Bone and soft-tissue sarcomas

0Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A dose-escalation clinical trial was first initiated in 1996 to evaluate the safety and efficacy of carbon ion radiotherapy (C-ion RT) for inoperable bone and soft-tissue sarcomas. The dose-escalation trial and a subsequent fixed-dose trial on patients with non-metastatic sar comas revealed that carbon ion radiotherapy provided good local control and offered a survival advantage with acceptable levels of morbidity. Ninety-five percent of the patients enrolled in the trials had axial sarcomas. The 3- and 5-year local control rates of the entire study population in the fixed-dose trial were 79 and 71%, respectively, with the corresponding 3 and 5-year overall survival rates being 71 and 59%. As of March 2013, over 900 patients were treated with carbon ion radiotherapy for bone and soft-tissue sarcomas in several trials. The most commonly treated sarcoma was sacral chordoma, followed by axial high-grade bone and soft-tissue sarcomas. This chapter deals with C-ion RT for unresectable sarcomas below C2.

Cite

CITATION STYLE

APA

Imai, R. (2014). Bone and soft-tissue sarcomas. In Carbon-Ion Radiotherapy: Principles, Practices, and Treatment Planning (pp. 271–285). Springer Japan. https://doi.org/10.1007/978-4-431-54457-9_31

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free