Skip to content

Subregional Radiomics-based Prediction of Neoadjuvant Immunotherapy Efficacy and Recurrence Risk in NSCLC

Subregional Radiomics-based Prediction of Neoadjuvant Immunotherapy Efficacy and Recurrence Risk in NSCLC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080287
Enrollment
Unknown
Registered
2024-01-25
Start date
2023-01-01
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

Lung cancer

Interventions

pCR group:The percentages of viable tumour cells, necrosis and stroma were respectively determined. The circumstance in which no viable tumour was observed was defined as a pathologic complete respons
Non-pCR group:The percentages of viable tumour cells, necrosis and stroma were respectively determined. The circumstance in which viable tumour was observed was defined as a non-pathologic complete re

Sponsors

Guangdong Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Aged over 18 years old; (2) Patients receiving radical lung cancer surgical resection after neoadjuvant immunotherapy combined with chemotherapy; (3) Pathologically confirmed stage IB-IIIB NSCLC patients; (4) Qualified 1 month before the first course of immunotherapy Chest CT data before surgery and surgery; (5) Follow-up time is no less than 6 months; (6) Complete clinical data

Exclusion criteria

Exclusion criteria: (1) There are no evaluable lung lesions, or the boundaries of the lesions are difficult to outline; (2) CT data have artifacts or the scan thickness is greater than 5 mm; (3) Clinical data or follow-up information are incomplete; (4) During immunotherapy Receive radiotherapy for the main target lesions; (5) Have a past or current history of other malignant tumors other than non-small cell lung cancer

Design outcomes

Primary

MeasureTime frame
Major pathological response;pathological complete response;

Secondary

MeasureTime frame
disease free survival ;overall survival;

Countries

China

Contacts

Public ContactHaiyu Zhou

Guangdong Provincial People's Hospital

lungcancer@163.com+86 137 1034 2002

Outcome results

None listed

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