SOGUGCOVID: Description of the Population With Genitourinary Tumors and COVID-19

Sponsor
Spanish Oncology Genito-Urinary Group (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04578132
Collaborator
(none)
408
32
22.2
12.8
0.6

Study Details

Study Description

Brief Summary

The identification of patients with genitourinary tumors who suffer from the infection by the Serious Acute Respiratory Syndrome Corona-Virus 2 (SARS-CoV-2) virus can represent multiple benefits both for themselves and for health professionals and the health system itself. We would be able to know more precisely the clinical evolution of these type of patient, to know their prognosis and being capable to select the most appropriate treatment modality for future pandemics.

SOGUG-COVID is an observational prospective-retrospective trial purely epidemiological, that aims to describe the population with genitourinary tumors (urothelial cancer, prostate cancer, testicular cancer and kidney cancer) infected by COrona VIrus Disease 19 (COVID-19) treated in Spanish hospitals, learn about the clinical presentation, therapeutic evolution and prognosis of said intercurrent infectious process, as well as its possible relationship with different clinical and therapeutic factors.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The study will be carried out in Spanish hospitals, with principal investigators belonging to the medical oncology services of the SOGUG group (Spanish Group of Genitourinary Oncology), who will act as promoter. Once the patients have been selected, the variables of interest will be collected and studied. The main variables to record will be:

    1. Patient characteristics

    2. Hospital center where the patient is recruited

    3. Pathological history:

    Concomitant pathology Usual drug treatment

    1. Tumor pathology:

    Tumor type, histology, and stage (initial and at diagnosis of infection) Cancer diagnosis date Active cancer treatment or follow-up Participation in clinical trial Type of treatment most recently received for the infection (Surgery; Radiotherapy; Chemotherapy, Immunotherapy ...) Treatment lines, initiation and last dose received of the most recent most recent cancer treatment

    1. COVID-19 infection:

    Confirmation date of COVID-19 infection PCR (Polymerase Chain Reaction) diagnostic test Immunoglobulin G (IgG) or Immunoglobulin M (IgM) serological diagnostic test Present symptoms, analytical alterations, thrombosis associated with COVID-19 infection, complications of infection Date of onset and disappearance of symptoms Days of fever and cough Radiological examination at the time of greatest severity Treatments received for COVID-19 Status upon discharge Date of discharge / exitus Negative presence of virus by PCR and PCR date

    1. For patients who are receiving or have received immunotherapy treatments, additional information will be collected:

    Immunotherapy treatment line and type Start / end date and last dose previous infection of the treatment with immunotherapy Adverse effects

    1. Prospective follow-up data (6 months from patient inclusion):

    Date of start or restart of cancer treatment after infection Change / suspension of cancer treatment after COVID-19 Date of surgery in neoadjuvant patients Recurrence of COVID-19 Best response obtained Date of progression to cancer treatment Current status and date of last contact The study will use the data obtained from the patient's medical history, with no plans to use other sources.

    The assignment of a patient to a specific therapeutic strategy has already been decided in advance by the usual clinical practice of medicine; The decision to prescribe a specific treatment is clearly dissociated from the decision to include a patient in the study. No intervention will be applied to patients, whether diagnostic or follow-up, that is not the usual clinical practice. Epidemiological methods will be used to analyze the collected data.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    408 participants
    Observational Model:
    Ecologic or Community
    Time Perspective:
    Other
    Official Title:
    Observational Retrospective-prospective Study in Patients With Genitourinary Tumors Presenting COVID-19 Infection (SOGUG-COVID-19)
    Actual Study Start Date :
    Nov 24, 2020
    Anticipated Primary Completion Date :
    Jun 1, 2022
    Anticipated Study Completion Date :
    Oct 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Genitourinary cancer patients that suffered COVID-19

    Patients diagnosed with genitourinary cancer (urothelial, kidney, prostate and germ) that suffered from COVID-19 infection prior to cancer treatment, during treatment, or after treatment.

    Outcome Measures

    Primary Outcome Measures

    1. Baseline characteristics [Through study completion, average 1 year]

      Describe the population infected by COVID-19 with genitourinary tumors (urothelial cancer, prostate cancer, testicular cancer and kidney cancer) treated in Spanish hospitals, know the clinical presentation: Age, gender, cancer type. Categorical variables will be presented as counts and percentages.

    2. Frequency of complications of COVID-19 intercurrent infection [Through study completion, average 1 year]

      Percentage of patients with complications associated to COVID-19 infection (classified by type and severity)

    3. Frequency of complications of COVID-19 infection in patients stratified by oncological treatment [Through study completion, average 1 year]

      To assess the possible relationship of the different oncological treatments administered to these patients with the clinical evolution of the COVID-19 infection. Complications will be classified by type and severity in groups of patients stratified by the oncological treatment received.

    4. Frequency of adverse events related to immunotherapy targeted to cancer (classified by type and severity) [Through study completion, average 1 year. Measured at 3 scenarios (during treatment, after treatment and therapies indicated after infection has passed)]

      To specifically assess the impact of COVID-19 infection on the toxicity of immunotherapy treatment (mainly pneumonitis) and the impact of immunotherapy on the evolution of the infectious picture in patients with tumors of genitourinary origin. three different scenarios: during treatment, after treatment and in patients who receive treatment after the infection has passed.

    5. Frequency of complications of COVID-19 infection in patients with prostate cancer stratified by anti-androgenic oncological treatment [Through study completion, average 1 year]

      To evaluate in patients with Prostate Cancer (PCa) the impact of androgen deprivation therapy (ADT) and new antiandrogenic agents (NAH) with or without corticosteroids on the infection COVID-19 as mean of frequency in complications of COVID-19 infection classified by type and severity

    Secondary Outcome Measures

    1. COVID-19 mortality rate in patients with genitourinary cancer [Through study completion, average 1 year]

      To assess the mortality associated with COVID-19 infection in the population with genitourinary tumors. Percentage of patients alive / dead at discharge.

    2. COVID-19 complication rate in patients with genitourinary cancer [Through study completion, average 1 year]

      Evaluate the rate (percentage) of complications that have required hospital admission and / or ICU treatment. Complications will be classified by type and severity and represented as percentage of patients presenting them.

    3. Asymptomatic rate [Through study completion, average 1 year]

      Describe the frequency of asymptomatic or minimally symptomatic COVID-19 infections.

    4. Frequency of delays/modifications on cancer treatment schedule [Through study completion, average 1 year]

      delays / modifications in cancer follow-up or treatment regimens. The average delay time and the number of modifications will be evaluated.

    5. Progression free survival in patients with genitourinary tumors that suffered COVID-19 [Through study completion, average 1 year]

      It is expected to obtain data on time to progression and overall survival of cancer patients, which can be compared with the reference values for each type of tumor pathology

    6. Overall survival in patients with genitourinary tumors that suffered COVID-19 [Through study completion, average 1 year]

      It is expected to obtain data on time to progression and overall survival of cancer patients, which can be compared with the reference values for each type of tumor pathology

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients ≥18 years old.

    • Diagnosed with genitourinary cancer (urothelial, kidney, prostate and germ).

    • COVID-19 infection prior to cancer treatment, during treatment, or after treatment.

    • The COVID-19 infection must be confirmed by PCR or serology, regardless of whether or not the patient requires hospitalization for the infection, additionally, a clinical and / or radiological determination must be available in those patients who present symptoms.

    Exclusion Criteria:
    • Not applicable

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Institut Català d'Oncologia L'Hospitalet Hospitalet de Llobregat Barcelona Spain
    2 Althaia Manresa Barcelona Spain
    3 Hospital Universitari Parc Taulí Sabadell Barcelona Spain
    4 Hospital Universitario Puerta de Hierro-Majadahonda Majadahonda Madrid Spain
    5 Hospital Universitario de Badajoz Badajoz Spain
    6 Hospital del Mar Barcelona Spain
    7 Hospital Santa Creu i Sant Pau Barcelona Spain
    8 Hospital Universitario Vall d Hebron Barcelona Spain
    9 Hospital Universitario de Burgos Burgos Spain
    10 Hospital de Ciudad Real Ciudad Real Spain
    11 Hospital Universitario Reina Sofía Córdoba Spain
    12 Instituto Catalán de Oncología- Girona Girona Spain
    13 Hospital Universitario Lucus Augusti Lugo Spain
    14 Fundación Jiménez Díaz Madrid Spain
    15 Hospital 12 de Octubre Madrid Spain
    16 Hospital Clínico San Carlos de Madrid Madrid Spain
    17 Hospital Infanta Leonor, Madrid Spain
    18 Hospital Universitario Gregorio Marañón Madrid Spain
    19 Hospital Universitario HM Sanchinarro Madrid Spain
    20 Hospital Universitario La Paz Madrid Spain
    21 Hospital Universitario La Princesa Madrid Spain
    22 Hospital Universitario Quironsalud Madrid Spain
    23 Hospital Universitario Ramón y Cajal Madrid Spain
    24 Complejo Hospitalario Universitario Ourense Orense Spain
    25 Clinica Universidad de Navarra Pamplona Spain
    26 Hospital Universitario Virgen Macarena Sevilla Spain
    27 Hospital Nuestra Señora del Prado Talavera De La Reina Spain
    28 Hospital Virgen de la Salud Toledo Spain
    29 Hospital Universitario Dr. Peset Valencia Spain
    30 Instituto Valenciano de Oncología Valencia Spain
    31 Hospital Txagorritxu Vitoria Spain
    32 Hospital Miguel Servet Zaragoza Spain

    Sponsors and Collaborators

    • Spanish Oncology Genito-Urinary Group

    Investigators

    • Study Chair: Miguel Ángel Climent, M.D., Ph.D., Instituto Valenciano de Oncología
    • Study Chair: Javier Puente, M.D., Ph.D., Hospital Clínico San Carlos de Madrid
    • Study Chair: Aránzazu González del Alba, M.D., Ph.D., Hospital Universitario Puerta de Hierro-Majadahonda
    • Study Chair: Sergio Vázquez Estevez, M.D., Ph.D., Hospital Universitario Lucus Augusti
    • Study Chair: Natalia Vidal, M.D., Ph.D., Hospital Clínico San Carlos de Madrid

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Spanish Oncology Genito-Urinary Group
    ClinicalTrials.gov Identifier:
    NCT04578132
    Other Study ID Numbers:
    • SOG-INM-2020-04
    First Posted:
    Oct 8, 2020
    Last Update Posted:
    Sep 22, 2021
    Last Verified:
    Mar 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Spanish Oncology Genito-Urinary Group
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 22, 2021