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NCT Number: NCT06528743

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis Stichting

Amsterdam, Netherlands

Location status: Recruiting

Location contact

Zeno Gouw

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • NSCLC (either pathology proven or sufficient clinical suspicion to be treated as NSCLC), referred for palliative radiotherapy of at least the primary tumor site.
  • Stage 2-4
  • WHO performance score 0-2.
  • Provision of signed, written and dated IC prior to any study specific procedures.

Exclusion criteria

  • Interstitial lung disease
  • Treatment with vascular endothelial growth factor receptor (VEGFR) inhibitors
  • Prior thoracic radiotherapy (>20 Gy EQD2 a/b 3) overlapping with the current planning target volume

Treatment and study plan

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

Radiation

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.

Primary outcomes

  1. the ability of patients to finish the radiotherapy schedule

    Time frame: 5 weeks

    The study is powered to find a decrease of response from 99% to no less than 84.15% (relative decrease of 15%).

Secondary outcomes

  1. Tumor response

    Time frame: at the end of treatment and after 3 months

    the relative volume change after radiotherapy vs the CTRT.

  2. treatment associated ≥ grade 2 non-hematologic toxicity according to the NCI Common Terminology Criteria of Adverse Events (CTCAE version 5.0) (from the first radiotherapy fraction until 6 months after radiotherapy)

    Time frame: from the first radiotherapy fraction until 6 months after radiotherapy

  3. Patient-reported outcome patient-reported outcome- Common Terminology Criteria of Adverse Events (PRO)-CTCAE

    Time frame: up to 1 year after radiation.

Study contacts

Contact information is provided by the study sponsor or research team.

Evelien Schouten

CONTACT

[email protected]

+31205129111

Zeno Gouw

CONTACT

[email protected]

+31205129111

Sponsors and collaborators

Lead sponsor

The Netherlands Cancer Institute

Other

Registry information

Acronym: PRIMER

Important dates

Study start
2024
Primary completion
2028
Study completion
2029
First posted
Jul 30, 2024
Registry last updated
Jan 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.