A Multicenter Trial Comparing Induction C/T Followed by CCRT v.s. CCRT Alone in Stage IV Nasopharyngeal Carcinoma
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Purpose
Investigate the effect of induction MEPFL chemotherapy followed by concurrent chemoradiotherapy (CCRT) on the disease control and survival in treatment of patients with advanced NPC.
| Condition | Intervention | Phase |
|---|---|---|
|
Nasopharyngeal Carcinoma |
Drug: Mitomycin C,Epirubicin,Cisplatin,5-Fluorouracil,Leucovorin |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Multicenter Phase III Trial Comparing Induction Chemotherapy Followed by Concurrent Chemoradiotherapy Versus Concurrent Chemoradiotherapy Alone in Stage IV Nasopharyngeal Carcinoma (NPC) |
- The primary endpoint is the disease-free survival.
- Secondary endpoints include overall survival and tumor response rate.
| Estimated Enrollment: | 480 |
| Study Start Date: | August 2003 |
| Estimated Study Completion Date: | December 2013 |
Rationale of induction chemotherapy:
Distant metastasis is the major cause of treatment failure and deaths in patients with loco-regionally advanced NPC.
Concurrent chemoradiotherapy may prolong survivals for patients with advanced NPC, but it is still flawed by high incidence of distant metastasis.
Induction chemotherapy with MEPFL has been shown to reduce the incidence of distant metastasis in a Phase II study.
Induction chemotherapy plus concurrent chemoradiotherapy may improve the survival of patients with advanced NPC.
Objectives:
Investigate the effect of induction MEPFL chemotherapy followed by concurrent chemoradiotherapy (CCRT) on the disease control and survival in treatment of patients with advanced NPC.
Study design:
This is a randomized, multi-center Phase III study. Patients will be randomized to CCRT with or without the MEPFL induction chemotherapy.
Type and number of patients:
Patients with stage IVA (T4) and/or IVB (N3) but without distant metastasis will be enrolled. A total of up to 480 patients will be randomized to detect an improvement of median overall survival from 5.8 to 8.7 years, with an a=0.05 and power of 0.8 using a two-sided logrank test with one interim analysis.
Treatment schedule:
Induction chemotherapy and CCRT:
Arm A: Weekly cisplatin concurrently with radiotherapy Arm B: Induction MEPFL three cycles followed with weekly cisplatin concurrently with radiotherapy.
Study endpoints:
The primary endpoint is the disease-free survival that will be calculated as the duration between the date of randomization and the date of recurrence of NPC at any site including persistent disease after +induction chemotherapy/CCRT, or death from any cause (failed), or the date of withdrawal (last contact date, censored), or the scheduled data analysis date (censored).( revised 8/27/2004)
Eligibility| Ages Eligible for Study: | up to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Histologically proved nasopharyngeal carcinoma.
- T4NxM0 or TxN3M0 disease by UICC/AJCC 1997 staging system. (30)
- Eastern Cooperative Oncology Group performance status < 2.
- A leukocyte count ≥3750/mL, Hb ≥ 10 g/dL, and a platelet count ≥100,000/mL.
- A serum bilirubin level < 1.5 mg/dL, serum creatinine level < 1.6 mg/dL or creatinine clearance > 60 mL/min.
- Age less than 70 years old
- An informed consent signed.
Exclusion Criteria:
- Evidence of metastatic disease.
- Presence of another malignancy other than treated squamous/basal cell carcinoma of the skin.
- Presence of uncontrolled hypertension, poorly controlled heart failure.
- Presence of active infection.
- Patients who have been or are being treated with chemotherapy, radiotherapy, immunotherapy, or other experimental therapies.
- Women who test positive for pregnancy.
Contacts and Locations| Contact: Wei-lien Feng, RN,MSN | 886-2-8792-3311 ext 17644 | winnif@nhri.org.tw |
| Taiwan | |
| Kaohsiung Medical University Hospital | Recruiting |
| Kaohsiung, Taiwan, 80708 | |
| Contact: Wei Te-Chih, B.S 886-7-3121101 ext 6109 hemawei@nhri.org.tw | |
| Principal Investigator: Shi-Long Lian, M.D. | |
| China Medical University Hospital | Recruiting |
| Taichung, Taiwan, 40447 | |
| Contact: Ya-Lin WU, B.S. 886-4-22052121 ext 5372 yalin@nhri.org.tw | |
| Principal Investigator: Ming-Hsui Tsai, M.D. | |
| National Taiwan University Hospital | Recruiting |
| Taipei, Taiwan, 115 | |
| Contact: Ling-Fang Lin., B.S. 886-2-2312-3456 ext 7677 dale@nhri.org.tw | |
| Principal Investigator: Ruey-Long Hong, M.D, PhD | |
| Chang-Gung Memorial Hospital(Lin-Kou), | Recruiting |
| Taoyuan, Taiwan, 333 | |
| Contact: Hsing-Hsun Chang, M.D 886-03-3281200 ext 2512 sissi566@nhri.org.tw | |
| Principal Investigator: Joseph T. Chang, M.D | |
| Principal Investigator: | Ruey-Long Hong, MD, PhD | Taiwan cooperative oncology group |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00201396 History of Changes |
| Other Study ID Numbers: | T1303 |
| Study First Received: | September 13, 2005 |
| Last Updated: | April 2, 2009 |
| Health Authority: | Taiwan: Department of Health |
Keywords provided by National Health Research Institutes, Taiwan:
|
A Multicenter Phase III Trial Induction Chemotherapy Concurrent Chemoradiotherapy |
Stage IV Nasopharyngeal Carcinoma (NPC) randomization disease-free survival |
Additional relevant MeSH terms:
|
Carcinoma Nasopharyngeal Neoplasms Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Pharyngeal Neoplasms Otorhinolaryngologic Neoplasms Head and Neck Neoplasms Neoplasms by Site Nasopharyngeal Diseases Pharyngeal Diseases Stomatognathic Diseases Otorhinolaryngologic Diseases Mitomycins Mitomycin |
Epirubicin Cisplatin Fluorouracil Leucovorin Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Pharmacologic Actions Nucleic Acid Synthesis Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Alkylating Agents Radiation-Sensitizing Agents Physiological Effects of Drugs Antimetabolites |
ClinicalTrials.gov processed this record on May 19, 2013