Skip to content

Clinical value of a follow-up intervention strategy based on multimodal integrated assessment in patients with stage N3 nasopharyngeal carcinoma after radiotherapy: a multicenter randomized controlled clinical trial

Clinical value of a follow-up intervention strategy based on multimodal integrated assessment in patients with stage N3 nasopharyngeal carcinoma after radiotherapy: a multicenter randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127994
Enrollment
Unknown
Registered
2026-07-12
Start date
2026-07-30
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Nasopharyngeal carcinoma

Interventions

Control group:Conventional follow-up
Intervention group:Multimodal integrated assessment-guided follow-up intervention

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Patients with histologically confirmed nasopharyngeal carcinoma at initial diagnosis, classified as stage N3 (any T stage, N3 disease according to the 9th edition of the AJCC/UICC staging system) without evidence of distant metastasis; 2.No prior history of neck lymph node dissection; 3.Age between 18 and 70 years; 4.Satisfactory performance status with an Eastern Cooperative Oncology Group (ECOG) score of 0–1; 5.Adequate organ function, defined as leukocyte count >= 4.0 × 10^9/L, absolute neutrophil count >= 2.0 × 10^9/L, hemoglobin >= 90 g/L, platelet count >= 100 × 10^9/L, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels = 60 mL/min; 6.The ability to be fully informed about the study and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients who have received other antitumor therapies or are currently participating in other interventional clinical trials. 2.Pregnant or lactating women; 3.Any serious comorbid conditions or risk factors that may lead to unacceptable risks or affect study compliance, such as severe cardiac disease (NYHA class III–IV), severe pulmonary dysfunction (grade 3 or higher), renal disease, or severe psychiatric disorders. 4.Except for adequately treated basal cell carcinoma of the skin, carcinoma in situ of the cervix, and superficial bladder tumors (Ta, Tis, and T1), patients with a history of other invasive malignancies within the past 5 years.

Design outcomes

Primary

MeasureTime frame
Failure-Free Survival, FFS;

Secondary

MeasureTime frame
Locoregional recurrence-free survival, LRRFS;Overall Survival, OS;Distant Metastasis-Free Survival, DMFS;Adverse Events;

Countries

China

Contacts

Public ContactXuelei Ma

West China Hospital of Sichuan University

drmaxuelei@gmail.com+86 13408410416

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026