Breast cancer therapy based on hormone receptor status with nanoparticles comprising taxane
The present invention relates to methods and kits for the treatment of breast cancer based on hormone receptor status of progesterone receptor and estrogen receptor comprising the administration of a taxane alone, in combination with at least one other and other therapeutic agents, as well as other treatment modalities useful in the treatment of breast cancer. In particular, the invention relates to the use of nanoparticles comprising paclitaxel and albumin (such as Abraxane®) either alone or in combination with other chemotherapeutic agents or radiation, which may be used for the treatment of breast cancer which does not express estrogen receptor and/or progesterone receptor.
1. A method for treating breast cancer in an individual, the method comprising:
(a) determining hormone receptor status of estrogen receptor and progesterone receptor;
(b) administering to the individual an effective amount of a composition comprising nanoparticles comprising paclitaxel and an albumin, and
(c) administering to the individual an effective amount of epirubicin and cyclophosphamide,
wherein the hormone receptor status of the individual is negative for both estrogen receptor and progesterone receptor.
2. The method of claim 1 , wherein the average diameter of the nanoparticles in the composition is no greater than about 200 nm.
3. The method of claim 1 , wherein the albumin is human serum albumin.
4. The method of claim 1 , wherein the weight ratio of the albumin and the paclitaxel in the nanoparticle composition is about 9:1 or less.
5. The method of claim 1 , wherein the individual is human.
6. The method of claim 1 , wherein the hormone receptor status of estrogen receptor and progesterone receptor is determined by immunohistochemistry.
7. The method of claim 1 , wherein the breast cancer expresses HER2 (HER2+).
8. The method of claim 1 , wherein the dosage of paclitaxel in the nanoparticle composition is 50-300 mg/m 2 .
9. The method of claim 1 , wherein the method is for treatment of breast cancer in a neoadjuvant setting.
10. The method of claim 1 , wherein the dosage of paclitaxel in the nanoparticle composition is 125 mg/m 2 .
11. The method of claim 1 , wherein the average diameter of the nanoparticles in the composition is no greater than about 150 nm.
12. The method of claim 1 , wherein the average diameter of the nanoparticles in the composition is about 130 nm.
13. The method of claim 1 , wherein the paclitaxel is coated with albumin.
14. The method of claim 2 , wherein the weight ratio of the albumin and the paclitaxel in the nanoparticle composition is about 9:1 or less, wherein the paclitaxel is coated with albumin.
15. The method of claim 2 , wherein the method is for treatment of breast cancer in a neoadjuvant setting.
16. The method of claim 2 , wherein the dosage of paclitaxel in the nanoparticle composition is 50-300 mg/m 2 .
17. The method of claim 14 , wherein the dosage of paclitaxel in the nanoparticle composition is 50-300 mg/m 2 .
18. The method of claim 11 , wherein the weight ratio of the albumin and the paclitaxel in the nanoparticle composition is about 9:1 or less, wherein the paclitaxel is coated with albumin.
19. The method of claim 12 , wherein the weight ratio of the albumin and the paclitaxel in the nanoparticle composition is about 9:1 or less, wherein the paclitaxel is coated with albumin.