US2017089906A1PendingUtilityA1

Biomarkers for ovarian cancer

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Assignee: VERMILLION INCPriority: Jun 24, 2005Filed: Nov 30, 2016Published: Mar 30, 2017
Est. expiryJun 24, 2025(expired)· nominal 20-yr term from priority
A61P 35/00G01N 33/5758G01N 33/57545G01N 2333/4725G01N 2333/775G01N 2333/4727G01N 33/6893G01N 2333/79G01N 33/543G01N 33/57484G01N 33/57449
44
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Claims

Abstract

The present invention provides protein-based biomarkers and biomarker combinations that am useful in qualifying ovarian cancer status in a patient. In particular, the biomarkers of this invention are useful to classify a subject sample as ovarian cancer, ovarian cancer of low malignant potential, benign ovarian disease or other malignant condition. The biomarkers can be detected by SELDI mass spectrometry.

Claims

exact text as granted — not AI-modified
1 . A method for qualifying ovarian cancer status in a subject comprising:
 (a) measuring by immunoassay or mass spectroscopy at least one biomarker in a biological sample selected from blood, serum, plasma, and ovarian cyst fluid from the subject using the composition of  claim 32 ; and   (b) correlating the measurement with ovarian cancer status.   
     
     
         2 - 6 . (canceled) 
     
     
         7 . The method of claim  1 L further comprising measuring a biomarker selected from the group consisting of ApoCl, Hemoglobin alpha/beta, ApoAII, ApoCII, Calcyclin, Calgranulin C, Calgranulin C (truncated form), Calgranulin A, IgG heavy chain, CA125 II, CA15-3, CAl 9-9, CA72-4, CA 195, CEA, creatine kinase B (CKB), Dianon NB 70/K, haptoglobin, transthyretin, ITIH4 beta 2-microglobulin, galactosyltransferase, haptoglobin, HE4, hepcidin, HER-2/neu, macrophage colony stimulating factor (M-CSF, CSF-I), prostatin, osteopontin, esoinophil-derived neurotoxin, extracellular domain of the epidermal growth factor receptor (p 11 OEGFR), kallikrein 6 and kallikrein 10, LASA, leptin, lysophosphatidic acid (LPA), placental alkaline phosphatase (PLAP), prolactin, SMRP, insulin-like growth factor L IGF-II, hemoglobin, urinary gonadotropin peptide, Sialyl TN, Tissue peptide antigen (TPA), tumor associated trypsin inhibitor (TATI), and modified forms thereof. 
     
     
         8 - 11 . (canceled) 
     
     
         12 . The method of  claim 1 , wherein the correlating is performed by a software classification algorithm. 
     
     
         13 . The method of  claim 1 , wherein ovarian cancer status is selected from benign ovarian disease, ovarian cancer of low malignant potential, ovarian cancer and other malignant conditions. 
     
     
         14 - 15 . (canceled) 
     
     
         16 . The method of  claim 1 , wherein the ovarian cancer status rules out the possibility of benign ovarian disease or rules out the possibility of ovarian cancer. 
     
     
         17 . (canceled) 
     
     
         18 . The method of  claim 1 , further comprising: (c) managing subject treatment based on the status. 
     
     
         19 . The method of  claim 1 , further comprising: (c) reporting the status to the subject. 
     
     
         20 . The method of  claim 1 , further comprising: (c) recording the status on a tangible medium. 
     
     
         21 - 22 . (canceled) 
     
     
         23 . The method of  claim 18 , wherein, if the measurement correlates with ovarian cancer, then managing subject treatment comprises administering a chemotherapeutic agent to the subject. 
     
     
         24 . The method of  claim 18 , further comprising: (d) measuring the at least one biomarker after subject management and correlating the measurement with disease progression. 
     
     
         25 - 31 . (canceled) 
     
     
         32 . A composition comprising CA125, HE4, transferrin, and ApoA1 for qualifying ovarian cancer in a subject. 
     
     
         33 . A composition for qualifying ovarian cancer comprising a panel of biospecific capture reagents, each of which specifically binds a biomarker, such that the panel binds CA125, HE4, transferrin, and ApoA1. 
     
     
         34 . The composition of  claim 33 , wherein the biospecific capture reagent is an antibody. 
     
     
         35 . The composition of  claim 33 , wherein each biospecific capture reagent is bound to a solid support. 
     
     
         36 . (canceled) 
     
     
         37 . A kit comprising the composition of  claim 33 , bound to
 a solid support; and   instructions for using the composition in the method of  claim 1 .   
     
     
         38 - 68 . (canceled) 
     
     
         69 . The composition of  claim 35 , wherein the solid support is selected from the group consisting of a bead, plate, membrane, array, or chip.

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