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A Phase III Study of Radiotherapy With or Without Adjuvant C/T in Advanced Stage Nasopharyngeal Carcinoma Patients

Primary Purpose

Nasopharyngeal Carcinoma

Status
Terminated
Phase
Phase 3
Locations
Taiwan
Study Type
Interventional
Intervention
Cisplatin,5-FU,Leucovorin
Sponsored by
National Health Research Institutes, Taiwan
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nasopharyngeal Carcinoma focused on measuring Radiotherapy, Adjuvant chemotherapy, Chemtherapy, Nasopharyngeal Carcinoma

Eligibility Criteria

undefined - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients must have histologically proven nasopharyngeal carcinoma who have just completed curative radiotherapy treatment. Original stage must be stage IV disease (M0) Patients must have a complete response, partial response or stable disease assessed 4 weeks after radiotherapy. Performance status scale ECOG grade 0,1. Creatinine ≦ 1.5mg/dl and bilirubin ≦ 2.0mg/dl, WBC ≧ 3,000/mm3 and PLT ≧ 100,000/mm3,or Creatinine Clearance > 45ml/min if Creatinine > 1.5mg/dl. Patients must be younger than 70 year-old. Patients must give signed informed consent. Exclusion Criteria: Patients had progressive disease after radiotherapy Patients had evidence of distant metastasis. Patients had completed radiotherapy for more than 7 weeks. The presence of life-threatening illness History of prior malignancy excluding basal cell carcinoma or squamous carcinoma of the skin or in-situ cervical cancer within 3 years of the diagnosis of NPC cancer. Previous chemotherapy. Pregnancy.

Sites / Locations

  • Veterans General Hospital-Taipei

Outcomes

Primary Outcome Measures

overall survival, relapse free survival,distant metastasis and local-regional control rates.

Secondary Outcome Measures

toxicities of the two treatment methods.

Full Information

First Posted
September 13, 2005
Last Updated
March 25, 2010
Sponsor
National Health Research Institutes, Taiwan
Collaborators
National Taiwan University Hospital, Tri-Service General Hospital, Kaohsiung Medical University, Kaohsiung Veterans General Hospital., Taipei Veterans General Hospital, Taiwan, Mackay Memorial Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00201344
Brief Title
A Phase III Study of Radiotherapy With or Without Adjuvant C/T in Advanced Stage Nasopharyngeal Carcinoma Patients
Official Title
A Phase III Study of Radiotherapy With or Without Adjuvant Chemotherapy in Advanced Stage Nasopharyngeal Carcinoma Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2009
Overall Recruitment Status
Terminated
Study Start Date
November 1994 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2000 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Health Research Institutes, Taiwan
Collaborators
National Taiwan University Hospital, Tri-Service General Hospital, Kaohsiung Medical University, Kaohsiung Veterans General Hospital., Taipei Veterans General Hospital, Taiwan, Mackay Memorial Hospital

4. Oversight

5. Study Description

Brief Summary
To investigate the efficacy of adjuvant PFL chemotherapy after radiotherapy vs radiotherapy alone in AJC stage IV nasopharyngeal carcinoma patients. The endpoints of the study includes : overall survival, relapse free survival, distant metastasis and local-regional control rates. To evaluate the toxicities of the two treatment methods.
Detailed Description
The head and neck contracts study tested induction and maintenance chemotherapy in patients with advanced head and neck cancers.There were no significant differences in survival between the two groups, but disease free survival was prolonged in the maintenance arm and not in the induction arm. Time to and frequency of distant metastases as the first site of relapse were significantly better for those on the maintenance arm. Many trials, designed several years ago, delivered single agent chemotherapy and were not particularly intensive. Most clinical trials were dealing with a heterogenous group of head and neck cancer patients. We felt that a better choice of adjuvant chemotherapy on cancers should include: (1) localized cancers with high metastatic potential following effective local treatment; (2) effective chemotherapy available; (3) chemotherapy should be intensive and effective enough to avoid the development of drug resistance. Of course, NPC had long been regarded as one of the most suitable head and neck cancers that may benefit from adjuvant chemotherapy due to its unique high response rate to chemotherapy and high metastatic potential after radiotherapy for localized, advanced staged disease. If radiotherapy plus adjuvant chemotherapy can improve the treatment results of standard radiotherapy by increasing the survival rate, decreasing the metastatic rate and local recurrence rate, then many NPC patients may benefit. Therefore, we propose this phase III study of radiotherapy with or without adjuvant PFL chemotherapy in advanced stage NPC patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma
Keywords
Radiotherapy, Adjuvant chemotherapy, Chemtherapy, Nasopharyngeal Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
320 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Cisplatin,5-FU,Leucovorin
Primary Outcome Measure Information:
Title
overall survival, relapse free survival,distant metastasis and local-regional control rates.
Secondary Outcome Measure Information:
Title
toxicities of the two treatment methods.

10. Eligibility

Sex
All
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients must have histologically proven nasopharyngeal carcinoma who have just completed curative radiotherapy treatment. Original stage must be stage IV disease (M0) Patients must have a complete response, partial response or stable disease assessed 4 weeks after radiotherapy. Performance status scale ECOG grade 0,1. Creatinine ≦ 1.5mg/dl and bilirubin ≦ 2.0mg/dl, WBC ≧ 3,000/mm3 and PLT ≧ 100,000/mm3,or Creatinine Clearance > 45ml/min if Creatinine > 1.5mg/dl. Patients must be younger than 70 year-old. Patients must give signed informed consent. Exclusion Criteria: Patients had progressive disease after radiotherapy Patients had evidence of distant metastasis. Patients had completed radiotherapy for more than 7 weeks. The presence of life-threatening illness History of prior malignancy excluding basal cell carcinoma or squamous carcinoma of the skin or in-situ cervical cancer within 3 years of the diagnosis of NPC cancer. Previous chemotherapy. Pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kwan-Hwa Chi, MD,
Organizational Affiliation
Taiwan cooperative oncology group
Official's Role
Principal Investigator
Facility Information:
Facility Name
Veterans General Hospital-Taipei
City
Taipei
ZIP/Postal Code
112
Country
Taiwan

12. IPD Sharing Statement

Learn more about this trial

A Phase III Study of Radiotherapy With or Without Adjuvant C/T in Advanced Stage Nasopharyngeal Carcinoma Patients

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