COr Loco-regional Advanced Lung Cancer Treated With Chemo-radiotherapy (COLA)

Sponsor
Odense University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05258448
Collaborator
(none)
100
1
106
0.9

Study Details

Study Description

Brief Summary

Patients with loco-regional NSCLC planned for curative treatment with chemoradiotherapy will be invited to participate in a prospective study; besides routine treatment, the patients will be followed with an ECG and cardiac MR for at least two years after radiotherapy treatment.

Condition or Disease Intervention/Treatment Phase
  • Other: Chemoradiotherapy

Detailed Description

Definitive chemo-radiotherapy is the treatment of choice for loco-regional advanced non-small cell lung cancer (LA-NSCLC). However, the treatment is associated with a range of side effects with radiation pneumonitis and esophagitis. In addition, the toxicity of the heart in lung cancer patients treated with radiotherapy has been offered less consideration. Therefore, it is essential to investigate the possible early and late toxicity to the heart and the baseline cardiac status of these patients. This study will describe cardiac comorbidity before radiotherapy treatment by a thorough history. Furthermore, we will evaluate heart function and evaluate possible heart disease by an ECG and cardiac MR. Patients will be followed with ECG and cardiac MR for two years after radiotherapy, detecting structural changes caused by radiotherapy and subclinical disease after radiotherapy.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Effect of Radiotherapy on the Heart in Loco-regional Advanced NSCLC Patients Treated With Definitive Radiotherapy Measured by Cardiac MR
Actual Study Start Date :
Aug 1, 2015
Anticipated Primary Completion Date :
Jan 1, 2023
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
COLA 1: Locally advanced non-small-cell lung cancer

Patients with locally advanced non-small-cell lung cancer treated with radiotherapy alone or in combination with chemotherapy with curative intent. Patients are included before initiation of the treatment. A Cardiac MR and ECG are performed at the beginning of the treatment, and at 6, 12, and 24 months after radiotherapy.

Other: Chemoradiotherapy
Cardiac Magnetic Resonance scan and ECG

COLA 2 Locally advanced non-small-cell lung cancer

Patients with locally advanced non-small-cell lung cancer treated with radiotherapy alone or in combination with chemotherapy with curative intent. Patients not included in COLA 1 cohort are offered one cardiac MR and ECG between 12-24 months after radiotherapy treatment.

Other: Chemoradiotherapy
Cardiac Magnetic Resonance scan and ECG

Outcome Measures

Primary Outcome Measures

  1. Overall survival [2 Years]

    All cause mortality

  2. Change in Left Ventricular Ejection Fraction [Baseline, at 6, 12 and 24 months.]

    Change from baseline, evaluated by cardiac MR

  3. Number of participants with treatment related adverse events and cardiac disease after radiotherapy as assesed by CTCAE v4.0. [2 years.]

    Assesed by patient interview and review of medical record.

  4. Cardiovascular specific mortality [2 years.]

    Assesed by patient interview and review of medical record

Secondary Outcome Measures

  1. Late enhacment [At Baseline, 6, 12 and 24 months.]

    Evaluated by cardiac MR.

  2. LVEDV changes [2 years]

    Left ventricular enddiastolic change in cMR

  3. LVESV changes [2 years]

    Left ventricular endsystolic change in cMR

  4. LV mass in gram [2 years]

    Left ventricular mass in gram.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age ≥ 18 Years

  • Inoperable and histologically/cytologically verified NSCLC.

  • Planned treatment with curative intent.

  • Capable of completing study procedures ECG and Cardiac MR.

  • Able of giving written and informed consent before study procedures are initiated.

Exclusion Criteria:
  • Vulnerable patients.

  • Patients with operable devices as pacemaker/ICD and cochlear implant or other conditions where MR scan is contraindicated.

  • Claustrophobia.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Odense University Hospital Odense C Denmark 5000

Sponsors and Collaborators

  • Odense University Hospital

Investigators

  • Principal Investigator: Tine Schytte, Professor, Odense University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Agon Olloni, Principal Investigator, MD, Phd Student, Odense University Hospital
ClinicalTrials.gov Identifier:
NCT05258448
Other Study ID Numbers:
  • S-20160086
First Posted:
Feb 28, 2022
Last Update Posted:
Feb 28, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 28, 2022