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Predictive model for anti-PD-1/PD-L1 treatment in lung cancer by single cell analysis

Predictive model for anti-PD-1/PD-L1 treatment in lung cancer by single cell analysis

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100054823
Enrollment
Unknown
Registered
2021-12-28
Start date
2021-01-01
Completion date
Unknown
Last updated
2022-12-12

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

Conditions

Lung cancer

Interventions

Gold Standard:Clinical outome
cell&#32
full&#32
sequencing

Sponsors

Shanghai Pulmonary Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The subjects should be aged 18-75 years old when they signed the informed consent form, both male and female; 2. Histologically or cytologically confirmed non-small cell lung cancer (NSCLC) and stage IIIB-IV tumor; 3. Provide relevant documents of the subject's EGFR mutation and ALK translocation status, which must be negative; 4. Must receive anti-PD1/PD-L1 immune monotherapy or immune combination chemotherapy; 5. According to RECIST 1.1 criteria, subjects must have measurable target lesions by CT or MRI; 6. Perform all screening laboratory tests as required by the protocol and within 14 days of the first dose. The values of laboratory tests done for screening must meet the criteria; 7. With my consent and signed informed consent, willing and able to comply with the planned visits, study treatments, laboratory tests and other experimental procedures.

Exclusion criteria

Exclusion criteria: No.

Design outcomes

Primary

MeasureTime frame
ACC, SEN, SPE, AUC of ROC;

Countries

China

Contacts

Public ContactWu Fengying

Shanghai Pulmonary Hospital

fywu@163.com+86 13167060870

Outcome results

None listed

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