RecruitingNot ApplicableNCT06528743

Feasibility of Primer Shot Radiotherapy for Non-small Cell Lung Cancer - PRIMER


Sponsor

The Netherlands Cancer Institute

Enrollment

34 participants

Start Date

Aug 8, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Intro/rationale: Radiotherapy employs uniform, equally spaced weekday fractions that do not account for changes in tumor radiosensitivity. However, radiobiological characteristics evolve during the radiotherapy schedule as reoxygenation increases radiosensitivity. In tumor-response simulations and preclinical experiments, it was superior to prime the tumor with one radiotherapy fraction, followed by a treatment break permitting mitotic cell death and reoxygenation of tumor cells. Objective: To determine the safety and feasibility of primer shot fractionation for NSCLC. Study design: A prospective non-randomized feasibility trial to test the safety of primer shot fractionation in a 3+3 phase with increasing treatment breaks, followed by an expansion cohort. Study population: Patients with NSCLC stage 2-4, referred for palliative radiotherapy of the primary tumor and possibly (lymph node) metastases. Patients are allowed to receive systemic treatments, except for VEGFR-inhibitors. The 3+3 phase is followed by an expansion phase of 22 patients. Intervention: All treatments are 5x6 Gy to all targets. Patients receive an increasing primer shot treatment break. In the 3+3 phase, the break between the first and the second radiotherapy fraction is: 1, 2 and 3 weeks. The maximum tolerated break length will be used for the expansion cohort. Main study parameters/endpoints: The main study endpoint is the ability of patients to finish the radiotherapy schedule as planned. Secondary endpoints are tumor response at the end of treatment and 3 months thereafter, and acute toxicity. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Based on simulations and preclinical data, primer shot treatment breaks increase tumor control. However, the increased overall treatment time could potentially increase the chance a patient drops out before the radiotherapy schedule is finished. Because of the gradually prolonged break, this risk is relatively small and acceptable for this population. Additionally, patients are asked to fill in PRO-CTCAE lung subset questionnaires at the start of treatment and during follow-up. They will also receive 1 additional CT with contrast at fraction 5.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new type of radiation treatment called "Primer Shot" radiotherapy for people with non-small cell lung cancer (NSCLC) who are receiving palliative (symptom-relieving) radiation. The goal is to see if this approach is practical and effective for managing symptoms. **You may be eligible if...** - You are 18 years or older - You have been diagnosed with non-small cell lung cancer (NSCLC), stage 2–4 - You have been referred for palliative radiotherapy to treat at least the primary tumor - You are in reasonably good health (able to perform basic self-care) **You may NOT be eligible if...** - Your cancer is not NSCLC - Your performance status is poor (largely confined to bed) - You are unable to sign an informed consent form - You have not been referred for palliative radiotherapy Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONRT (5x6 Gy) to the primary tumor and, if indicated, to lymph node and/or distant metastases.

Patients will receive RT (5x6 Gy) to the primary tumor and, if indicated, to lymph node and/or distant metastases. Enrolled patients will receive a fractionation scheme with increasing break length.


Locations(1)

Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis Stichting

Amsterdam, Netherlands

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NCT06528743