University Hospital Essen
Essen, Germany
Location status: Recruiting
NCT Number: NCT06247163
There is a prospective risk-adapted evaluation of the optimal dose of radiotherapy for definitive radiotherapy of locally advanced small cell lung cancer within the corridor recommended as standard therapy according to the current interdisciplinary S3 guideline of the German Cancer Society/Cancer Aid/AWMF
Interested in participating?
Request Info18 year and older
All sexes
Observational
Essen, Germany
Location status: Recruiting
The main objective of this study is to determine whether patients with SCLC who have a metabolically active residual tumor in the fluorodeoxyglucose (FDG) PET/CT scan after two to three cycles of induction chemotherapy have a similarly low local recurrence rate with higher dose. There is a prospective risk-adapted evaluation of the optimal dose of radiotherapy for definitive radiotherapy of locally advanced small cell lung cancer within the corridor recommended as standard therapy according to the current interdisciplinary S3 guideline of the German Cancer Society/Cancer Aid/AWMF. Allocation to PET boost, if confirmed vital tumor rest by PET CT and biopsy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
An Interim PET CT will be performed. If there is residual vital tumor, a higher radiation dose will be applied.
Time frame: 2 months to 5 years
Local recurrence free survival
Time frame: 2 months to 5 years
Distant recurrence free survival
Time frame: 2 months to 5 years
Overall survival
Contact information is provided by the study sponsor or research team.
University Hospital, Essen
Other
Prospective PET-guided Radiotherapy for Patients With Small Cell Lung Cancer.
Acronym: PET-ART
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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