odds ratio (OR) reflected the association between the choice of treatment and the risk of biochemical recurrence. The OR also indicated the association between the treatments and the risk of either urinary incontinence or sexual dysfunction. Review Manager Version 5.3 software (Cochrane Collaboration, Oxford, UK) designed for composing Cochrane Reviews, was employed for meta-analysis while the Chi-square test was used to assess statistical heterogeneity. The frequencies of biochemical recurrence, urinary incontinence, and erectile dysfunction following either prostatectomy or BT were determined using a fixed-effect pairwise meta-analysis. Random effects analysis was performed in case a significant statistical heterogeneity was observed. The I2 statistic was used as an indicator of percentage heterogeneity among studies and was interpreted as follows: I2<50%, low heterogeneity; 50–75%, moderate heterogeneity; >75%, high heterogeneity. The funnel plot asymmetry was used to assess the publication bias of a meta-analysis that included more than 10 studies.

Results

Following a screening of the available databases, 1,756 potentially relevant publications were identified, including 1,486 from PubMed, 121 from EMBASE, and 149 from Cochrane Library. In total, 18 articles identified as duplicate search results were omitted, 1,702 studies were excluded by scanning titles and abstracts, and full texts of 36 citations were obtained. All the remaining articles, including their respective references, were carefully read according to the predefined inclusion and exclusion criteria. Ultimately, 25 studies were selected for the present meta-analysis. A flow diagram detailing the literature selection process is shown in .

Figure 1

The flow chart of the selection process.

Clinical characteristics of included studies

A total of 2 RCT and 22 comparative observational studies were included in this analysis. In the studies, a total of 61,752 patients underwent primary radical treatment, with 45,002 being treated by RP and 16,750 by BT. Further characterization of the included studies is detailed in (15-29). All the studies were published within the last 2 decades. In terms of country of publication, 12 studies were conducted in the USA, while the remaining 13 studies were conducted in China, Spain, Italy, Canada, France, Germany, and The Netherlands. The number of participants in each treatment cohort varied from 93 to 41,395. The maximum follow-up period for most of the groups in the meta-analysis was 13 years; 6 studies followed up patients for 5 years, and 3 studies followed up for 6 years. The other studies followed up patients ranging from one and a half years to 12 years. Most of the included studies were retrospective with a low evidence level. As a result, additional statistical analysis based on these data was performed.

Table 1

Clinical characteristics of included studies

Study	Author	Year	Country	NOS	Follow-up, Y	Study type	Age		Clinical stage	PSA		Sample size
							RP	BT		RP	BT	RP	BT
1	Ramos et al.	1999	USA	6	7	RS	62±7	70	T1a-T2c	NA	NA	299	122
2	Wei et al.	2002	USA	5	4	PS	63.5±7.8	67.2±7.3	T1-T3	NA	NA	570	61
3	Anthony et al.	2003	USA	6	2	RS	60	62	T1c	NA	NA	299	186
4	Bradley et al.	2004	USA	5	1.5	RS	60.4	68.5	T1-T3	5.3	6.5	60	154
5	Miller et al.	2005	USA	6	4	RS	67.2	70.4	T1-T3	5.7	6.7	480	65
6	Potters et al.	2004	USA	7	7	RS	61.8	69.4	T1a-T2b	8.8	9.15	746	733
7	Sharkey et al.	2005	USA	7	12	RS	63.1	71.9	T1-T2	NA	NA	1177	281
8	Tward et al.	2006	USA	5	3.8	RS	66	69	T1c-T2b	NA	NA	34,758	6,637
9	Buron et al.	2007	French	5	2	RS	62.7±6.0	65.2±6.3	T1-T2	8.9±4.0	7.5±2.7	127	308
10	Colberg et al.	2007	USA	7	13	RS	59	67	T1c-T2	NA	NA	391	350
11	Frank et al.	2008	USA	5	3	RS	61	64	T1-T2	NA	NA	234	74
12	Ferrer et al.	2008	Spain	7	2	PS	64.0±5.5	66.9±6.5	T1c-T2a	7.9±3.3	6.9±2.3	134	275
13	Giberty et al.	2009	Italy	/	5	RCT	65.2	65.6	T1c-T3b	7.8	7.5	100	100
14	Walz et al.	2008	Germany	7	5	RS	NA	NA	NA	NA	NA	1,124	171
15	Andrew et al.	2010	USA	5	5	RS	62	69	T1-T2c	6.7	7.3	418	256
16	Pardo et al.	2010	Spain	5	3	PS	64.2±5.5	66±7.0	T1-T2	8.0±3.3	6.8±2.1	123	185
17	Crook et al.	2010	Canada	6	5	RS	59.4±5.9	61.4±6.2	NA	5.3±2.8	5.5±2.1	64	105
18	Arvold et al.	2011	USA	7	4.2	RS	62.9	71	T1c-T2c	NA	NA	2,935	5,902
19	Po Hui et al.	2016	China	7	5	RS	63.53±6.71	71.92±7.03	T1-T3a	16.08±23.38	23.34±20.4	97	161
20	Daniel et al.	2016	Canada	6	4	RS	61	64	T1-T2	5.78±2.63	5.77±2.39	254	321
21	Ronald et al.	2017	USA	5	2	RS	62±6.8	66±7.3	T1-T3	NA	NA	130	16
22	Giberti et al.	2017	Italy	/	2	RCT	62.6±6.0	63.0±5.4	T1c-T2a	6.6±1.9	7.2±2.5	77	79
23	Cristina et al.	2017	Spain	5	1	RS	60	64	NA	6.3	5.8	42	51
24	Marie Anne et al.	2018	The Netherlands	6	1	RS	66.7±5.4	65.4±5.7	T1-T2	NA	NA	152	39
25	Zhou et al.	2019	China	7	5	RS	65.28±6.49	73.41±5.21	T1c-T3a	NA	NA	211	218

RP, radical prostatectomy; BT, brachytherapy; NOS, Newcastle-Ottawa scale; Y, year; RCT, randomized controlled trial; RS, retrospective studies; PS, prospective study; PSA, prostate-specific antigen; NA, not available.

Quality of included studies

Cochrane collaborative tools were used to assess the risk of bias in the RCTs, and the results are presented in . The NOS score adapted for prospective and retrospective cohort studies ranged from 5 to 7. The results are displayed in . The overall quality of all the studies was medium, and the highest score was 9.

Figure 2

Risk of bias graph.

Figure 3

Risk of bias summary.

Prostate cancer-specific mortality (PCSM)

Out of the 25 studies included, only Arvold et al., Potters et al., and Tward et al. reported PCSM while the remaining 22 studies compared BCR, urinary incontinence rate, and erectile dysfunction rate between RP and BT groups. A total of 51,713 patients were included in the studies. The results of this study showed that the PCSM rates of the 2 groups were 1.1% for RP and 0.5% for BT (OR =1.62; 95% CI: 0.86–3.04), and there was no significant difference between the 2 groups (P=0.13, I2=59%) (). The funnel plot showed that there were no significant deviations in PCSM rates.

Figure 4

Forest plot of the PCSM rate between RP and BT. PCSM, prostate cancer-specific mortality; RP, radical prostatectomy; BT, brachytherapy.

Biochemical recurrence rate (BCR)

Estimation of the BCR of the 2 groups incorporated a total of 8,385 patients. The results showed that the BCR of the 2 groups was 16.8% and 15.9%, respectively (OR =1.24, 95% CI: 0.91–1.68, P=0.17). There was no statistically significant difference between the BCR of the 2 groups (P=0.17, I2=77%, ). To further explore the heterogeneity among studies investigating the patients with BCR after these 2 treatments, we performed meta-regression analysis across various factors, including the sample size and follow-up years of studies, and the time of the studies conducted, and we found these factors were not significantly associated with the heterogeneity (). The funnel plot in shows no significant deviation in BCR between the 2 groups.

Figure 5

Forest plot of BCR rate between RP and BT. BCR, biochemical recurrence rate; BT, brachytherapy.

Figure 6

The meta-regression for follow-up years and BCR rate. BCR, biochemical recurrence rate.

Figure 7

Funnel plot for primary outcome (BCR rate). BCR, biochemical recurrence rate.

Urinary incontinence rate

A total of 6 studies reported the urinary incontinence rate, and a total of 1,468 patients were enrolled in the reviews. The urinary incontinence rates in the RP and BT groups were 21.8% and 9.7%, respectively (OR =4.62; 95% CI: 2.33–9.16). Significant differences in the urinary incontinence rate of the 2 groups were recorded (P<0.0001, I2=48%, ).

Figure 8

Forest plot of the urinary incontinence rate between RP and BT. RP, radical prostatectomy; BT, brachytherapy.

Erectile dysfunction rate

The erectile dysfunction rate was obtained from 6 studies comprising a total of 1,001 patients. The meta-analysis showed that the erectile dysfunction rate in the RP and BT groups was 54.5% and 31.5%, respectively (OR =2.06; 95% CI: 1.15–3.70), and the difference between the 2 groups was statistically significant (P=0.002, I2=74%, ).

Figure 9

Forest plot of the erectile dysfunction rate between RP and BT. RP, radical prostatectomy; BT, brachytherapy.

PRO of urinary incontinence

The PRO of urinary incontinence using Expanded Prostate Cancer Index Composite (EPIC) scores between RP and BT had a standard mean difference of (SMD) of −11.52 (95% CI: −18.32–4.72). Significant differences in the EPIC scores of the 2 groups were recorded (P=0.0009, I2=87%, ).

Figure 10

Forest plot of the PRO of urinary incontinence. PRO, patient-reported outcomes.

PRO of sexual function

A total of 6 studies on PRO of sexual function were included in this meta-analysis. The results of this analysis showed that sexual function scores between the RP and BT groups had an SMD of −5.62 and a 95% CI of −13.82–2.57. There was no significant difference in sexual functionality between the 2 groups (P=0.18, I2=89%) ().

Publication biases

The BCR funnel plot for RP and BT is presented in . A general overview of the image indicated that the distribution of each study in the triangle was relatively symmetrical. To be certain, we also used the Begg’s test to evaluate and verify the statistical symmetry of the funnel plot by calculating the P value. The results are shown in . P<0.05 is regarded as a significant publication bias. The result reveals that the funnel plot was statistically symmetrical. There was, therefore, no significant publication bias in the study.

Figure 11

Forest plot of the PRO of sexual dysfunction. PRO, patient-reported outcomes.

Figure 12

Begg’s test for the studies investigating BCR rate. BCR, biochemical recurrence rate.

Discussion

PCa is the second most prevalent malignant tumor in men worldwide (30,31). Prostatectomy (RP), the current standard treatment for PCa patients, is highly effective in tumor control. However, RP has been associated with several adverse effects, such as the possibility of impaired sexual and urinary function, which decreases the quality of life for PCa patients (32). Consequently, several alternatives to PR, such as active surveillance, EBRT plus ADT, and BT, have been proposed. However, whether active surveillance improves the survival and quality of life of patients remains to be explored (1,12). The EBRT plus ADT treatment option has often been compared with RP, and various studies concluded that EBRT plus ADT could have the same tumor control effect as RP. This treatment option, however, demanded a long period of hospitalization and caused several complications including radiocystitis, urethrostenosis, intestinal dysfunction and irritability, and osteoporosis. Subsequently, some patients preferred the more convenient and economical BT which did not require hospitalization. BT was reported to have an oncologic control capacity similar to that of RP, and better functional preservation than RP, while different studies reported the opposite outcome (33). From the perspectives of most doctors, the relative merits of BT and RP have not yet been made apparent. This uncertainty motivated the design of our review which compared the effectiveness of BT and RP on tumor control and functional preservation. This study forms the first highly comprehensive and up-to-date meta-analysis that simultaneously compares the oncological and functional outcomes of these 2 treatments.

This meta-analysis compared the BCR and PCSM rates of patients treated by BT versus those treated by RP. No significant differences in both the BCR (OR: 1.24; 95% CI: 0.91, 1.68) and PCSM (OR: 1.62; 95% CI: 0.86, 3.04) between the 2 therapies were noted during the observation period. Previous studies have reported that BT selectively kills tumor cells with little effect on healthy tissues and was, therefore, a minimally invasive therapy for PCa. However, it has been reported that BT does not remove both the prostate gland and the surrounding potentially oncogenic tissues as thoroughly as RP does (34). Our findings indicated that BT was superior to RP on functional preservation. Our results revealed that patients treated via BT had much higher sexual dysfunction and urinary incontinence rates than those treated by BT in both short-term post-operative reports (OR: 2.06; 95% CI: 1.15, 3.70 and OR: 4.62; 95% CI: 2.33, 9.16) and long-term PRO (OR: −5.62; 95% CI: −13.81, 2.57 and OR: −11.52; 95% CI: −18.32, −4.72), which was consistent with the expectations of many urologists and radiologists. RP involving the removal of the prostate and seminal vesicles is highly demanding for both surgeons and patients. Even surgeons who have performed thousands of prostatectomies may still damage the neurovascular bundle which is crucial to urinary and sexual function. One reason for the difficulty of this treatment is the anatomical complexity of the neurovascular bundle potentially being be attached to the prostate. In this condition, the prostate cannot be removed entirely without damaging the neurovascular bundles (35). Even after strictly adhering to the nerve-sparing RP suggested by Walsh, about 30% of patients suffered sexual dysfunction after the surgery. The failure indicated that the surgeon’s knowledge about the anatomy of the neurovascular bundles was still insufficient, and the distribution of these bundles may not be limited to the side and back of the prostate, as described by Walsh (36). The neurovascular bundles could also be located at the front part of the prostate (37). For patients, at clinical stages, T2c, T3, or greater, or Gleason score >7, preservation of the neurovascular bundle was not recommended in cases where the positive margin could be found in the pathological report (38). Also, for patients where the preoperative evaluation allowed for the preservation of the neurovascular bundles, the localization of a tumor invasion on the pelvis fascia meant that neurovascular bundles should equally be removed (39). For this reason, it was difficult to protect the crucial neurovascular bundles during RP, especially due to the anatomical variations among patients. Other factors thought to be related to urinary incontinence include posterior fascia reconstruction, preservation of the bladder neck during surgery, and regular exercise of pelvic floor muscles (40). These factors further increase the complexity of RP, with surgeons expected to do their best to of preserve both the urinary and sexual functions of patients. On the contrary, BT provides a rapid dose diffusion at a distance from the radioactive source. As a result, the tissues surrounding the tumor are only exposed to limited doses of radiation and are thus protected from the immense damage that characterizes RP (41). A combination of these factors may explain why patients treated by BT could obtain better functional preservation than those treated with RP. To enhance the reliability and comprehensiveness of our study, we also integrated the PRO on the urinary incontinence and sexual function using EPIC scores. No significant differences between the 2 treatment options were observed in sexual function scores, but significant differences were observed in urinary incontinence scores. This may be explained by the fact that even though BT is a relatively minimally invasive treatment and causes less injury to the normal tissues compared to RP, the patients inevitably suffer from impairment in physical, cognitive, and social functions owing to persistent discomfort and complications such as bowel irritation which exert a negative effect on sexual function (22).

We included studies from different researchers treating patients in variable conditions, and a vast discrepancy was, therefore, predictable. Variations in age, race, and clinical stages of patients, preoperative serum concentration of PSA, the Gleason scores, preoperative urinary and sexual function, the surgeons’ expertise in RP, the forms of RP adopted by surgeons, and implantation quality of BT could all lead to diverse outcomes. It has been reported that the patients diagnosed with PCa at a younger age may have poorer tumor differentiation which may lead to an adverse prognosis (42). Another example is that the patients with clinical stage ≤ T2 were reported to have better outcomes in the BCR rate than that of patients with clinical stage ≥ T3 after RP (43). Moreover, after RP, the BCR rate for patients with Gleason scores of 4+3 was believed to be higher than that of patients with the Gleason scores of 3+4 (44). In addition, the forms of RP could be divided into intrafascial, interfascial, and extrafascial ones, sharing the same name but actually leading to distinct outcomes in tumor control and functional preservation (45). Compared to the laparoscope, the use of the da Vinci surgical robot for radical prostatectomy (RP) in some qualified hospitals may also generate variability, owing to sufficient exposure and a shorter learning curve (46). Another possible cause of this discrepancy could be the use of different statistical methods by the various researchers of our included studies. For instance, we observed different definitions of BCR. Some researchers reported that patients might experience BCR when PSA >0.5 ng/mL following BT, while others thought that PSA should exceed the PSA nadir +2.0 ng/mL. The observed discrepancy may contribute to a statistical difference and, thus, influence the findings of our study.

The present study indicates that BT is superior to RP in the preservation of urinary continence and sexual function, while it is similar in tumor control capacity; this does not suggest that BT is a perfect replacement for surgery since this study did not explore other aspects like the bowel irritation involved in these 2 treatments. Another additional factor that needs to be examined is the effect on the intestinal tract, mostly reported by patients receiving BT. Moreover, the studies included in this review are from 1999 to 2019, which was a significant period. Within these 2 decades, significant advances in both techniques and instrumentation have been achieved. Currently practicing urologists have, for instance, witnessed the transition from open RP to robotic-assisted RP, which offers better preservation of both urinary and sexual function. The outcomes of our study should, therefore, be verified by conducting larger RCTs that incorporate more contemporary techniques.

Limitations

There are several limitations to this study. Firstly, most of the included studies were either case series or prospective cohort studies, and both case-control and randomization were absent in most of the included studies. Secondly, irritation of the intestinal tract, another crucial complication of BT, was not involved in our article, but this factor can greatly influence the quality of life of patients. Owing to the lack of comparative data in this field, the conclusions of this study may be limited. Further standardized studies involving large cohorts and randomized design should, therefore, be conducted to obtain more accurate results.

Conclusions

BT for PCa was associated with a similar risk of PCSM and BCR compared with RP, and a lower incidence of sexual dysfunction and urinary incontinence. This study tentatively confirms BT as an alternative to RP for patients seeking a curative treatment with minimal risks of urinary incontinence and sexual dysfunction. Additionally, more large samples and multi-center studies with standardized reports of perioperative parameters and clinical outcomes are needed for further evaluation in the future.

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