Benefit of Adding Chemotherapy for Advance Nasopharyngeal Carcinoma (T1-4N2-3M0)
NCT ID: NCT00563927
Last Updated: 2010-07-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
340 participants
INTERVENTIONAL
1999-03-31
2009-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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Conventional RT
Cisplatin
5-fluorouracil
Eligibility Criteria
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Inclusion Criteria
* Tumor staged as N2-3
* No evidence of distant metastasis M0
* Performance status:0-2
* Marrow: WBC \>= 4 and platelet \>= 100
* Renal: creatinine clearance \>= 60
* Informed consent
Exclusion Criteria
* Age \>= 70
* Palliative intent or tumor extent mandating AP opposing facio-cervical fields
* Prior malignancy except adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease-free for 5 years
* Previous radiotherapy (except non-melanomatous skin cancers outside the intended RT treatment volume
* Previous chemotherapy
* Patient is pregnant or lactating
70 Years
ALL
No
Sponsors
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Hong Kong Nasopharyngeal Cancer Study Group Limited
OTHER
Hospital Authority, Hong Kong
OTHER_GOV
Principal Investigators
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Wai Hon LAU, Dr
Role: PRINCIPAL_INVESTIGATOR
Department of Clinical Oncology, Queen Elizabeth Hospital
Locations
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Pamela Youde Nethersole Eastern Hospital
Hong Kong, , China
Queen Elizabeth Hospital
Hong Kong, , China
Queen Mary Hospital
Hong Kong, , China
Tuen Mun Hospital
Hong Kong, , China
Countries
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Other Identifiers
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HARECCTR0500023
Identifier Type: -
Identifier Source: secondary_id
NPC99-01
Identifier Type: -
Identifier Source: secondary_id
L/M-77 TO PYH08/79
Identifier Type: -
Identifier Source: org_study_id
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