⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Chemo-immunotherapy Plus Thoracic Radiotherapy in Extensive Stage Small-cell Lung Cancer

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: Chemo-immunotherapy Plus Thoracic Radiotherapy in Extensive Stage Small-cell Lung Cancer

Official Title: Randomized Phase III Trial Investigating the Survival Benefit of Adding Thoracic Radiotherapy to Durvalumab (MEDI4736) Immunotherapy Plus Chemotherapy in Extensive Stage Small-cell Lung Cancer

Study ID: NCT05223647

Study Description

Brief Summary: Studies have shown that combining chemotherapy and immune checkpoint inhibitors (ICI) prolongs survival compared with chemotherapy alone in extensive stage small-cell lung cancer (ES SCLC), but the survival benefit is modest. The main aim of this trial is to investigate whether there is a synergistic/additive effect of concurrent thoracic radiotherapy in ES SCLC patients receiving carboplatin/etoposide/durvalumab.

Detailed Description: Studies show that adding ICI therapy to standard chemotherapy prolongs survival in ES SCLC. The survival benefit, however, is modest, and there is a need for more effective therapy. It has been hypothesized that there is a synergistic effect of combining ICI with radiotherapy. In this randomized phase III study, the main aim is to investigate whether concurrent thoracic radiotherapy of 30 Gy/10 fractions improves survival in ES SCLC patients receiving carboplatin/etoposide/durvalumab. It is currently not possible to classify the patients who benefit from ICIs in SCLC. In this study, biological material (tissue, blood, feces) which will be analyzed for potential predictive and prognostic biomarkers. Prophylactic cranial irradiation in ES SCLC is debated, mainly due to the potentially detrimental effect on cognition. Thus, frequency and timing of brain metastases and cognitive function will be assessed before, during and after study treatment.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

North Estonia Medical Centre, Tallinn, , Estonia

Landspitali University Hospital, Reykjavík, , Iceland

Erasmus MC, Rotterdam, , Netherlands

Haukeland Universitetssykehus, Bergen, , Norway

Nordlandssykehuset HF, Bodø, , Norway

Drammen sykehus - Vestre Viken, Drammen, , Norway

Innlandet hospital Gjøvik, Gjøvik, , Norway

Haugesund hospital, Haugesund, , Norway

Sykehuset Levanger, Levanger, , Norway

Akershus Universitetssykehus AHUS, Oslo, , Norway

Oslo University Hospital Ullevål, Oslo, , Norway

Stavanger University Hospital, Stavanger, , Norway

University Hospital of North Norway, Pulmonology Department, Tromsø, , Norway

Cancer Clinic at St. Olavs Hospital, Trondheim, , Norway

Ålesund Hospital, Ålesund, , Norway

Gävle hospital, Gävle, , Sweden

Sahlgrenska Sjukehuset, Göteborg, , Sweden

Linköping University Hospital, Linköping, , Sweden

Lund University Hospital, Skåne, , Sweden

Karolinska University Hospital, Stockholm, , Sweden

Contact Details

Name: Magnus Steigedal, PhD

Affiliation: Department of Clinical and Molecular Medicine, NTNU

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: