Low intensity focused ultrasound for treating cancer and metastasis
Systems and methods for treating cancer and for preventing metastasis using low intensity focused ultrasound in combination with an anti-cancer therapy are disclosed.
1. A method for priming a subject having a tumor, the method comprising:
a. applying a priming therapy comprising non-ablative ultrasound comprising at least two ultrasound beams to a treatment zone in the subject having the tumor, wherein the at least two ultrasound beams have different frequencies, and wherein the at least two ultrasound beams have a beam profile waist at −3 dB that is not less than 5 mm in the treatment zone; and
b. administering a chemotherapeutic agent to the subject, wherein the chemotherapeutic agent comprises a heat shock protein 90 (HSP90) inhibitor, wherein applying the priming therapy induces a stress in cells of the tumor in the treatment zone without ablating the cells.
2. The method of claim 1 , wherein the HSP90 inhibitor comprises 17AAG (tanespimycin).
3. The method of claim 1 , wherein one of the at least two ultrasound beams has a frequency in the range of 0.01 to 10 MHz and a spatial peak temporal average acoustic output intensity (I spta ) of between 1 and 1000 W/cm 2 in the treatment zone.
4. The method of claim 3 , wherein the frequency of the one of the at least two ultrasound beams is in the range of 30 to 300 kHz.
5. The method of claim 3 , wherein another of the at least two ultrasound beams has a frequency in the range of 300 kHz to 3 MHz.
6. The method of claim 3 , wherein the spatial peak temporal average acoustic output intensity (I spta ) of the one of the at least two ultrasound beams is between 10 and 300 W/cm 2 in the treatment zone.
7. The method of claim 1 , wherein the at least two ultrasound beams are applied for 0.5 to 5 seconds.
8. The method of claim 1 , wherein the priming therapy is applied to the cells of the tumor in the treatment zone to increase a non-ablative stress in the cells.
9. The method of claim 8 , wherein the priming therapy is applied to the cells of the tumor in the treatment zone to increase endoplasmic reticulum (ER) stress in the cells.
10. The method of claim 9 , wherein the increased ER stress increases intensity and effectiveness of a T-cell mediated response to the anti-tumor therapy.
11. The method of claim 1 , wherein the priming therapy is applied to the cells of the tumor in the treatment zone are to induce a release of an immunomodulatory factor.
12. The method of claim 11 , wherein the immunomodulatory factor comprises a heat shock protein.
13. The method of claim 1 , wherein the ultrasound is applied to the treatment zone in the subject before the chemotherapeutic agent.
14. The method of claim 1 , wherein the ultrasound is applied to the treatment zone in the subject concurrent with the chemotherapeutic agent.
15. The method of claim 1 , wherein the at least two ultrasound beams are applied sequentially.
16. The method of claim 1 , wherein the at least two ultrasound beams are applied simultaneously.
17. The method of claim 1 , wherein the tumor comprises a tumor of the prostate, breast, nasopharynx, pharynx, lung, bone, brain, sialaden, stomach, esophagus, testes, ovary, uterus, endometrium, liver, small intestine, appendix, colon, rectum, bladder, gall bladder, pancreas, kidney, urinary bladder, cervix, vagina, vulva, prostate, thyroid or skin, head or neck, glioma or soft tissue sarcoma.
18. The method of claim 1 , wherein the tumor has become resistant to the chemotherapeutic agent when the chemotherapeutic agent was previously administered to the subject.
19. The method of claim 1 , wherein the ultrasound delivers an energy in the range of 300 to 3000 J/cm 3 in the treatment zone of the subject.
20. The method of claim 1 , wherein the treatment zone is configured to reach a maximum temperature of less than 55° C.