Impact of an Early Warning System on the Prognosis of Patients With Hematological Malignancies Receiving Intensive Chemotherapy With or Without Hematopoietic Cell Transplantation.

NCT ID: NCT06409767

Last Updated: 2025-09-24

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

RECRUITING

Clinical Phase

NA

Total Enrollment

2224 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-10

Study Completion Date

2028-07-11

Brief Summary

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Patients with hematologic malignancies requiring intensive chemotherapy are at risk for life-threatening complications. Organ failure may appear rapidly and delay in initiating life-sustaining interventions may result in increased mortality. This encourages great alertness although not all patients require close monitoring. It is therefore critical to identify which patients are the most at risk for clinical deterioration to consider increased surveillance in these patients. The benefit of early intensive care unit (ICU) admission, as soon as the first signs of organ dysfunction appear, must also be clarified. Such an intervention could increase survival of patients by close monitoring and early initiation of organ-specific interventions but could also be responsible for anxiety and increased use of ICU resources.

Many teams have analyzed the impact of early warning systems (EWS) including vital signs to detect organ dysfunction early on. It has been shown that these EWS could positively impact survival in many medical fields (pre-hospital, medicine or surgery departments). A few retrospective studies have explored the impact of EWS in hematology, with overall good prediction for ICU admission and mortality. Until now, it has however not been formally demonstrated that early ICU admission, as soon as the first signs of organ dysfunction appear, could benefit patients with hematologic malignancies. A randomized controlled trial studying the impact of early intervention would clarify the role of such a strategy.

In this study, the investigators will prospectively evaluate the implementation of the National Early Warning Score (NEWS), with systematic referral to the ICU in high-score patients, to improve the survival of patients receiving intensive chemotherapy in ten academic centers. This score is one of the most performant and most frequently used to predict organ failure. Its calculation only requires vital signs such as respiratory rate, peripheral oxygen saturation, need for oxygen therapy, body temperature, arterial pressure, heart rate, and level of consciousness. The investigators will therefore study the impact of ICU admission in patients with high NEWS in a randomized, controlled trial. A cluster randomization is planned in which the centers will be randomized between usual care (control group) and interventional care with transfer to the ICU in the event of a NEWS score ≥7 (interventional group). Each parameter used to calculate the NEWS will be collected at least three times a day by the attending nurse.

Detailed Description

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Conditions

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Leukemia Lymphoma Multiple Myeloma

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Cluster randomized trial
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Interventional arm

Group Type EXPERIMENTAL

Real-time calculation of the NEWS with ICU admission if NEWS ≥ 7.

Intervention Type OTHER

The calculation of NEWS requires vital signs such as respiratory rate, peripheral oxygen saturation, need for oxygen therapy, body temperature, arterial pressure, heart rate, and level of consciousness. Each parameter used to calculate the NEWS will be collected least three times a day by the attending nurse.

Control arm

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Real-time calculation of the NEWS with ICU admission if NEWS ≥ 7.

The calculation of NEWS requires vital signs such as respiratory rate, peripheral oxygen saturation, need for oxygen therapy, body temperature, arterial pressure, heart rate, and level of consciousness. Each parameter used to calculate the NEWS will be collected least three times a day by the attending nurse.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adult patient
* Hospitalization in a protected unit of a hematology department for induction therapy of acute myeloid leukemia or acute lymphoblastic leukemia induction, intensive chemotherapy with autologous hematopoietic cell transplantation, allogeneic hematopoietic cell transplantation
* Expected length of stay in the hematology department of at least 7 days
* Patient with social security
* Signed informed consent form

Exclusion Criteria

* Decision of care limitation with decision not to transfer to ICU or not initiate organ support
* Pregnant, parturient or breastfeeding woman
* Person deprived of liberty by judicial or administrative decision
* Person under forced psychiatric care
* Person under legal protection
* Person unable to express consent
* Hospitalization for Chimeric Antigenic Receptor (CAR) T-cell therapy
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centre Hospitalier Amiens-Picardie

Amiens, , France

Site Status RECRUITING

Centre Hospitalier Universitaire d'Angers

Angers, , France

Site Status RECRUITING

Centre Hospitalier Universitaire Besancon

Besançon, , France

Site Status RECRUITING

Centre Hospitalier Universitaire Brest

Brest, , France

Site Status RECRUITING

Centre Hospitalier universitaire Nancy

Nancy, , France

Site Status RECRUITING

Centre Hospitalier Universitaire Nantes

Nantes, , France

Site Status RECRUITING

Centre Hospitalier Universitaire poitiers

Poitiers, , France

Site Status RECRUITING

centre Hospitalier Universitaire Saint etienne

Saint-Etienne, , France

Site Status RECRUITING

centre Hospitalier Universitaire Strasbourg

Strasbourg, , France

Site Status NOT_YET_RECRUITING

centre Hospitalier Universitaire Tours

Tours, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Corentin Orvain, MD PhD

Role: CONTACT

02 41 35 36 37 ext. +33

Aurélie Hautefort

Role: CONTACT

02 41 35 36 37 ext. +33

Facility Contacts

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Delphine LEBON, PhD

Role: primary

03 22 45 59 14 ext. +33

Corentin Orvain, PhD

Role: primary

02 41 35 44 75 ext. +33

Yohan Desbrosses, PhD

Role: primary

03 81 66 82 32 ext. +33

Marie-Anne Couturier, PhD

Role: primary

02 98 22 30 37

Caroline Bonmati, PhD

Role: primary

03 83 15 32 82 ext. +33

Pierre Peterlin, PhD

Role: primary

02 40 08 32 71

Maria-Pilar Gallego-Hernanz, PhD

Role: primary

05 49 44 43 07 ext. +33

Emmanuelle Tavernier, PhD

Role: primary

04 77 91 70 60

Célestine Simand, PhD

Role: primary

03 68 76 74 07 ext. +33

Alban Villate, PhD

Role: primary

02 47 47 37 12 ext. +33

Other Identifiers

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ID-RCB

Identifier Type: OTHER

Identifier Source: secondary_id

49RC23_0425

Identifier Type: -

Identifier Source: org_study_id

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