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A Retrospective Cohort Study on the Association Between Liposomal Doxorubicin and Risk of Infectious Pneumonia in Breast Cancer Patients

A Retrospective Cohort Study on the Association Between Liposomal Doxorubicin and Risk of Infectious Pneumonia in Breast Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129015
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-07-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Breast cancer

Interventions

Liposomal doxorubicin group:None
Epirubicin group:None

Sponsors

The Fifth Affiliated hospital of Sun Yet-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years. 2. Female. 3. Pathologically confirmed breast cancer. 4. Undergoing chemotherapy at the Fifth Affiliated Hospital of Sun Yat-sen University between January 1, 2022 and March 31, 2025. 5. Chemotherapy regimen includes at least one cycle of liposomal doxorubicin or epirubicin. 6. Complete medical records, including demographic information, tumor staging, chemotherapy details, lab test results (blood tests before and after chemo), imaging reports (chest CT/X-ray), and infection-related diagnosis records.

Exclusion criteria

Exclusion criteria: 1.Definite diagnosis of infectious pneumonia within 2 weeks prior to the initiation of chemotherapy; 2.Comorbidity with active autoimmune diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus, etc.); 3.Concurrent use of other immunosuppressive agents (e.g., calcineurin inhibitors, anti-TNF agents, etc.) during or prior to chemotherapy, excluding glucocorticoids used for antiemetic therapy of chemotherapy-induced nausea and vomiting; 4.Comorbidity with human immunodeficiency virus (HIV) infection, active tuberculosis, or other chronic infectious diseases; 5.Incomplete medical records with missing key data (e.g., chemotherapy regimen, diagnostic basis for pneumonia, laboratory indicators) that preclude completion of the study analysis.

Design outcomes

Primary

MeasureTime frame
Incidence of infectious pneumonia;

Secondary

MeasureTime frame
Main pathogen types;composition of pneumonia etiologies;Risk factors;

Countries

China

Contacts

Public ContactPeijian Peng

The Fifth Affiliated hospital of Sun Yet-sen University

pengpjian@163.com+86 756 2528015

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026