Atezolizumab After Concurrent Chemo-radiotherapy Versus Chemo-radiotherapy Alone in Limited Disease Small-cell Lung Cancer

NCT03540420 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 212

Last updated 2026-04-13

No results posted yet for this study

Summary

Some patients with limited disease small-cell lung cancer (LD SCLC) are cured after chemo-radiotherapy, but the majority relapse and die from their cancer. Better therapy is needed. Immunotherapy represents the largest advance in cancer therapy in recent years and has demonstrated promising activity in SCLC. In this study we will investigate whether atezolizumab prolongs survival in LD SCLC patients who have undergone chemo-radiotherapy.

Conditions

  • Small-cell Lung Cancer

Interventions

DRUG

Atezolizumab

atezolizumab 1200 mg intravenous every 3 weeks in 12 months

Sponsors & Collaborators

  • University Hospital of North Norway

    collaborator OTHER
  • Alesund Hospital

    collaborator OTHER
  • Vestre Viken Hospital Trust

    collaborator OTHER
  • University Hospital, Akershus

    collaborator OTHER
  • Helse Nord-Trøndelag HF

    collaborator OTHER
  • Helse Stavanger HF

    collaborator OTHER_GOV
  • Haukeland University Hospital

    collaborator OTHER
  • Sorlandet Hospital HF

    collaborator OTHER_GOV
  • Ullevaal University Hospital

    collaborator OTHER
  • Molde Hospital

    collaborator OTHER
  • Helse Fonna

    collaborator OTHER
  • Nordlandssykehuset HF

    collaborator OTHER
  • Volda Hospital

    collaborator OTHER
  • Kristiansund Hospital

    collaborator OTHER
  • Sahlgrenska University Hospital

    collaborator OTHER
  • Skane University Hospital

    collaborator OTHER
  • Karolinska University Hospital

    collaborator OTHER
  • Ôrebro University Hospital

    collaborator UNKNOWN
  • Gävle Hospital

    collaborator OTHER
  • University Hospital, Linkoeping

    collaborator OTHER
  • Odense University Hospital

    collaborator OTHER
  • Aalborg University Hospital

    collaborator OTHER
  • Rigshospitalet, Denmark

    collaborator OTHER
  • National Cancer Center Affiliate of Vilnius University Hospital Santaros Klinikos

    collaborator OTHER
  • Kantonsspital Winterthur KSW

    collaborator OTHER
  • University Hospital, Basel, Switzerland

    collaborator OTHER
  • Insel Gruppe AG, University Hospital Bern

    collaborator OTHER
  • Kantonsspital Graubünden

    collaborator OTHER
  • Freiburger Spital

    collaborator OTHER
  • Klinik Hirslanden, Zurich

    collaborator OTHER
  • Kantonsspital Olten

    collaborator OTHER
  • Spital STS AG

    collaborator INDUSTRY
  • Ente Ospedaliero Cantonale, Bellinzona

    collaborator OTHER
  • Cantonal Hospital of St. Gallen

    collaborator OTHER
  • St. Olavs Hospital

    collaborator OTHER
  • Oslo University Hospital

    collaborator OTHER
  • Rijnstate Hospital

    collaborator OTHER
  • Isala

    collaborator OTHER
  • Zuyderland Medisch Centrum

    collaborator OTHER
  • The Netherlands Cancer Institute

    collaborator OTHER
  • St. Antonius Hospital

    collaborator OTHER
  • Amphia Hospital

    collaborator OTHER
  • Medisch Spectrum Twente

    collaborator OTHER
  • Erasmus Medical Center

    collaborator OTHER
  • Norwegian University of Science and Technology

    lead OTHER

Principal Investigators

  • Torstein B Rø, MD, PhD · Norwegian University of Science and Technology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-31
Primary Completion
2024-04-01
Completion
2027-04-01

Countries

  • Denmark
  • Lithuania
  • Netherlands
  • Norway
  • Sweden
  • Switzerland

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 NCT03540420 on ClinicalTrials.gov