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The prospective,multicenter, randomized clinical trial to compare weekly cisplatin CCRT and every three weeks cisplatin CCRT in advanced nasopharyngeal carcinoma

The prospective,multicenter, randomized clinical trial to compare weekly cisplatin CCRT and every three weeks cisplatin CCRT in advanced nasopharyngeal carcinoma

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12001979
Enrollment
Unknown
Registered
2012-01-08
Start date
2011-10-01
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

A:cisplatin CCRT every three weeks
B:cisplatin CCRT every week

Sponsors

Nasopharyngeal Carcinoma Department of Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Histologic diagnosis of nasopharyngeal carcinoma; 2. Aged between 18 and 65 years; 3. T3N0-2M0, T4N0-2M0, T1-4N2M0(UICC 7th edition); 4. KPS>=80; 5. No distant metastasis; 6. WBC count>=4*10^9/L, Hemoglobin>=100g/L, platelet count>=100*10^9/L; 7. ALT or AST<2*ULN, bilirubin<1.5*ULN; 8. Serum creatinine<1.5*ULN.

Exclusion criteria

Exclusion criteria: 1. Distant metastases; 2. Previously treated (surgery, chemotherapy, radiotherapy, EGFR targeted therapy or immunotherapy); 3. Second malignancy within 5 years; 4. Precious therapy with an investigational agent; 5. Uncontrolled seizure disorder or other serious neurologic disease; 6. Allergic reaction (>=Grade III) to any drug including in this study; 7. Clinically significant cardiac or respiratory disease; 8. Creatinine clearance <30ml/min; 9. Drug or alcohol addiction; 10. Do not have full capacity for civil acts; 11. With severe complications or active infection; 12. Concurrent immunotherapy or hormone therapy for other diseases; 13. Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
failure free survive rate;

Secondary

MeasureTime frame
overall survival rate;locoregional failure-free rate;disease free survival rate;distant metastasis free survival;Quality of life;

Countries

China

Contacts

Public ContactGuo Xiang
guoxiang@sysucc.org.cn+86 020 87343359

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 26, 2026