Osteosarcoma is a disease in which the recent lack of progress in improving patient survival strongly suggests the need for novel treatment approaches. A panel of well characterized osteosarcoma patient derived xenografts with genetic changes recapitulating the disease, have been tested by our laboratory as part of the Pediatric Preclinical Testing Program. These efforts thus far have been highly successful in identifying several drugs which are currently being or about to be tested in osteosarcoma clinical trials conducted by the Children's Oncology Group - specifically eribulin and glembatumumab vedotin. Numerous additional osteosarcoma patient derived xenograft models have been developed potentially permitting expansion of the panel of tumors assessed. In this proposal exploration of using a more efficient approach to screen for drug activity in the established models may permit utilization of a broader panel of osteosarcoma patient derived xenografts. In this proposal eltrombopag will be explored for activity in the treatment of osteosarcoma based on promising in vitro data. Building on prior findings, eribulin will be tested for additive activiy with agents routinely used in the treatment of osteosarcoma including cisplatin, cyclophosphamide and etoposide. Finally, a novel ALK inhibitor that also has IGF-1R inhibitory activity, certinib, will be tested as a single agent and in combination with rapamycin for activityin the osteosarcoma patient derived xenografts. These results can be informative for future osteosarcoma clinical trials development as well as potentially identify novel agents that can be considered for clinical trials.

Public Health Relevance

Osteosarcoma the most common primary malignant bone tumor in children, adolescents and young adults, is a disease in which progress in improving survival has stagnated for the past three decades highlighting the need for novel therapies. In this proposal a highly informative and representative panel of osteosarcoma tumor samples obtained from patients and grown in immuno-deficient mice will be used to identify novel drugs and drug combinations that may be effective in clinical trials in osteosarcoma patients.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01CA199221-05
Application #
9293259
Study Section
Special Emphasis Panel (ZCA1)
Program Officer
Smith, Malcolm M
Project Start
2015-07-10
Project End
2020-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
5
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Pediatrics
Type
Hospitals
DUNS #
800772139
City
Houston
State
TX
Country
United States
Zip Code
77030
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