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Clinical Impact of Thoracic Scanographic Characteristics of Hematologic Malignancy Patients

Clinical Impact of Thoracic Scanographic Characteristics of Hematologic Malignancy Patients with Mediastinal Mass Syndrome Admitted to the Intensive Care Unit

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05694806
Acronym
MED-HEM
Enrollment
125
Registered
2023-01-23
Start date
2022-06-01
Completion date
2024-12-01
Last updated
2024-09-25

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

Conditions

Mediastinal Diseases

Keywords

Mediastinal mass syndrome

Brief summary

The mediastinum can be the site of benign or malignant tumors, including 10 to 20% of hematological malignancies. Mediastinal mass syndrome (MMS) includes symptoms due to irritation, invasion or compression of the organs of the mediastinum. This syndrome includes respiratory manifestations that may be secondary to compression of the tracheobronchial tree, venous vascular manifestations with the superior vena cava syndrome or arterial manifestations, cardiac manifestations, digestive or nervous manifestations. The management of a mediastinal syndrome is a diagnostic and therapeutic emergency requiring the collaboration of several disciplines in order to achieve the most effective but least deleterious way possible to diagnostic imaging, etiological biopsy, and the possible implementation of life-saving symptomatic measures before the initiation of etiological treatment. Diagnostic thoracic imaging relies primarily on thoracic computed tomography (CT) to determine the size and nature of the mediastinal mass, the presence and extent of tracheobronchial or great vessel compression, the presence of pleural and/or pericardial effusion, pulmonary embolism, parenchymal lesions, and possibly subdiaphragmatic lesions. However, the potential severity of MMS is often under-diagnosed in adult patients, particularly in the context of hematologic malignancy. Indeed, we have very little literature on the initial management of these patients at risk. The present study propose to conduct the first multicenter study to analyze the characteristics (clinical, scanographic, echocardiographic, hematological and resuscitation) of the initial management of patients with symptomatic MMS at diagnosis or at relapse of a patient with MH admitted to the Intensive Care Unit (ICU).

Interventions

analysis of thoracic scans realised in standard care

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Hematologic malignancy at diagnosis or relapse * Symptomatic mediastinal mass syndrome * Admission to the ICU, Continuous Medical Surveillance (CMS) or Intensive Care (IC) for symptomatology related to MMS * Chest CT (after maximum 48 hours of corticosteroid therapy (1mg/kg/ Prednisone equivalent), maximum 15 days before and 5 days after admission to ICU) * Maximum administration of corticosteroid therapy 48 hours before admission to the ICU (maximum 1mg/kg/ Prednisone equivalent) * No prior pleural or pericardial drainage * Study period: 01/01/2014 - 31/12/2021 (8 years)

Exclusion criteria

* No diagnosis of hematologic malignancy * Diagnosis of solid benign or malignant tumor * No mediastinal mass syndrome * No admission to ICU/CMS * No chest CT scan meeting inclusion criteria * Administration of corticosteroids for more than 48 hours prior to admission to the ICU and/or prior to chest CT * Lack of social security affiliation.

Design outcomes

Primary

MeasureTime frameDescription
To identify prognostic thoracic scan factors of severe mediastinal mass syndrome1 weekTo identify prognostic thoracic scan factors of severe mediastinal mass syndrome defined by the occurrence of severe respiratory, hemodynamics and/or neurological failures.

Countries

France

Contacts

Primary ContactMuriel Picard, MD
picard.m@chu-toulouse.fr0561756105

Outcome results

None listed

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