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Study on the safety and efficacy of bronchial artery microsphere embolization combined with apatinib in the treatment of central pulmonary squamous cell carcinoma

Study on the safety and efficacy of bronchial artery microsphere embolization combined with apatinib in the treatment of central pulmonary squamous cell carcinoma

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023806
Enrollment
Unknown
Registered
2019-06-12
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

central pulmonary squamous cell carcinoma

Interventions

case series:bronchial artery microsphere embolization combined with apatinib

Sponsors

The Second People's Hospital of Yibin
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Pathologically confirmed squamous cell carcinoma of the lung; Imaging showed central lung cancer with at least one measurable lesion (RECIST1.1). No surgery opportunity, clinical stage IV or III B; ECOG score is 0-2; Expected survival =3 months; The patient had previously received the first-line chemotherapy regimen with platinum-containing drugs combined with two drugs, and was failure or lesion progression by imaging evaluation; Routine laboratory examination (blood routine, liver and kidney function, coagulation function, etc.) was not significant abnormal. Subjects volunteered to participate in this study and signed informed consent, with good compliance and follow-up.

Exclusion criteria

Exclusion criteria: A history of surgery or radiation therapy; Intractable hypertension beyond the control of drugs;Brain metastasis; Severe abnormal coagulation function; Patients with severe cardiopulmonary dysfunction or inability to lie flat; Other antiangiogenic agents (such as endor, bevacizumab, etc.) were used before enrollment.Pregnant or lactating women;Patients with fertility are unwilling or unable to take effective contraceptive measures; Contraindications specified in the instructions for apatinib; Patients are participating in other clinical trials; During the study, the patients were lost to follow-up and the interventional embolization was unsuccessful. Medical imaging examination showed the progress of the disease, and the researchers considered it inappropriate to continue taking apatinib. Patients with NCI-CTC grade 3 or above, bleeding or other toxic side effects, cannot be tolerated after dose adjustment and symptomatic treatment.

Design outcomes

Primary

MeasureTime frame
progression free survival;

Secondary

MeasureTime frame
overall survival;objective response rate;Disease control rate;quality of life;hemoptysis;abnormal rate of laboratory test;Incidence of adverse events and serious adverse events;

Countries

China

Contacts

Public ContactZhu Jun

The Second People's Hospital of Yibin

865149749@qq.com+86 13890960428

Outcome results

None listed

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