Claims for Patent: 7,507,704

Summary for Patent: 7,507,704

Title:	Receptor modulated cancer protocols
Abstract:	The present invention discloses that prior art protocols that administer HER receptor blockers concurrently with phase specific cytotoxic chemotherapeutics result in antagonistic function that prevents subsequent administrations of phase specific cytotoxic from functioning. The present invention provides protocols that allow the two classes of drugs to function synergistically. Moreover, the present invention also identifies that gompertzian tumor growth results in heterogeneity of cell cycle times in a tumor and that chemotherapeutic depopulation of the tumor results in accelerating cell cycle times, both of which preclude synchronicity of successive administrations of S-Phase cytotoxics relative to the progression of the S-Phase in the cancer cell population under prior art protocols. Present invention provides novel \"synchronous\" protocols for S-Phase cytotoxics, using HER blockers, to overcome this problem. Present invention also discloses how to integrate protocols of U.S. Pat. No. 6,486,146 for HER+ cancers that are also endocrine dependent.
Inventor(s):	Zamoyski; Mark (San Jose, CA)
Assignee:
Application Number:	11/809,264
Patent Claims:	1. A method of progressively reducing the size of a tumor or tumors over expressing human epidermal growth factor receptor proteins (HER1 tumors) comprising interlaced administrations of S-Phase specific cell cycle active cytotoxic chemotherapeutic or chemotherapeutics in therapeutically effective amounts to reduce tumor size and HER1 blocker or blockers in therapeutically effective amounts to inhibit tumor regrowth between successive administrations of said S-Phase specific cell cycle active cytotoxic chemotherapeutic or chemotherapeutics and for a period of time that does not interfere with the utility of successive administrations of said S-Phase specific cell cycle active cytotoxic chemotherapeutic or chemotherapeutics. 2. The method of claim 1 wherein said HER1 blocker is erlotinib. 3. The method of claim 1 wherein said HER1 blocker is cetuximab. 4. The method of claim 1 wherein said HER1 blocker is gefitinib. 5. The method of claim 1 wherein when said HER1 tumor or tumors are also estrogen, progesterone, or testosterone dependent then estrogen, progesterone or testosterone is administered at a point in time prior to, or concurrent with, or both prior to and concurrent with, administration of said S-Phase specific cell cycle active cytotoxic chemotherapeutic or chemotherapeutics in therapeutically effective amounts to insure progression of said estrogen, progesterone, or testosterone dependent tumor or tumors through the cell cycle. 6. The method of claim 1 wherein when said HER1 tumor or tumors are also estrogen, progesterone, or testosterone dependent then estrogen, progesterone or testosterone blockers or downregulators are administered in conjunction with said HER1 blocker or blockers in therapeutically effective amounts to inhibit progression of said estrogen, progesterone, or testosterone dependent tumor or tumors through the cell cycle and estrogen, progesterone, or testosterone is administered at a point in time prior to, or concurrent with, or both prior to and concurrent with, administration of said S-Phase specific cell cycle active cytotoxic chemotherapeutic or chemotherapeutics in therapeutically effective amounts to insure progression of said estrogen, progesterone, or testosterone dependent tumor or tumors through the cell cycle. 7. The method of claim 1 wherein the VEGF blocker bevacizumab is administered in therapeutically effective amounts to prevent blood vessel cells from progressing through the cell cycle and said VEGF blocker bevacizumab is administered a point in time sufficiently prior to administration of said S-Phase specific cell cycle active chemotherapeutic or chemotherapeutics to prevent said blood vessel cells from being in the S-Phase of the cell cycle during administration of said S-Phase specific cell cycle active cytotoxic chemotherapeutic or chemotherapeutics.

Details for Patent 7,507,704

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Eli Lilly And Company	ERBITUX	cetuximab	Injection	125084	02/12/2004		2022-11-15
Eli Lilly And Company	ERBITUX	cetuximab	Injection	125084	03/28/2007		2022-11-15
Genentech, Inc.	AVASTIN	bevacizumab	Injection	125085	02/26/2004		2022-11-15