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Risk stratification for men with localised prostate cancer

Authoring team

NICE suggest that urological cancer Multidisciplinary teams should assign a risk category to all newly diagnosed men with localised prostate cancer

This is based on the PSA, Gleason score and clinical stage of the prostate cancer.

PSA

Gleason score

Clinical stage

Low risk

< 10 ng/ml

and

<= 6

and

T1-T2a

Intermediate risk

10-20 ng/ml

or

7

or

T2b-T2c

High risk*

> 20 ng/m

or

8-10

or

T3-T4

*High-risk localised prostate cancer is also included in the definition of locally advanced prostate cancer.

Notes:

  • Gleason grading system is based on glandular architecture - nuclear atypia is not evaluated
    • Gleason grading system defines five histological patterns or grades with decreasing differentiation. The primary and secondary pattern, i.e. the most prevalent and the second most prevalent pattern, are added to obtain a Gleason score or sum
      • Gleason pattern 1
        • composed of a very well circumscribed nodule of separate, closely packed glands which do not infiltrate into adjacent benign prostatic tissue
        • glands are of intermediate size, and similar in size and shape
        • pattern is usually seen in transition zone cancers
        • Gleason pattern 1 is exceedingly rare
      • Gleason pattern 2
        • composed of round or oval glands with smooth ends. The glands are more loosely arranged and not quite as uniform in size and shape as those of Gleason pattern 1
        • may be minimal invasion by neoplastic glands into the surrounding non-neoplastic prostatic tissue
        • glands are of intermediate size and larger than in Gleason pattern 1
        • variation in glandular size and separation between glands is less than that seen in pattern 3.
        • Gleason pattern 2 is usually seen in transition zone cancers but may occasionally be found in the peripheral zone
      • Gleason pattern 3
        • the most common histological pattern
        • the glands are more infiltrative and the distance between them is more variable than in patterns 1 and 2
          • malignant glands often infiltrate between adjacent non-neoplastic glands
          • glands of pattern 3 vary in size and shape and are often angular
            • small glands are typical for pattern 3, but there may also be large, irregular glands
              • each gland has an open lumen and is circumscribed by stroma
      • Gleason pattern 4
        • glands appear fused, cribriform or they may be poorly defined. Fused glands are composed of a group of glands that are no longer completely separated by stroma
        • edge of a group of fused glands is scalloped and there are occasional thin strands of connective tissue within this group
        • hypernephroid pattern described by Gleason is a rare variant of fused glands, with clear or very pale-staining cytoplasm
      • Gleason pattern 5
        • an almost complete loss of glandular lumina, with only occasional lumina apparent
        • epithelium forms solid sheets, solid strands or single cells invading the stroma

    • Gleason score is based on the sum of two numbers:
      • the first number is the score of the most common tumour pattern, the second number is the score of the second most common pattern if there are three patterns the first number is the most common and the second is the one with the highest grade
        • for example, if the most common tumor pattern was grade 3, but some cells were found to be grade 4, the Gleason Score would be 3+4 = 7
        • Gleason Score ranges from 0 to 10, with 10 having the worst prognosis
          • for Gleason Score 7, a Gleason 4+3 is a more aggressive cancer than a Gleason 3+4. Also, there is not really any difference between the aggressiveness of a Gleason Score 9 or 10 tumour
          • low grade tumours are with a score of 5 or below ; intermediate grade with a score of 6 & high grade of 7 or more till 10
    • Gleason scores of 7-10 are associated with worse prognoses, and tumours with Gleason scores 5-6 are associated with lower progression rates after definitive therapy

Reference:


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