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A study of the effect of immune checkpoint inhibitor infusion duration on the prognosis of patients with advanced non-small cell lung cancer

A study of the effect of immune checkpoint inhibitor infusion duration on the prognosis of patients with advanced non-small cell lung cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099097
Enrollment
Unknown
Registered
2025-03-18
Start date
2025-01-16
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

advanced non-small-cell lung cancer

Interventions

Experimental group:The observation group received immune checkpoint inhibitors between 6:00 and 7:00 in the morning (before 7:00 am)
control group:The control group received immune checkpoint inhibitors before 10:00-13:00 in the morning (until 13:00)

Sponsors

Henan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: To be included in this study, all of the following selection criteria must be met: 1. Diagnosed with non-small cell lung cancer, in accordance with the Clinical Diagnosis and Treatment Guidelines for Lung Cancer of the Oncology Branch of the Chinese Medical Association (2021 edition), all confirmed by histological evidence, and clinically classified as tumor node metastasis (TNM) stage III-IV; 2. Age >= 18 years old; 3. Expected survival period >= 6 months; 4. The treatment plan adopts immune checkpoint inhibitors combined with chemotherapy for patients; 5. Good compliance, able to comply with clinical trial requirements and medication regulations; 6. The subject or guardian has signed an informed consent form.

Exclusion criteria

Exclusion criteria: Any of the following will not be included in this study: 1.Merge tumors other than lung cancer; 2. Individuals allergic to any ingredient in the medication; 3. Merge cognitive impairment, mental disorders, or unwillingness to cooperate; 4. Patients who take protective medical measures; 5. Individuals with severe liver and kidney dysfunction; 6. The researchers believe that patients who did not participate in this study are not eligible.

Design outcomes

Primary

MeasureTime frame
PFS,Progression free survival;

Secondary

MeasureTime frame
ORR,Objective response rate;DCR,Disease control rate;OS,overall survival;Survival rate (1-year, 2-year, 3-year survival rate);The occurrence of immune related adverse events;

Countries

China

Contacts

Public ContactQiming Wang; Gao Yana

Henan Cancer Hospital

qimingwang1006@126.com+86 137 8359 0691

Outcome results

None listed

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