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Endostatin in combination with docetaxel for patients with NSCLC who resistant to the prior EGFR-TKI agent treatment

Endostatin in combination with docetaxel for patients with NSCLC who resistant to the prior EGFR-TKI agent treatment

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-09000355
Enrollment
Unknown
Registered
2009-09-24
Start date
2009-03-01
Completion date
Unknown
Last updated
2017-04-18

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:Docetaxel: 75mg/m2, intravenous drip, day1, repeated every 21 days. Endostatin: 15mg, intravenous drip, day1-14, repeated every 21 days.

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Pathologically proved non small cell lung cancer; 2. Over age of 18; 3. At least one EGFR-TKI was prior used; 4. One and only one chemotherapy regimen was administered ahead of EGFR-TKI; 5. Tumor progression was detected after EGFR-TKI treatment; 6. No chemotherapy or radiation was administered after EGFR-TKI treatment; 7. Evaluable tumor mass was present; 8. Performance status as ECOG 0-2; 9. No contraindication to chemotherapy; 10. Expectation of life was over 12 weeks; 11. Voluntary participation and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Not controlled brain metastasis; 2. Only unevaluable tumor was present; 3. Target tumor needs local treatment; 4. Hypersensitiveness to bacillus coli praeparatum; 5. Combined with any unstable systemic diseases; 6. Disturbances of blood coagulation, active bleeding or hemorrhagic tendency; 7. Having contraindications to docetaxel or endostatin according to the directions; 8. Pregnancy or lactation; 9. Having serious heart disease; 10. Any conditions that the investigator regards to be not suitable for current study.

Design outcomes

Primary

MeasureTime frame
Response Rate;Progression Free Survival;Grade 4 toxicities;

Secondary

MeasureTime frame
Overall Survival;

Countries

China

Contacts

Public ContactDr. Jiang Zhu
zhujiang1@medmail.com.cn+86 0 13880087086

Outcome results

None listed

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