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Reduced-dose vs Standard-dose Irradiation for Low-risk Clinical Target Volume in Nasopharyngeal Carcinoma.

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Sun Yat-sen University

Status and phase

Enrolling
Phase 3

Conditions

Nasopharyngeal Cancinoma (NPC)

Treatments

Radiation: Radiation Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT07201337
2025-FXY-299

Details and patient eligibility

About

To evaluate the locoregional control, survival rate, toxicity, and quality of life in patients with nasopharyngeal carcinoma treated with reduced prophylactic irradiation doses to the Low-Risk Clinical Target Volume (CTV).

Full description

This phase 3, multicenter, non-inferiority, randomized controlled clinical trial recruits patients with newly diagnosed, untreated, non-distant metastatic, non-keratinizing nasopharyngeal carcinoma (NPC). The intervention involves comparing reduced-dose prophylactic irradiation to standard-dose prophylactic irradiation for the low-risk clinical target volume (CTV). The objective is to compare the locoregional control, survival rate, toxicity, and quality of life between the two groups.

Enrollment

550 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Newly diagnosed, untreated, non-distant metastatic, and non-keratinizing NPC; aged between 18 and 70 years; Eastern Cooperative Oncology Group performance score of 0-1; adequate hematologic function (neutrophil count ≥ 1.5 × 10^9/L, platelet count ≥100×109/L, and hemoglobin≥ 90 g/L); adequate renal function (creatinine ≤ 1.5 upper limit of normal [ULN]) or calculated creatinine clearance (CrCl) ≥ 60 mL/min (Cockcroft-Gault formula); and adequate hepatic function (serum bilirubin ≤ 2.0×ULN, and alanine aminotransferase and aspartate aminotransferase ≤ 2.5×ULN).

Exclusion criteria

Previous chemotherapy treatment, surgery (except diagnostic) or radiotherapy to the neck or nasopharyngeal regions; previous malignancy (except for cured basal cell carcinoma or carcinoma in situ of the cervix); lactation or pregnancy; or severe coexisting illness.

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Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

550 participants in 2 patient groups

Reduced-dose Radiotherapy for Low-risk CTV
Experimental group
Treatment:
Radiation: Radiation Therapy
Radiation: Radiation Therapy
Standard-dose Radiotherapy for Low-risk CTV
Active Comparator group
Treatment:
Radiation: Radiation Therapy
Radiation: Radiation Therapy

Trial contacts and locations

1

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Central trial contact

Hai-Qiang Mai, Ph. D.

Data sourced from clinicaltrials.gov

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