NCT07035470

Brief Summary

This retrospective study evaluates whether biological age, calculated using the PhenoAge model, predicts short-term outcomes in patients with advanced cancer who were hospitalized. The main goal is to investigate associations between biological age and short-term mortality, functional status (ECOG), comorbidity burden (mCCI), and length of hospital stay. All data were collected from medical records without any patient intervention.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
1,615

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

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

November 5, 2022

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 16, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 25, 2025

Completed
Last Updated

June 29, 2025

Status Verified

June 1, 2025

Enrollment Period

2.2 years

First QC Date

June 16, 2025

Last Update Submit

June 25, 2025

Conditions

Keywords

Biological AgePhenoAgeAdvanced CancerHospitalized Patients

Outcome Measures

Primary Outcomes (1)

  • 90-Day All-Cause Mortality

    All-cause mortality within 90 days following the date of hospital admission (index hospitalization).

    Up to 90 days post-admission

Secondary Outcomes (1)

  • Modified Charlson Comorbidity Index (mCCI)

    Baseline (Day of hospital admission)

Study Arms (1)

Hospitalized Advanced Cancer Patients

Patients hospitalized with advanced solid tumors (Stage III or IV) in the oncology clinic were retrospectively analyzed. Biological age was calculated using the PhenoAge model. Clinical outcomes such as mortality, ECOG score, mCCI, and length of stay were assessed.

Other: PhenoAge-Based Biological Age Assessment

Interventions

Biological age was retrospectively calculated using the PhenoAge algorithm, based on nine routine laboratory parameters and chronological age. This model estimates phenotypic aging and was used to predict short-term outcomes including mortality, functional status, comorbidity burden, and hospital length of stay. No new intervention was administered; all data were collected from existing medical records.

Hospitalized Advanced Cancer Patients

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

This study includes adult patients (≥18 years old) with advanced-stage solid tumors who were hospitalized at Etlik City Hospital, Turkey, between November 5, 2022, and December 31, 2024. Only patients with at least 48 hours of hospitalization and complete laboratory data necessary for PhenoAge calculation were included. The study population represents a real-world sample of hospitalized cancer patients at elevated risk of short-term adverse outcomes.

You may qualify if:

  • Hospitalized in the Medical Oncology Department between November 5, 2022, and December 31, 2024
  • Histologically confirmed advanced-stage (stage III-IV) solid tumors
  • Age ≥18 years
  • Hospital stay of at least 48 hours
  • Actively receiving chemotherapy or received it within the last 6 months
  • Availability of all 9 required laboratory tests (albumin, creatinine, glucose, CRP, lymphocyte %, MCV, RDW, ALP, WBC) for PhenoAge calculation during the first admission

You may not qualify if:

  • Elective hospitalizations (e.g., planned chemotherapy, biopsy)
  • Patients who died during the first admission
  • Missing required laboratory parameters
  • ICU patients and unconscious patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Etlik City Hospital

Ankara, Yenimahalle, 06210, Turkey (Türkiye)

Location

Study Design

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

Study Record Dates

First Submitted

June 16, 2025

First Posted

June 25, 2025

Study Start

November 5, 2022

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

June 29, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations