Clinical and Molecular Study With Digital Support of Patients With Inoperable Lung Cancer

NCT ID: NCT05372081

Last Updated: 2022-05-13

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

2022-03-23

Study Completion Date

2025-03-31

Brief Summary

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The purpose of this study is to provide high quality oncology services to patients with inoperable Non-Small Cell Lung Cancer (NSCLC) in Greece. These services will be based on 3 pillars:

1. Clinical: personalized treatment will be administered and its effectiveness and safety will be recorded and evaluated.
2. Molecular: the gene footprint of each patient at the beginning of his treatment, the molecular identity of his tumor will be analyzed and recorded based on analysis with modern Next Generation Sequencing (NGS) techniques.
3. Digital: Patients will have access to the digital platform where they will record the adverse reactions they will face during their treatment.

Detailed Description

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Lung cancer is the primary cause of cancer death worldwide regardless of gender or age group. Based on the most recent statistics for our country, every year about 9000 new cases of lung cancer are diagnosed. Lung cancer is the most common type of cancer in Greece in both men and women. It is estimated that about 8000 people lose their lives annually from this disease, while the total number of deaths from lung cancer seems to exceed in number the sum of deaths due to breast, prostate and colorectal cancer.

For many decades chemotherapy was the cornerstone and the only treatment option for lung cancer. In the last 20 years, the discovery and study of various molecular subtypes in non-small cell lung cancer has led to the development of targeted therapies. Modern oncology has multiple targeted therapies for corresponding molecular subtypes, such as ROS-1 rearrangements, amplifications and mutations of the MET gene, RET rearrangements, mutations of the BRAF gene, NTRK gene fusions, HER2 gene mutations, as well as KRAS mutations.The detection of molecular pathways, targeted mutations and biomarkers is a critical step in the diagnosis and treatment of patients with non-small cell lung cancer, in both early and advanced stage.The use of NGS (Next Generation Sequencing) technology as modern tool for accessing genetic material is adopted by more and more clinicians worldwide. The molecular analysis of the tumor with the technique of NGS, is considered as a necessity in the practice of modern oncology in order the patients to receive the best treatments for their disease.

a) Clinical pillar: In this study will be included 200 patients, 18 years old and older, with PS 0-2, treated for inoperable NSCLC stage IV. Patient will be treated according to the local standard of care based on their medical history. b)After signing the Informed Consent patients will provide biological material (blood samples and Formalin fixed paraffin embedded tissues) in order to proceed with the molecular arm of the study and the extended NGS analysis. In addition to molecular analysis, an economic analysis of the use of health resources will follow for a detailed understanding of the relevant financial aggregates and the improvement of the performance of existing resources. c) On the digital arm each patient will have access in the digital platform of CAREACCROSS which allows continuous and remote access for both patient and their physician with absolute security and data privacy.

All patients will be included in the digital monitoring and information program from their mobile phone and will have contact the investigator and the study team.

Conditions

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Non-Small Cell Carcinoma of Lung, TNM Stage 4

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients who will receive digital assistant

Patients will receive digital assistance (in a few words text format) for any symptoms/adverse events they will include in their profile in the digital platform.

Digital platform

Intervention Type OTHER

Patients will be randomized (1:1) in the way they will receive or not any assistance from the digital platform.

Patients who will not receive digital assistant

Patients will just include any symptoms/adverse events in their profile in the digital platform.

Digital platform

Intervention Type OTHER

Patients will be randomized (1:1) in the way they will receive or not any assistance from the digital platform.

Interventions

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Digital platform

Patients will be randomized (1:1) in the way they will receive or not any assistance from the digital platform.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with non-small cell lung cancer stage IV
* No younger than 18 years old patients
* Performance status: 0-2
* Existence of biological material for the molecular analysis
* Patients who have not been treated with any other treatment than adjuvant
* Ability to use a mobile device or computer for digital communication

Exclusion Criteria

* Childbearing women
* Patients with PS \> 3
* Limited ability to use a mobile device for basic digital communication
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stavros Niarchos Foundation

UNKNOWN

Sponsor Role collaborator

Care Across Ltd

UNKNOWN

Sponsor Role collaborator

Hellenic Cooperative Oncology Group

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Paris Kosmidis, MD

Role: PRINCIPAL_INVESTIGATOR

YGEIA Hospital

Locations

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Ygeia Hospital

Psychikó, Attica, Greece

Site Status RECRUITING

MITERA Hospital

Athens, Marousi, Greece

Site Status RECRUITING

General University Hospital of Larissa

Larissa, Mezourlo, Greece

Site Status RECRUITING

3rd Dept of Medical Oncology, Agii Anargiri Cancer Hospital

Athens, Nea Kifisia, Greece

Site Status RECRUITING

4th Dept of Medical Oncology, Metropolitan Hospital

Athens, Neo Faliro, Greece

Site Status RECRUITING

Henry Dunant Hospital Center

Athens, , Greece

Site Status RECRUITING

EUROCLINIC of Athens

Athens, , Greece

Site Status RECRUITING

401 General Military Hospital of Athens

Athens, , Greece

Site Status RECRUITING

1st Dept of Medical Oncology, Metropolitan Hospital

Athens, , Greece

Site Status RECRUITING

2nd Dept of Medical Oncology, Metropolitan Hospital

Athens, , Greece

Site Status RECRUITING

General Hospital of Kavalas

Kavala, , Greece

Site Status RECRUITING

General Hospital of Patra "Agios Andreas"

Pátrai, , Greece

Site Status RECRUITING

Division of Oncology, Dept of Internal Medicine, University Hospital of Patras

Pátrai, , Greece

Site Status RECRUITING

2nd Dept of Medical Oncology, EUROMEDICA General Clinic of Thessaloniki

Thessaloniki, , Greece

Site Status RECRUITING

General Hospital of Thessalonikis "G. Papanikolaou"

Thessaloniki, , Greece

Site Status RECRUITING

Countries

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Greece

Central Contacts

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Paris Kosmidis, MD

Role: CONTACT

+30 210 6867105

Facility Contacts

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Paris Kosmidis, MD

Role: primary

00302106867105

Ilias Athanasiadis, MD

Role: primary

Athansios Kotsakis, MD

Role: primary

Joseph Sgouros, MD

Role: primary

00302103501273

Helena Linardou, MD

Role: primary

+302104809852

Ioannis Mountzios, MD

Role: primary

00302106972346

Christos Panopoulos, MD

Role: primary

Nikolaos Tsoukalas, MD

Role: primary

Dimitrios Bafaloukos, MD

Role: primary

Epameinontas Samantas, MD

Role: primary

Anastasios Vagionas, MD

Role: primary

Athina Christopoulou, MD

Role: primary

Angelos Koutras, Ass. Prof.

Role: primary

Eleni Fountzilas, MD

Role: primary

00302310683136

Sofia Lampaki, MD

Role: primary

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Other Identifiers

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HE2SN/21

Identifier Type: -

Identifier Source: org_study_id

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