| PATHOLOGICAL
EXTENSION OF PROSTATE CANCER AS DEFINED BY GLEASON SCORE ON BIOPSY
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MARCOS F. DALL’OGLIO,
ALEXANDRE CRIPPA, MARIO PARANHOS, LUCIANO J. NESRALLAH, KATIA R. LEITE,
MIGUEL SROUGI
Division
of Urology, Paulista School of Medicine, Federal University of Sao Paulo,
UNIFESP, Sao Paulo, SP, Brazil
ABSTRACT
Introduction:
Based on the importance of the Gleason score on the behavior of prostate
adenocarcinoma, this study attempts to predict the extension of prostate
adenocarcinoma pre-operatively, as defined by the Gleason score on biopsy,
in individuals who will undergo radical prostatectomy.
Materials and Methods: We selected 899 individuals
who underwent retropubic radical prostatectomy from 1988 to 2004. Clinical
and pathological data obtained in the preoperative period were retrospectively
analyzed through digital rectal examinations of the prostate, initial
serum PSA levels and pathological data provided by biopsy. The Gleason
score on biopsy was assessed and divided into 3 groups: 2 to 6, 7, and
8 to 10, and correlated with the possibility of the disease being confined
to the prostate.
Results: From the 899 selected patients,
654 (74%) showed Gleason scores of 2 to 6, 165 (18%) had a score of 7
and 80 (9%) had scores of 8 to 10 on biopsy. The likelihood of confined
diseases, extraprostatic extensions, invasion of seminal vesicles and
lymph nodal involvement were respectively: 74%, 18%, 8% and 0.8% for a
Gleason score of 2 to 6, 47%, 30%, 19% and 4% for a Gleason score of 7,
and 49%, 29%, 18% and 4% for a Gleason score of 8 to 10.
Conclusion: In patients who will undergo
radical prostatectomy due to prostate adenocarcinoma, a Gleason score
of 7 on biopsy shows the same behavior as a Gleason score of 8 to 10 in
relation to extension of disease.
Key
words: prostatic neoplasms; neoplasm staging; biopsy; needle;
pathology
Int Braz J Urol. 2005; 31: 326-30
INTRODUCTION
The
risk for progression of prostate cancer following radical prostatectomy
(RP) is predicted by Gleason score, and pathological and surgical margins
(1). The histological grade is regarded as a highly relevant prognostic
factor (2,3), and in tumors with high Gleason score, the disease is often
associated with aggressive biological behavior and risk of occult disease
(4,5). Attempting to determine the extension of the disease preoperatively
is fundamental, since even tumors with a high Gleason score, but in a
confined disease, present a disease-free outcome in 60% to 71% of cases
(6). It is known that the recurrence of prostate cancer is higher in individuals
with Gleason scores of 8 to 10 than with a score of 7, as defined by the
surgical specimen. In such cases, the disease is confined in 43.1% and
9.2% for Gleason 7 and 8-10 respectively (7).
Preoperative prediction of the extension
of the disease, which is determined by simply discriminating the Gleason
score in the histopathology of biopsy fragments, will allow us to anticipate
the possibility of extraprostatic disease in patients who will undergo
RP.
Since there are no accurate data establishing
if the Gleason score on biopsy could predict the location of prostate
cancer (confined versus extraprostatic), this study aimed to compare prostate
tumors with Gleason scores of 2 to 6, 7 and 8 to 10 as defined by biopsy,
and to verify the presence of extraprostatic disease following radical
prostatectomy through the pathological parameters of the surgical specimen.
MATERIALS
AND METHODS
We
retrospectively studied 961 patients undergoing retropubic radical prostatectomy
with bilateral selective iliac lymphadenectomy due to prostate adenocarcinoma,
in the period from September 1988 to December 2002. The patient age range
was from 40 to 83 years, with a mean age of 62.9 ± 7.4 years.
The study included patients whose medical
records indicated the total number of fragments removed on biopsy, the
number of fragments with cancer, Gleason score, PSA and pathological study
of the surgical specimen. Fifty-four patients who received neoadjuvant
treatment were excluded, as were another 8 who were diagnosed through
endoscopic resection of the prostate or transvesical prostatectomy, thus
totaling 899 patients. The mean PSA was 10.1 ± 7.7 ng/mL (ranging
from 0.3 to 72 ng/mL). In relation to clinical stage, 432 (48%) patients
were classified as T1c, 219 (24%) as T2a, 173 (19.3%) as T2b, 68 (7.6%)
as T2c and 7 (0.8%) as T3a. The mean percentage of affected fragments
was 41% ± 24% (ranging from 5% to 100%). The mean Gleason score
on biopsy was 5.8 ± 1.3.
Pathological
Assessment
All surgical specimens, consisting of prostate,
seminal vesicles and obturator lymph nodes, were assessed by the same
pathologist. Specimens were fixed in 10% formalin for 6 hours in average
and underwent a routine of measuring and weighing the gland on a digital
balance with 2 decimal places of precision. Thin transversal sections
were performed in the surgical margins relative to the bladder neck and
the prostate apex. Using the urethra as a reference, the remaining gland
had its margins stained with India ink, and was then sequentially sliced
each 0.3 millimeters. Eight to 10 sections from each lobe were included
for histological study. Seminal vesicles were sectioned at their base,
and longitudinal sections were subsequently made for histological examination.
Obturator lymph nodes were dissected and sliced for inclusion in the study.
The material underwent the usual processing
in preparation for microscopic examination, with dehydration in alcohol,
clearing in xylol and embedding in paraffin. Fragments were stained with
hematoxylin and eosin and then analyzed under a binocular light microscope.
The assessed parameters were:
Histological grade and Gleason score –
The Gleason histological classification was used for assessing tumor differentiation,
considering exclusively the acinar pattern.
Surgical margins – Positive margins
were defined as the presence of a tumor in the surgical transection margins,
as defined by the presence of India ink.
Infiltration of periprostatic tissue –
Invasion of fat tissue and periprostatic neurovascular plexus was considered
as non-confined disease.
Infiltration of seminal vesicles –
Involvement of seminal vesicles was considered only when the tumor invaded
their parenchyma, and not the adventitial area.
Lymph nodal metastases – Obturator
lymph nodes containing tumor are considered as positive metastases.
Statistical analysis was performed with
the qui-square test with values of p < 0.05 being defined as significant.
RESULTS
Table-1
summarizes the pathological data for the Gleason score on biopsy and the
location of prostate adenocarcinoma. Of the 899 selected patients, we
observed that 654 (73%) had a Gleason score of 2 to 6. Another 165 (18%)
presented a Gleason score of 7, and 80 (9%) had a Gleason score of 8 to
10, as identified by biopsy. Among the patients with a Gleason score of
7, 78 (47%) had organ-confined location, 50 (30%) presented extraprostatic
invasion, 31 (19%) had involvement of seminal vesicle and 6 (4%) showed
lymph nodal involvement. Those tumors with a Gleason score of 8 to 10
presented prostate-confined disease in 39 (49%) of patients, 23 of them
(29%) had extraprostatic disease and 3 (3%) showed lymph nodes affected
by the disease.
There was a significant difference only
when comparing Gleason scores of 2 to 6 with a 7 or an 8 to 10, with no
significant difference observed between the latter 2 groups.
COMMENTS
Our
study showed that in individuals undergoing prostate biopsy, the presence
of Gleason pattern 4 or 5 determines a risk of 51 to 53% for extraprostatic
disease in the surgical specimen.
Merely dividing the Gleason score into ranges
of 2 to 6 and 7 to 10 seems reasonable for predicting the extension of
disease, since in univariate analysis the behavior of a Gleason score
7 was statistically identical to the behavior of patients with Gleason
scores of 8 to 10. In our opinion, the similarity in findings of extraprostatic
disease between 7 and 8 to 10 can be explained by the presence of a pattern
of 4 or 5 (8), which is invariably present. Patients with up to 10% of
pattern 4 or 5 in the surgical specimen have more than a 70% probability
of becoming disease-free, while individuals with more than 50% of pattern
4 or 5 present progressive disease in 82% of cases (9).
The percentage of positive fragments on
biopsy correlates to tumor volume. Additionally, the presence of a 4 or
5 pattern in the surgical specimen also determines a worse prognosis concerning
outcome (10), however, as we have demonstrated, the chance of identifying
confined disease is the same for 7 and for 8 to 10. Moreover, we could
observe that patients with a Gleason score lower than 7 present a recurrence
of the disease in 13% of cases, and this rate approaches 60% with a Gleason
score between 7 and 10 (11). In our sample, we showed that 49% of individuals
with a Gleason score between 8 and 10 had confined disease, 19% had neoplastic
involvement of the seminal vesicles, and in only 8% of patients with a
score lower than or equal to 6 were the seminal vesicles affected by the
tumor. There is some controversy as whether a Gleason score of 7 has a
different outcome from a score of 8 to 10 in relation to confined disease
and recurrence (5). As we know, the Gleason score is composed of the 2
volumetrically prevalent patterns in the specimen, thus a Gleason score
of 7 can be 3 + 4 or 4 + 3. Since the percentage of pattern 4 influences
whether the disease is confined or not (10), studies comparing Gleason
scores of 7, 4 + 3 and 3 + 4 have been published. Chan et al. (12) observed
34.7% of confined disease in patients undergoing radical prostatectomy
with a Gleason score of 7 in the surgical specimen. However, the risk
of progression was 20% higher with scores of 4 + 3 than in the 3 + 4 group
after a 10-year follow-up. However, in order to obtain the results, many
of these studies derived from the surgical specimen and not from the biopsy
(5), which may not be equal if we calculate the difference between Gleason
scores of 3 + 4 and 4 + 3 from the biopsy fragments. A study conducted
by Grober et al. (13) demonstrated that there was no difference between
the 2 groups (3 + 4 and 4 + 3) of Gleason score 7 on biopsy in terms of
the disease being confined or not, having extraprostatic extension or
showing involvement of the seminal vesicles, which agrees with our data.
In fact, a score 7 on biopsy should take into account not only the first
score pattern, but PSA levels and the number of positive fragments on
biopsy as well (14); if we have 4 + 3 with 2 or less fragments affected
by tumor in 68.7% of patients, the disease will be confined. On the other
hand, if the score is 3 + 4 with more than 2 affected fragments, this
number will drop to 41.1%. These data have been confirmed by Peller et
al. (15) who, when comparing patients with Gleason scores of 7 and 100%
positive fragments on biopsy with a Gleason score of 8 and the same number
of positive fragments, were able to show agreement in 97% of cases for
predicting confined disease.
When comparing our results with Tefilli
et al. (7), we verified that when the Gleason score is between 2 and 6,
74% of the patients have confined disease versus 69% with non-confined
disease. On the other hand, with a score of 7, we see 47% versus 43%;
that is, quite similar values. However, when comparing patients with a
Gleason score between 8 and 10, we found 48.8% of patients with confined
disease versus only 9.2% with non-confined disease. This difference can
be explained by the fact that the mean PSA in patients with a score of
7 was 12 ng/mL versus 25 ng/mL in patients with a Gleason score between
8 to 10 (7). Epstein et al. (1) found a rate of confined disease of 30%
in men with a Gleason score of 7, and, of them, approximately 70% were
disease-free after 10 years.
In relation to a Gleason score ≥ 8,
we found 9.5% to 31% of patients with confined disease (7). It is relevant
that these patients had localized disease, because 82% of these individuals
are not likely to have recurrent disease during a 5-year follow-up, despite
the high Gleason score (16). Egan & Bostwick (17) demonstrated that
individuals with a Gleason score of 7 had confined disease in 48% of cases
versus 53% in men with a Gleason score of 8. In our study, we found 48.8%
of confined disease with a score between 8 and 10. As shown previously,
there is a wide variation in results when we attempt to use isolated parameters
for predicting confined disease, and this is due to several factors that
are involved in prostate adenocarcinoma. Since the construction of the
first nomogram for predicting confined disease using PSA, clinical stage
and Gleason score, more than one parameter is used in order to reduce
the probability of error (3).
CONCLUSION
It
is important to consider the presence of Gleason grade 4 or 5 on prostate
biopsy for planning the management of prostate cancer. In these cases,
the disease is organ-confined in the pathological examination of the surgical
specimen in only half the cases.
_____________
Adriana Sanudo
performed the statistical analysis.
REFERENCES
- Epstein JI, Pound CR, Partin AW, Walsh PC. Disease progression following
radical prostatectomy in men with Gleason score 7 tumor. J Urol 1998;
160:97-100; discussion 101.
- Lerner SE, Blute ML, Bergstralh EJ, Bostwick DG, Eickholt JT, Zincke
H: Analysis of risk factors for progression in patients with pathologically
confined prostate cancers after radical retropubic prostatectomy. J
Urol 1996; 156: 137-43.
- Partin AW, Yoo J, Carter HB, Pearson JD, Chan DW, Epstein JI, Walsh
PC. The use of prostate specific antigen, clinical stage and Gleason
score to predict pathological stage in men with localized prostate cancer.
J Urol 1993; 150: 110-4.
- Lau WK, Bergstralh EJ, Blute ML, Slezak JM, Zincke H: Radical prostatectomy
for pathological Gleason 8 or greater prostate cancer: influence of
concomitant pathological variables. J Urol 2002; 167: 117-22. Erratum
in: J Urol. 2004; 171: 811.
- Herman CM, Kattan MW, Ohori M, Scardino PT, Wheeler TM: Primary Gleason
pattern as a predictor of disease progression in Gleason score 7 prostate
cancer: a multivariate analysis of 823 men treated with radical prostatectomy.
Am J Surg Pathol 2001; 25: 657-60.
- Tefilli MV, Gheiler EL, Tiguert R, Banerjee M, Sakr W, Grignon D,
Wood DP Jr, Pontes JE: Role of radical prostatectomy in patients with
prostate cancer of high Gleason score. Prostate 1999; 39: 60-6.
- Tefilli MV, Gheiler EL, Tiguert R, Sakr W, Grignon DJ, Banerjee M,
Pontes JE, Wood DP Jr: Should Gleason score 7 prostate cancer be considered
a unique grade category? Urology 1999; 53:372-7.
- Pan CC, Potter SR, Partin AW, Epstein JI: The prognostic significance
of tertiary Gleason patterns of higher grade in radical prostatectomy
specimens: a proposal to modify the Gleason grading system. Am J Surg
Pathol. 2000; 24:563-9.
- Stamey TA, McNeal JE, Yemoto CM, Sigal BM, Johnstone IM: Biological
determinants of cancer progression in men with prostate cancer. JAMA
1999; 281: 1395-400.
- Rubin MA, Mucci NR, Manley S, Sanda M, Cushenberry E, Strawderman
M, et al.: Predictors of Gleason pattern 4/5 prostate cancer on prostatectomy
specimens: can high grade tumor be predicted preoperatively? J Urol
2001; 165: 114-8.
- Sakr WA, Tefilli MV, Grignon DJ, Banerjee M, Dey J, Gheiler EL, et
al.: Gleason score 7 prostate cancer: a heterogeneous entity? Correlation
with pathologic parameters and disease-free survival. Urology. 2000;
56: 730-4.
- Chan TY, Partin AW, Walsh PC, Epstein JI: Prognostic significance
of Gleason score 3+4 versus Gleason score 4+3 tumor at radical prostatectomy.
Urology. 2000; 56: 823-7.
- Grober ED, Tsihlias J, Jewett MA, Sweet JM, Evans AJ, Trachtenberg
J, et al.: Correlation of the primary Gleason pattern on prostate needle
biopsy with clinico-pathological factors in Gleason 7 tumors. Can J
Urol. 2004; 11: 2157-62.
- Makarov DV, Sanderson H, Partin AW, Epstein JI. Gleason score 7 prostate
cancer on needle biopsy: is the prognostic difference in Gleason scores
4 + 3 and 3 + 4 independent of the number of involved cores? J Urol.
2002; 167: 2440-2.
- Peller PA, Young DC, Marmaduke DP, Marsh WL, Badalament RA: Sextant
prostate biopsies. A histopathologic correlation with radical prostatectomy
specimens. Cancer 1995; 75:530-8.
- Mian BM, Troncoso P, Okihara K, Bhadkamkar V, Johnston D, Reyes AO,
et al.: Outcome of patients with Gleason score 8 or higher prostate
cancer following radical prostatectomy alone. J Urol. 2002; 167: 1675-80.
- Egan AJ, Bostwick DG. Prediction of extraprostatic extension of prostate
cancer based on needle biopsy findings: perineural invasion lacks significance
on multivariate analysis. Am J Surg Pathol. 1997; 21:1496-500.
_______________________
Received: February 1, 2005
Accepted after revision: May 5, 2005
_______________________
Correspondence address:
Dr. Marcos F. Dall’Oglio
Rua Barata Ribeiro, no. 398, 5o. Andar
Sao Paulo, SP, 01308 - 000, Brazil
Fax: + 55 11 3159-3618
E-mail: marcosdallogliouro@terra.com.br |