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Immune Boost In Non-Small Cell Lung Cancer

A Randomized Phase II Study of Radiation Induced Immune Boost in Operable Non-small Cell Lung Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02319408
Acronym
RadImmune
Enrollment
36
Registered
2014-12-18
Start date
2016-04-30
Completion date
2020-02-29
Last updated
2022-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer

Brief summary

Insufficient migration and activation of tumour specific effector T cells seems to be the one important reason for inadequate host anti-tumour immune response. Ionizing radiation can induce a variety of immune responses. The goal of this randomized trial is to assess if a preoperative single fraction low dose radiation is able to improve anti-tumour immune response in operable early stage lung cancer.

Interventions

Lobectomy for lung cancer following preoperative radiation

Sponsors

German Cancer Research Center
CollaboratorOTHER
Heidelberg University
CollaboratorOTHER
University Hospital Heidelberg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologically proven clinical stage I to IIA pulmonary adenocarcinoma * Lung tumor is felt to be curatively resectable by the treating physicians * Sufficient pulmonary function for lobectomy according to current guidelines * The patient is free of distant metastases as confirmed by contrast-enhanced chest and upper abdomen CT-scan and by contrast-enhanced CT or MRI of the brain * Age over 50years at the time of consent due to federal radiation protection law * In female patients of childbearing potential there must be a negative pregnancy test * Eastern Cooperative Oncology Group performance status of 0,1, 2 or 3 at the time of randomization * Patients who the investigator believes can and will comply with the requirements of this protocol * Written informed consent according to good clinical practise and national/regional regulations

Exclusion criteria

* The patient shows clinical signs of pneumonia * The patient receives immunosuppressive drugs (alkylating agents, antimetabolites, methotrexate, azathioprine, mercaptopurine, cytotoxic antibodies, ciclosporin, tacrolimus, sirolimus, interferon, mycophenolate, small biological agents) * The patient has been diagnosed with a potential immune mediated disease * Elevated blood leukocyte count or erythrocyte sedimentation rate * Pregnancy * The patient has received any cancer specific treatment, including radiotherapy, immunotherapy, hormonal therapy or chemotherapy * The patient is diagnosed with a concomitant malignancy and/or has a history of malignancy within the past five years or has had a malignancy that has been in complete remission for less than 5 years * The patient needs chronic long term oxygen therapy * The patient has undergone splenectomy * The patient is known to be HIV positive * The patient has an uncontrolled bleeding disorder

Design outcomes

Primary

MeasureTime frameDescription
Cluster of differentiation (CD)8+ T cells in resected NSCLC7 daysFrequencies of CD8+ T cells in resected NSCLC tumors determined by immunohistochemistry

Secondary

MeasureTime frameDescription
T cell subtypes in resected NSCLC7 daysFrequencies of CD3+, CD4+, CD45RO and Foxp3+ T cells in resected NSCLC tumors determined by immunohistochemistry and flow cytometry

Other

MeasureTime frameDescription
Tumor reactive T cells3 monthsFrequencies of tumor reactive T cells in blood and bone marrow before radiotherapy and after surgery

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026