A Multicenter Trial Comparing Induction C/T Followed by CCRT v.s. CCRT Alone in Stage IV Nasopharyngeal Carcinoma

National Health Research Institutes, Taiwan

Status and phase: Completed; Phase 3

Conditions: Nasopharyngeal Carcinoma

Treatments: Radiation: CCRT; Drug: Mitomycin C,Epirubicin,Cisplatin,5-Fluorouracil,Leucovorin

Study type: Interventional

Funder types: Other

Identifiers

NCT00201396

T1303

Details and patient eligibility

About

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.

Full description

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)

Enrollment: 480 patients

Sex: All

Ages: Under 70 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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480 participants in 2 patient groups

A arm

Active Comparator group

Description:

CCRT

Treatment:

Radiation: CCRT

B arm

Experimental group

Description:

Induction/CCRT

Treatment:

Radiation: CCRT

Drug: Mitomycin C,Epirubicin,Cisplatin,5-Fluorouracil,Leucovorin