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

NCT05223647 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 239

Last updated 2026-01-28

No results posted yet for this study

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.

Conditions

  • Small-cell Lung Cancer

Interventions

PROCEDURE

Thoracic radiotherapy

30Gy/10 fractions thoracic radiotherapy given between 2nd and 3rd course of chemo-immunotherapy.

DRUG

Chemo-immunotherapy

Four courses of carboplatin/etoposide/durvalumab every 3 weeks followed by durvalumab every 4 weeks until intolerable toxicity, progressive disease leading to a need for other treatment, or until the patient no longer wishes to continue treatment.

Sponsors & Collaborators

  • St. Olavs Hospital

    collaborator OTHER
  • Haukeland University Hospital

    collaborator OTHER
  • University Hospital of North Norway

    collaborator OTHER
  • Alesund Hospital

    collaborator OTHER
  • Helse Stavanger HF

    collaborator OTHER_GOV
  • Oslo University Hospital

    collaborator OTHER
  • Helse Nord-Trøndelag HF

    collaborator OTHER
  • Helse Fonna

    collaborator OTHER
  • Drammen sykehus

    collaborator OTHER
  • University Hospital, Akershus

    collaborator OTHER
  • Erasmus Medical Center

    collaborator OTHER
  • Sahlgrenska University Hospital

    collaborator OTHER
  • Karolinska University Hospital

    collaborator OTHER
  • Gävle Hospital

    collaborator OTHER
  • Sykehuset Innlandet HF

    collaborator OTHER
  • North Estonia Medical Centre

    collaborator OTHER
  • Nordlandssykehuset HF

    collaborator OTHER
  • Landspitali University Hospital

    collaborator OTHER
  • Lund University Hospital

    collaborator OTHER
  • University Hospital, Linkoeping

    collaborator OTHER
  • Norwegian University of Science and Technology

    lead OTHER

Principal Investigators

  • Magnus Steigedal, PhD · Department of Clinical and Molecular Medicine, NTNU

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-11
Primary Completion
2025-09-04
Completion
2025-09-04

Countries

  • Estonia
  • Iceland
  • Netherlands
  • Norway
  • Sweden

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05223647 on ClinicalTrials.gov