OncoMatch

OncoMatch/Clinical Trials/NCT04136886

Concurrent Chemotherapy for Recurrent T3/T4 Nasopharyngeal Carcinoma

Is NCT04136886 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies Cisplatin for nasopharyngeal carcinoma.

Phase 3RecruitingSun Yat-sen UniversityNCT04136886Data as of Jun 2026Location: China

Treatment: CisplatinThe purpose of this study is to determine whether concurrent chemotherapy and IMRT is effective in the treatment of locally stage T3/T4 recurrent nasopharyngeal carcinoma patients compared with IMRT alone.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

Cisplatin

Cancer type

Head and Neck Squamous Cell Carcinoma

Disease stage

Required: Stage RT3, RT4

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 70

Prior therapy

Must have received: radiation therapy — first course

More than 1 year from the end of the first course of radiotherapy

Cannot have received: anti-tumor treatment

Prior anti-tumor treatment after diagnosis of local recurrence

Lab requirements

Blood counts

WBC count ≥4×10^9/L, neutrophile granulocyte count ≥1.5×10^9/L, PLT count ≥100×10^9/L, Hb ≥9g/L

Kidney function

creatinine ≤ 1.5 times of upper normal limits

Liver function

Total bilirubin, AST, ALT ≤ 2.0 times of upper normal limits

WBC count ≥4×10^9/L, neutrophile granulocyte count≥1.5×10^9/L, PLT count ≥100×10^9/L, Hb ≥9g/L; Total bilirubin, AST, ALT≤2.0 times of upper normal limits; creatinine ≤1.5 times of upper normal limits

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

Frequently asked questions

Is NCT04136886 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-tumor treatment disqualifies patients from enrollment.

What disease stage is eligible?

Stage RT3 or RT4 is required.

Is there an age limit?

Yes. Patients must be 70 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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