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Phase II trial of etoposide/cisplatin with RH-endostain for patients with extensive-stage small-cell lung cancer

Phase II trial of etoposide/cisplatin with RH-endostain for patients with extensive-stage small-cell lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNC-10000823
Enrollment
Unknown
Registered
2010-04-04
Start date
2009-05-01
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

small-cell lung cancer

Interventions

treatment group:Cisplatin 25mg/m2 was administered intravenously over 30 to 60 minuteson on day 1-3
Etoposide 120mg/m2 was administered intravenously over 60 minutes on days 1-4
Endostar 15 mg was administered over 90 minutes by IV infusion on days 1-14
Repeated every 3 weeks for up to four cycles.

Sponsors

The First College Of Clinical Medical Science, China Three Gorges University &Yichang Central People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients with previously untreated, histologically or cytologically confirmed ED-SCLC were eligible; age 18 years or older; measurable disease; an ECOG performance status (PS) of 0 to 2; life expectancy of greater than 12 weeks; adequate hematologic, hepatic and renal functions; gave written informed consent prior to registration

Exclusion criteria

Exclusion criteria: Prior chemotherapy; unmeasurable disease; pregnancy and breastfeeding; CNS metastases; active infection and unhealing wounds, hepatic and renal functions deficiency; serious cardio-cerebrovascular disease such as coronary heart disease, unstable angina pectoris, myocardial infarction, cardiac arrhythmias, cerebral infarction and haemorrhage or psychiatric illness that would have affected compliance.

Design outcomes

Primary

MeasureTime frame
progession-free survival;

Secondary

MeasureTime frame
overall survival;toxicity;response rate;

Countries

China

Contacts

Public ContactZheng-Tao Zhou
zhouzhengtao@126.com+86 15972698932

Outcome results

None listed

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