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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02910895
Other study ID # N16STS
Secondary ID NL58626.031.16
Status Recruiting
Phase N/A
First received
Last updated
Start date September 9, 2017
Est. completion date September 2024

Study information

Verified date June 2024
Source The Netherlands Cancer Institute
Contact Rick Haas, MD, PhD
Phone +31 20 512 9111
Email r.haas@nki.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 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 Exclusion Criteria: - Known coagulation disorder and/or anticoagulant medication in as far it might interfere with a safe biopsy procedure (to the discretion of the treating physician and attending radiologist) - Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the study

Study Design


Intervention

Other:
tumor biopsy
biopsy

Locations

Country Name City State
Netherlands Netherlands Cancer Institute Amsterdam

Sponsors (2)

Lead Sponsor Collaborator
The Netherlands Cancer Institute KU Leuven

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary A platform of Patient Derived Xenografts (PDX) of Soft Tissue Sarcomas of patients with sarcomas take rate 4 months
Primary The take-rate of fresh human PDX tumour material in nude mice. take rate 4 months
Primary A consistent system for further anti-sarcoma therapy (both RT and chemotherapy experiments) take rate 2 years after start of study
Primary A platform of 2D/3D cell cultures (organoids) of Soft Tissue Sarcomas. take rate 6 weeks
Primary A model for translational research take rate 2 years after start of study
Secondary The passage possibilities of human PDX tumour material by freezing, storing, thawing and re-inoculating in nude mice take rate of continuous growth of implantation of tumor material 4 months after implantation of tumour material
Secondary Fractionation sensitivity on several STS subtypes in PDX. take rate 4 months
Secondary To study the passage possibilities of 2D/3D cell cultures by freezing, storing and thawing take rate of continuous growth 1 month
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