Clinical trial Recruiting at 1 site Interventional Ages 18 and up

New radiotherapy approach for advanced lung cancer

Official title: HERAN-Heterogeneously Hypofractionated Radiotherapy for Locally Advanced NSCLC

Run by Danish Lung Cancer Group · NCT03742687 · Data updated 2026-11-12

This study is testing a new type of radiotherapy for patients with advanced lung cancer who can't have regular treatment to see if it can help them live longer and feel better.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment151 (estimated)
SponsorDanish Lung Cancer Group
Academic / other
Drugs / interventionschemotherapy, radiation
Locations1 site (Aarhus)
StatusRecruiting
StartedNovember 22, 2018
Main results expectedDecember 30, 2023
Study endsDecember 30, 2026
Registry record updatedSeptember 11, 2023
Trial IDNCT03742687 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older with histologically confirmed, inoperable locally advanced NSCLC and a performance status of 0-2.

Probably not a fit

Patients with uncontrolled metastatic disease or other active malignancies are unlikely to benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates a novel treatment method called heterogeneously hypofractionated radiotherapy for patients with locally advanced non-small cell lung cancer (NSCLC) who cannot undergo standard chemoradiotherapy. The study aims to assess both the effectiveness and safety of this treatment option, which is designed to minimize damage to healthy tissue while providing adequate control of the cancer. Patients are categorized based on their ability to tolerate standard treatment, allowing for a tailored approach to their care. The goal is to improve survival rates and quality of life for these patients.

Why it matters

Potential benefit: If successful, this treatment could offer a viable alternative for patients with advanced lung cancer who currently have limited options.

How similar studies have gone: While this approach is innovative, similar studies have shown promise in improving treatment outcomes for patients with advanced lung cancer.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Histologically or cytological confirmed locally advanced, inoperable NSCLC.
* Age ≥18 years.
* Signed informed consent.
* Performance status 0-2.
* Able to comply with study and follow-up procedures.
* Fertile women must have a negative pregnancy test. Fertile men and women must use effective contraception. Fertile women included in the study must use the pill, spiral, depot injection of gestagen, subdermal implantation, hormonal vaginal ring or transdermal patch for the duration of study treatment and one month thereafter.

Exclusion Criteria:

* Prior radiotherapy to the thorax, unless there is no significant overlap of current treatment volumes with previous treatment fields.
* Dose plan conforming to protocol planning criteria not possible.
* Uncontrolled metastatic disease.
* Other active malignant disease.

Where it's running

  • Aarhus University Hospital
    Aarhus, Denmark
    Recruiting

Study contacts

  • Principal investigator: Azza A Khalil, MD, PhD — Aarhus University Hospital
  • Study coordinator: Azza A Khalil, MD, PhD
  • Email: azzakhal@rm.dk
  • Phone: +4578462556

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Curative chest re‑irradiation for thoracic cancers

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.