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Efficacy of Chemotherapy Combined with Anlotinib for the Second Line Treatment of Patients with Squamous Cell Carcinoma of the Head and Neck: a Retrospective Study Based on Medical Records

Efficacy of Chemotherapy Combined with Anlotinib for the Second Line Treatment of Patients with Squamous Cell Carcinoma of the Head and Neck

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100043233
Enrollment
Unknown
Registered
2021-02-09
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

head and neck squamous cell carcinoma

Interventions

cohort 1:paclitaxel combined with cisplatin plus an Anlotinib
cohort2:paclitaxel combined with cisplatin

Sponsors

Daping Hospital, Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 255 patients with head and neck squamous cell carcinoma diagnosed in the army characteristic medical center of the Army Medical University from May 2018 to June 2020 were included.

Exclusion criteria

Exclusion criteria: 1. Pregnancy or breast feeding; 2. Patients with hypertension and antihypertensive medication can not be reduced to normal range (systolic blood pressure > 150 mmHg, diastolic blood pressure > 100 mmHg); 3. Patients with grade II or higher myocardial infarction, arrhythmia, grade III~IV cardiac function or cardiac ejection fraction 1.5 or PT > ULN+4s or APTT > 1.5 ULN), with bleeding tendency, or receiving thrombolytic or anticoagulant therapy; 5. Urine protein positive patients; 6. Accompanied by serious uncontrollable infection or medical diseases; 7. A person who has been confirmed to be allergic to Anlotinib and/or its excipients; 8. Patients with central nervous system metastases; 9. Patients with a history of psychotropic substance abuse who are unable to quit or have a mental disorder; 10. With severe heart, lung, liver, kidney and other important organ dysfunction;

Design outcomes

Primary

MeasureTime frame
progression-free survival;

Secondary

MeasureTime frame
overall survival;

Countries

China

Contacts

Public ContactZhao-Yang Zhong

Daping Hospital, Army Medical University

zhongzhaoyang08@hotmail.com+86 13883932762

Outcome results

None listed

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