Sublobar Wedge Resection or Stereotactic Radiotherapy Treatment of High-risk Patients With Early-stage Lung Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAarhus University Hospital

About this trial

In low-risk patients with stage I non-small cell lung cancer (NSCLC) surgical treatment with an anatomical resection is currently the standard of care.

For medically inoperable patients with stage I NSCLC, radiation therapy is currently the standard treatment. The latest generation of radiation therapy modalities is Stereotactic Body Radiation Therapy (SBRT).

In high-risk patients, minimal invasive surgery in terms of sublobar resection (wedge resection) with lymph node sampling is currently the recommended treatment approach for these patients, even though the evidence is limited. Additionally, SBRT is an alternative treatment option but the use in these patients is also based on weak evidence. So, it is highly warranted to compare these two treatment options in this group of patients in a randomized, controlled trial where selection bias can be eliminated. It is the specific aim of this study to provide such a trial allowing an evidence-based approach when deciding between surgery and SBRT as treatment for NSCLC in high-risk patients.

The STRADOS study (STereotactic RADiotherapy Or Surgery) is an open randomized, controlled national multicenter study in which high-risk patients with stage I non-small-cell lung cancer (NSCLC) are randomized to receive either surgical treatment with minimal invasive wedge resection with lymph node sampling, or SBRT.

The overall purpose of the study is to investigate the disease-free survival (DFS) after surgical treatment when compared to SBRT. The primary endpoint is DFS after 3 years. Secondary endpoint is quality of life after 1, 3, 6, 12 and 36 months. Tertiary endpoints are overall survival (OS) after 3 and 5 years; DFS after 5 years; re-admission adverse events and complications after 1, 3, 6, 12 and 36 months; health-care related costs within 12 and 36 months; PRO data - other than quality of life (QoL) (health condition, symptoms and functional level) after 1, 3, 6, 12 and 36 months and lung function test after 12 month.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Biopsy-proven NSCLC

Diagnostic codes: DC34, DC 34.1, DC 34.2, DC 34.3 or DC 34.9

Clinical stage I NSCLC according to the 9th edition of TNM

Disqualifiers

Declared terminally ill or life expectancy shorter than one year.

Multifocal disease

PS ≥ 3

Centrally located tumors not eligible to SBRT

Trial design

Treatments tested in this trial

  • Stereotactic radiation therapy intervention
  • Surgical intervention

Treatment groups

182 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Aarhus University Hospital

Lead sponsor

Odense University Hospital

Collaborator

Aalborg University Hospital

Collaborator

Rigshospitalet, Denmark

Collaborator

Copenhagen University Hospital at Herlev

Collaborator

Bispebjerg Hospital

Collaborator

University Hospital, Gentofte, Copenhagen

Collaborator

Vejle Hospital

Collaborator

Zealand University Hospital

Collaborator

Aalborg University

Collaborator

University of Aarhus

Collaborator