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Stages and prognosis of prostate cancer
Especially from the tumor spread results for treatment planning and prognosis important tumor stage. The individual prognosis depends on many factors and can be estimated using nomograms.

After the tests were completed, the clinical tumor spread according to the TNM-system dependent (see are investigation ) and the taken in prostate biopsy tissue histology (histological) assessed (see Classification ). Using the findings, you can make a classification in clinical (as determined by tests) tumor stages and groups with similar prognosis:

Staging
The clinical tumor stage is most easily cleaned after the tumor spread specify. This is usually done according to the TNM system, rarely by Whitmore-Jewett-American system (eg, T2b N0 M0 = B2, and details on both see the growth and spread ). A summary is understandable and easier to choose the right treatment and estimating prognosis:
  • Locally limited prostate cancer: T1-2 N0 M0
  • Locally advanced prostate cancer: T3-4 N0 M0
  • Metastatic (advanced) prostate cancer: T1-4 and N1 and / or M1
Another classification according to the tumor spread is in the TNM system included (according to UICC, 7th edition, 2009):
  • Stage I: T1 N0 M0 2a
  • Stage II: T2b-c N0 M0
  • Stage III: T3 N0 M0
  • Stage IV: T4 N0 M0 or T1-4 N1 M0 or T1-4 N0-1 M1
In other staging systems in addition to the tumor spread, other findings are included as the PSAvalue and the grade of tumor (its viciousness, see Classification ). This has been aimed to assess the prognosis better (see below).

Forecast
The position of an individual forecast (forecast) over the course of the disease is very difficult.It depends on numerous factors, including the age and health of the person concerned, the clinical tumor stage (see above), the biopsy report and the proposed treatment.
If left untreated, the disease usually continues slowly. The following table shows the average values ​​for the risk of metastases (secondary tumors) and for mortality (mortality) of untreated patients depending on the clinical tumor spread according to the TNM system (after R. Hautmann, H. Huland: Urology Springer, Heidelberg 2006. , p.233):

TNM stageMetastases
present at
Mortality (without treatment)
T1a0%2% in 5-10 years
T1b25%20% in 5-10 years
T2a15%20% in 5-10 years
T2c35%70% in 5-10 years
T350%75% in 5-10 years
N1-3, M1100%over 50% in 3 years
The histological findings of prostate biopsy contributes significantly to the prognosis and treatment planning. It also allows conclusions about the probable pathological TNM stage (would that observed after surgery). For a more favorable prognosis if treated properly speaking (for explanations see classification ):
  • Tumor type: Adenocarcinoma
  • Gleason score to 7a (= 3 +4)
  • Helpap grading to GIIa
  • Low or mäßiggradiges prostate cancer (low grade or intermediate grade)
  • Low number of positive (infected) Punching cylinders (small tumor)
  • Low proportion of the total tumor biopsy material (small tumor)
  • Unilateral involvement of the prostate
  • Large distance of the tumor to the prostate capsule
  • No tumor ingrowth into the nerve sheath (no perineural infiltration)
  • No tumor ingrowth into the seminal vesicles
When you combine the tumor spread according to the TNM system with the PSA level and the Gleason score, to allow groups with similar prognosis form (according to UICC, 7th edition, 2009, PSA level or Gleason score may be missing both not available, a grouping is not possible):
GroupTNMPSA (ng / ml)Gleason score
IT1a-cN0M0<10Up to 6
T2aN0M0<10Up to 6
IIAT1a-cN0M0<207
T1a-cN0M0As of 10 <20Up to 6
T2aN0M0As of 10 <20Up to 6
T2aN0M0<207
T2bN0M0<20Up to 7
IIBT2cN0M0Each valueEach value
T1-2N0M0As of 20Each value
T1-2N0M0Each valueFrom 8
IIIT3a-bN0M0Each valueEach value
IVT4N0M0Each valueEach value
T1-4N1M0Each valueEach value
T1-4N0-1M1Each valueEach value
The risk groups for progression of the tumor in locally confined prostate cancer see treatment planning .

Risk assessment with nomograms
To improve the individual prediction, known as nomograms have been developed. Here are lists or charts that help can predict the pathological (identified by operation) TNM stage and various treatment outcomes and survival probabilities based on examination findings. An illustration is omitted here because they are constantly being revised. There are numerous nomograms, the most important are:

Partin Tables: They serve the pathological TNM stage predict (pT and pN). Depending on the PSA level and Gleason score tables from 2011 show for the clinical stage T1c, T2a, T2b and T2c, respectively, the probabilities for a localized tumor (pT2), a capsule exceeded (pT3a), a seminal vesicle invasion (pT3b) and lymph node metastasis (pN1).

Kattan nomograms: With the aid of such a failure to progression (a progression) predict the disease, depending on, for example, PSA level, Gleason score and clinical TNM stage. There are nomograms for the probability of progression-free after radical prostatectomy (after 5 and 10 years and after 7 years if it was already operating), LDR brachytherapy (after 5 years, seeradiotherapy ) and percutaneous irradiation (after 5 years, see radiotherapy ).

More nomograms: The probability of a localized tumor can be predicted with the nomogram of Steuber that for a lymph node involvement with the nomogram of Briganti.
Outlook: Special computer programs (ANN, artificial = artificial neural networks), a far more findings into account at the same time as nomograms. They promise so that in the future a more accurate risk assessment. In addition, numerous changes (eg in the form of biomarkers) can be determined in the excised tissue in the prostate biopsy, which based on the classical Typing and Grading (see classification beyond) and the prognosis might be able to facilitate future.

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