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Clinical Trial Summary

Non-interventional study consisting of a population of patients who had received for soft tissue sarcoma by at least 2 courses of Yondelis® at a dose of 1.5 mg / m² / 3 weeks after failure or intolerance to doxorubicin / ifosfamide from 2007 to 2011.


Clinical Trial Description

Patient selection is based on a database of retrospectively within the GSF / GETO.

The tumor assessment must be made by scanner at baseline and post-C2 or C3 and should be available and sent to sponsor.

The comparative reading of the imaging is centralized and made without the knowledge of the local assessment:

- sum of the large diameter for 2 imagery (baseline and 1st evaluation

- tumor density on areas of interest for the 2 imaging (baseline and 1st evaluation

- Rank patients according to two methods (Choi and RECIST): complete response, partial response, stability, progress and non-assessable. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01650077
Study type Observational
Source Centre Oscar Lambret
Contact
Status Completed
Phase
Start date September 21, 2012
Completion date October 28, 2014

See also
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