SAR-Reg

Sarcoma
Soft tissue sarcomas, Other sarcoma diseases, Bone sarcomas, GIST (gastrointestinal stromal tumor)
Register and supportive Studies
Aim of the study Intensive research into biological correlations and their translation into clinical application is continuously working to improve the treatment of malignant diseases. The individual treatment options result from the combination of a detailed biological characterization of the tumour cells and a comprehensive assessment of the condition of the respective patient. You have been diagnosed with a sarcoma or there is a strong suspicion that you have a sarcoma. With this letter we invite you to participate in a research project for the systematic data collection and characterization of sarcoma diseases. The Sarcoma Registry Study is a study that aims to systematically investigate and characterize the biological and clinical aspects of sarcoma diseases. The collection and archiving of clinical data serves the purpose of medical research. Your consent to the use of associated data is voluntary. If you do not wish to participate or wish to withdraw your consent at a later date, you will not suffer any disadvantages as a result. The aim of the sarcoma study is to carry out analyses of the data and samples obtained, but also to make the samples and data obtained available to future projects researching malignant diseases. Translated with DeepL.com (free version)
Aim of the study Intensive research into biological correlations and their translation into clinical application is continuously working to improve the treatment of malignant diseases. The individual treatment options result from the combination of a detailed biological characterization of the tumour cells and a comprehensive assessment of the condition of the respective patient. You have been diagnosed with a sarcoma or there is a strong suspicion that you have a sarcoma. With this letter we invite you to participate in a research project for the systematic data collection and characterization of sarcoma diseases. The Sarcoma Registry Study is a study that aims to systematically investigate and characterize the biological and clinical aspects of sarcoma diseases. The collection and archiving of clinical data serves the purpose of medical research. Your consent to the use of associated data is voluntary. If you do not wish to participate or wish to withdraw your consent at a later date, you will not suffer any disadvantages as a result. The aim of the sarcoma study is to carry out analyses of the data and samples obtained, but also to make the samples and data obtained available to future projects researching malignant diseases.