Randomised trial of proton vs. carbon ion radiation therapy in patients with chordoma of the skull base, clinical phase III study HIT-1-Study

BMC Cancer

Study Protocol

Irini Karapanagiotou-Schenkel¹  Jürgen Debus²  Anna V Nikoghosyan²  Stephanie E Combs²  Marc W Münter²  Alexandra D Jensen² 

[1] Biometrics and Data Management, DKFZ G040, Patient and NCT Clinical Trial Center, Im Neuenheimer Feld 581, 69120, Heidelberg, Germany;Dept. of Clinical Radiology, University of Heidelberg, INF 400, 69120, Heidelberg, Germany;

关键词: Interim Analysis;    Local Control Rate;    Chordomas;    Relative Biologic Effectiveness;    Proton Therapy;   

DOI  :  10.1186/1471-2407-10-607

 received in 2010-08-17, accepted in 2010-11-05,  发布年份 2010

来源: Springer

【 摘 要 】

BackgroundChordomas of the skull base are relative rare lesions of the bones. Surgical resection is the primary treatment standard, though complete resection is nearly impossible due to close proximity to critical and hence also dose limiting organs for radiation therapy. Level of recurrence after surgery alone is comparatively high, so adjuvant radiation therapy is very important for the improvement of local control rates. Proton therapy is the gold standard in the treatment of skull base chordomas. However, high-LET beams such as carbon ions theoretically offer biologic advantages by enhanced biologic effectiveness in slow-growing tumors.Methods/designThis clinical study is a prospective randomised phase III trial. The trial will be carried out at Heidelberger Ionenstrahl-Therapie centre (HIT) and is a monocentric study.Patients with skull base chordoma will be randomised to either proton or carbon ion radiation therapy. As a standard, patients will undergo non-invasive, rigid immobilization and target volume delineation will be carried out based on CT and MRI data. The biologically isoeffective target dose to the PTV in carbon ion treatment (accelerated dose) will be 63 Gy E ± 5% and 72 Gy E ± 5% (standard dose) in proton therapy respectively. Local-progression free survival (LPFS) will be analysed as primary end point. Toxicity and overall survival are the secondary end points. Additional examined parameters are patterns of recurrence, prognostic factors and plan quality analysis.DiscussionUp until now it was impossible to compare two different particle therapies, i.e. protons and carbon ions directly at the same facility.The aim of this study is to find out, whether the biological advantages of carbon ion therapy can also be clinically confirmed and translated into the better local control rates in the treatment of skull base chordomas.Trial registrationClinicalTrials.gov identifier: NCT01182779

【 授权许可】

CC BY   
© Nikoghosyan et al; licensee BioMed Central Ltd. 2010