Skip to content

Multicenter prospective clinical study for treatment options for partial release in patients with locally advanced laryngeal and hypopharyngeal cancer after TPF-induction chemotherapy

Multicenter prospective clinical study for treatment options for partial release in patients with locally advanced laryngeal and hypopharyngeal cancer after TPF-induction chemotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021844
Enrollment
Unknown
Registered
2019-03-12
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-03-18

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

Conditions

Laryngeal and hypopharyngeal cancer

Interventions

Group 2:radical radiotherapy or concurrent chemoradiotherapy
Group 1:surgery+ postoperative adjuvant radiotherapy

Sponsors

Beijing Tongren Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with advanced or advanced throat cancer (local tumor T2-4, any N) who achieved PR after induction chemotherapy in 2-3 cycles [segment reference to the eighth edition of AJCC-TNM staging]; 2. aged 18-75 years old; 3. initial treatment Patients (primary, no surgery, radiotherapy and chemotherapy history); 4. KPS score 80 points and above; 5. blood, heart, lung, liver, kidney and other major organs function is basically normal. WBC=3.5×10^9/L, ANC=1.5×10^9/L, PLT=100×10^9/L, Hb=80g/L, total plasma bilirubin=1.5×the upper limit of normal value, ALT, AST or AKP=2.5× Upper limit of normal value, urea nitrogen, creatinine = 1.25 × upper limit of normal value; 6. improved neck and chest enhancement CT and endoscopy before enrollment; 7. pathological examination before enrollment (differentiation degree, immunological index - Ki-67, EGFR, HPV); 8. Signed informed consent, good compliance.

Exclusion criteria

Exclusion criteria: 1. distant metastasis patients; 2. patients with advanced tracheotomy; 3. patients who can be resected by laser minimally invasive surgery; 4. have uncontrollable seizures, central nervous system disorders or self-knowledge due to mental illness loss; 5. serious controlled infection; 6. major organ dysfunction (including heart, lung, liver, kidney, etc.); 7. can not tolerate general anesthesia; 8. other or two years of malignant tumors.

Design outcomes

Primary

MeasureTime frame
Overall survival;Progression free survival;Laryngeal preserve survival;

Countries

China

Contacts

Public ContactFang Jugao

Beijing Tongren Hospital, Capital Medical University

fangjg19651110@163.com+86 18811612211

Outcome results

None listed

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