Cardiovascular Morbidities and Lung Cancer Treatment: a Prospective Registry

NCT ID: NCT03368820

Last Updated: 2021-08-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-12-04

Study Completion Date

2023-12-31

Brief Summary

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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

Detailed Description

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Conditions

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Lung Neoplasm

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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No intervention

Treatment left at the discretion of the participant

Intervention Type OTHER

Eligibility Criteria

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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).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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European Lung Cancer Working Party

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Thierry Berghmans, MD, PhD

Role: STUDY_CHAIR

ELCWP

Locations

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Department of Intensive Care Unit and Thoracic Oncology Institut Jules Bordet

Brussels, , Belgium

Site Status RECRUITING

Hôpital Saint-Joseph

Charleroi, , Belgium

Site Status RECRUITING

CHU Tivoli

La Louvière, , Belgium

Site Status RECRUITING

Hôpital Ambroise Paré

Mons, , Belgium

Site Status RECRUITING

CH Peltzer-La Tourelle

Verviers, , Belgium

Site Status RECRUITING

Hôpital Mont-Godinne

Yvoir, , Belgium

Site Status RECRUITING

Countries

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Belgium

Central Contacts

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Thierry Berghmans, MD, PhD

Role: CONTACT

00322541311 ext. 3192

Anne-Pascale Meert, MD, PhD

Role: CONTACT

003225413111 ext. 3192

Facility Contacts

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Thierry Berghmans, MD

Role: primary

0032/2/5390496

Benoit Colinet, MD

Role: primary

Ingrid CsToth, MD

Role: primary

Stéphane Holbrechts, MD

Role: primary

Yves Bonduelle, MD

Role: primary

Sebahat Ocak, MD, PhD

Role: primary

Other Identifiers

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01151

Identifier Type: -

Identifier Source: org_study_id

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