Why the study?
Osteosarcoma survival has seen no improvement in four decades despite chemotherapy and surgery, creating a strong need for new therapies targeting metastatic potential and the tumor microenvironment.
This review highlights the need for and recent advances in targeted therapies for osteosarcoma to improve survival and manage metastatic disease.
May prompt targeted therapy development in metastatic osteosarcoma; leaves open which microenvironment interventions improve survival.
Osteosarcoma is the most common bone cancer in adolescents and young adults, but it is a rare cancer with no improvement in patient survival in the last four decades. The main problem of this bone tumor is its evolution toward lung metastatic disease, despite the current treatment strategy (chemotherapy and surgery). To further improve survival, there is a strong need for new therapies that control osteosarcoma cells with metastatic potential and their favoring tumor microenvironment (ME) from the diagnosis. However, the complexity and heterogeneity of those tumor cell genomic/epigenetic and biology, the diversity of tumor ME where it develops, the sparsity of appropriate preclinical models, and the heterogeneity of therapeutic trials have rendered the task difficult. No tumor- or ME-targeted drugs are routinely available in front-line treatment. This article presents up-to-date information from preclinical and clinical studies that were recently published or presented in recent meetings which we hope might help change the osteosarcoma treatment landscape and patient survival in the near future.
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Gaspar et al. (2020) studied this question.
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