Metastasis accounts for over 90% of all cancer associated suffering and death, and arguably presents the most formidable challenges in cancer management. The central innovation and overall goal of this project is the development of new design radiotherapy biomaterials that could be employed to significantly boost pancreatic/lung/prostate cancer cure rate: including treatment of metastasis and overcoming radioresistance, all at no additional inconvenience to patients. The new biomaterials are designed to simply replace the inert biomaterials (fiducials/spacers), which are currently routinely implanted to ensure spatial accuracy during radiotherapy. These new biomaterials specifically incorporate a payload of non-toxic targeted radiosensitizing gold nanoparticles (GNP), and immunoadjuvants in a biodegradable polymer matrix. Once in place, the new design biomaterials controllably release the payload directly into the tumor as the polymer degrades. During radiotherapy, the released GNP will significantly enhance local tumor cell kill, substantially boosting dose to radioresistant tumor cells via Einstein?s photoelectric effect, with minimal toxicity to healthy tissue. Meanwhile, antigens from irradiated tumor cells work with the released immunoadjuvant to prime a robust T cell response, which may kill metastatic cells distant from the irradiated site (abscopal effect) and establish immune memory to prevent cancer recurrence. Slow in-situ release of the payload will minimize systemic/overlapping toxicities, which are currently a critical barrier/concern with competing approaches. Overall, our low risk, potential high-reward innovation could significantly enhance survival and quality of life for pancreatic/ung/prostate cancer patients.

Public Health Relevance

Pancreatic cancer has a dismal 5-year survival rate, in part because most newly diagnosed patients already have metastatic or radioresistant disease. If successful, this project will meet the public health goals of NIH and the NCI in significantly increasing the survival and quality of life for cancer patients, particularly those with pancreatic cancer, for whom current treatments are limited. This can be extended to enhance treatment for some of the other most deadly cancers: lung, and metastatic prostate cancer. In addition, the technology we are developing in the project could prevent the cancer from recurring, which is usually one of the greatest fears of cancer patients treated with curative intent.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21CA205094-01A1
Application #
9302964
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Soyombo-Shoola, Abigail Adebisi
Project Start
2017-09-25
Project End
2019-03-31
Budget Start
2017-09-25
Budget End
2018-03-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Dana-Farber Cancer Institute
Department
Type
DUNS #
076580745
City
Boston
State
MA
Country
United States
Zip Code
02215
Ngwa, Wilfred; Irabor, Omoruyi Credit; Schoenfeld, Jonathan D et al. (2018) Using immunotherapy to boost the abscopal effect. Nat Rev Cancer 18:313-322
Moreau, Michele; Yasmin-Karim, Sayeda; Kunjachan, Sijumon et al. (2018) Priming the Abscopal Effect Using Multifunctional Smart Radiotherapy Biomaterials Loaded with Immunoadjuvants. Front Oncol 8:56