Development of a Platform of Patient Derived Xenografts (PDX) and 2D/3D Cell Cultures of Soft Tissue Sarcomas (STS): Protocol to Obtain Tumour Material From Patients With STS.

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Outside the setting of well-designed prospective clinical studies, the current standard preoperative RT should be a conventionally 1.8-2 Gy fractionated regimen to a total dose of 50 Gy in 5-6 weeks. However, given the vast diversity of sarcoma subtypes, it is also unlikely to assume a uniform therapeutic management to be optimal for all sarcomas alike. Other than 2 Gy fraction sizes and/or 50 Gy total dose series have been investigated in the past and should be further exploited in the future, but the practical implementation in humans is hampered by the rarity of the disease. The current systemic treatment of sarcomas consists of both the older cytotoxic chemotherapies and the newer targeted therapies like tyrosine kinase inhibitors. But it is hard to predict which patients will respond to which specific systemic treatment. This leads to worse prognoses and unnecessary toxicity for sarcoma patients. Despite the fact that the number of sarcoma patients in current studies is too small with a mix of different subtypes, some subtypes show a better response than other subtypes. This platform may form the basis for preclinical translational investigations with radiotherapy and various systemic treatments.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically confirmed diagnosed (non-) metastatic intermediate to high grade STS

• Local recurrences are allowed

• Age ≥ 18 years

• Able and willing to undergo tumour biopsies or tumour sampling during surgery

• Localization of sarcoma enables safe biopsy or surgery

• Written informed consent

Locations
Other Locations
Netherlands
Netherlands Cancer Institute
RECRUITING
Amsterdam
Contact Information
Primary
Rick Haas, MD, PhD
r.haas@nki.nl
+31 20 512 9111
Backup
Astrid Scholten, MD, PhD
a.scholten@nki.nl
+31 20 512 9111
Time Frame
Start Date: 2017-09-09
Estimated Completion Date: 2024-09
Participants
Target number of participants: 40
Treatments
Other: single arm
single tumor biopsy
Related Therapeutic Areas
Sponsors
Leads: The Netherlands Cancer Institute
Collaborators: KU Leuven

This content was sourced from clinicaltrials.gov

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