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A Phase 2, Single Arm, Multi Center Trial Evaluating the Efficacy of the COmbination of Sirolimus and cYclophosphamide in Metastatic or Unresectable Myxoid Liposarcoma and chOndrosarcoma
Chondrosarcoma and liposarcoma consists of different subtypes with a wide range of patient survival. Current treatment options consist of wide surgical resection, however for patients with a local recurrence or metastatic disease the outcome is poor. New treatment options being evaluated and mouse models show in vivo that mammilian target of rapamycin (mTOR) inhibition can prevent tumour growth. mTOR is an kinase that is present in two complexes and thereby activates multiple pathways. Aberrant mTOR signalling is known to be involved in cancer cell survival. Several clinical studies for patients with bone or soft tissue sarcoma treated with mTOR inhibitors have been conducted and they show promising results. From these studies the investigators can conclude that the combination of an mTOR inhibitor with cyclophosphamide shows promising results in chondrosarcoma. With the lack of other treatment options for unresectable and metastatic chondrosarcoma or myxoid liposarcoma the Eurosarc consortium (www.eurosarc.eu) decided to treat these patients in a standardised way according to a common protocol with the combination of sirolimus and cyclophosphamide using the growth modulation index for evaluation in the current clinical study protocol.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
LUMC
Leiden, Netherlands
Hospital de Sant Pau
Barcelona, Spain
Hospital Val d'Hebron
Barcelona, Spain
CIO Clara Campal
Madrid, Spain
Hospital Universitario Virgen del Rocío
Seville, Spain
Hospital Universitario y Politécnico de La Fe
Valencia, Spain
Instituto Valenciano de Oncología
Valencia, Spain
Start Date
June 1, 2014
Primary Completion Date
December 1, 2021
Completion Date
December 1, 2021
Last Updated
April 20, 2022
70
ACTUAL participants
sirolimus and cyclophosphamide
DRUG
Lead Sponsor
Leiden University Medical Center
NCT02048371
NCT03397186
Data Source & Attribution
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