Skip to content

Induction chemotherapy followed by chrono-chemotherapy concurrent with intensity-modulated radiotherapy in the treatment of locally advanced nasopharyngeal carcinoma phase ?clinical randomized study

Induction chemotherapy followed by chrono-chemotherapy concurrent with intensity-modulated radiotherapy in the treatment of locally advanced nasopharyngeal carcinoma phase ?clinical randomized study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004607
Enrollment
Unknown
Registered
2014-01-05
Start date
2014-06-01
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

2:Cisplatin chrono-chemotherapy concurrent with intensity-modulated radiation therapy
1:Induction chemotherapy followed by cisplatin conventional chemotherapy concurrent combined with intensity-modulated radiation therapy

Sponsors

Guizhou Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The pathological diagnosis of early cure III-IV stage of patients with advanced nasopharyngeal carcinoma (according to the 2010 UICC staging criteria, T3-4, N0-3), no evidence of distant metastasis (M0). Have a measurable tumor lesions; 2. Karnofsky score=70; 3. Aged 18-70 years old, male or female; 4. No major organ dysfunction; Normal bone marrow hematopoietic function (white blood cell =4.0×10^9/L; Platelet=100×10^9/L; Hemoglobin =100g/L) normal liver function (total bilirubinalanine aminotransferase aspartate aminotransferase =1.5 times the upper limit of normal)normal renal function (creatinine =1.5 times the upper limit of normal) electrocardiogram does not affect the normal treatment; 5. To understand this study and sign informed consent form.

Exclusion criteria

Exclusion criteria: 1. A distant metastasis; 2. Patients with physical or mental illness, and researchers think that patients can't fully or adequately understand the possible complications of this study; 3. Pregnancy (confirmed by serum or urine ß-HCG test) or between lactation period; 4. Serious complications, such as uncontrollable hypertension, heart function failure, diabetes, etc.; 5. Who had received radiation and chemotherapy.

Design outcomes

Primary

MeasureTime frame
Toxicity;Curative effect;

Countries

China

Contacts

Public ContactFeng Jin

The Affiliated Hospital of Guiyang Medical College/The Affiliated Cancer Hospital of Guiyang Medical College/Guizhou Cancer Hospital

jinf8865@gmail.com+86 13985124806

Outcome results

None listed

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