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The relationship between body composition and the efficacy of Camrelizumab in the treatment of solid tumors,a observational study

The relationship between body composition and the efficacy of Camrelizumab in the treatment of solid tumors,a observational study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097894
Enrollment
Unknown
Registered
2025-02-27
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

NSCLC

Interventions

Observation group:None

Sponsors

The first people's hospital of ziyang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Eligible participants were adults aged >=18,both men and women; 2.ECOG PS 0-2; 3.Histologically or cytologically con?rmed limiting stage or advanced stage NSCLCESCC; 4.Had no previous systemic chemotherapy; 5.Had at least one measurable lesion per Response Evaluation Criteria in Solid Tumors version 1.1; 6.Had a life expectancy of at least 12 weeks; 7.Vital organ functions meet the following requirements; 8.Human body composition analysis was performed before the first treatment of Camrelizumab; 9.All patients provided written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with active or untreated CNS metastases by CT/MRI were excluded from the study. 2.Had other malignant tumors or malignant diseases in the three years prior to enrollment; 3.Confirmed or suspected to have interstitial pneumonia, autoimmune diseases, and serious cardiovascular and cerebrovascular diseases; 4.Received any other drug treatment or participated in another clinical study within 4 weeks prior to signing the ICF; 5.Known allergy to Camrelizumab or excipients, known severe allergic reactions to any of the mabs; 6.The researchers determined that other conditions were not suitable for inclusion in the study;

Design outcomes

Primary

MeasureTime frame
ORR,Objective response rate;

Secondary

MeasureTime frame
PFS,progression-free survival;Safety;OS,Overall survival;

Countries

China

Contacts

Public ContactJieyan Luo

The first people's hospital of ziyang

20537389@qq.com+86 15082608690

Outcome results

None listed

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