Methods for diagnosing prostatic adenocarcinoma

• US 5,710,007 A
• Filed: 09/29/1995
• Issued: 01/20/1998
• Est. Priority Date: 09/29/1995
• Status: Expired due to Fees

• Current Assignee: Albert A. Luderer, Chen, Ya-Ting, Grant D. Carlson, Thiel, Robert P., Thomas F. Soriano
• Original Assignee: Albert A. Luderer, Chen, Ya-Ting, Grant D. Carlson, Thiel, Robert P., Thomas F. Soriano
• Inventors: Chen, Ya-Ting, Soriano, Thomas F., Thiel, Robert P., Carlson, Grant D., Luderer, Albert A.
• Primary Examiner(s): Feisee, Lila
• Assistant Examiner(s): EYLER, YVONNE L
• Application Number:
  US08/536,215
• Time in Patent Office: 844 Days
• Field of Search: 435/7.9, 435/7.92, 435/7.23, 435/7.1, 436/63, 436/64, 436/518
• US Class Current: 435/7.1
• CPC Class Codes: G01N 33/57434 of prostate
• CPC Class Codes: G01N 33/57488 involving compounds identifable in body fluids

Abstract

The present invention relates to a method for diagnosing prostatic adenocarcinoma (CAP) in a male human patient without requiring a biopsy. The total prostate specific antigen (PSA) level in the blood or serum of the patient is measured. If the patient has a total PSA level of between 2.5 ng/ml and 20.0 ng/ml, then the free PSA level in the blood or serum of the patient is measured. The proportion of free PSA to total PSA is calculated. If this proportion is less than about 7%, then the patient is diagnosed as having CAP. The present method can also be used on patients that have a total PSA of at least 10.1 ng/ml, but have also had a negative prostate biopsy.

Claims

1. A method for diagnosing prostatic adenocarcinoma (CAP) in a male human patient without requiring a prostate biopsy comprising:

a) measuring the total prostate specific antigen (PSA) level in the blood or serum of the patient;

b) measuring the free PSA level in the blood or serum of a patient only if he has a total PSA level of between 2.5 ng/ml and 20.0 ng/ml;

c) calculating the proportion of free PSA to total PSA; and

d) diagnosing the patient as having CAP if the calculated proportion of free PSA to total PSA is less than about 7%.

2. A method for diagnosing prostatic adenocarcinoma (CAP) in a male human patient who has a measured total prostate specific antigen (PSA) level of at least 10.1 ng/ml and has had a negative prostate biopsy without requiring a further prostate biopsy to confirm CAP comprising:

a) measuring the free PSA level in the blood or serum of the patient;

b) calculating the proportion of free PSA to total PSA; and

c) diagnosing the patient as having CAP if the calculated proportion of free PSA to total PSA is less than about 7%.

3. The method for diagnosing prostatic adenocarcinoma (CAP) as in claim 2 wherein one also re-measures the total prostate specific antigen (PSA) level in the blood or serum of the patient.

4. The method for diagnosing prostatic adenocarcinoma (CAP) as set forth in claim 2 wherein the total prostate specific antigen (PSA) level in the blood or serum of the patient is between 10.1 ng/ml and 20.0 ng/ml.

5. The method for diagnosing prostatic adenocarcinoma (CAP) as set forth in claim 3 wherein the total prostate specific antigen (PSA) level in the blood or serum of the patient is between 10.1 ng/ml and 20.0 ng/ml.