US2015190397A1PendingUtilityA1
Treatment of Cancers Expressing p95 ErbB2
Est. expiryAug 1, 2023(expired)· nominal 20-yr term from priority
G01N 2333/71A61K 31/517A61K 39/39558A61P 35/00A61K 2039/545G01N 2333/91205A61K 31/519C12Q 1/6886G01N 33/57557G01N 33/57515G01N 33/5759G01N 33/57492
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Claims
Abstract
The truncated ErbB2 receptor (p95ErbB2) is shown to differ from the full-length ErbB2 receptor in its association with other ErbB receptors. The truncated receptor preferentially associated with ErbB3, whereas full length ErbB2 heterodimerizes with 5 either EGFR or ErbB3. Consistent with p95ErbB2 heterodimerization with ErbB3, it is shown that heregulin (an ErbB3 ligand) stimulates p95ErbB2 phosphorylation in breast cancer cell lines. Described herein are methods of identifying patients suitable for treatment with a p95ErbB2 inhibitor, and methods of treating such patients.
Claims
exact text as granted — not AI-modified1 . A method of treating a human patient having a solid tumor comprising the steps of:
obtaining at least one sample from said patient, testing for the presence of p95 ErbB2 in said sample; and treating said patient with GW572016 if p95 ErbB2 is detected in said sample.
2 . The method of claim 1 , wherein said solid tumor is selected from breast, ovarian, colon, head and neck, bladder, renal, and lung.
3 . The method of claim 1 , wherein said solid tumor is a breast tumor.
4 . The method of claim 1 , wherein said sample is a tumor sample.
5 . The method of claim 1 , wherein said sample is a blood sample.
6 . (canceled)
7 . The method of claim 1 , further comprising treating said human patient with a second compound that inhibits either p95 ErbB2 or p185 ErbB2 .
8 . (canceled)
9 . The method of claim 7 , wherein the second compound is trastuzumab.
10 . The method of claim 1 , wherein the expression of p95 ErbB2 is determined by an immunohistochemical method.
11 . The method of claim 1 , wherein the expression of p95 ErbB2 is determined by measuring ErbB2 extracellular domain in a sample of a subject's serum.
12 . The method of claim 4 , wherein said tumor sample is selected from, breast, ovarian, colon, head and neck, bladder, renal, and lung.
13 . The method of claim 1 , wherein said solid tumor is a solid epithelial tumor.
14 . The method of claim 12 , wherein said tumor sample is a breast tumor.
15 . The method of claim 1 , wherein said human patient has previously been treated with trastuzumab.
16 . A method of claim 1 , wherein the presence of p95 ErbB2 level is at least 5% of full-length ErbB2 receptor level in said sample.
17 . A method of treating a human patient for breast cancer, comprising the steps of:
obtaining at least one sample from said patient; testing for expression of p95 ErbB2 in said sample; and treating said patient with a GW572016 if p95 ErbB2 is detected in said sample.
18 . A method of treating a human subject having a solid tumor that overexpresses ErbB2, said method comprising:
determining whether said solid tumor exhibits trastuzumab resistance, and treating said patient with GW572016 if said tumor is trastuzumab resistant.
19 . The method of claim 18 , wherein said tumor expresses p95 ErbB2 at a level at least equal to about 5%, 10%, 20%, 25% or more of full-length ErbB2 receptor expression level.
20 . A method of selecting therapy for a human subject having a solid tumor that overexpresses ErbB2, said method comprising:
determining whether said solid tumor expresses p95 ErbB2 , and correlating the measurement of p95 ErbB2 expression with an improved likelihood of response to a p95 ErbB2 inhibitor wherein expression of p95 ErbB2 is at least 5% of full-length ErbB2 expression.Join the waitlist — get patent alerts
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