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Biological Age Predicts 90-Day Mortality in Advanced Cancer

Biological Age as a Prognostic Marker in Hospitalized Patients With Advanced Cancer: A Retrospective Analysis Based on PhenoAge Model

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07035470
Acronym
BIOAGE-CAN
Enrollment
1615
Registered
2025-06-25
Start date
2022-11-05
Completion date
2024-12-31
Last updated
2025-06-29

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

Conditions

Advanced Solid Tumors Cancer, Hospitalizations

Keywords

Biological Age, PhenoAge, Advanced Cancer, Hospitalized Patients

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.

Detailed description

This is a retrospective observational study including hospitalized adult patients with stage III or IV solid tumors admitted to Etlik City Hospital between November 5, 2022 and December 31, 2024. Patients were included if they stayed for ≥48 hours and had all required laboratory values for calculating biological age using the Levine PhenoAge model. The study aimed to evaluate the association between biological age and (1) 30- and 90-day mortality, (2) ECOG performance score, (3) modified Charlson Comorbidity Index (mCCI), and (4) hospital length of stay. Regression and survival analyses were used to identify prognostic factors. All data were anonymized and collected retrospectively from hospital records.

Interventions

OTHERPhenoAge-Based Biological Age Assessment

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.

Sponsors

Ankara Etlik City Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* 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 Patients with multiple hospitalizations who meet the inclusion criteria will be included

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
90-Day All-Cause MortalityUp to 90 days post-admissionAll-cause mortality within 90 days following the date of hospital admission (index hospitalization).

Secondary

MeasureTime frameDescription
Modified Charlson Comorbidity Index (mCCI)Baseline (Day of hospital admission)The Modified Charlson Comorbidity Index (mCCI) is a validated scoring system used to quantify comorbidity burden. It includes 19 comorbid conditions with weighted values and incorporates age adjustment. Scores range from 0 to 33. In this study, age points are added only for patients aged 50 years and above: +1 point for ages 50-59, +2 for 60-69, +3 for 70-79, and +4 for ≥80. Higher mCCI scores indicate greater comorbidity burden and are associated with poorer clinical outcomes. The score is calculated retrospectively from documented diagnoses in the medical records at baseline.

Countries

Turkey (Türkiye)

Outcome results

None listed

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