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Efficacy and safety of irinotecan combined with systemic chemotherapy in the treatment of cervical cancer with CalliSpheres loaded drug embolization microspheres: a prospective, single center clinical trial

Efficacy and safety of irinotecan combined with systemic chemotherapy in the treatment of cervical cancer with CalliSpheres loaded drug embolization microspheres: a prospective, single center clinical trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800016151
Enrollment
Unknown
Registered
2018-05-14
Start date
2018-05-14
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Cervical cancer

Interventions

Case series:CalliSpheres loaded drug embolic microspheres loaded with irinotecan with DEB-TACE

Sponsors

Department of gynaecology in the west coast of Affiliated Hospital of Qingdao University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) understanding and signing informed consent; 2) Aged 18-75 years; 3) cervical cancer is diagnosed by histopathology or clinical diagnosis (refer to the 2016 edition of NCCN clinical practice guideline cervical cancer); 4) patients with stage B1, stage I, B2, II A and stage II B cervical cancer; 5) a recurrent tumor that can not be completely removed by a variety of factors; patients with intermediate and late tumor, who are unexcised or unwilling to be excised, have a preoperatively descending patient; 6) hemorrhage of tumor and metastasis; 7) the expected survival time is more than 3 months; 8) the physical capacity of ECOG is less than 2.

Exclusion criteria

Exclusion criteria: 1) patients with or without other malignancies (except cured basal or squamous cell carcinoma or cervical carcinoma in situ); 2) a history of major diseases involving heart, kidney, bone marrow or lung and central nervous system; 3) recent infection needs antibiotics; 4) there are four clinical trials involving other experimental drugs or devices within four weeks; 5) can cause the subjects to fail to follow the research plan or even endanger the patient's safety complications or social environment.

Design outcomes

Primary

MeasureTime frame
PFS;

Secondary

MeasureTime frame
????;ORR;DCR;

Countries

China

Contacts

Public ContactYao Qin

West Coast Hospital area, Affiliated Hospital of Qingdao University Medical College, Huangdao District, Qingdao, Shandong, China

dr_yaoqin@126.com+86 186561806573

Outcome results

None listed

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