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OncoMatch/Clinical Trials/NCT06239727

Reduced-dose Radiotherapy for Stage III Nasopharyngeal Carcinoma Based on the Treatment Response

Is NCT06239727 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies multiple treatments for nasopharyngeal carcinoma.

Phase 3RecruitingSun Yat-sen UniversityNCT06239727Data as of Jun 2026Location: China

Treatment: PD-1 blocking antibody · Gemcitabine · Cisplatin (80 mg/m2) · Cisplatin (100 mg/m2) · CapecitabineThis is an Open Label, Non-Inferiority, Multicenter, Randomized Phase 3 Trial aimed to investigate the impact of reduced-dose radiotherapy in combination with chemotherapy and immunotherapy on patients' prognosis and complication compared with conventional-dose radiotherapy in combination with chemotherapy and immunotherapy for treatment-sensitive stage III NPC patients screened out according to the treatment response.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

GemcitabineCisplatin (80 mg/m2)Cisplatin (100 mg/m2)Capecitabine

Other

PD-1 blocking antibody

Cancer type

Head and Neck Squamous Cell Carcinoma

Disease stage

Required: Stage III

Excluded: Stage T3N0

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 65

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Must have received: induction chemotherapy (GP regimen, Camrelizumab) — induction

Receive 3 cycles of indction chemotherapy (GP regimen + Camrelizumab)

Cannot have received: radiotherapy

Exception: non-melanoma skin cancer located outside the target volume of radiotherapy for nasophayngeal carcinoma

History of radiotherapy, except for non-melanoma skin cancer located outside the target volume of radiotherapy for nasophayngeal carcinoma

Cannot have received: other local or regional therapy

Receive treatment for the local or regional disease other than that specified in the research plan

Lab requirements

Blood counts

white blood cell count > 4×10^9/l, hemoglobin > 90g/l, platelet count > 100×10^9/l

Kidney function

creatinine clearance rate ≥ 60 ml/min

Liver function

total bilirubin ≤ 1.5 × uln, alanine transaminase and aspartate transaminase ≤ 2.5 × uln, alkaline phosphatase ≤ 2.5 × uln

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06239727 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

What disease stage is eligible?

Stage III is required.

Is there an age limit?

Yes. Patients must be 65 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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