SERIAL ANALYSIS OF BIOMARKERS FOR DISEASE DIAGNOSIS
The present invention generally relates to serial analysis of biomarkers for disease diagnosis. In certain embodiments, the invention provides methods for diagnosing a disease including obtaining a sample from a subject, conducting a first assay to determine whether a first biomarker in the sample is positive or negative for a disease, and conducting a second assay to determine whether a second biomarker in the sample is positive or negative for the disease if the first assay produced a negative result.
1 . A method for diagnosing a disease state, the method comprising:
obtaining a sample from a subject;
conducting a first assay to determine whether a first biomarker is positive or negative for a disease; and
conducting a second assay to determine whether a second biomarker is positive or negative for the disease if the first assay produced a negative result.
2 . The method according to claim 1 , further comprising conducting at least one additional assay on the sample, wherein the additional assays are conducted serially and each assay is conducted on a different biomarker.
3 . The method according to claim 2 , wherein the assays are conducted until a positive result with respect to a biomarker indicative of the disease is detected.
4 . The method according to claim 1 , wherein the first biomarker is a nucleic acid biomarker.
5 . The method according to claim 4 , wherein the first assay detects presence or absence of a mutation, wherein presence of the mutation is indicative of a positive result for the disease.
6 . The method according to claim 1 , wherein the second biomarker is a protein biomarker.
7 . The method according to claim 6 , wherein the second assay measures a level of the protein in the sample.
8 . The method according to claim 7 , wherein a level exceeding a predetermined threshold for the protein is indicative of a positive result for the disease.
9 . The method according to claim 7 , wherein a level below a predetermined threshold for the protein is indicative of a positive result for the disease.
10 . The method according to claim 1 , wherein the first and second markers have a known standard-of-care threshold for disease diagnosis.
11 . A method for diagnosing a disease, the method comprising:
obtaining a sample from a subject;
conducting a first set of assays on a first set of biomarkers;
assigning a value for each of the biomarkers in the first set based upon a standard-of-care threshold for disease diagnosis for each biomarker in the first set;
aggregating the values into a first single output score, wherein the first score is indicative of a positive or a negative diagnosis of a disease;
conducting a second set of assays on a second set of biomarkers if the first single output score is indicative of a negative diagnosis of the disease;
assigning a value for each of the biomarkers in the second set based upon a standard-of-care threshold for disease diagnosis for each biomarker in the second set; and
aggregating the values into a second single output score, wherein the second score is indicative of a positive or a negative diagnosis of the disease.
12 . The method according to claim 11 , further comprising conducting at least one additional set of assays on the sample, wherein the additional sets of assays are conducted serially and each set of assays comprises a different set of biomarkers.
13 . The method according to claim 12 , wherein the assays are conducted until an aggregated single output score with respect to a set of biomarkers is obtained that is a positive result for the disease to be diagnosed.
14 . The method according to claim 11 , wherein the value for each of the biomarkers in the first set and the value for each of the biomarkers in the second set are binary values.
15 . The method according to claim 14 , wherein the first set of biomarkers are nucleic acid biomarkers.
16 . The method according to claim 15 , wherein the first set of assays detects presence or absence of a mutation for each biomarker in the first set.
17 . The method according to claim 16 , wherein presence of a mutation for a biomarker in the first set is assigned an output of “1”, and absence of a mutation for a biomarker in the first set is assigned an output of “0”.
18 . The method according to claim 14 , wherein the second set of biomarkers are protein biomarkers.
19 . The method according to claim 18 , wherein the second set of assays measure levels of the proteins in the sample.
20 . The method according to claim 19 , wherein a level exceeding a predetermined threshold for each protein in the second set is assigned an output of “1”, and a level below a predetermined threshold for each protein in the second set is assigned an output of “0”.
21 . The method according to claim 19 , wherein a level below a predetermined threshold for each protein in the second set is assigned an output of “1”, and a level exceeding a predetermined threshold for each protein in the second set is assigned an output of “0”.
22 . A method for diagnosing a disease, the method comprising:
obtaining a sample from a subject; and
conducting a plurality of assays on the sample, wherein the assays are conducted serially and each assay is conducted on a different biomarker, wherein a further assay is conducted only if a previously conducted assay produced a negative result with respect to the biomarker being assayed.
23 . The method according to claim 22 , wherein the assays are conducted until a positive result with respect to a biomarker indicative of the disease is detected.
24 . The method according to claim 22 , wherein nucleic acid biomarkers are assayed before protein biomarkers.
25 . The method according to claim 22 , wherein the biomarkers have a known standard-of-care threshold for disease diagnosis.