ConditionNasopharyngeal 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 groupsSponsors and collaborators
Source ClinicalTrials.gov