Nedaplatin Versus Cisplatin in Treatment for Nasopharyngeal Carcinoma

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAffiliated Cancer Hospital & Institute of Guangzhou Medical University

About this trial

To compare the effectiveness and toxicity of nedaplatin versus cisplatin in induction chemotherapy combined with concurrent chemoradiotherapy for locoregionally advanced nasopharyngeal carcinoma.

Eligibility criteria

Qualifiers

Patients with newly histologically confirmed non-keratinizing nasopharyngeal carcinoma, including WHO II or III

Original clinical staged as III-IVa (except T3-4N0) according to the 8th edition American Joint Committee on Cancer staging system

No evidence of distant metastasis (M0)

Age between 18-65

Disqualifiers

Histologically confirmed keratinizing nasopharyngeal carcinoma (WHO I)

Age >65 or < 18 years

Treatment with palliative intent

Prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer

Trial design

Treatments tested in this trial

  • Docetaxel, nedaplatin, fluorouracil
  • Docetaxel, cisplatin, fluorouracil
  • Nedaplatin
  • Cisplatin
  • Intensity modulated-radiotherapy

Treatment groups

352 Participants
are divided into 2 treatment groups