|Year : 2014 | Volume
| Issue : 4 | Page : 410-417
Role of robot-assisted radical prostatectomy in the management of high-risk prostate cancer
Akshay Sood, Wooju Jeong, Deepansh Dalela, Dane E Klett, Firas Abdollah, Jesse D Sammon, Mani Menon, Mahendra Bhandari
Vattikuti Urology Institute, Henry Ford Hospital, Detroit, MI, USA
|Date of Web Publication||1-Oct-2014|
Vattikuti Urology Institute, Henry Ford Health System, 2799 W. Grand Boulevard, Detroit, Michigan, 48202
Source of Support: None, Conflict of Interest: None
| Abstract|| |
We aimed to evaluate the role of robot-assisted radical prostatectomy (RARP) in the management of high-risk prostate cancer (PCa), with a focus on oncological, functional and perioperative outcomes. Further, we also aimed to briefly describe our novel modification to conventional RARP that allows immediate organ retrieval and examination for intra-operative surgical margin assessment. A literature search of PubMed was performed for articles on the management of high-risk PCa. Papers written in English and concerning clinical outcomes following RARP for locally advanced and high-risk PCa were selected. Outcomes data from our own center were also included. A total of 10 contemporary series were evaluated. Biopsy Gleason score ≥ 8 was the most common cause for classification of patients into the high-risk PCa group. Biochemical failure rate, in the few series that looked at long-term follow-up, varied from 9% to 26% at 1 year. The positive surgical margin rate varied from 12% to 53.3%. Urinary continence rates varied from 78% to 92% at 1 year. The overall complication rates varied from 2.4% to 30%, with anastomotic leak and lymphocele being the most common complications. Long-term data on oncological control following RARP in high-risk patients is lacking. Short-term oncological outcomes and functional outcomes are equivalent to open radical prostatectomy (RP). Safety outcomes are better in patients undergoing RARP when compared with open RP. Improved tools for predicting the presence of organ-confined disease (OCD) are available. High-risk patients with OCD would be ideal candidates for RARP and would benefit most from surgery alone.
Keywords: Functional outcomes, High-risk, oncological outcomes, prostate cancer, robotics
|How to cite this article:|
Sood A, Jeong W, Dalela D, Klett DE, Abdollah F, Sammon JD, Menon M, Bhandari M. Role of robot-assisted radical prostatectomy in the management of high-risk prostate cancer
. Indian J Urol 2014;30:410-7
|How to cite this URL:|
Sood A, Jeong W, Dalela D, Klett DE, Abdollah F, Sammon JD, Menon M, Bhandari M. Role of robot-assisted radical prostatectomy in the management of high-risk prostate cancer
. Indian J Urol [serial online] 2014 [cited 2019 Jul 17];30:410-7. Available from: http://www.indianjurol.com/text.asp?2014/30/4/410/142067
| Introduction|| |
Prostate-specific antigen (PSA) screening was introduced in the US in the late 1980s for early detection of prostate cancer (PCa), and has resulted in both an increase in PCa diagnoses and an earlier identification of these tumors. Despite the downward stage migration associated with PSA testing and the growing number of low-risk and organ-confined (OC) tumors, roughly 14.8% and 3.5% of men with newly diagnosed PCa are currently found to have high-risk and locally advanced disease (cT3NX/+M0), respectively. , Although these proportions have declined when compared with the pre-PSA screening era, they remain significant and have remained relatively stable over the past decade. Those men with high-risk PCa at the time of presentation have increased rates of secondary therapy and metastasis and contribute disproportionately to PCa mortality. ,, Improved treatments for such men would have a significant positive impact on overall morbidity and mortality due to this disease.
There is no consensus on the ideal management of these high-risk PCa patients. Multiple challenges exist in optimally treating men with high-risk disease, including, but not limited to, the biologic behavior of the cancer and the lack of staging accuracy of current diagnostic tools; furthermore, breakdown of various nomograms at these extremes make prognostic and outcome assessment difficult.  Significant differences may exist within the high-risk group because patients may have anywhere from one to three high-risk features and yet be similarly classified. 
With robot-assisted radical prostatectomy (RARP) being increasingly utilized for PCa treatment, , in this review, we discuss oncological, functional and perioperative outcomes following RARP, the general role of surgery for the management of high-risk disease and technical modifications that may help improve patient outcomes.
| Materials and methods|| |
A literature search of PubMed was performed to retrieve all published articles on the management of high-risk PCa. We used the search terms "high-risk prostate cancer" AND "radical prostatectomy" OR "robotic radical prostatectomy." Papers written in English and concerning clinical outcomes following RARP for high-risk PCa were selected. Reference lists of retrieved papers were scrutinized for additional relevant articles. Outcomes data following RARP from our own center were also included.
[Table 1] summarizes the studies evaluating outcomes of RARP in high-risk PCa. We found 10 studies evaluating the role of RARP in high-risk PCa. All studies represent contemporary experiences and were published between 2008 and 2013. In 90% of the studies, data were collected prospectively and the mean cohort size was 104 patients (range 30-160 patients).
|Table 1: Summary of series evaluating outcomes after robot-assisted radical prostatectomy in patients with high-risk PCa|
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| Results and discussion|| |
Definition of high-risk PCa and epidemiology
High-risk PCa is characterized by the following criteria [D'Amico], either
- PSA value >20 ng/mL or
- Biopsy Gleason score (GS) of ≥8 or
- Clinical stage (cT) of T2c or above
- A combination of either of these. 
The National Comprehensive Cancer Network (NCCN) and UCSF Cancer of the Prostate Risk Assessment (UCSF-CAPRA) classifications are other widely used criteria for defining high-risk PCa [Figure 1]. NCCN differs from the D'Amico criteria with regard to the clinical stage assignment for high risk,  where clinical stage T3a or higher is considered high risk. In the UCSF-CAPRA classification,  points (0-4) are assigned to individual risk factors and a score of ≥6 is considered high-risk disease. Most studies included in the current review utilized D'Amico risk stratification (70.0%) for defining high-risk PCa. Nguyen et al. compared the predictive value of six different definitions of high-risk PCa (consisting of varying combinations of clinical stage, serum PSA and GS) and found 5-year and 10-year BCRFS to range from 36% to 58% and 25% to 43% respectively, concluding that BCRFS for high-risk PCa did not differ significantly regardless of the definition used. 
With respect to epidemiology, as mentioned previously, the overall incidence of high-risk PCa has decreased since the advent of PSA screening, and currently stands at 14.8% as compared with 40.9% in the late 1980s. At present, approximately 9.8%, 8.1% and 3.5% of men newly diagnosed with PCa present with GS ≥ 8, PSA > 20 ng/dL and cT ≥ T2c, respectively.  Accordingly, GS is currently the major factor determining patient assignment to the high-risk category, followed by PSA and then by clinical stage with 61.5%, 50.8% and 21.9% of high-risk patients having GS ≥ 8, PSA > 20 ng/dL and cT ≥ T2c, respectively.  This trend was evident in the current review as well, as in all the series reviewed that used > 1 risk factor to define high-risk PCa, 91.6-29.7% of patients had GS ≥ 8 and 30.0-15.9% had a PSA > 20 ng/dL [Table 1].
Literature review of outcomes following RARP in high-risk PCa patients
[Table 2] summarizes the oncological outcomes in patients with high-risk PCa. Long-term follow-up data were not available in all the series. In the studies that did assess long-term oncological control, the rate of biochemical recurrence (BCR) varied from 9% to 26% at 1 year. , At 3 years, it was between 14%  and 55%.  Sukumar et al. looked at the oncological outcomes of 4803 patients with PCa undergoing RARP, including 1556 patients with non-organ confined disease (OCD).  They demonstrated a BCR of 18.3% in this group of patients over a period of mean follow-up of 34.6 months (range 1-116.7 months). All studies used a PSA ≥ 0.2 ng/mL as the definition of BCR, except for Shikanov et al.,  who defined BCR as a PSA > 0.1 ng/mL and reported an 18% BCR rate at 1 year.
|Table 2: Summary of oncological outcomes in series looking at robot-assisted radical prostatectomy outcomes in patients with high-risk PCa|
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The positive surgical margin (PSM) rate varied from 12.0%  to 53.3%.  However, in most studies, the PSM rate was between 20% and 30%. ,,,,, The lymph node positivity rate was also widely variable, from 1.4% to 33.3% overall. A 33.3% positivity rate was reported by Yuh et al.  in their study specifically assessing the role of robotic-extended lymph node dissection in intermediate and high-risk PCa, and might reflect the most accurate lymph node involvement rate in this subset of patients. That being said, the PSM and the lymph node positivity results from these reports should be interpreted cautiously as many of these studies did not provide details on the protocol used for sampling radical prostatectomy (RP) specimens and the extent of lymph node dissection performed, both of which are well-know factors affecting the PSM rate  and lymph node positivity rate. , respectively.
These BCR and PSM rates are comparable to the results reported by Briganti et al. in their review of open RP (ORP) outcomes, where they found a mean BCR rate of 31% at 5 years and a mean PSM rate of 45% following ORP in patients with high-risk disease.  Harty et al. compared the PSM rates for open versus minimally invasive RP in 445 high-risk PCa patients and found that they were not significantly different: 52.9% in ORP, 50% in RARP and 41.4% in laparoscopic RP (LRP) (P = 0.13).  The PSM rate did not differ when comparing ORP with a combined group of RARP and LRP (P = 0.16). Similar results were seen by Pierorazio et al. when they compared 913 men undergoing open versus minimally invasive RARP and LRP for high-risk PCa at a single center over a 10-year period and found no significant difference in the PSM or BCR rates across the groups. 
Sukumar et al., in the study mentioned previously, looked at 99 patients with node-positive disease (N1), which, even though not strictly classified under high-risk PCa, represents an aggressive cohort with a relatively high risk of BCR.  In their series, this group had a mean PSA of 12.3 ng/mL; 46.5% of them had a biopsy GS of 8-10 and 15.2% had cT2c-cT3 disease. BCR for this cohort was 58.6% over a mean follow-up of 34.6 months (range 1-116.7 months). Actuarial 5-year BCR-free survival, metastasis-free survival and cancer-specific survival (CSS) were 26.3% (SE: 7.3), 77.7% (SE: 11.7) and 96.1% (SE: 2.7), respectively, for these patients with N1 disease.
[Table 3] summarizes the functional outcomes. The 12-month continence rates using a 0-1 safety pad definition varied from 78% to 92%. , Ou et al., using a 0 pad definition for continence, reported a 95% continence rate in men undergoing RARP for high-risk disease.  Potency rates varied from 52% to 60% at 12 months. , Rogers et al. reported a 33.3% potency rate at 26 months, but their study population was aged ≥ 70 years.  In select patients with high-risk disease who underwent bilateral nerve sparing, Ou et al. found potency rates of 71%. 
|Table 3: Summary of functional outcomes in series looking at robot-assisted radical prostatectomy outcomes in patients with high-risk PCa|
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[Table 4] provides details on the perioperative outcomes of RARP. The mean operative time was 168 min, with operative times ranging from 111 to 186 min and mean estimated blood loss was 189 mL (range 84-200 mL). Length of hospital stay (LOS) varied from 1 to 3.4 days. The overall complication rates ranged from 2.4% to 30%, although many series did not fulfill the Martin criteria requirement for reporting of complications,  and this could lead to underreporting of adverse events. The most common complications reported were urethrovesical anastomotic leaks in approximately 10% of the patients,  lymphocele (range 6.6-2.4%) , and deep venous thrombosis in approximately 3.3% of patients.  Rectal injuries were extremely rare. 
|Table 4: Summary of perioperative outcomes in a series looking at robot-assisted radical prostatectomy outcomes in patients with high-risk PCa|
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In a retrospective, propensity score-matched analysis comparing the perioperative outcomes of 1512 patients with high-risk PCa undergoing RARP versus ORP, Gandaglia et al. found no significant differences in complications (P = 0.6), PSM (P = 0.4) or additional therapy needed after surgery (P = 0.2) between patients treated with RARP and ORP.  In multivariable analyses, however, patients undergoing RARP were less likely to receive a blood transfusion (P = 0.002) or to experience a prolonged LOS (P = 0.001) compared with men treated with ORP.
Similar results were obtained by Punnen et al., who retrospectively analyzed oncological and perioperative outcomes of 410 patients undergoing ORP versus RARP at a single center and found that, beside a longer LOS, more blood loss and higher transfusion rate (all P = 0.01), more men undergoing RARP had a complete nerve-sparing procedure compared with men undergoing ORP (54% vs. 34%, P = 0.01).  Oncological outcomes measured, in terms of PSM and BCR-free survival, did not differ significantly between the two groups.
Role of surgery in high-risk PCa
Randomized studies specifically looking at the comparative effectiveness of different treatment modalities for high-risk PCa are lacking, but significant information may be gleaned from high-risk subsets of randomized controlled trials (RCTs) evaluating various treatment modalities for all-risk PCa. In the supplement to the landmark paper published by Wilt et al. in 2012 comparing RP versus observation for treatment of localized PCa, they performed a subset analysis of patients with high-risk PCa.  The subset analysis [Figure 2] showed that cancer-specific mortality (CSM) was greatly reduced in high-risk PCa patients who underwent RP versus those who underwent observation (11.5% vs. 20.0%, respectively, P = 0.05). The overall mortality was also lower in patients undergoing RP as compared with observation, although it was not statistically significant (55% vs. 59%, respectively, P = 0.25). Their subset analysis showed survival benefit after RP was greater in patients with high-risk PCa in comparison with patients with low-risk PCa. Similarly, Bill-Axelson et al. in their Scandinavian Prostate Cancer Group-4 RCT showed that patients who have high-risk PCa are benefited by surgery as compared with watchful waiting. 
|Figure 2: (a) Overall survival trend in patients with high-risk prostate cancer. (b) Cancer-specific survival trend in patients with high-risk prostate cancer (Adapted with permission from Supplementary Data to Wilt et al., 2012 New England Journal of Medicine. All rights belong to the Massachusetts Medical Society.)|
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In addition to the aforementioned RCTs, multiple other studies , substantiate the favorable outcomes of surgery for high-risk disease patients. A recent study by Briganti et al., which evaluated outcomes in 1366 patients after RP with 15 years of follow-up, found that the CSS was as high as 91.0% at 10 years.  Boorjian et al. in their study looking at the comparative effectiveness of RP vs. external-beam radiotherapy (EBRT) in high-risk PCa patients found that overall survival (OS) was significantly better in patients who underwent RP compared with patients who underwent EBRT with or without androgen-deprivation therapy (ADT) (RP OS: 77% compared with the patients who received EBRT + ADT OS: 67% or EBRT alone OS: 52%; P = 0.001).  Similarly, Abdollah et al.  showed that the 10-year CSM rates were significantly better in patients who underwent RP as compared with radiotherapy or observation (3.6%, 6.5% and 10.8%, respectively; P = 0.001).
RP offers several distinct advantages. First, and most importantly, it provides pathologic specimens for more accurate staging. Recent studies have shown that up to 35% of patients are staged inaccurately,  and up to 50% of high-risk, post-RP patients have more favorable disease on final pathological review.  Thus, RP allows clinicians to offer targeted therapy based on more accurate staging and to avoid morbidity associated with unnecessary adjuvant treatment. Second, RP provides excellent local cancer control. Inman et al. reported a recurrence rate of just 13% in men who underwent RP as compared with a recurrence rate of 41-61% in men who underwent EBRT.  Third, EBRT, which is considered the main alternative to RP, is associated with significant morbidity including late-onset erectile dysfunction, chronic bladder irritation, hemorrhagic cystitis, infertility, strictures, bowel/bladder incontinence and secondary risk of cancer [Ischia et al.,]. In addition, men undergoing RP are 3.5 times less likely to require ADT, and they also have significantly longer intervals of ADT-free survival compared with men undergoing EBRT.  ADT is associated with significant morbidity including hyperlipidemia, metabolic syndrome, diabetes, cardiovascular disease, anemia, osteoporosis, periodontal disease, infertility, sexual dysfunction, fatigue, hot flashes and/or cognitive deficits.  Finally, primary tumors play a significant role in tumor shedding and cytokine/growth factor production. Therefore, RP provides definitive tumor debulking (i.e. removal of the primary tumor) and may improve overall outcomes. 
These RCTs and cohort studies constitute level-1b and 2b evidence, respectively, and clearly demonstrate the beneficial role of surgery in high-risk PCa. Having said that, we should recognize that the high-risk PCa group is a heterogeneous group, as shown by Yossepowitch et al., Yossepowitch et al. compared eight high-risk subsets in nearly 6000 men undergoing RP and found varying rates of BCRFS, need for secondary therapy and metastatic progression, with 10-year PCa-specific mortality ranging from 3% to 11%.  Thus, patients falling under the umbrella of high-risk PCa should ideally be treated on a case-to-case basis, as a patient with high PSA and high GS but with an OCD would benefit most from surgery alone while a patient with non-OCD might benefit more from a non-surgical option.
This review demonstrates many points. First, outcomes following RARP for the management of high-risk PCa are equivalent to ORP in terms of functional and short-term oncological outcomes, but better in terms of safety outcomes. Second, RARP is an effective and safe option for select high-risk patients. Third, functional outcomes for patients with high-risk PCa are highly variable, and in general are inferior when compared with all-risk or low-risk PCa.  Fourth, surgery as part of a multimodal management strategy seems to offer the best survival rates as compared with other modalities alone or in combination, but there is a need for better stratification of these high-risk patients for their optimal management, which can only be achieved by devising better modalities of stage assessment and prediction of biological behavior of the disease utilizing various imaging and translational tumor markers, which are still in discovery and testing phase. At this time, it can be said that RARP is as effective as other available modalities, but may be the best choice for select patients with localized, high-risk PCa.
RARP for high-risk PCa - Our MORE technique
We recently developed a Modification to the Vattikuti Institute Prostatectomy technique ,,,, of RP, which allows immediate Organ Retrieval after excision for intra-operative Examination and frozen-section analysis (the MORE technique).
Briefly, with the help of a GelPOINT TM platform (Applied Medical, Rancho Santa Margarita, CA, USA), a hand-access platform, the excised RP specimen, is easily extracted without needing to undock the robot or any loss of pneumoperitoneum. The specimen is then examined on-table by the surgeon. Frozen-section biopsies may be taken from areas that appear suspicious for PSM on inspection and/or bimanual examination, and after carefully marking the samples for anatomical orientation they are sent for analysis. Biopsies that are positive or suspicious for cancer result in more tissue being removed. While waiting for the results of the frozen section analysis, the surgeon continues with lymph node dissection and hence there is no increase in the overall operative time.
With this technical modification, we showed an absolute risk reduction of 26.6% (P = 0.04) in the PSM rate in patients with pT3a disease. MORE is a promising technique and a prospective trial is currently underway in our institution.
| Conclusions|| |
There is substantial evidence to support that RP with or without robotic assistance achieves extremely favorable oncological outcomes in patients with high-risk PCa compared with other treatment modalities. In addition, patients who are considered to have high-risk disease are an internally heterogeneous group, and all patients should not be treated alike. The key is to predict which patients, despite having high-risk characteristics, may harbor OCD. The current literature suggests that at least 40%  of patients classified as high risk fall into this category, but the proportion may be as high as 80%.  With new nomograms specifically tailored for predicting OCD in high-risk disease patients,  and the improvement in the accuracy of magnetic resonance imaging technology in assessing nodal disease/non-OCD, patients with a high likelihood of having OCD, despite being high risk, would be ideal candidates for RP and would gain the most benefit from surgery alone.
| References|| |
|1.||Cooperberg MR, Lubeck DP, Mehta SS, Carroll PR. Time trends in clinical risk stratification for prostate cancer: Implications for outcomes (data from CaPSURE). J Urol 2003;170:S21-5. |
|2.||Gallina A, Chun FK, Suardi N, Eastham JA, Perrotte P, Graefen M, et al. Comparison of stage migration patterns between Europe and the USA: An analysis of 11 350 men treated with radical prostatectomy for prostate cancer. BJU Int 2008;101:1513-8. |
|3.||D'Amico AV, Whittington R, Malkowicz SB, Schultz D, Blank K, Broderick GA, et al. Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer. JAMA 1998;280:969-74. |
|4.||Rider JR, Sandin F, Andren O, Wiklund P, Hugosson J, Stattin P. Long-term outcomes among noncuratively treated men according to prostate cancer risk category in a nationwide, population-based study. Eur Urol 2013;63:88-96. |
|5.||Yossepowitch O, Eggener SE, Serio AM, Carver BS, Bianco FJ Jr., Scardino PT, et al. Secondary therapy, metastatic progression, and cancer-specific mortality in men with clinically high-risk prostate cancer treated with radical prostatectomy. Eur Urol 2008;53:950-9. |
|6.||Gallina A. Editorial comment on: Outcome of prostate cancer patients with initial PSA>or=20 ng/ml undergoing radical prostatectomy. Eur Urol 2007;52:1065-6. |
|7.||Yossepowitch O, Eastham JA. Radical prostatectomy for high-risk prostate cancer. World J Urol 2008;26:219-24. |
|8.||Trinh QD, Sammon J, Sun M, Ravi P, Ghani KR, Bianchi M, et al. Perioperative Outcomes of Robot-Assisted Radical Prostatectomy Compared With Open Radical Prostatectomy: Results From the Nationwide Inpatient Sample. Eur Urol 2012;61:679-85. |
|9.||Tsui C, Klein R, Garabrant M. Minimally invasive surgery: National trends in adoption and future directions for hospital strategy. Surg Endosc 2013;27:2253-7. |
|10.||Ou YC, Yang CK, Wang J, Hung SW, Cheng CL, Tewari AK, et al. The trifecta outcome in 300 consecutive cases of robotic-assisted laparoscopic radical prostatectomy according to D'Amico risk criteria. Eur J Surg Oncol 2013;39:107-13. |
|11.||Rogers CG, Sammon JD, Sukumar S, Diaz M, Peabody J, Menon M. Robot assisted radical prostatectomy for elderly patients with high risk prostate cancer. Urol Oncol 2013;31:193-7. |
|12.||Zugor V, Witt JH, Heidenreich A, Porres D, Labanaris AP. Surgical and oncological outcomes in patients with preoperative PSA>20 ng/ml undergoing robot-assisted radical prostatectomy. Anticancer Res 2012;32:2091-5. |
|13.||Lavery HJ, Nabizada-Pace F, Carlucci JR, Brajtbord JS, Samadi DB. Nerve-sparing robotic prostatectomy in preoperatively high-risk patients is safe and efficacious. Urol Oncol 2012;30:26-32. |
|14.||Sagalovich D, Calaway A, Srivastava A, Sooriakumaran P, Tewari AK. Assessment of required nodal yield in a high risk cohort undergoing extended pelvic lymphadenectomy in robotic-assisted radical prostatectomy and its impact on functional outcomes. BJU Int 2013;111:85-94. |
|15.||Yuh BE, Ruel NH, Mejia R, Wilson CM, Wilson TG. Robotic extended pelvic lymphadenectomy for intermediate- and high-risk prostate cancer. Eur Urol 2012;61:1004-10. |
|16.||Connolly SS, Cathcart PJ, Gilmore P, Kerger M, Crowe H, Peters JS, et al. Robotic radical prostatectomy as the initial step in multimodal therapy for men with high-risk localised prostate cancer: Initial experience of 160 men. BJU Int 2012;109:752-9. |
|17.||Jayram G, Decastro GJ, Large MC, Razmaria A, Zagaja GP, Shalhav AL, et al. Robotic radical prostatectomy in patients with high-risk disease: A review of short-term outcomes from a high-volume center. J Endourol 2011;25:455-7. |
|18.||Yee DS, Narula N, Amin MB, Skarecky DW, Ahlering TE. Robot-assisted radical prostatectomy: Current evaluation of surgical margins in clinically low-, intermediate-, and high-risk prostate cancer. J Endourol 2009;23:1461-5. |
|19.||Shikanov SA, Thong A, Gofrit ON, Zagaja GP, Steinberg GD, Shalhav AL, et al. Robotic laparoscopic radical prostatectomy for biopsy Gleason 8 to 10: Prediction of favorable pathologic outcome with preoperative parameters. J Endourol 2008;22:1477-81. |
|20.||Mohler JL, Armstrong AJ, Bahnson RR, Boston B, Busby JE, D'Amico AV, et al. Prostate cancer, Version 3.2012: Featured updates to the NCCN guidelines. J Natl Compr Canc Netw 2012;10:1081-7. |
|21.||Punnen S, Freedland SJ, Presti JC Jr, Aronson WJ, Terris MK, Kane CJ, et al. Multi-institutional Validation of the CAPRA-S Score to Predict Disease Recurrence and Mortality After Radical Prostatectomy. Eur Urol 2014;65:1171-7. |
|22.||Nguyen CT, Reuther AM, Stephenson AJ, Klein EA, Jones JS. The specific definition of high risk prostate cancer has minimal impact on biochemical relapse-free survival. J Urol 2009;181:75-80. |
|23.||Sukumar S, Rogers CG, Trinh QD, Sammon J, Sood A, Stricker H, et al. Oncological Outcomes after Robot-Assisted Radical Prostatectomy: Long Term Follow-up in 4,803 patients. British Journal of Urology International 2013. |
|24.||Iremashvili V, Lokeshwar SD, Jorda M, Pelaez L, Soloway MS. Prognostic implications of partial sampling of radical prostatectomy specimens: Comparison of 3 methods. J Urol 2013;190:84-90. |
|25.||Mattei A, Fuechsel FG, Bhatta Dhar N, Warncke SH, Thalmann GN, Krause T, et al. The template of the primary lymphatic landing sites of the prostate should be revisited: Results of a multimodality mapping study. Eur Urol 2008;53:118-25. |
|26.||Briganti A, Joniau S, Gontero P, Abdollah F, Passoni NM, Tombal B, et al. Identifying the best candidate for radical prostatectomy among patients with high-risk prostate cancer. Eur Urol 2012;61:584-92. |
|27.||Harty NJ, Kozinn SI, Canes D, Sorcini A, Moinzadeh A. Comparison of positive surgical margin rates in high risk prostate cancer: Open versus minimally invasive radical prostatectomy. Int Braz J Urol 2013;39:639-46. |
|28.||Pierorazio PM, Mullins JK, Eifler JB, Voth K, Hyams ES, Han M, et al. Contemporaneous comparison of open vs minimally-invasive radical prostatectomy for high-risk prostate cancer. BJU Int 2013;112:751-7. |
|29.||Martin RC 2 nd , Brennan MF, Jaques DP. Quality of complication reporting in the surgical literature. Ann Surg 2002;235:803-13. |
|30.||Gandaglia G, Abdollah F, Hu J, Kim S, Briganti A, Sammon JD, et al. Is Robot-Assisted Radical Prostatectomy Safe in Men with High-Risk Prostate Cancer? Assessment of Perioperative Outcomes, Positive Surgical Margins, and Use of Additional Cancer Treatments. J Endourol 2014;28:784-91. |
|31.||Punnen S, Meng MV, Cooperberg MR, Greene KL, Cowan JE, Carroll PR. How does robot-assisted radical prostatectomy (RARP) compare with open surgery in men with high-risk prostate cancer? BJU Int 2013;112:E314-20. |
|32.||Wilt TJ, Brawer MK, Jones KM, Barry MJ, Aronson WJ, Fox S, et al. Radical prostatectomy versus observation for localized prostate cancer. N Engl J Med 2012;367:203-13. |
|33.||Bill-Axelson A, Holmberg L, Filen F, Ruutu M, Garmo H, Busch C, et al. Radical prostatectomy versus watchful waiting in localized prostate cancer: The Scandinavian prostate cancer group-4 randomized trial. J Natl Cancer Inst 2008;100:1144-54. |
|34.||Spahn M, Joniau S, Gontero P, Fieuws S, Marchioro G, Tombal B, et al. Outcome predictors of radical prostatectomy in patients with prostate-specific antigen greater than 20 ng/ml: A European multi-institutional study of 712 patients. Eur Urol 2010;58:1-7. |
|35.||Walz J, Joniau S, Chun FK, Isbarn H, Jeldres C, Yossepowitch O, et al. Pathological results and rates of treatment failure in high-risk prostate cancer patients after radical prostatectomy. BJU Int 2011;107:765-70. |
|36.||Boorjian SA, Karnes RJ, Viterbo R, Rangel LJ, Bergstralh EJ, Horwitz EM, et al. Long-term survival after radical prostatectomy versus external-beam radiotherapy for patients with high-risk prostate cancer. Cancer 2011;117:2883-91. |
|37.||Abdollah F, Sun M, Thuret R, Jeldres C, Tian Z, Briganti A, et al. A competing-risks analysis of survival after alternative treatment modalities for prostate cancer patients: 1988-2006. Eur Urol 2011;59:88-95. |
|38.||Reese AC, Sadetsky N, Carroll PR, Cooperberg MR. Inaccuracies in assignment of clinical stage for localized prostate cancer. Cancer 2011;117:283-9. |
|39.||Ploussard G, Masson-Lecomte A, Beauval JB, Ouzzane A, Bonniol R, Buge F, et al. Radical prostatectomy for high-risk prostate cancer defined by preoperative criteria: Oncologic follow-up in national multicenter study in 813 patients and assessment of easy-to-use prognostic substratification. Urology 2011;78:607-13. |
|40.||Inman BA, Davies JD, Rangel LJ, Bergstralh EJ, Kwon ED, Blute ML, et al. Long-term outcomes of radical prostatectomy with multimodal adjuvant therapy in men with a preoperative serum prostate-specific antigen level>or=50 ng/mL. Cancer 2008;113:1544-51. |
|41.||Meng MV, Elkin EP, Latini DM, Duchane J, Carroll PR. Treatment of patients with high risk localized prostate cancer: Results from cancer of the prostate strategic urological research endeavor (CaPSURE). J Urol 2005;173:1557-61. |
|42.||Ischia J, Gleave M. Radical prostatectomy in high-risk prostate cancer. Int J Urol 2013;20:290-300. |
|43.||Kaplan RN, Rafii S, Lyden D. Preparing the "soil": The premetastatic niche. Cancer Res 2006;66:11089-93. |
|44.||Menon M, Bhandari M, Gupta N, Lane Z, Peabody JO, Rogers CG, et al. Biochemical Recurrence Following Robot-Assisted Radical Prostatectomy: Analysis of 1384 Patients with a Median 5-year Follow-up. Eur Urol 2010;58:838-46. |
|45.||Menon M, Tewari A, Peabody J. Vattikuti Institute prostatectomy: Technique. J Urol 2003;169:2289-92. |
|46.||Menon M, Tewari A, Baize B, Guillonneau B, Vallancien G. Prospective comparison of radical retropubic prostatectomy and robot-assisted anatomic prostatectomy: The Vattikuti Urology Institute experience. Urology 2002;60:864-8. |
|47.||Menon M, Shrivastava A, Kaul S, Badani KK, Fumo M, Bhandari M, et al. Vattikuti Institute prostatectomy: Contemporary technique and analysis of results. Eur Urol 2007;51:648-57. |
|48.||Menon M, Shrivastava A, Bhandari M, Satyanarayana R, Siva S, Agarwal PK. Vattikuti Institute prostatectomy: Technical modifications in 2009. Eur Urol 2009;56:89-96. |
|49.||Jeong W, Sood A, Ghani KR, Pucheril D, Sammon JD, Gupta NS, et al. Bimanual Examination Of The Retrieved Specimen And Regional Hypothermia During Robot-Assisted Radical Prostatectomy: A Novel Technique For Reducing Positive Surgical Margin And Achieving Pelvic Cooling. British Journal of Urology International Int 2013. |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4]