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Test Code P2PHI [-2]Pro Prostate-Specific Antigen with Prostate Health Index, Serum


Specimen Required


Patient Preparation:

1. Specimens for testing should be collected prior to prostate manipulations such as digital rectal examination (DRE), prostatic massage, transrectal ultrasound (TRUS), and prostatic biopsy.

2. A 6-week waiting period between needle biopsy and specimen collection is recommended.

3. Specimens should not be collected from patients receiving therapy with high biotin (vitamin B7) doses (ie, >5 mg/day) until at least 8 hours following the last biotin administration.

Collection Container/Tube: Red top (serum gel/SST are not acceptable)

Submission Container/Tube: Plastic vial

Specimen Volume: 1 mL

Collection Instructions: Within 3 hours of collection, centrifuge, aliquot serum into a plastic vial, and refrigerate. Freeze sample within 24 hours of collection and send frozen.


Useful For

As an aid in distinguishing prostate cancer from benign prostatic conditions in men aged 50 years and older with total PSA between 4.0 and 10.0 ng/mL and digital rectal examination findings that are not suspicious for cancer.

Method Name

Immunoenzymatic Assay

Reporting Name

p2PSA with Prostate Health Index, S

Specimen Type

Serum Red

Specimen Minimum Volume

0.75 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Red Frozen (preferred) 150 days
  Ambient  24 hours
  Refrigerated  24 hours

Reject Due To

Gross hemolysis Reject
Gross icterus Reject

Clinical Information

Prostate-specific antigen (PSA) is a glycoprotein produced by the prostate gland, the lining of the urethra, and the bulbourethral gland. Normally, very little PSA is secreted in the blood. In conditions of increase glandular size and tissue damage, PSA is released into circulation. Measurement of serum PSA is useful for determining the extent of prostate cancer and assessing the response to prostate cancer treatment. PSA is also used as a screening tool for prostate cancer detection, although its use in screening has become controversial in recent years. While an elevated serum PSA is associated with prostate cancer, a number of benign conditions, such as benign prostatic hyperplasia (BPH) and prostatitis might lead to elevated serum PSA concentrations. As a consequence, PSA lacks specificity for prostate cancer detection.

 

Several PSA isoforms have been identified that can further increase the specificity of PSA for prostate cancer. In particular, the [-2] form of proPSA (p2PSA) shows improved performance over either total or free PSA for prostate cancer detection on biopsy. The prostate health index (phi) is a formula that combines all 3 PSA forms (total PSA, free PSA, and p2PSA) into a single score. phi is calculated using the following formula: (p2PSA/free PSA) x square root (PSA).

 

In a multicenter study that compared the performance of total PSA, free PSA, p2PSA, and phi in men undergoing prostate biopsy due to a serum PSA concentration between 4 and 10 ng/mL, phi was the best predictor of any prostate cancer, high-grade cancer, and clinically significant cancer. At 95% clinical sensitivity, the clinical specificity of phi was 16.0%, compared to 8.4% for free PSA and 6.5% for total PSA.

Reference Values

Females: Not applicable

 

PROSTATE-SPECIFIC ANTIGEN (PSA) MALES:

Age

Reference range

<40 Years

≤2.0 ng/mL

40-49 Years

≤2.5 ng/mL

50-59 Years

≤3.5 ng/mL

60-69 Years

≤4.5 ng/mL

70-79 Years

≤6.5 ng/mL

≥80 Years

≤7.2 ng/mL

 

PERCENT FREE PSA MALES:

When total PSA is in the range of 4-10 ng/mL

% Free PSA

Probability of cancer

≤10%

56%

11-15%

28%

16-20%

20%

21-25%

16%

>25%

8%

 

PROSTATE HEALTH INDEX (phi) MALES:

When PSA is in the range of 4-10 ng/mL

phi range

Probability of cancer

95% Confidence interval

0-26.9

9.8%

5.2-15.4%

27.0-35.9

16.8%

11.3-22.2%

36.0-54.9

33.3%

26.8-39.9%

≥55.0

50.1%

39.8-61.0%

Interpretation

The prostate health index (phi) may be used to determine the probability of prostate cancer on biopsy in men 50 years of age and older with total prostate-specific antigen (PSA) in the 4.0 to 10.0 ng/mL range. Low phi scores are associated with a lower probability of finding prostate cancer on biopsy, and higher phi scores are associated with an increased probability of finding prostate cancer on biopsy. The choice of an appropriate phi score to be used in guiding clinical decision making may vary for each patient and may depend on other clinical factors or family history. The table below indicates the probability of finding prostate cancer on biopsy when total PSA is in the range of 4.0 to 10.0 ng/mL and may be used as guidance for interpreting the phi score.

 

phi range

Probability of cancer

95% Confidence interval

0-26.9

9.8%

5.2%-15.4%

27.0-35.9

16.8%

11.3%-22.2%

36.0-54.9

33.3%

26.8%-39.9%

55.0+

50.1%

39.8%-61.0%

Cautions

Specimens for [-2] pro-prostate-specific antigen (p2PSA) testing should be collected prior to prostate manipulations such as digital rectal examination (DRE), prostatic massage, transrectal ultrasound (TRUS), and prostatic biopsy. DRE may cause a transient increase in p2PSA, free PSA, and PSA.

 

Transrectal needle biopsy has also been shown to cause transient increases in p2PSA, free PSA, and PSA elevations, thus a 6-week waiting period between needle biopsy and p2PSA, free PSA, and PSA sampling is recommended.

 

The prostate health index (phi) results should be interpreted in light of the total clinical presentation of the patient, including symptoms, clinical history, data from additional tests, and other appropriate information. phi should not be interpreted as absolute evidence for the presence or absence of prostate cancer. Elevated PSA concentrations, increased phi, or decreased free PSA may be observed in patients with nonmalignant disorders, as well as those with prostate cancer.

 

Routine use of 5 alpha-reductase inhibitor drugs typically lower PSA, free PSA, and p2PSA levels in patients. Other drugs used to treat benign prostatic hyperplasia (BPH) may also affect PSA levels. Care should be taken in interpreting results from patients taking these drugs.

 

In rare cases, some individuals can develop antibodies to mouse or other animal antibodies (often referred to as human anti-mouse antibodies [HAMA] or heterophile antibodies), which may cause interference in some immunoassays. Caution should be used in interpretation of results and the laboratory should be alerted if the result does not correlate with the clinical presentation.

 

For patient samples containing elevated levels of total protein (>8 g/dL), the possibility exists for interference by total protein. Carefully evaluate the results of patients suspected of having elevated total protein levels.

 

Free PSA specimens can potentially be falsely decreased by biotin. Biotin should not strongly affect total PSA or p2PSA values.

 

The use of the prostate health index (phi) has not been validated when PSA values are outside of the range of 4.0 to 10.0 ng/mL.

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

84153-Total PSA

84154-Free PSA

86316-[-2]ProPSA

LOINC Code Information

Test ID Test Order Name Order LOINC Value
P2PHI p2PSA with Prostate Health Index, S 53764-7

 

Result ID Test Result Name Result LOINC Value
PSAT Prostate Specific Antigen, S 83112-3
PSAF Free PSA, S 83113-1
PSAP2 [-2]ProPSA, S 97149-9
PSAP3 % Free PSA 12841-3
PSAP4 Prostate Health Index 97150-7

Day(s) Performed

Monday through Saturday

Report Available

1 to 3 days