NCT07408661

Brief Summary

This study aimed to develop a more accurate way to predict the 30-day survival of cancer patients admitted to the intensive care unit (ICU). The researchers focused on markers of iron metabolism, as imbalances in iron are common in cancer and severe illness. The study analyzed data from 1,137 critically ill cancer patients. Using artificial intelligence (AI), specifically a model called TabPFN, the study combined these iron markers with other routine clinical data (like blood cell counts and lactate levels) to create a new prediction tool.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,137

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2015

Longer than P75 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2015

Completed
9.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2024

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

February 6, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
Last Updated

February 13, 2026

Status Verified

February 1, 2026

Enrollment Period

9.8 years

First QC Date

February 6, 2026

Last Update Submit

February 12, 2026

Conditions

Keywords

Critical careCancerArtificial IntelligenceRisk stratificationFerritin

Outcome Measures

Primary Outcomes (1)

  • All-cause Mortality at 30 Days

    The primary outcome is the incidence of death from any cause within 30 days following the date of ICU admission. Mortality status will be determined by a review of the hospital discharge records and associated death records in the MIMIC-IV database.

    30 days from the date of ICU admission.

Study Arms (1)

Critically Ill Cancer Patients

This group comprises adult cancer patients who were admitted to the intensive care unit (ICU). The primary interest is in their 30-day all-cause mortality following ICU admission. The cohort includes 1,137 patients whose clinical data was extracted from the MIMIC-IV database. Key variables of interest include iron metabolism markers (ferritin, serum iron, TIBC), routine blood tests, and vital signs, all assessed at or near ICU admission. This retrospective observational study investigates the prognostic value of these markers and aims to develop a machine learning model for predicting mortality risk.

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of adult cancer patients who were critically ill, requiring intensive care unit admission. This retrospective cohort is derived from the MIMIC-IV database, comprising patients with a cancer diagnosis who had their first ICU stay during hospitalization and for whom complete data on the key predictors and outcome are available.

You may qualify if:

  • Adult patients (age ≥ 18 years).
  • Diagnosis of any type of cancer, as recorded in the hospital database.
  • First ICU admission during the hospital stay (only the first ICU stay is considered for patients with multiple admissions).

You may not qualify if:

  • Length of ICU stay less than 24 hours.
  • Missing or unavailable data for the key study variables, specifically iron metabolism markers (ferritin, serum iron, total iron-binding capacity) or essential clinical parameters needed for analysis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neoplasms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Professor

Study Record Dates

First Submitted

February 6, 2026

First Posted

February 13, 2026

Study Start

January 1, 2015

Primary Completion

October 1, 2024

Study Completion

December 1, 2025

Last Updated

February 13, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share