Nasopharyngeal Carcinoma Clinical Trials

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A Prospective Phase II Clinical Study of Proton Therapy for Recurrent Nasopharyngeal Carcinoma

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device, Radiation
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The above studies show that most of the supportive evidence for the reduction of toxicity and improvement of efficacy of proton therapy for recurrent Nasopharyngeal carcinoma(NPC) comes from various observational and retrospective studies, lacking high-level evidence-based medical evidence. The conduct of this study will explore the safety and efficacy of intensity-modulated proton radiotherapy for recurrent NPC and provide more high-quality evidence-based medical evidence for proton therapy of recurrent cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Non-metastatic squamous cell carcinoma of the nasopharynx with biopsy confirmation, at stage ≥ T2b and/or with positive lymph nodes, (2) Pathological type WHO I-III

• PS score (according to Eastern Cooperative Oncology Group (ECOG) standard) 0-1.

• Age ≥ 18 years.

• Expected survival period ≥ 6 months

• Before treatment, evaluate the tumor range and size of the patient.

• Nutritional and general physical condition must be able to tolerate the recommended radiotherapy and chemotherapy.

Locations
Other Locations
China
Guangzhou Concord Cancer Center
RECRUITING
Guangzhou
Guangzhou concord cancer center
RECRUITING
Guanzhou
Contact Information
Primary
Taize Yuan, M.D., Ph.D.
taize.yuan@ccm.cn
8620-32506195
Time Frame
Start Date: 2025-03-10
Estimated Completion Date: 2028-03-10
Participants
Target number of participants: 52
Treatments
Experimental: Proton therapy group
All patients received proton therapy, with a prescribed dose of 60-66 Gy in 30-33 fractions, 5 days per week, for a total of 6-6.5 weeks.
Related Therapeutic Areas
Sponsors
Leads: Guangzhou Concord Cancer Center

This content was sourced from clinicaltrials.gov

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