Skip to content

A randomized, controlled trial for radiosensitization of calcium folinate in locally advanced nasopharyngeal carcinoma

A randomized, controlled Phase II trial for radiosensitization of calcium folinate for untreated locoregionally advanced nasopharyngeal carcinoma

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019912
Enrollment
Unknown
Registered
2018-12-08
Start date
2018-12-10
Completion date
Unknown
Last updated
2018-12-10

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

Conditions

Local advanced nasopharyngeal carcinoma

Interventions

Intervention group:Intravenous infusion of calcium folinate started 3 days before chemotherapy
Control group:Without calcium folinate

Sponsors

the Fifth Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Nasopharyngeal carcinoma (NPC) was diagnosed by pathology at the age of 18-70. Its clinical stage was locally advanced (stage III or IVa); 2. No antineoplastic treatment before; 3. The survival time more than 3 months; 4. Patients'whole body state score should be less than 2 points according to ECOG (Eastern Cooperative Oncology Group) score; 5. The patient must meet all of the following conditions: white blood cell count at 4,000-10,000/mm3; neutrophil count at or above 2,000/mm3; platelet count at or above 100,000/mm3; hemoglobin at or above 11.0 g/dL; aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 1.5 times the upper limit of normal value; total bilirubin at or below 24 umol/L and creatinine at or below 85umol/L.

Exclusion criteria

Exclusion criteria: 1. Distant metastasis in clinical stage (M1); 2. Malignant tumors were diagnosed and treated with radiotherapy and chemotherapy within 5 years before admission; 3. There are the following serious diseases: uncontrollable infections, severe heart failure and myocardial infarction in the past six months; 4. pregnancy.

Design outcomes

Primary

MeasureTime frame
white blood cell;platelet;Glutamic pyruvic transaminase;glutamic-oxalacetic transaminase;creatinine;

Countries

China

Contacts

Public ContactHuaili Zhou

Department of thoracic oncology, the cancer center of the fifth affiliated hospital of Sun Yat-sen University

zhouh_li@163.com+86 13543009576

Outcome results

None listed

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