Prostate cancer staging

Prostate cancer staging is the process by which physicians evaluate the spread of prostate cancer. This is important because in a good cancer stagingsystem, the stage of disease helps determine prognosisand assists in selecting therapies. A combination of physical examination, blood tests, and medical imagingis used to determine the clinical stage; if tissue is obtained via biopsyor surgery, examination of the tissue under a microscope can provide pathologic staging.

There are two schemes commonly used to stage prostate cancer. The most common is the TNMsystem, which evaluates the size of the tumor, the extent of involved lymph nodes, and any metastasis(distant spread). As with many other cancers, these are often grouped into four stages (I–IV). Another scheme, used less commonly, is the Whitmore-Jewett stage.

Briefly, Stage I disease is cancer that is found incidentally in a small part of the sample when prostate tissue was removed for other reasons, such as benign prostatic hypertrophy, and the cells closely resemble normal cells. Stage II cancer cells less closely resemble normal cells, or more of the prostate is involved. In Stage III, the tumor has spread through the prostatic capsule. In Stage IV disease, the tumor has invaded nearby structures, or has spread to lymph nodes or other organs.

TNM staging

From the AJCC6th edition (2002) and UICC6th edition.

Evaluation of the (primary) tumor ('T')

• TX: cannot evaluate the primary tumor
• T0: no evidence of tumor
• T1: tumor present, but not dectable clincally or with imaging
  • T1a: tumor was incidentally found in less than 5% of prostate tissue resected (for other reasons)
  • T1b: tumor was incidentally found in greater than 5% of prostate tissue resected
  • T1c: tumor was found in a needle biopsyperformed due to an elevated serum PSA
• T2: the tumor can be felt (palpated) on examination, but has not spread outside the prostate
  • T2a: the tumor is in half or less than half of one of the prostate gland's two lobes
  • T2b: the tumor is in more than half of one lobe, but not both
  • T2c: the tumor is in both lobes
• T3: the tumor has spread through the prostatic capsule(if it is only part-way through, it is still T2)
  • T3a: the tumor has spread through the capsule on one or both sides
  • T3b: the tumor has invaded one or both seminal vesicles
• T4: the tumor has invaded other nearby structures

Evaluation of the regional lymph nodes ('N')

• NX: cannot evaluate the regional lymph nodes
• N0: there has been no spread to the regional lymph nodes
• N1: there has been spread to the regional lymph nodes

Evaluation of distant metastasis ('M')

• MX: cannot evaluate distant metastasis
• M0: there is no distant metastasis
• M1: there is distant metastasis
  • M1a: the cancer has spread to lymph nodes beyond the regional ones
  • M1b: the cancer has spread to bone
  • M1c: the cancer has spread to other sites (regardless of bony involvement)

Evaluation of the histologic grade ('G')

Usually, the gradeof the cancer (how different the tissue is from normal tissue) is evaluated separately from the stage; however, for prostate cancer, grade information is used in conjuction with TNM status to group cases into four overall stages.

• GX: cannot assess grade
• G1: the tumor closely resembles normal tissue (Gleason2–4)
• G2: the tumor somewhat resembles normal tissue (Gleason 5–6)
• G3–4: the tumor resembles normal tissue barely or not at all (Gleason 7–10)

Overall staging

The tumor, lymph node, metastasis, and grade status can be combined into four stages of worsening severity.

Whitmore-Jewett staging

The Whitmore-Jewett system is similar to the TNM system, with approximately equivalent stages. Roman numeralsare sometimes used instead of Latin letters for the overall stages (for example, Stage I for Stage A, Stage II for Stage B, and so on).

• A: tumor is present, but not detectable clinically; found incidentally
  • A1: tissue resembles normal cells; found in a few chips from one lobe
  • A2: more extensive involvement
• B: the tumor can be felt on physical examination but has not spread outside the prostatic capsule
  • BIN: the tumor can be felt, it does not occupy a whole lobe, and is surrounded by normal tissue
  • B1: the tumor can be felt and it does not occupy a whole lobe
  • B2: the tumor can be felt and it occupies a whole lobe or both lobes
• C: the tumor has extended through the capsule
  • C1: the tumor has extended through the capsule but does not involve the seminal vesicles
  • C2: the tumor involves the seminal vesicles
• D: the tumor has spread to other organs

Risk groups

While TNM staging is important, the TNM stage alone is not sufficient for deciding what treatment is best for a patient with prostate cancer. Instead, a different category called "risk groups" is used, which is based on the T-stage of the TNM system and adds additional information from the Gleason scoreand prostate specific antigen(PSA) value. The risk can be described as low risk, intermediate risk, or high risk. The risk is a useful predictor of having extraprostatic extension, which is spread of the cancer beyond the prostate gland itself. Although slightly different criteria are used for assigning risk, one such system defines low risk as a PSA less than 10, a Gleason score of 6 or lower, and a T-stage of T2a or lower; high risk is a PSA more than 20, a Gleason score of 8 or higher, or T2c; intermediate risk is a PSA of 10 to 20, T2b, or a Gleason of 7.

Patients with low risk disease may be treated with prostatectomyor radiotherapyalone. Patients with intermediate risk disease are usually treated with radiotherapy and a short duration (less than 6 months) of hormonal ablation (medical castration using a gonadotropin-releasing hormone analog), and those with high risk disease are usually treated with radiotherapy and a long duration of hormonal ablation.

This article is licensed under the GNU Free Documentation License.
It uses material from the http://en.wikipedia.org/wiki/Prostate+cancer+staging Wikipedia article Prostate cancer staging.