Skip to content

Comprehensive treatment of head and neck rhabdomyosarcoma: a single-arm, open, multicenter, prospective clinical study

Comprehensive treatment of head and neck rhabdomyosarcoma: a single-arm, open, multicenter, prospective clinical study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032156
Enrollment
Unknown
Registered
2020-04-21
Start date
2020-04-20
Completion date
Unknown
Last updated
2020-04-27

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

Conditions

Rhabdomyosarcoma

Interventions

experimental group:chemotherapy, radiotherapy and surgery

Sponsors

Eye Ear Nose and Throat Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 16 years old, < 70 years old; 2. ECOG performance status of 0-1; 3. Patients have a histologically confirmed diagnosis of head and neck rhabdomyosarcoma and no prior exposure to chemotherapy or radiotherapy; 4. Patients with risk divided into the IRSG middle-risk group; 5. No obvious heart, liver, kidney dysfunction and blood system diseases; 6. Prohibit the use of other drugs for the treatment of neutropenia or drugs that affect hemogram, such as Medroxyprogesterone, megestrol, adrenocortical hormone, etc.; 7. The patient and his family members signed the chemotherapy consent form and informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with poor compliance or refusal to use treatment; 2. Those with concomitant diseases that seriously impair patient safety or affect patients' inability to complete clinical trials; 3. Patients with intolerable and/or serious or life-threatening adverse events during application; 4. Women during lactation or pregnancy (urine ß-HCG positive); 5. Those who have a history of drug abuse; 6. Patients with active mental disorders or other cognitive disorders that affect the ability to sign informed consent and comprehension; 7. Other conditions that the researcher judges are not suitable for enrollment.

Design outcomes

Primary

MeasureTime frame
progression-free survival ;

Secondary

MeasureTime frame
overall survival;objective remission rate;

Countries

China

Contacts

Public ContactShu Tian

Eye Ear Nose and Throat Hospital, Fudan University

tianshueent@163.com+86 13611672263

Outcome results

None listed

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