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Compare the 5 - fluorouracil and capecitabine in combination with cisplatin synchronous intensity-modulated radiotherapy in the treatment of locally advanced nasopharyngeal carcinoma clinical research

Compare the 5 - fluorouracil and capecitabine in combination with cisplatin synchronous intensity-modulated radiotherapy in the treatment of locally advanced nasopharyngeal carcinoma clinical research

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIQ-16008412
Enrollment
Unknown
Registered
2016-05-03
Start date
2016-06-01
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

1:5 - fluorouracilcapecitabine in combination with cisplatin synchronous intensity-modulated radiotherapy (CCRT)
2:capecitabine in combination with cisplatin synchronous intensity-modulated radiotherapy(CCRT)

Sponsors

The Second People's Hospital of Neijiang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. By pathological or cytological diagnosis of nasopharyngeal carcinoma patients and treated first; 2. UICC2003 stage for III, a and bIV IV (local middle-late); 3. Without radiation and chemotherapy absolute contraindications; 4. Signed informed consent before treatment; 5. Aged 18 to 80 years old, physical status ECOG 0 ~ 2 or KPS acuity 70; 6. Subjects were no vital organ dysfunction, routine blood, lung, liver, kidney, blood coagulation function and cardiac function were all normal; 7. Patients who had good compliance treatment and follow-up.

Exclusion criteria

Exclusion criteria: 1. Do not accord with the standard set of staging and survival of patients; 2. Nasopharyngeal carcinoma recurrence after chemotherapy; patient who ever accept any form of external andcavities beam radiation therapy; 3. patient with high blood pressure, diabetes, history of unstable angina pectoris can't be controlde and history of myocardial infarction, or seen in the past 12 months have symptoms of congestive heart failure or unable to control arrhythmia;Electrocardiogram (ecg) prompt a ischemic change or clinical diagnosis of heart valve disease; Bacteria, fungi or viruses infection disease activity; Mental disorders; 4. Patients with pregnancy or lactation; 5. With allergic constitution and known or suspected patients allergic to any drugs applyde to research 6. Poor compliance of patients; 7. Researchers think that is unfavorable to the subject.

Design outcomes

Primary

MeasureTime frame
OS;

Secondary

MeasureTime frame
local control rate;side effect;

Countries

China

Contacts

Public ContactDu Chi

The Second People's Hospital of Neijiang

duchi@vip.163.com+86 13990551326

Outcome results

None listed

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