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NCT06747026Completed

Real-World Immuno-Radiotherapy for Advanced NSCLC

Real-world Survival Outcomes and the Evaluation of Optimal Strategies for Immuno-Radiotherapy in Advanced Non-Small-Cell Lung Cancer: a Territory-wide Study (OCEANUS Study)

Source: ClinicalTrials.gov · Last updated 24 Dec 2024

Brief summary (registry, in English)

The optimal combination strategy for radiotherapy combined with immunotherapy (iRT) in advanced non-small-cell lung cancer (NSCLC) remains unclear, and there is a lack of real-world data to validate its efficacy. The objective of this study is to confirm the survival benefits of iRT in advanced NSCLC and to identify the optimal combination strategy for its use.

Status (registry)
Completed
Study type
Observational
Enrollment
338 (actual)
First submitted
18 Dec 2024
Start date
1 Jan 2015
Primary completion date
1 Dec 2024
Lead sponsor
Fengming Kong
Diseases
Lung cancer
NCT number
NCT06747026

What you commit to

  • Study type: Observational
  • Participants enrolled: 338
  • From 1 Jan 2015 to the primary completion date, 1 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who did not receive radiotherapy or who did not undergo radiotherapy within 90 days before or after immunotherapy

Other illness

  • Patients with multiple primary cancers or a pathological diagnosis of small cell lung cancer

Who the study is looking for

  • NSCLC patients who received immunotherapy between 2015 and 2021
  • For unresectable locally advanced NSCLC: definitive thoracic radiotherapy must have been administered as the initial treatment, with immunotherapy initiated within 90 days after RT or concurrently with RT
  • For de novo metastatic NSCLC: radiotherapy targeting the primary lung tumor or metastatic lesions must have been administered as the initial treatment, with immunotherapy initiated within 90 days after RT or concurrently with RT
  • For post-treatment progressive NSCLC: salvage radiotherapy must have been performed during immunotherapy or within 90 days after the cessation of immunotherapy
  • Age \>= 18 years old

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Queen Mary Hospital
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.