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Multimodal interventional treatment under the guidance of PTC technology for stage III non-small cell lung cancer patients who are not suitable for operation or intolerant or refractory to radio-chemotherapy

Multimodal interventional treatment under the guidance of PTC technology for stage III non-small cell lung cancer patients who are not suitable for operation or intolerant or refractory to radio-chemotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061042
Enrollment
Unknown
Registered
2022-06-15
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

non-small cell lung cancer

Interventions

PTC-Multimodal interventional treatment :Multimodal interventional treatment

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-85 years, with biopsy proven NSCLC; 2. American Joint Committee on Cancer (AJCC)Version 8, TNM StageIII NSCLC; 3. Patients who cannot be resected surgically, fail radiotherapy and chemotherapy, or are intolerant; 4. Estimated survival > 3 months; 5. ECOG PS 0-3; 6. Radio-chemotherapy failure was defined as dynamic re-examination of enhanced CT every 6-8 weeks after receiving first-line chemotherapy according to RECIST 1.1. as disease progression; 7. Patients who could not receive radiotherapy and chemotherapy included patients with ECOG PS score of 3 and refused to receive first-line chemotherapy due to old age or personal wishes; 8. The functional level of major organs must meet the following requirements: (1) CBC neutrophils >= 1.5x10^9/L, PLT >= 90x10^9/L, HGB >= 90g/L; (2) Blood biochemistry TB <= upper limit of normal value(ULN), ALT & AST <= 1.5xULN, nitrogen & creatinine <= 1.5xULN.

Exclusion criteria

Exclusion criteria: 1. < 18 years old; 2. Previously received TKI or immunotherapy; 3. Estimated survival < 3 months; 4. At the same time, he received anti-tumor therapy in other clinical trials, including immunotherapy, TKI and so on; 5. A history of immune deficiency or other acquired congenital immune deficiency diseases or a history of organ transplantation; 6. Other circumstances in which the investigator determines that it is not appropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
PSF;

Secondary

MeasureTime frame
ORR;DCR;OS;QoL;

Countries

China

Contacts

Public ContactLi Xiao-Guang

Beijing Hospital, National Center of Gerontology

xglee88@126.com+86 13683383783

Outcome results

None listed

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