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Clinical study of anlotinib hydrochloride combined with concurrent chemoradiotherapy in the treatment of locally advanced cervical cancer

Clinical study of anlotinib hydrochloride combined with concurrent chemoradiotherapy in the treatment of locally advanced cervical cancer

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062885
Enrollment
Unknown
Registered
2022-08-22
Start date
2022-08-19
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

cervical cancer

Interventions

Anlotinib combined with concurrent chemoradiotherapy:Anlotinib combined with concurrent chemoradiotherapy

Sponsors

Yili Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participate and sign informed consent in writing; 2. Aged 18-75 years; 3. Histologically confirmed cervical cancer; 4. Clinical stage IB3, IIA2-IV; 5. Primary treatment (have not received anti-tumor therapy such as radiotherapy, chemotherapy, molecular targeting, and immunity before); 6. The primary tumor is measurable; 7. No distant organ metastases; 8. Karnofsky score > 70; 9. Survival expected >= 3 months; 10. Women of childbearing potential should ensure contraception during study entry; 11. Hemoglobin >= 100 g/L, WBC >= 4x10^9/L, platelets >= 100x10^9/L; 12. Liver function: ALT, AST 50%, the percentage of DLCO (diffusing function of lung) measured value and predicted value > 80%; 15. The patient has good compliance with the treatment and follow-up received.

Exclusion criteria

Exclusion criteria: 1. The primary tumor or lymph nodes have been surgically treated (except biopsy); 2. Diagnosis of other malignancies (other than cured in situ cervical carcinoma/basal cell carcinoma of the skin/bladder epithelial tumor) 5 years prior to the start of the study; 3. Subjects who have received other drug trials within the past 1 month; 4. Pregnant or breastfeeding women and women who refuse contraception during the treatment observation period; 5. Those with a history of severe allergies or idiosyncratic constitutions; 6. Those with a history of severe lung or heart disease; 7. People who are drug or alcohol addicts; 8. Persons with personality or mental disorders, no capacity for civil conduct or limited capacity for civil conduct.

Design outcomes

Primary

MeasureTime frame
Safety;radiotherapy response;2- and 3-year local control rates;2- and 3-year DFSR (Disease-Free Survival rate);2- and 3-year OSR (overall survival rate);BIOMARKER;

Countries

China

Contacts

Public ContactHongfei Liu

Yili Friendship Hospital

153682320@qq.com+86 15894126011

Outcome results

None listed

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