Registry on NEN Patients and COVID-19

Sponsor
European Institute of Oncology (Other)
Overall Status
Recruiting
CT.gov ID
NCT04444401
Collaborator
(none)
50
1
18
2.8

Study Details

Study Description

Brief Summary

A huge number of initiatives about COVID-19 are ongoing and a growing number of publications regard the correlation between cancer patients in general and SARS-CoV-2 infection. Although it has been reported that cancer patients are at a higher risk of SARS-CoV-2 infection and COVID-19 complications, data collection about cases of NEN patients SARS-CoV-2 positive are scattered and related to single countries or institutions. Because of that and due to the rarity and heterogeneity of NEN it will be hard to have homogeneous, reliable, representative and reproducible data for drawing adequate clinical recommendations about NEN patients and COVID-19.

Therefore we propose a global collection of data through an international database to describe and monitor NEN patients with SARS-CoV-2 infection. This retrospective/prospective collection of data can create a solid basis to check frequence of events, clinical management, clinical outcome, demographic, geographical, clinical and biological correlations. This will be helpful for the clinical and scientific community to get reliable information for a homogeneous clinical management of NEN patients during COVID-19 pandemic.

The main goal is to get the as wide as possible representativity of the world situation.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    At the end of December 2019, several cases of pneumonia of unknown origin were diagnosed in Wuhan, in the province of Hubei, China. These cases have been linked to a new beta-coronavirus (COVID-19), identified with RT-PCR method from samples taken from the bronchoalveolar samples of a patient with pneumonia of unknown etiology in the Wuhan Jinyintan hospital. Severe acute respiratory coronavirus 2 syndrome (SARS-CoV-2) has spread rapidly worldwide causing a pandemic.

    Cancer patients are considered at greater risk of viral infection and its complications, including SARS-CoV-2. Certain types of cancer, such as thoracic cancers, and underlying clinical conditions, for instance concomitant immunosuppressive therapies or immune-related comorbidities, are factors potentially predisposing to an increased risk of infection and eventually complications of COVID-19.

    In this context, it is difficult to understand where and how to identify patients with neuroendocrine neoplasia (NEN).

    We propose a global collection of data through an international database to describe and monitor NEN patients with COVID-19. This retrospective/prospective collection of data can create a large basis to check frequency of events, clinical management, clinical outcome, demographic, geographical, clinical and biological correlations.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    50 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Other
    Official Title:
    InterNaTional rEgistry oN Sars-cov-2posItiVe nEuroendocrine Neoplasm Patients (INTENSIVE)
    Actual Study Start Date :
    Jun 15, 2020
    Anticipated Primary Completion Date :
    Dec 15, 2021
    Anticipated Study Completion Date :
    Dec 15, 2021

    Outcome Measures

    Primary Outcome Measures

    1. Correlation between clinical parameters and SARS-CoV-2 infection [01/2020 - 12/2020]

      To evaluate the correlation between SARS-CoV-2 infection and the following parameters: major comorbidities, severe overall events (including death), chemotherapy for neuroendocrine tumor (NET), chemotherapy for neuroendocrine carcinoma (NEC), everolimus therapy, immunotherapy, peptide receptor radionuclide therapy (PRRT) and surgery or radiotherapy within the last 2 months.

    2. Clinical outcome of SARS-CoV-2 Infection [01/2020 - 12/2020]

      To evaluate the impact of SARS-CoV-2 Infection in NEN patients

    Secondary Outcome Measures

    1. major demographic features [01/2020 - 12/2020]

      demographic features of SARS-CoV-2 infected NEN patients

    2. type of NEN [01/2020 - 12/2020]

      Rate of grade, stage, status and primary site of NENs

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients > 18 y.o.

    • Patients with a NEN of any type with a positive SARS-CoV-2 swab (RT-PCR).

    • Patients with SARS-CoV-2 positivity (RT-PCR) who are asymptomatic or with symptoms/signs of COVID-19.

    • Patients with a NEN on active treatment.

    • Patients with macroscopic evidence of NEN or with no evidence of NEN (if they received surgical +/- locoregional non-surgical treatments within the last 2 months)

    • Able to provide signed written informed consent

    Exclusion Criteria:
    • Patients with NEN and symptoms suspected for COVID-19 who did not undergo SARS-CoV-2 swab (RT-PCR).

    • Patients with small cell lung cancer.

    • Patients with non-pure NEN (e.g. MiNEN).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 European Institute of Oncology, IEO, IRCCS Milan MI Italy 20141

    Sponsors and Collaborators

    • European Institute of Oncology

    Investigators

    • Principal Investigator: Nicola Fazio, M.D., Ph.D., European Institute of Oncology, IEO, IRCCS

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    European Institute of Oncology
    ClinicalTrials.gov Identifier:
    NCT04444401
    Other Study ID Numbers:
    • IEO-1291
    First Posted:
    Jun 23, 2020
    Last Update Posted:
    Aug 13, 2021
    Last Verified:
    Aug 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by European Institute of Oncology
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 13, 2021