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Grant: Operating Grant - Priority Announcement: Breast Cancer

University of Toronto

$0.00

Targeted Polymeric Nanotechnology for Multi-Modality Treatment of HER2 Positive Breast Cancer

EF 2013-14

Résumé
Breast cancer (BC) is a heterogeneous disease that can be divided into different subtypes based on evaluation of specific markers on BC cells. Human epidermal receptor 2 (HER2) is one of the markers that is commonly evaluated for subtype identification. HER2 positive (HER2+) BC is associated with a significantly worse prognosis than HER2- BC and increased risk of recurrence and death. Approximately 15-30% of BC cases are reported to be HER2+. The introduction of the HER2 targeted therapy, trastuzumab, administerd in combination with effective chemotherapies such as docetaxel has transformed treatment for patients with HER2+ disease resulting in significant improvements in overall outcomes. However, once patients develop metastatic BC there are not curative options and the disease will eventually progress in all patients. Indeed, it is the development of trastuzumab resistance that remains a significant therapeutic challenge. The proposed research directly addresses this clinical challenge through the development of powerful new nanotechnology which has been engineered to deliver Indium-111 as radiotherapy and docetaxel as chemotherapy to trastuzumab resistant, HER2+ BC cells. This research builds on recent clinical data that show that targeting of a cytotoxic agent to HER2+, trastuzumab resistant tumours can overcome resistance. In our proposed treatment strategy, we use pharmaceutically safe materials to deliver the cytotoxic agents, Indium-111 and docetaxel, for the selective killing of HER2+ BC cells, as a synergistic and potent combination therapy.
Programme
Operating Grant - Priority Announcement: Breast Cancer
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
297889
Name
Allen Christine J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Avon Foundation for Women - Canada
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Cancer Progression & Therapeutics
Projecttitle
Targeted Polymeric Nanotechnology for Multi-Modality Treatment of HER2 Positive Breast Cancer
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$0
Cihrequipment2
$0
Programname2
Operating Grant - Priority Announcement: Breast Cancer
Keyworddelim
Auger Electron Radiotherapy; Block Copolymer Micelles; Breast Cancer; Docetaxel; Drug Delivery; Her-2; Imaging; Nanotechnology
Abstract
Breast cancer (BC) is a heterogeneous disease that can be divided into different subtypes based on evaluation of specific markers on BC cells. Human epidermal receptor 2 (HER2) is one of the markers that is commonly evaluated for subtype identification. HER2 positive (HER2+) BC is associated with a significantly worse prognosis than HER2- BC and increased risk of recurrence and death. Approximately 15-30% of BC cases are reported to be HER2+. The introduction of the HER2 targeted therapy, trastuzumab, administerd in combination with effective chemotherapies such as docetaxel has transformed treatment for patients with HER2+ disease resulting in significant improvements in overall outcomes. However, once patients develop metastatic BC there are not curative options and the disease will eventually progress in all patients. Indeed, it is the development of trastuzumab resistance that remains a significant therapeutic challenge. The proposed research directly addresses this clinical challenge through the development of powerful new nanotechnology which has been engineered to deliver Indium-111 as radiotherapy and docetaxel as chemotherapy to trastuzumab resistant, HER2+ BC cells. This research builds on recent clinical data that show that targeting of a cytotoxic agent to HER2+, trastuzumab resistant tumours can overcome resistance. In our proposed treatment strategy, we use pharmaceutically safe materials to deliver the cytotoxic agents, Indium-111 and docetaxel, for the selective killing of HER2+ BC cells, as a synergistic and potent combination therapy.
Competitiondate
201309
Approvedterm2
1 yr 0 mth
Pinamesdelim
Allen, Christine J; Reilly, Raymond M; Sridhar, Srikala S
Approvedterm
1 an 0 mois