Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Jan;11(1):511-520.
doi: 10.3892/ol.2015.3962. Epub 2015 Nov 24.

Strategies and developments of immunotherapies in osteosarcoma

Affiliations

Strategies and developments of immunotherapies in osteosarcoma

Jia Wan et al. Oncol Lett. 2016 Jan.

Abstract

Osteosarcoma (OS) is a frequently observed primary malignant tumor. Current therapy for osteosarcoma consists of comprehensive treatment. The long-term survival rate of patients exhibiting nonmetastatic OS varies between 65-70%. However, a number of OS cases have been observed to be resistant to currently used therapies, leading to disease recurrence and lung metastases, which are the primary reasons leading to patient mortality. In the present review, a number of pieces of evidence provide support for the potential uses of immunotherapy, including immunomodulation and vaccine therapy, for the eradication of tumors via upregulation of the immune response. Adoptive T-cell therapy and oncolytic virotherapy have been used to treat OS and resulted in objective responses. Immunologic checkpoint blockade and targeted therapy are also potentially promising therapeutic tools. Immunotherapy demonstrates significant promise with regard to improving the outcomes for patients exhibiting OS.

Keywords: adoptive T-cell immunotherapy; immunologic checkpoint blockade; immunomodulation; immunotherapy; oncolytic virotherapy; osteosarcoma; targeted therapy; vaccines.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Sakamoto A, Iwamoto Y. Current status and perspectives regarding the treatment of osteo-sarcoma: Chemotherapy. Rev Recent Clin Trials. 2008;3:228–231. doi: 10.2174/157488708785700267. - DOI - PMC - PubMed
    1. Mori K, Rédini F, Gouin F, Cherrier B, Heymann D. Osteosarcoma: Current status of immunotherapy and future trends (Review) Oncol Rep. 2006;15:693–700. - PubMed
    1. Loeb DM. Is there a role for immunotherapy in osteosarcoma? Cancer Treat Res. 2009;152:447–457. doi: 10.1007/978-1-4419-0284-9_25. - DOI - PubMed
    1. Habel N, Hamidouche Z, Girault I, Patiño-García A, Lecanda F, Marie PJ, Fromigué O. Zinc chelation: A metallothionein 2A's mechanism of action involved in osteosarcoma cell death and chemotherapy resistance. Cell Death Dis. 2013;4:e874. doi: 10.1038/cddis.2013.405. - DOI - PMC - PubMed
    1. Wilky BA, Goldberg JM. Immunotherapy in sarcoma: A new frontier. Discov Med. 2014;17:201–206. - PubMed

LinkOut - more resources