Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2000-08-09
2002-08-13
Goldberg, Jerome D. (Department: 1614)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C514S312000, C514S314000, C514S569000
Reexamination Certificate
active
06432979
ABSTRACT:
This invention relates to the use of a combination of an NSAID and a epidermal growth factor receptor (EGFR) kinase inhibitor in the treatment and inhibition of colonic polyps and colorectal cancer.
Colonic Polyps occur in both a familial pattern (familial adenomatous polyps; FAP) and sporadically. FAP afflicts approximately 25,000 patients in the US; while it is estimated that sporadic adenomatous polyps (SAP) occur in approximately 2 million people per year in the US alone. All these patients are at risk for developing adenocarcinoma of the colon. In the case of FAP, that risk is virtually 100% and these patients usually undergo a colectomy at an early age. Patients with sporadic polyps are treated with polypectomy and require periodic colonoscopic examination because of their inherent risk of developing recurrent polyps. In fact, parents and siblings of these patients are also at increased risk for developing colorectal cancer.
The genetic basis for FAP has been linked to the presence of mutations in the APC gene. Similar APC mutations have been found in patients with sporadic polyps. Biochemically, the APC mutation occurs in conjunction with the increased expression of cyclooxygenase enzymes, particularly COX-2. These enzymes are essential for the production of prostenoids, (prostaglandin's; (PG's)) that mediate a number of functions in the bowel including motility, vascular tone, angiogenesis and mucosal protection. PG's are also purported to discourage apoptosis and this is proposed as an explanation for polyp formation.
The therapy of FAP and SAP has focused on inhibiting COX enzymes. Considerable evidence exists for the efficacy of COX inhibitors in reducing polyp formation. These COX inhibitors are predominantly NSAID's such as clinoril, sulindac, piroxicam and etodoloc, all of which appear to be equivalent in their action. A major problem with NSAID therapy has been the development of serious side effects including peptic ulceration, and cholestatic hepatitis and renal papillary necrosis. Long term therapy with NSAIDs for the treatment of polyps is therefore considered to be impractical.
Protein tyrosine kinases are a class of enzymes that catalyze the transfer of a phosphate group from ATP or GTP to tyrosine residue located on protein substrates. Protein tyrosine kinases clearly play a role in normal cell growth. Many of the growth factor receptor proteins function as tyrosine kinases and it is by this process that they effect signaling. The interaction of growth factors with these receptors is a necessary event in normal regulation of cell growth. However, under certain conditions, as a result of either mutation or overexpression, these receptors can become deregulated; the result of which is uncontrolled cell proliferation which can lead to tumor growth and ultimately to the disease known as cancer [Wilks A. F.,
Adv. Cancer Res.,
60, 43 (1993) and Parsons, J. T.; Parsons, S. J.,
Important Advances in Oncology,
DeVita V. T. Ed., J.B. Lippincott Co., Phila., 3 (1993)]. Among the growth factor receptor kinases and their proto-oncogenes that have been identified and which are targets of the compounds of this invention are the epidermal growth factor receptor kinase (EGF-R kinase, the protein product of the erbB oncogene), and the product produced by the erbB-2 (also referred to as the neu or HER2) oncogene. Since the phosphorylation event is a necessary signal for cell division to occur and since overexpressed or mutated kinases have been associated with cancer, an inhibitor of this event, a protein tyrosine kinase inhibitor, will have therapeutic value for the treatment of cancer and other diseases characterized by uncontrolled or abnormal cell growth. For example, overexpression of the receptor kinase product of the erbB-2 oncogene has been associated with human breast and ovarian cancers [Slamon, D. J., et. al.,
Science,
244, 707 (1989) and
Science,
235, 1146 (1987)]. Deregulation of EGF-R kinase has been associated with epidermoid tumors [Reiss, M., et. al.,
Cancer Res.,
51, 6254 (1991)], breast tumors [Macias, A., et. al.,
Anticancer Res.,
7, 459 (1987)], and tumors involving other major organs [Gullick, W. J.,
Brit. Med. Bull.,
47, 87 (1991)]. Because of the importance of the role played by deregulated receptor kinases in the pathogenesis of cancer, many recent studies have dealt with the development of specific PTK inhibitors as potential anti-cancer therapeutic agents [some recent reviews: Burke. T. R.,
Drugs Future,
17, 119 (1992) and Chang, C. J.; Geahlen, R. L.,
J. Nat. Prod.,
55, 1529 (1992)].
It has recently been proposed that the activation and overexpression of COX-2 in adenomatous polyps is due to activation of the EGFR. EGFR stimulation by one of it's ligands—amphiregulin (AR), induces the nuclear targeting of COX-2, release of PG's and subsequent mitogenesis, in polarized colonic epithelial cells. COX-2 inhibitors have been shown to prevent this series of events.
Colon cancer results from an accumulation of a number of genetic abnormalities that occur over the lifetime of the developing tumor. The primary genetic change is a mutation in a gene called APC and this gene mutation occurs prior to the development of adenomas. Subsequent changes include mutations in the K-Ras, DCC and P53 genes as well as other changes that have not as yet been defined. What is known is that there is a clear progression from dysplastic cells within the colon through early adenomas (polyps) to intermediate adenomas, late adenomas to carcinoma and its metastases.
There are a number of diseases that begin as polyps and progress to cancer. The best defined of these is FAP (familial adenomatous polyposis) which has a population incidence of 1 in 7,000. The APC mutation, or a mutation in a gene associated with the function of APC, occurs in close to 100% of these patients. A similar occurrence of the APC mutation is present in sporadic adenomas and sporadic cancers. These adenomas occur with a population and incidence of 1 and 20.
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Discafani-Marro Carolyn M.
Frost Philip
American Cyanamid Company
Goldberg Jerome D.
Hogan Jr. John W.
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