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A Registry Study of Endocrine Adverse Events Related to Anticancer Drugs in Solid Tumor Patients

A Registry Study of Endocrine Adverse Events Related to Anticancer Drugs in Solid Tumor Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113453
Enrollment
Unknown
Registered
2025-11-28
Start date
2025-04-17
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Endocrine Adverse Events Related to Anticancer Drugs

Interventions

Case series:NA

Sponsors

Shanghai Fourth People's Hospital affiliated to Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Male or female 18 years of age or older; 2. Histologically or cytologically confirmed diagnosis of solid tumors, including but not limited to lung cancer, gastric cancer, head and neck squamous cell carcinoma, esophageal cancer, and other solid tumors, who are receiving antineoplastic drug therapy such as chemotherapy, targeted therapy, immune checkpoint inhibitors, or novel therapeutic agents (including but not limited to monoclonal or bispecific antibodies targeting immune or angiogenic pathways, and antibody–drug conjugates [ADCs]). 3. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 3; 4. Provision to sign and date the informed consent, and stated willingness to comply with all study procedures and remain available for the duration of the study.

Exclusion criteria

Exclusion criteria: 1. Known human immunodeficiency virus (HIV) infection or active tuberculosis; 2. Known pregnancy or lactation; 3. Any other condition that, in the opinion of the investigator, would make the patient unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Incidence of endocrine adverse events related to anticancer drugs;Time to onset of endocrine adverse events related to anticancer drugs;Severity of endocrine adverse events related to anticancer drugs;Risk factors of endocrine adverse events related to anticancer drugs;Disease-Free Survival (DFS);

Secondary

MeasureTime frame
Overall Survival (OS);Progression-Free Survival (PFS);Objective Response Rate (ORR);Disease Control Rate (DCR);Duration of Response (DoR);

Countries

China

Contacts

Public ContactCongrong Wang

Shanghai Fourth People's Hospital affiliated to Tongji University

wcr601@163.com+86 21 5560 3123

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026