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The 3 d - DSA technology in CalliSpheres @ carrier drug microsphere by the body, the pulmonary artery targeted chemotherapy embolization treatment of locally advanced non-small cell lung cancer clinical application and evaluation

The 3 d - DSA technology in CalliSpheres @ carrier drug microsphere by the body, the pulmonary artery targeted chemotherapy embolization treatment of locally advanced non-small cell lung cancer clinical application and evaluation

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026087
Enrollment
Unknown
Registered
2019-09-20
Start date
2019-09-09
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

Advanced non-small cell lung cancer

Interventions

Case series:CalliSpheres @ carrier drug microsphere

Sponsors

Yongchuan Hospital Affiliated to Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) with definite pathological diagnosis, there are 1 or more measurable lesions according to the mRECIST standard; (2) Aged 35-80 years old; (3) ECOG PS score 0-2, and the expected survival >3 months; (4) the gene test was wild-type and could not tolerate or reject standard chemoradiotherapy; (5) on the basis of the international union of cancer (UICC) TNM staging standards are set by the 2002 patients with stage III-IVa; (6) without interventional therapy, radiotherapy, chemotherapy and molecular targeted therapy within one month; Sign written informed consent.

Exclusion criteria

Exclusion criteria: (1) the presence of metastatic lesions at sites other than the lung; (2) renal dysfunction (urea nitrogen >430.0 mg/dL or blood creatinine >42.0 mg/dL); (3) uncontrollable hypertension, diabetes, cardiovascular disease with obvious symptoms, and large amount of pleural effusion; (4) loss of follow-up, failure of interventional embolization or death of non-research related factors during the study; (5) Other researchers determined that participants were unfit to participate.

Design outcomes

Primary

MeasureTime frame
mRECIST;

Secondary

MeasureTime frame
Adverse Reation;

Countries

China

Contacts

Public ContactYang Jianhua

Yongchuan Hospital Affiliated to Chongqing Medical University

269302295@qq.com+86 13709410898

Outcome results

None listed

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