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Therapeutic effect of CalliSperes microballoon bronchial artery chemoembolization on refractory non-small cell lung cancer with pleural effusionTherapeutic effect of CalliSperes microballoon bronchial artery chemoembolization on refractory non-small cell lung cancer with pleural effusion: a historical control study

Therapeutic effect of CalliSperes microballoon bronchial artery chemoembolization on refractory non-small cell lung cancer with pleural effusion: a historical control study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033063
Enrollment
Unknown
Registered
2020-05-19
Start date
2019-06-01
Completion date
Unknown
Last updated
2020-05-25

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

treatment group:Intercostal artery infusion chemotherapy combined with bronchial artery embolization

Sponsors

PLA 309th Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) aged 18-75 years, gender not limited; (2) histopathological diagnosis of lung adenocarcinoma and squamous cell carcinoma of live small cell lung cancer; (3) TNM stage is IIIB or IV A; (4) have 1 or more measurable lesions according to RECIST1.1 standard; (5) refusal of chemotherapy or poor effect after chemotherapy; (6) ECOG score of physical fitness 6 months; (8) signed the consent of treatment protocol.

Exclusion criteria

Exclusion criteria: (1) patients with extensive uncontrolled extra-pulmonary metastases; (2) patients with mutations in gene detection can be treated with targeted drugs; (3) patients who have had or are currently experiencing other malignancies (except for cured basal or squamous cell skin cancer or carcinoma in situ of the cervix); (4) leukocyte 2mg/L; Twice the normal upper limit of AST and/or ALT >); (6) coagulation dysfunction (INR > 1.5) or known bleeding disease, or anticoagulant therapy; (7) patients with combined active infection requiring antibiotic treatment; (8) uncontrollable hypertension, diabetes, cardiovascular disease with obvious symptoms and a large amount of hydrothorax; (9) death due to unsuccessful embolization or non-study related factors; (10) hypersensitivity to contrast agents; (11) women with combined pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Complete response rate;

Secondary

MeasureTime frame
Partial remission rate;progression of disease;Overall survival rate;

Countries

China

Contacts

Public ContactWeiguo Zhao

PLA 309th Hospital

694466576@qq.com+86 18538737790

Outcome results

None listed

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