Patients treated with radical prostatectomy with positive digital rectal examination findings in the intermediate‑risk group are prone to PSA recurrence

  • Authors:
    • Nobuki Furubayashi
    • Takahito Negishi
    • Shintaro Ura
    • Jun Mutaguchi
    • Kenichi Taguchi
    • Mototsugu Shimokawa
    • Motonobu Nakamura
  • View Affiliations

  • Published online on: April 20, 2016     https://doi.org/10.3892/ol.2016.4485
  • Pages: 3882-3888
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Abstract

The present study aimed to evaluate the possibility of performing radical prostatectomy (RP) alone to achieve a radical cure for prostate cancer in the intermediate‑risk group. Samples were collected from 638 Japanese patients who underwent antegrade RP between August 1998 and May 2013; subsequently, 157 patients were excluded. According to the D'Amico criteria, the low‑, intermediate‑ and high‑risk groups comprised 107, 222 and 152 patients, respectively. The 5‑year prostate‑specific antigen (PSA) failure‑free survival rates in the low‑, intermediate‑, and high‑risk groups were 96.5, 88.9 and 72.6%, respectively (P<0.001; degrees of freedom=2). In the intermediate‑risk group, the difference in PSA failure‑free survival between the 0<PSA≤10 and 10<PSA≤20 ng/ml, and the biopsy Gleason score 6 and 7 groups were not statistically significant, according to the log‑rank test (P=0.2266 and P=0.1329, respectively). However, the difference in PSA failure‑free survival between the clinical tumor stage (cT)1c and cT2a/b groups was statistically significant based on the log‑rank test (P<0.0001). The results of the multivariate analysis revealed that, of the preoperative characteristics, only the cT was a significant predictor in patients with and without PSA failure (P<0.001). Therefore, patients classified into the intermediate‑risk group with cT2a/b stage, according to positive digital rectal examination findings, and are not considered to be likely to achieve a complete cure with RP surgery alone. In summary, for patients meeting these criteria in the intermediate‑risk group, RP surgery alone is likely to be insufficient, and other additional treatments may be considered subsequent to RP.

Introduction

Prostate cancer varies from insignificant lesions to locally advanced prostate tumors, even in cases without distant metastasis (1,2). Thus, it is necessary to develop a finer stage classification system in order to determine the most appropriate therapy for patients with prostate cancer that require more treatment options.

Diagnostic imaging is not as useful for prostate cancer as it is for other malignant tumors. Although digital rectal examination (DRE), ultrasound and magnetic resonance imaging are commonly used to evaluate the clinical tumor stage (cT), these diagnostic imaging modalities lack accuracy (35). By contrast, the prostate-specific antigen (PSA) level is an excellent tumor marker available for prostate cancer diagnosis (6). In addition, the grade of the tumor (Gleason score) can be determined using a prostate needle biopsy (7). Therefore, the disease stage is classified using multiple factors. The risk classification of prostate cancer corresponds with this concept, with the D'Amico classification being the most widely used (8). According to the D'Amico criteria, for convenience, the intermediate-risk group includes patients with cT2b lesions, a biopsy Gleason score (bGS) of 7 or a PSA level of >10 to ≤20 ng/ml. In the D'Amico classification, cases that do not belong to the low-risk or high-risk groups are also assigned to the intermediate-risk group. As a result, the breadth of cases included in the intermediate-risk group is wide.

In the low-risk group, there is a high probability that prostate cancer is localized in the prostate, and this group is considered most likely to achieve a cure with radical prostatectomy (RP) alone. By contrast, RP for patients in the low-risk group also presents the possibility of over-treatment (9). Conversely, in the high-risk group, radiation therapy in combination with endocrine therapy is common (10,11); however, there is no reason not to treat with RP (12). There is a high possibility, although lower than for the low-risk group, that RP will achieve a cure in the intermediate-risk group. When considering the control of cancer and postoperative quality of life, the intermediate-risk group may receive the most benefit from surgery.

Therefore, the present study assessed the outcomes of radical prostatectomy (RP) in Japanese intermediate-risk patients with prostate cancer who received no pre-surgical treatment. The possibility of achieving a complete cure with RP alone was evaluated.

Patients and methods

Patient characteristics and risk-group classification

Patients who underwent prostate biopsies and received a diagnosis of adenocarcinoma at the National Kyushu Cancer Center (Fukuoka, Japan) or additional associated institutions were assessed in the present study. Embedded whole-mount antegrade RP tissue specimens obtained from 638 patients who underwent RP between August 1998 and May 2013 were evaluated. The patients underwent pelvic lymph node dissection during the same time period. Of the specimens obtained, 157 patients were excluded from the study, including 151 patients due to a history of receiving hormonal therapy and 6 patients due to unclear biopsy or prostatectomy specimen findings. All patients were Japanese (median age, 66 years; range, 47–77 years), and the PSA levels ranged between 0.623 and 39.413 ng/ml (median, 7.491 ng/ml). The median follow-up period after surgery was 54.1 months.

The patients were classified into three risk groups according to the D'Amico criteria (3). The low-risk (stage T1c/T2a, PSA level ≤10 ng/ml and bGS of ≤6), intermediate-risk (stage T2b, bGS of 7 or PSA level between >10 and ≤20 ng/ml) and high-risk (stage T2c, PSA level >20 ng/ml or bGS of ≥8) groups comprised 107 (22.2%), 222 (46.2%) and 152 (31.6%) patients, respectively. The breadth of cases included in the intermediate-risk group was wide, therefore, the patients were subdivided according to factors for risk classification, including the PSA level, cT status and bGS. The PSA levels were divided into two subgroups of 0<PSA≤10 and 10<PSA≤20, the cT status was divided into two subgroups of cT1c and cT2a, and the bGS score was divided into two subgroups of bGS 6 and bGS 7. cT was diagnosed using only DRE. Two pathologists evaluated the degree of malignancy in the preoperative biopsy and RP specimens according to the 2005 International Society of Urological Pathology Consensus Conference on Gleason grading system (13) and determined the pathological stage based on the 2009 TNM classification (14).

Methods

The whole-organ prostate specimens obtained by RP were fixed in 15% neutral-buffered formalin (Wako Pure Chemical Industries, Ltd., Osaka, Japan) for 48–96 h, and were serially sectioned perpendicular to the rectal surface at 5-mm intervals. Sections that were predominantly caudal and cephalic were cut in the sagittal plane at 5-mm intervals in order to assess the bladder neck and apical margins. The specimens were subsequently embedded in paraffin (Merck KGaA, Darmstadt, Germany), cut into 5-µm sections and stained with hematoxylin and eosin (Sakura Finetek Japan, Co., Ltd., Tokyo, Japan). Extraprostatic extension (EPE) was defined as the extension of the tumor from the prostate to the periprostatic soft tissue. The presence of tumor cells at the stained resection margin (RM) was defined as a positive RM. The follow-up schedule after RP involved a PSA assay performed using ARCHITECT® Automated Immunoassay Analyzer, ARCHITECT Total PSA Calibrators (catalog no., 7K70-01) and ARCHITECT Total PSA Controls (catalog no., 7k70-10) (Abbott Japan Co., Ltd., Chiba, Japan) every 3 months for the first 2 years, followed by every 4 months for the next 3 years and every 6 months thereafter. Disease recurrence and/or PSA failure were defined as the detection of a serum PSA level of >0.2 ng/ml, or the use of RP if the PSA level did not decrease to <0.2 ng/ml following surgery. A number of patients who underwent RP were subsequently treated with radiation and/or hormone therapy before the serum PSA level exceeded 0.2 ng/ml. Therefore, in these patients, the time point of adjuvant therapy was defined as the date of disease recurrence. All patients provided their written informed consent to participate in this study, and the study protocol was approved by the ethics committee of the National Kyushu Cancer Center.

Statistical analysis

Statistical analysis was performed using the JMP Pro software package (version 11.0.0; SAS Institute, Inc., Cary, NC, USA). The PSA failure-free survival rate was determined according to the Kaplan-Meier method, and the significance of clinicopathological parameters associated with PSA failure was assessed using the Cox proportional hazards regression model. The log-rank test was used to determine differences between the risk groups. P<0.05 was considered to indicate a statistically significant difference.

Results

Clinicopathological characteristics according to risk group

The clinicopathological characteristics of the three risk groups are shown in Table I. According to the D'Amico criteria, the low-risk group, intermediate-risk group and high-risk group each contained 107 (22.2%), 222 (46.2%) and 152 (31.6%) patients, respectively. No differences were observed in the age of the patients between the groups. Based on the RP Gleason score, 9.3% (10/107), 15.3% (34/222) and 42.1% (64/152) of the patients in the low-, intermediate- and high-risk groups had high-grade (bGS ≥8) tumors, respectively. A total of 17.8% (19/107), 35.1% (78/222) and 54.0% (82/152) of patients in the low-, intermediate- and high-risk groups had a pathological stage of ≥T3, respectively. Furthermore, lymph node involvement was observed in 1 patient in the low-risk group, 5 patients in the intermediate-risk group and 7 patients in the high-risk group.

Table I.

Clinicopathological characteristics according to the risk group classification.

Table I.

Clinicopathological characteristics according to the risk group classification.

Risk group

CharacteristicLowIntermediateHigh
Total patients, n107222152
Median age (range), years66 (47–77)66 (57–76)67 (48–77)
cT, n (%)
  1c84 (78.5)157 (70.7)77 (50.7)
  2a/b23 (21.5)65 (29.3)47 (30.9)
  2c21 (13.8)
  37 (4.6)
Preoperative PSA, n (%)
  ≤10 ng/ml107 (100)151 (68.1)83 (54.6)
  10≤20 ng/ml71 (31.9)36 (23.7)
  >20 ng/ml33 (21.7)
Biopsy Gleason score, n (%)
  ≤6107 (100)19 (8.6)8 (5.2)
  7203 (91.4)27 (17.8)
  ≥8117 (77.0)
RP Gleason score, n (%)
  ≤645 (42.1)18 (8.2)6 (3.4)
  752 (48.6)170 (76.5)82 (53.9)
  ≥810 (9.3)34 (15.3)64 (42.1)
pT, n (%)
  2a/b18 (16.8)27 (12.2)9 (5.9)
  2c70 (65.4)117 (52.7)61 (40.1)
  3a17 (15.9)71 (32.0)64 (42.1)
  3b2 (1.9)7 (3.1)18 (11.9)
EPE, n (%)17 (15.9)66 (29.7)65 (42.8)
Positive RM, n (%)13 (12.1)45 (20.3)35 (23.0)
sv, n (%)2 (1.9)7 (3.2)18 (11.8)
pN, n (%)1 (0.9)5 (2.3)7 (4.6)

[i] Clinical and pathological staging was based on the 2009 TNM classification; Gleason grading based on the 2005 International Society of Urological Pathology Consensus Conference. P<0.05 was considered to indicate a statistically significant difference. cT, clinical tumor stage; PSA, prostate-specific antigen; RP, radical prostatectomy; pT, pathological tumor stage; EPE, extraprostatic extension; RM, resection margin; sv, seminal vesicle invasion; pN, pathological lymph node metastasis.

PSA failure-free survival rates according to the risk group classification

The 5-year PSA failure-free survival rates in the low-, intermediate- and high-risk groups were 96.5, 88.9 and 72.6%, respectively (Fig. 1). The difference between the low- and intermediate-risk groups was statistically significant, according to the log-rank test (P=0.0113). In addition, the difference between the intermediate- and high-risk groups was statistically significant, according to the log-rank test (P=0.0004).

Correlations between clinicopathological characteristics and PSA failure in the intermediate-risk group

The correlations between clinicopathological characteristics and PSA failure in the intermediate-risk group are shown in Table II. According to Cox proportional hazards analysis in this group, cT was the only preoperative variable that was a significant predictor of PSA failure (P<0.001), whereas the postoperative variables of RP Gleason score, pathological tumor stage, EPE, seminal vesicle invasion and positive lymph nodes were found to be significant predictors, based on the univariate analysis.

Table II.

Correlations between the clinicopathological characteristics and PSA failure in the intermediate-risk group.

Table II.

Correlations between the clinicopathological characteristics and PSA failure in the intermediate-risk group.

VariableHazard ratioP-value95% CI
Univariate analysis
  Age, <70 vs. ≥70 yearsa1.1800.7050.518–3.022
  PSA, 0–10 vs. >10–20 ng/mla1.6250.2420.709–3.551
  cT, 1c vs. 2a/ba10.274<0.0014.350–28.227
  RP Gleason score, ≤7 vs. ≥83.1880.0101.354–7.020
  pT, 2 vs. 33.6270.0011.653–8.516
  EPE, 0 vs. 13.2400.0031.470–7.240
  RM, 0 vs. 11.1980.7030.438–2.816
  sv, 0 vs. 16.3780.0061.834–17.017
  pN, 0 vs. 118.860<0.0014.207–62.156
Multivariate analysis
  Age, <70 vs. ≥70 yearsa1.6550.2450.718–4.279
  PSA, 0–10 vs. >10–20 ng/mla1.2370.6360.494–2.872
  cT, 1c vs. 2a/ba11.481<0.0014.754–32.310
  RP Gleason score, ≤7 vs. ≥81.7280.2370.684–4.074
  pT, 2 vs. 32.3490.0681.001–5.717
  EPE, 0 vs. 12.2520.0611.033–5.063
  RM, 0 vs. 11.6140.3340.581–3.875
  sv, 0 vs. 18.5380.0032.383–24.473
  pN, 0 vs. 12.9140.1990.529–12.559

a Preoperative variable. Clinical and pathological staging was based on the 2009 TNM classification system; Gleason grading based on the 2005 International Society of Urological Pathology Consensus Conference. P<0.05 was considered to indicate a statistically significant difference. PSA, prostate-specific antigen; cT, clinical tumor stage; RP, radical prostatectomy; pT, pathological tumor stage; EPE, extraprostatic extension; RM, resection margin; sv, seminal vesicle invasion; pN, pathological lymph node metastasis; 0, negative; 1, positive; CI, confidence interval.

In the multivariate analysis, statistically significant differences were observed for the cT stage (P<0.001) and seminal vesicle invasion (P=0.003) in the patients with and without PSA failure.

PSA failure-free survival rates according to PSA subgroups in the intermediate-risk group (Fig. 2)

Based on the range of the PSA level, the intermediate-risk group was divided into two subgroups with values of 0<PSA≤10 and 10<PSA≤20 ng/ml. A value of 10<PSA≤20 ng/ml was identified in 31.9% (71/222) of the patients. The 5-year PSA failure-free survival rates in the 0<PSA≤10 and 10<PSA≤20 ng/ml groups were 91.7 and 82.5%, respectively, although the difference between these groups was not statistically significant according to the log-rank test (P=0.2266).

PSA failure-free survival rates according to the bGS subgroups in the intermediate-risk group (Fig. 3)

Based on the bGSs, the intermediate-risk group was divided into two subgroups of bGS 6 and 7. A bGS of 6 was identified in only 8.6% (19/222) of the patients, and there were no cases of PSA failure (100% 5-year PSA failure-free survival). The 5-year PSA failure-free survival rate in the bGS 7 group was 87.9%, and the difference between the bGS 6 and bGS 7 groups was not statistically significant according to the log-rank test (P=0.1329).

PSA failure-free survival rates based on the primary Gleason pattern in the bGS 7 subgroup within the intermediate-risk group (Fig. 4)

In the intermediate-risk group, a bGS of 7 was identified in 91.4% (203/222) of the patients, and bGSs of 3+4 and 4+3 were identified in 128 and 74 patients, respectively. Only 1 patient had a bGS of 5+2. The 5-year PSA failure-free survival rates in the bGS 3+4 and 4+3 groups were 92.7 and 79.9%, respectively, and the difference between the bGS 3+4 and 4+3 groups was statistically significant according to the log-rank test (P=0.0298).

PSA failure-free survival rates according to the cT subgroups in the intermediate-risk group (Fig. 5)

The cT was diagnosed using only DRE. In the intermediate-risk group, a cT2a/b status was identified in 29.3% (65/222) of the patients. The 5-year PSA failure-free survival rates in the cT1c and cT2a/b groups were 94.0 and 76.4%, respectively, and the difference between the cT1c and cT2a/b groups was statistically significant according to the log-rank test (P<0.0001).

Discussion

RP is selected as a treatment for prostate cancer to achieve a cure by resecting the cancer lesion. However, depending on the patient's clinical condition, it may be difficult to resect the prostate cancer completely and/or distant metastasis may develop even if the entire local prostate tumor is successfully resected. This treatment is considered to be successful if the postoperative PSA level remains stable at a low value. Therefore, it is understood that RP should be performed in cases with a low likelihood of PSA recurrence. However, surgical intervention may result in overtreatment when the indication for surgery is limited to only patients whose clinical condition is not likely to lead to PSA failure, as other treatments are expected to have equivalent outcomes, and certain types of prostate cancer may be monitored with active surveillance or a ‘watchful waiting’ strategy.

According to the 2012 version of the clinical practice guidelines for prostate cancer in Japan (15), RP is recommended for patients who are not expected to develop PSA recurrence, such as those with a bGS ≤7, a PSA level of <10 ng/ml and a cT of cT1c-T2c. This guideline is based on the results of a variety of prognostic studies with large RP samples (1619), although these studies were retrospective. However, there is no definitive reason as to why RP is should not be used, even in high-risk cases of PSA recurrence (2023). In other words, a complete cure with surgery alone is possible in these cases.

In patients with prostate cancer, as in other malignancies, it is important to assess the degree of malignancy and determine the prognosis in order to select the appropriate treatment. Risk classification, the grouping of patients based on several clinical factors, is widely used in the clinical setting. Several pre-treatment risk classification models for prostate cancer have been proposed to date, with the D'Amico classification being the most widely applied (8). However, in the D'Amico classification, cases that do not belong to the low-risk or high-risk groups are assigned to the intermediate-risk group. Hence, the range of cases included in the intermediate-risk group is wide.

Therefore, the present study aimed to assess the outcomes of RP in intermediate-risk Japanese patients who received no pre-surgical treatment in order to investigate the possibility of achieving a complete cure with RP alone. According to the D'Amico criteria, indicated in Table I, the low-, intermediate- and high-risk group each contained 107 (22.2%), 222 (46.2%) and 152 (31.6%) patients, respectively. Based on the bGS, high-grade (bGS ≥8) tumors were only noted in patients in the high-risk group (77.0%; 117/152); by comparison, high-grade RP Gleason scores were observed in 9.3% (10/107), 15.3% (34/222) and 42.1% (64/152) of the patients in the low-, intermediate- and high-risk groups, respectively, which emphasizes that high-grade Gleason scores may be present in a proportion of patients of in the intermediate-risk group.

The present study determined the cT classification based on only the results of the DRE, in accordance with the original study by D'Amico et al (8). The PSA failure-free survival rates for each risk group are shown in Fig. 1. The 5-year PSA failure-free survival rates in the low-, intermediate- and high-risk groups were 96.5, 88.9 and 72.6%, respectively (Fig. 1). The difference between the intermediate- and high-risk groups (P=0.0004), and the difference between the intermediate- and low-risk groups (P=0.0113) were statistically significant according to the log-rank test. The results indicate that the rate of a complete cure with RP alone in the intermediate-risk group was lower than that observed in the low-risk group and higher than that observed in the high-risk group.

In addition, correlations between clinicopathological characteristics and PSA failure were examined in the intermediate-risk group (Table II). There were no cases of PSA failure among the bGS 6 cases, therefore, the preoperative variable of bGS was not analyzed in the univariate or multivariate Cox proportional hazards regression model. According to the results of multivariate analysis, cT was the only significant predictor in the patients with and without PSA failure (P<0.001) among the preoperative variables. Univariate and multivariate analyses did not reveal any other statistically significant differences in the preoperative variables, including the preoperative PSA level (P=0.242), which is a component of the risk profile in the D'Amico risk classification. The postoperative variables of RP Gleason score, pathological tumor stage, EPE and positive lymph nodes were found to be significant predictors based on the univariate analysis (P=0.010, P=0.001, P=0.003 and P<0.001, respectively), while the only postoperative variable identified to be a significant predictor in the univariate and multivariate analyses was seminal vesicle invasion (P=0.006 and P=0.003, respectively). However, the intermediate-risk group included only cases that did not belong to the low- or high-risk groups; as a result, the breadth of cases included in the intermediate-risk group was unexpectedly wide. Therefore, additional analyses were performed in the intermediate-risk group, including factors used for risk stratification, such as the PSA level, bGS and cT status.

First, the patients were divided into two groups based on the PSA values: 0<PSA≤10 and 10<PSA≤20 ng/ml (Fig. 2). Values of 0<PSA≤10 and 10<PSA≤20 ng/ml were identified in 68.1% (151/222) and 31.9% (71/222) of the patients, respectively. Pathological organ-confined disease is known to occur in 80% of patients with a PSA level <4.0 ng/ml, 66% of those with a PSA level between 4.0 and 10.0 ng/ml and <50% of those with a PSA level >10.0 ng/ml (24,25). Therefore, it is expected that the rate of organ-confined disease decreases as the PSA value increases and, thus, the risk of recurrence increases. Compared with that observed in the low-risk group, the intermediate-risk group demonstrated a wide range of PSA values according to the D'Amico risk classification. However, the 5-year PSA failure-free survival rates in the 0<PSA≤10 and 10<PSA≤20 ng/ml groups were 91.7 and 82.5%, respectively, and the difference between the 0<PSA≤10 and 10<PSA≤20 ng/ml groups was not statistically significant according to the log-rank test (P=0.2266).

Next, the patients were divided into two groups based on the bGS: bGS 6 and bGS 7 (Fig. 3). bGS 6 was identified only in 8.6% (19/222) of the patients and bGS 7 was identified in 91.4% (203/222) of the patients. There were no episodes of PSA failure in the bGS 6 group (PSA failure-free survival rate, 100%), and the 5-year PSA failure-free survival rate in the bGS 7 group was 87.9%. The difference between the bGS 6 and 7 groups was not statistically significant according to the log-rank test (P=0.1329). This result is considered to be a contributory factor to the lack of PSA failure among bGS 6 cases. Furthermore, the bGS 7 pattern is additionally considered to be a contributory factor, as the intermediate-risk group consisted largely of patients with a bGS 7 score. According to the bGS 7 pattern in the intermediate-risk group, the bGS 3+4 and 4+3 subgroups contained 128 (63.1%) and 74 (36.5%) patients, and the bGS 5+2 subgroup contained 1 patient. In the present study, among all of the bGS7 cases, excluding the single case of bGS 5+2, the 5-year PSA failure-free survival rates in the bGS 3+4 and 4+3 groups were 92.7 and 79.9%, respectively (Fig. 4). The difference between the bGS 3+4 and 4+3 groups was statistically significant according to the log-rank test (P=0.0298).

Although numerous grading systems exist for evaluating prostate adenocarcinoma, the Gleason grading system is the most widely accepted (26). The Gleason system is based on the glandular pattern of the tumor, as identified at relatively low magnification; cytological features have no role in the grade of the tumor. The primary (predominant) and secondary (second most prevalent) architectural patterns are identified and assigned a grade between 1 and 5, with 1 being the most differentiated and 5 being the least differentiated. As both the primary and secondary patterns are influential for predicting the prognosis, the Gleason sum score is obtained by adding the primary and secondary grades. It is important to recognize Gleason pattern 4 tumors, as tumors with this pattern are associated with a significantly worse prognosis than those with pure Gleason pattern 3 (27,28). It has also been demonstrated in RP specimens that tumors with a Gleason score of 4+3=7 exhibit a worse prognosis than those with a Gleason score of 3+4=7 (29). These descriptions are consistent with the observations made in the present study.

Finally, the patients in the present study were divided into two groups based on the cT status: cT1c and cT2a/b. cT1c and cT2a/b was identified in 70.7% (157/222) and 29.3% (65/222) of the patients, respectively. Numerous imaging modalities are applied for staging prostate cancer; however, no technique is reliably sensitive for detecting extraprostatic disease. The inability to image microscopic disease limits the accuracy of current modalities (30). In the current study, the cT classification was determined based only on the results of DRE, in accordance with the original study by D'Amico et al (8). The 5-year PSA failure-free survival rates in the clinical cT1c and cT2a/b groups were 94.0 and 76.4%, respectively (Fig. 5), and the difference between the cT1c and cT2a/b groups was statistically significant according to the log-rank test (P<0.0001). An abnormal DRE was recently reported to be associated with an increased risk of detecting high-grade (Gleason score >7) prostate cancer lesions in a screened population (3134). These descriptions are consistent with the observations obtained in the present study.

In summary, the present study retrospectively assessed the outcomes of performing RP alone in Japanese patients with intermediate-risk prostate cancer based on the D'Amico risk classification. Patients classified into the intermediate-risk group with cT2a/b stage, based on positive DRE findings, are not considered to be likely to achieve a complete cure with RP surgery alone. Furthermore, the current findings for intermediate-risk group RP patients demonstrated that tumors with a bGS of 4+3=7 are associated with poorer PSA failure-free survival rates than those with a bGS of 3+4=7 in the bGS 7 group. Therefore, for patients meeting these criteria in the intermediate-risk group, RP surgery alone is likely to be insufficient, and other additional treatments may be considered subsequent to RP.

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June-2016
Volume 11 Issue 6

Print ISSN: 1792-1074
Online ISSN:1792-1082

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Spandidos Publications style
Furubayashi N, Negishi T, Ura S, Mutaguchi J, Taguchi K, Shimokawa M and Nakamura M: Patients treated with radical prostatectomy with positive digital rectal examination findings in the intermediate‑risk group are prone to PSA recurrence. Oncol Lett 11: 3882-3888, 2016
APA
Furubayashi, N., Negishi, T., Ura, S., Mutaguchi, J., Taguchi, K., Shimokawa, M., & Nakamura, M. (2016). Patients treated with radical prostatectomy with positive digital rectal examination findings in the intermediate‑risk group are prone to PSA recurrence. Oncology Letters, 11, 3882-3888. https://doi.org/10.3892/ol.2016.4485
MLA
Furubayashi, N., Negishi, T., Ura, S., Mutaguchi, J., Taguchi, K., Shimokawa, M., Nakamura, M."Patients treated with radical prostatectomy with positive digital rectal examination findings in the intermediate‑risk group are prone to PSA recurrence". Oncology Letters 11.6 (2016): 3882-3888.
Chicago
Furubayashi, N., Negishi, T., Ura, S., Mutaguchi, J., Taguchi, K., Shimokawa, M., Nakamura, M."Patients treated with radical prostatectomy with positive digital rectal examination findings in the intermediate‑risk group are prone to PSA recurrence". Oncology Letters 11, no. 6 (2016): 3882-3888. https://doi.org/10.3892/ol.2016.4485