OncoMatch

OncoMatch/Clinical Trials/NCT05514275

Radiotherapy Combined With Endostatin and Capecitabine for NPC

Is NCT05514275 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Endostatin and Capecitabine for nasopharyngeal carcinoma.

Phase 2RecruitingZhejiang Cancer HospitalNCT05514275Data as of Jun 2026Location: China

Treatment: Endostatin and CapecitabineRadiotherapy combined with recombinant human endostatin and capecitabine for patients with nasopharyngeal carcinoma (NPC) resistant to induction chemotherapy.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

Endostatin and Capecitabine

Cancer type

Head and Neck Squamous Cell Carcinoma

Disease stage

Required: Stage T3-4N1, N2-3 (8th American Joint Commission on Cancer edition)

Tumor staged as T3-4N1/N2-3 (according to the 8th American Joint Commission on Cancer edition). No evidence of distant metastasis (M0).

Demographics

Ages ≤ 65

Prior therapy

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

Must have received: neoadjuvant chemotherapy — neoadjuvant

unsatisfactory tumor response (stable or progressive disease) after neoadjuvant chemotherapy (NACT)

Cannot have received: chemotherapy

Exception: except neoadjuvant chemotherapy

Prior chemotherapy or surgery (except diagnostic) to primary tumor or nodes

Cannot have received: surgery

Exception: except diagnostic

Prior chemotherapy or surgery (except diagnostic) to primary tumor or nodes

Cannot have received: radiotherapy

Exception: except for non-melanomatous skin cancers outside intended RT treatment volume

History of previous radiotherapy (except for non-melanomatous skin cancers outside intended RT treatment volume)

Lab requirements

Blood counts

leucocyte count ≥4000/μL, hemoglobin ≥90g/L, platelet count ≥100000/μL

Kidney function

creatinine clearance ≥60 ml/min

Liver function

ALT, AST <1.5×ULN; ALP ≤2.5×ULN; bilirubin ≤ULN

Adequate marrow: leucocyte count ≥4000/μL, hemoglobin ≥90g/L and platelet count ≥100000/μL. Normal liver function test: Alanine Aminotransferase (ALT)、Aspartate Aminotransferase (AST) <1.5×upper limit of normal (ULN) concomitant with alkaline phosphatase (ALP) ≤2.5×ULN, and bilirubin ≤ULN. Adequate renal function: creatinine clearance ≥60 ml/min.

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

Frequently asked questions

Is NCT05514275 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 T3-4N1 or N2-3 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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