Skip to content

Human recombinant endostatin (Endostar) combined with concurrent radiochemotherapy in patients with cervical squamous cell cancer: a prospective, randomized controlled clinical study

Human recombinant endostatin (Endostar) combined with concurrent radiochemotherapy in patients with cervical squamous cell cancer: a prospective, randomized controlled clinical study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17011374
Enrollment
Unknown
Registered
2017-05-12
Start date
2017-05-16
Completion date
Unknown
Last updated
2017-05-22

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

Conditions

cervical cancer

Interventions

1:Human recombinant endostatin (Endostar) combined with concurrent radiochemotherapy
2:concurrent radiochemotherapy

Sponsors

The Cancer Hospital of Gansu Province
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 70 years old; 2. KPS grade 80-90; 3. The disease was diagnosed as cervical carcinoma with histopathology and cytology; Pathologic types include squamous cell carcinoma and adenocarcinoma; 4. FIGO stage IIB ~ IVb; 5. The laboratory criteria: the blood routine, liver, kidney function and heart function are basically normal, WBC?4*10^9/L; neutrophil? 2*10^9/L; platelet ? 100*10^9/L; Hemoglobin?90g/L; 6. Expected survival =12weeks; 7. Voluntary participation and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. The history of allergy to biological agents; 2. Undering Other anti-cancer treatments; 3. other as following : History of important viscera dysfunction and severe heart disease including congestive heart failure,arrhythmia, beyond the control of the require long-term drug treatment of angina pectoris, heart valve disease, myocardial infarction, and patients with resistant hypertension, pregnancy or lactation women, infective wound in delay no more, have the spirit of not easy to control.

Design outcomes

Primary

MeasureTime frame
Objective Respond Rate;Progression-free Survival, PFS;Overall Survival, OS;Toxity and side-effect;

Countries

China

Contacts

Public ContactFengju Zhao

The Cancer Hospital of Gansu Province

18215113598@163.com+86 13919219021

Outcome results

None listed

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