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Brief Title: Addition of Radiotherapy to Standard Medical Treatment for Stage IV NSCLC
Official Title: Multicentre Phase III Study: Addition of Radiotherapy to Standard Medical Treatment for Stage IV NSCLC
Study ID: NCT04530708
Brief Summary: The hypothesis for this study is that addition of a moderate dose of radiotherapy to the primary tumor and mediastinal nodes after three months of medical treatment could reduce the tumor burden, partly as an abscopal effect, and thereby improving quality of life and possible also prolonging survival for stage IV NSCLC.
Detailed Description: Primary objective: To assess whether the addition of radiotherapy to the remaining thoracic tumor burden following standard medical treatment results in a superior quality of life measured with lung cancer symptom scale (LCSS) in patients with stage IV non-small cell lung cancer. The comparison will be made at three months after randomization. Secondary objectives: Overall survival, progression-free survival, toxicity and longitudinal quality of life measurements. Design: Multicentre, randomized, phase III trial. Patients will be registered for the study up-front but randomization will be performed after evaluation of response, three months after initiating medical treatment with chemotherapy/ chemo-immunotherapy or immunotherapy. Randomization will be to thoracic radiotherapy or follow-up (1:1).
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Department of Oncology, Norrlands Universitetssjukhus, Umeå, Norrland, Sweden
Department of Oncology, Karolinska University Hospital, Stockholm, Stockholm County, Sweden
Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Västra Götaland, Sweden
Name: Jan Nyman, Ass.prof
Affiliation: Sahlgrenska University Hospital, Sweden
Role: PRINCIPAL_INVESTIGATOR
Name: Thomas Björk-Eriksson, Prof.
Affiliation: Regionalt Cancercentrum Väst
Role: STUDY_DIRECTOR