SSTR-targeted conjugates and particles and formulations thereof
Conjugates of an active agent such as DM1 attached to a targeting moiety, such as a somatostatin receptor binding moiety, via a linker, and particles comprising such conjugates have been designed. Such conjugates and particles can provide improved temporospatial delivery of the active agent, improved biodistribution and penetration in tumor, and/or decreased toxicity. Methods of making the conjugates, the particles, and the formulations thereof are provided. Methods of administering the formulations to a subject in need thereof are provided, for example, to treat or prevent cancer.
1. A method of reducing proliferation of cells, wherein the cells are neuroendocrine cancer cells and wherein the cells are not small cell lung cancer cells, comprising administering a conjugate to the cells, wherein the conjugate is
2. The method of claim 1 , wherein the cells express a somatostatin receptor (SSTR).
3. The method of claim 2 , wherein the cells express SSTR2.
4. The method of claim 1 , wherein the cells are selected from pheochromocytoma, neuroblastoma, ganglioneuroma, paraganglioma, carcinoids, gastrinoma, glucagonoma, vasoactive intestinal polypeptide-secreting tumor, pancreatic polypeptide-secreting tumor, nonfunctioning gastroenteropancreatic tumors, meduallary thyroid cancer, Merkel cell tumor of the skin, pituitary adenoma, and pancreatic cancer cells.
5. A method of reducing the growth of a tumor, wherein the tumor is a neuroendocrine cancer and wherein the tumor is not small cell lung cancer, comprising administering a conjugate to the subject, wherein the conjugate is
6. The method of claim 5 , wherein the tumor expresses a somatostatin receptor (SSTR).
7. The method of claim 6 , wherein the tumor expresses SSTR2.
8. The method of claim 5 , wherein the neuroendocrine cancer is selected from pheochromocytoma, neuroblastoma, ganglioneuroma, paraganglioma, carcinoids, gastrinoma, glucagonoma, vasoactive intestinal polypeptide-secreting tumor, pancreatic polypeptide-secreting tumor, nonfunctioning gastroenteropancreatic tumors, meduallary thyroid cancer, Merkel cell tumor of the skin, pituitary adenoma, and pancreatic cancer.
9. The method of claim 5 , wherein the method further comprises the subject having a positive scan result detected with SSTR scintigraphy or positron emission tomography (PET).
10. The method of claim 9 , wherein Indium-111-labelled pentetreotide is used in the SSTR scintigraphy or 68Ga-DOTA-TATE, 68Ga-DOTA-TOC, and 68Ga-DOTA-NOC in PET.