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Drug Sensitivity Testing in Osteosarcoma: A Case Report
Ines Lohse1,2,3,4, Giselle Dutcher5, Hassan Al-Ali5,6,7
1Center for Therapeutic Innovation, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.
Abstract:
Precision medicine approaches using ex-vivo drug sensitivity testing (DST) have received attention in the cancer research community as a means to improve treatment stratification in populations where multiple treatment attempts are not feasible, or no standard-of-care treatment exists, such as ultra-rare cancers with a significant clinical need for effective treatment options, like osteosarcoma. DST has the potential to supplement existing patient stratification approaches by providing tumor-specific response data to aid in treatment selection at the time of treatment decision. We present the case of a pediatric osteosarcoma patient who was evaluated using DST at the time of standard-of-care treatment to evaluate treatment sensitivity. The DST screen indicated significant treatment sensitivity to anthracyclines and methotrexate, consistent with the first-line standard-of-care therapy (MAP). Clinical follow-up showed treatment sensitivity to standard-of-care MAP treatment and pathology results of 90% necrosis. The present case shows that DST screening is feasible from a technical standpoint, can be performed in a clinically relevant time frame that does not delay treatment start, and provides personalized drug sensitivity information on clinically available agents, and the DST results align with the clinical treatment response.
Insights
Ex-vivo drug sensitivity testing (DST) shows promise for guiding cancer treatment. In a pediatric osteosarcoma case, DST accurately predicted response to standard therapy, demonstrating its clinical utility.
Area of Science:
- Oncology
- Precision Medicine
- Pharmacology
Background:
- Precision medicine aims to tailor cancer treatments to individual patients.
- Ex-vivo drug sensitivity testing (DST) offers a method for personalized treatment selection.
- Osteosarcoma, particularly in pediatric cases, presents challenges due to limited effective treatment options.
Observation:
- A pediatric osteosarcoma patient underwent DST alongside standard-of-care treatment.
- The DST identified sensitivity to anthracyclines and methotrexate, key components of the MAP regimen.
- Clinical outcomes and pathology confirmed sensitivity to the MAP treatment, with 90% tumor necrosis.
Findings:
- DST is technically feasible and can be completed within a clinically relevant timeframe.
- The testing provides personalized drug sensitivity data for available agents.
- DST results correlated with the patient's clinical response to therapy.
Implications:
- DST can supplement existing stratification methods by providing tumor-specific drug response data.
- This approach can aid in treatment selection for rare cancers like osteosarcoma.
- The findings support the integration of DST into clinical decision-making for improved cancer care.

