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4 cycles neoadjuvant chemotherapy withTPF regimen followed by concurrent chemotherapy for stage IVB nasopharyngeal carcinoma

4 cycles neoadjuvant chemotherapy withTPF regimen followed by concurrent chemotherapy for stage IVB nasopharyngeal carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-16007739
Enrollment
Unknown
Registered
2016-01-12
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nasopharyngeal carcinoma

Interventions

four cycles chemotherapy:four cycles chemotherapy

Sponsors

Department of Radiation Oncology, Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 70 years; 2. Eastern Cooperative Oncology Group (ECOG) status of 0-2; 3. Pathologically diagnosed with NPC; 4. NPC patients with T1-4N3M0 IVB stage based on the 7th version of the American Joint Committee on Cancer (AJCC) staging system; 5. No hematological diseases, white blood cell counts of at least 4*10^9/L, hemoglobin level of at least 80 g/L, platelet counts of at least 100*10^9/L, alanine transaminase (ALT) levels at least 2.5-fold below the upper limit of normal, and normal kidney function (creatinine clearance rate >=60 mL/min.

Exclusion criteria

Exclusion criteria: 1. Newly diagnosed with metastasis; 2. Serious heart, liver and kidney function damage; 3. With a history of other malignant tumors; 4. With radiotherapy or chemotherapy,ectomy of nasopharynx,lymph node biopsy or topical treatment; 5. Pregnant or lactating women; 6. Mental abnormality; 7. Eastern Cooperative Oncology Group (ECOG) status >=3.

Design outcomes

Primary

MeasureTime frame
Progression-free survival rate;

Secondary

MeasureTime frame
The objective response rate;Overall survival rate;Distant metastasis-free survival rate;Locoregional relapse-free survival rate;Acute adverse event;Late adverse event;

Countries

China

Contacts

Public ContactXu Benhua
benhuaxu@163.com+86 13696884375

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026