Skip to content

Analysis of induction chemotherapy regimens and prognostic risk factors for advanced hypopharyngeal squamous cell carcinoma

Otolaryngology

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062391
Enrollment
Unknown
Registered
2022-08-04
Start date
2022-08-03
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

hypopharyngeal squamous cell carcinoma

Interventions

one:Induction chemotherapy + surgery + radiotherapy
two:Surgery + radiotherapy or concurrent chemoradiation

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Obtain signed written informed consent or telephone authorization; - Age at the time of surgery>= 18 years and = (see Appendix 1 for details on KPS scoring criteria); - Good follow-up compliance.

Exclusion criteria

Exclusion criteria: - Failure to obtain signed written informed consent and failure to obtain consent such as the patient's telephone; - at the time of admission the patient's TNM is diagnosed in stages of T1, N0 and specific T2, N0 and T4b, N0-3; - Clear distant metastases M1 of hypopharyngeal carcinoma or other malignant neoplasms complicated by hypopharyngeal carcinoma during the period of occurrence; - Patients who have previously been diagnosed with squamous cell carcinoma of the lower pharynx and have been treated with traditional Chinese medicine; - Previous treatment of patients who have not been carried out in accordance with the standard protocol for diagnosis and treatment; - Patients who have developed any malignant tumors in the past 5 years (cured cutaneous basal cell carcinoma or cervical in situ except for cancer); - Anaphylaxis of grade 3-4 known to any drug in the treatment that leads to suspension or reduction of the dose of the drug; - Peripheral neuropathy > grade 1; - any unstable systemic diseases (including active infections, uncontrolled hypertension, unstable angina, angina that has begun to attack in the last 3 months, congestive heart failure, myocardial infarction that occurred within 12 months before admission, severe arrhythmias requiring medical therapy, liver, kidney or metabolic diseases); - Known human immunodeficiency virus (HIV) infection; - Pregnant or lactating women; - Drug/alcohol abuse, or suffering from a mental or psychiatric disorder that may interfere with the study of compliance; - patients with epilepsy who require medication (for example, steroids or antiepileptic drugs); - Situations where the researcher deems it inappropriate to join the group.

Design outcomes

Primary

MeasureTime frame
Overall svrvival;

Secondary

MeasureTime frame
disease-free survival;Throat preservation rate;Objective response rate;Local control rate;quality of life;security;

Countries

China

Contacts

Public ContactLixiao Chen

Shanghai General Hospital

chenlixiao1201@163.com+86 13651698736

Outcome results

None listed

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