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OpenTrials
Completed

NCT Number: NCT02488850

Determination of Peripheral Immune Cell Activity During Treatment With Either Surgery or Radiotherapy in Patients With Early Stage NSCLC

Rationale: An anatomical surgical resection is considered to be the standard of care in fit patients who present with early stage non-small cell lung cancer (NSCLC). However, surgery is less frequently performed in both elderly patients (aged ≥75 years), who represent the fastest-growing group of patients with stage I/II NSCLC, and in patients who have significant co-morbidity. Following the introduction of stereotactic ablative radiotherapy (SABR), an outpatient treatment that is typically delivered in between 3-8 fractions, the median survival of all elderly patients undergoing radiotherapy in The Netherlands increased by 9.3 months. Randomized trials comparing SABR and surgery have yet to be completed and results of the ongoing ACOSOG Z4032 studies will not be available in the within 5 years. A recent data retrospective study comparing both modalities has raised interesting questions about the impact of local therapy on recurrence patterns. It was found that a better loco-regional disease control rate was achieved with SABR.

Objective: To study the effect of surgery and SABR on both immunostimulatory (with primary endpoint CD8 positive cells) and immunosuppressive cells in peripheral blood in patients with early stage non-small cell lung cancer who are treated with either modality.

Study population: 40 patients with cT1-2aN0M0 either cytologically or histologically proven NSCLC.

Main study parameters/endpoints: To determine whether an increase in CD8 activity can be established after SABR in patients with early stage lung cancer and to compare this increase with that in patients undergoing a surgical intervention. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Only risks in participation are the risks with drawing blood. Subjects will not have any benefits. This pilot study will be used to generate information concerning both treatments useful for the decision to plan a future study in a larger series of patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Erasmus MC Cancer Institute, Rotterdam, South Holland, Netherlands

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Cytologically or histologically proven cT1-2aN0M0 NSCLC
  • Patients ≥ 18 years old
  • Patients should be fit to undergo both treatments in accordance with institutional protocols

Exclusion criteria

  • Patients with any signs of any co-existing infectious disease or immunosuppressive treatment (inhalation steroids are permitted)
  • Mentally incapacitated subjects

Treatment and study plan

Surgery

Procedure

SABR

Radiation

Primary outcomes

  1. Number of IFN-gamma/ Granzyme B producing CD8 T cells

    Time frame: Baseline (week 0)

    Number and activation status of peripheral CD8+ T cells

  2. Number of IFN-gamma/ Granzyme B producing CD8 T cells

    Time frame: Week 1

    Number and activation status of peripheral CD8+ T cells

  3. Number of IFN-gamma/ Granzyme B producing CD8 T cells

    Time frame: Week 2

    Number and activation status of peripheral CD8+ T cells

  4. Number of IFN-gamma/ Granzyme B producing CD8 T cells

    Time frame: Week 3

    Number and activation status of peripheral CD8+ T cells

  5. Number of IFN-gamma/ Granzyme B producing CD8 T cells

    Time frame: Week 6

    Number and activation status of peripheral CD8+ T cells

Secondary outcomes

  1. CD4/CD8 ratio in peripheral blood

    Time frame: Baseline

  2. CD4/CD8 ratio in peripheral blood

    Time frame: Week 1

  3. CD4/CD8 ratio in peripheral blood

    Time frame: Week 2

  4. CD4/CD8 ratio in peripheral blood

    Time frame: Week 3

  5. CD4/CD8 ratio in peripheral blood

    Time frame: Week 6

  6. number of regulatory T cells

    Time frame: Baseline

  7. number of regulatory T cells

    Time frame: Week 1

  8. number of regulatory T cells

    Time frame: Week 2

  9. number of regulatory T cells

    Time frame: Week 3

  10. number of regulatory T cells

    Time frame: Week 6

  11. Activation marker expression on T cells

    Time frame: Baseline

  12. Activation marker expression on T cells

    Time frame: Week 1

  13. Activation marker expression on T cells

    Time frame: Week 2

  14. Activation marker expression on T cells

    Time frame: Week 3

  15. Activation marker expression on T cells

    Time frame: Week 6

Sponsors and collaborators

Lead sponsor

Erasmus Medical Center

Other

Registry information

Official study title

Determination of Peripheral Immune Cell Activity During Treatment With Either Surgery or Radiotherapy in Patients With Early Stage Non-small Cell Lung Cancer HAMLET Study

Acronym: HAMLET

Important dates

Study start
2012
Primary completion
2022
Study completion
2022
First posted
Jul 2, 2015
Registry last updated
Nov 7, 2024

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.

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