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Spots Global Cancer Trial Database for Addition of Radiotherapy to Standard Medical Treatment for Stage IV NSCLC

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

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

Study Description

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).

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

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

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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