Skip to content

Different administration of Endostar Combined with Paclitaxel and Carboplatin in the Treatment of Advanced Non Small Cell Lung Cancer

Different administration of Endostar Combined with Paclitaxel and Carboplatin in the Treatment of Advanced Non Small Cell Lung Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015862
Enrollment
Unknown
Registered
2018-04-25
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-04-30

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

Pumping group:endostar continuous intravenous infusion by pumping
Normal infusion group:endostar normal infusion group

Sponsors

Fujian Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) 18-75 years of age; (2) Cytologically or histologically proven diagnosis of NSCLC; (3) Stage IV according to AJCC (7th edition of 2010); (4) ECOG performance status 0-2; (5) No prior chemotherapy and immunotherapy (postoperative adjuvant therapy must be completed=6 months); (6) Radiotherapy must be completed=4 weeks and the acute toxicities must been restored; previous radiotherapy lesion cannot be target tumor lesion unless progress; (7) EGFR and ALK mutations treated with mono corresponding targeted drugs and progressive; (8) At least one target tumor lesion can be measured by CT or MRI(the long diameter of tumor lesion=10mm, the short diameter of lymph node lesions=15mm and the target lesions not be treated with radiotherapy or freezing and so on); (9) Life expectancy of at least 3 months; (10) Adequate hematologic, hepatic and renal function to accept chemotherapy; electrocardiogram was normal; (11) Follow research requirements and follow-up procedures, signed informed consent form; (12) clinical data integrity.

Exclusion criteria

Exclusion criteria: (1) Serious violation of the inclusion criteria; (2) Can not follow the research requirements and follow-up procedures; (3) the change or death occurring during follow-up and no related to the experimental factors.

Design outcomes

Primary

MeasureTime frame
objective response rate;progression free survival;

Countries

China

Contacts

Public ContactJiang Kan

Fujian Cancer Hospital

jasmine9576@sina.com+86 13600886062

Outcome results

None listed

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