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Cardiovascular Morbidities and Lung Cancer Treatment: a Prospective Registry

Cardiovascular Morbidities and Lung Cancer Treatment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03368820
Enrollment
200
Registered
2017-12-11
Start date
2017-12-04
Completion date
2023-12-31
Last updated
2021-08-23

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

Conditions

Lung Neoplasm

Keywords

lung neoplasms, cardiovascular co-morbidity

Brief summary

Therapeutic algorithms for lung cancer are mainly based on randomised controlled trials which excluded patients with severe co-morbidities. Smoking, the main risk factor for lung cancer, is associated with cardiovascular events that may impact on the therapeutic decision. The aim of this registry is to determine if and how cardiovascular co-morbidities impact on the physicians' decision for anticancer treatment in lung cancer patients by comparing it to the European Lung Cancer Working Party (ELCWP) guidelines

Interventions

OTHERNo intervention

Treatment left at the discretion of the participant

Sponsors

European Lung Cancer Working Party
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Histological diagnosis of lung cancer, either NSCLC or SCLC patients and carcinoid tumours * Untreated lung cancer of any stage and any treatment (including palliative care only). * Availability for participating in the detailed follow-up of the protocol. * Signed informed consent. * Age above 18 years. * Presence of at least one co-morbidity: * Any active or past cardiac ischemia * Reduced left ventricular ejection fraction (\< 50%) * Obstructive cardiomyopathy * Valvular dysfunction (3 or 4/4; valvular replacement) * Arrhythmia (atrial flutter or fibrillation, significant ventricular arrhythmia, 2nd-3rd degree auriculo-ventricular block, Wolf-Parkinson-White and other similar aberrant conduction, bifascicular block, arrhythmogenic right ventricular dysplasia) * Uncontrolled hypertension (systolic blood pressure (BP) \> 160 millimeter of mercury (mmHg) or diastolic BP \> 100 mmHg on ≥ 1 hypotensive drug) or controlled hypertension on ≥ 2 concurrent hypotensive drugs * Active or treated peripheral arteritis (grade 2 or more) * Cerebrovascular events * Pulmonary embolism and/or thrombophlebitis or patients at high risk of thrombophilia (homozygous Leiden factor…) * Aortic aneurism

Exclusion criteria

* Thymoma and thymic malignancies, pleural mesothelioma. * Patient previously treated for lung cancer. * Tumours for which complete staging cannot be assessed. * History of prior malignant tumour, except non-melanoma skin cancer or in situ carcinoma of the cervix or of the bladder or cured malignant tumour (more than 5-year disease free interval).

Design outcomes

Primary

MeasureTime frameDescription
Treatment decision adequacy1 yearComparison of physician's treatment decision to current ELCWP guidelines

Secondary

MeasureTime frameDescription
Treatment decision adequacy according to histology1 yearComparison of physician's treatment decision to current ELCWP guidelines separately in small (SCLC) and non-small lung cancer (NSCLC)
Response rateEvery 3 cycles for chemotherapy (9 weeks) or 1 month after completion of radiochemotherapy (15 weeks)Response rate in patients with cardiovascular co-morbidities and adapted treatment using (World Health Organisation (WHO) criteria
Overall survival1 yearSurvival will be measured from the day of diagnostic biopsy. All patients have to be followed until death

Countries

Belgium

Contacts

Primary ContactThierry Berghmans, MD, PhD
thierry.berghmans@bordet.be00322541311
Backup ContactAnne-Pascale Meert, MD, PhD
nathalie.leclercq@bordet.be003225413111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026