Transient Protection of Hematopoietic Stem and Progenitor Cells Against Ionizing Radiation
This invention is in the area of improved compounds and methods for transiently protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC), from the damage associated with ionizing radiation (IR) exposure using selective radioprotectants.
1 . A method for reducing the effect of ionizing radiation exposure on hematopoietic stem cells and/or progenitor cells (HSPCs) in a subject undergoing at least three ionizing radiation treatments within a week for a cyclin dependent kinase 4/6 replication independent cancer, the method comprising:
a. administering to the subject an effective amount of a compound having the formula:
wherein R is C(X) 2 ,
wherein the two X groups together form an alkyl bridge to form a spiro compound;
or its pharmaceutically acceptable salt thereof; and,
b. exposing the subject to the ionizing radiation;
wherein the subject is administered an effective amount of the compound prior to exposing the subject to each of the at least three ionizing radiation treatments.
2 . The method of claim 1 , wherein the subject is a human.
3 . The method of claim 1 , wherein the subject is being treated for a CDK4/6 replication independent cancer selected from small cell lung cancer, triple-negative breast cancer, HPV-positive head and neck cancer, retinoblastoma, Rb-negative bladder cancer, Rb negative prostate cancer, osteosarcoma or cervical cancer.
4 . The method of claim 3 , wherein the cancer is small cell lung cancer.
5 . The method of claim 3 , wherein the cancer is triple-negative breast cancer.
6 . The method of claim 3 , wherein the cancer is HPV-positive head and neck cancer, retinoblastoma.
7 . The method of claim 3 , wherein the cancer is Rb-negative bladder cancer.
8 . The method of claim 3 , wherein the cancer is Rb negative prostate cancer.
9 . The method of claim 3 , wherein the cancer is osteosarcoma.
10 . The method of claim 3 , wherein the cancer is cervical cancer.
11 . The method of claim 1 , wherein the compound is administered to the subject less than about 24 hours prior to exposure to the ionizing radiation.
12 . The method of claim 1 , wherein the compound is administered to the subject prior to exposure to the ionizing radiation such that the compound reaches peak serum levels during exposure to the ionizing radiation.
13 . The method of claim 1 , wherein the compound is administered to the subject less than about 4 hours prior to exposure to the ionizing radiation.
14 . The method of claim 1 , further comprising administering to the subject a hematopoietic growth factor.
15 . The method of claim 14 , wherein the hematopoietic growth factor is granulocyte colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), M-CSF (macrophage colony stimulating factor), thrombopoietin, interleukin (IL)-12, SCF (stem cell factor) and erythropoietin (EPO).
16 . The method of claim 15 , wherein the hematopoietic growth factor is G-CSF.
17 . The method of claim 15 , wherein the hematopoietic growth factor is GM-CSF.
18 . The method of claim 15 , wherein the hematopoietic growth factor is EPO.
19 . The method of claim 15 , wherein the hematopoietic growth factor is thrombopoietin.
20 . The method of claim 1 , wherein subject is exposed to the ionizing radiation 3 times within a week.
21 . The method of claim 1 , wherein the subject is exposed to the ionizing radiation 4 times within a week.
22 . The method of claim 1 , wherein the subject is exposed to the ionizing radiation 5 times a week.