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Retrospective real-world study of the efficiency of radiotherapy and safety of patients with locally advanced nasopharyngeal cancer: different uses for different nasopharyngeal cancer patients based on biological characteristics

Retrospective real-world study of the efficiency of radiotherapy and safety of patients with locally advanced nasopharyngeal cancer: different uses for different nasopharyngeal cancer patients based on biological characteristics

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055700
Enrollment
Unknown
Registered
2022-01-16
Start date
2006-01-01
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

nasopharyngeal carcinoma

Interventions

case series:Nil

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with newly diagnosed stage III-IV nasopharyngeal carcinoma confirmed by histopathology and imaging, who receive concurrent radiotherapy and chemotherapy; 2. Aged 18-70 years (inclusive); 3. Physical function status KPS score >= 70 points; 4. The patient's lung, liver, kidney function, blood picture, and urine routine are within the agreed range (inclusion criteria in CRF), and the electrocardiogram must be within the normal range; 5. No other radiotherapy sensitizers were used in combination with Ximena during radiotherapy; 6. The use of Ximena radiotherapy sensitization cases has ended; 7. No other tumor diseases in the past, except for cured cervical carcinoma in situ, skin basal cancer or malignant diseases cured for 5 years; 8. Without AIDS, active tuberculosis and other serious immune abnormal diseases; 9. The radiotherapy technique adopts intensity-modulated radiation therapy; 10. The treatment plan is induction chemotherapy + concurrent chemoradiotherapy/concurrent chemoradiotherapy; 11. Complete treatment and follow-up data.

Exclusion criteria

Exclusion criteria: 1. Serious, uncontrolled diseases and infections; 2. History of active hepatitis; 3. Some obvious diseases that the researcher believes should be excluded from this study; 4. Other patients who are not considered suitable for inclusion in this study by the investigator.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Objective mitigation rate ;Progression-free survival ;No distant metastasis for survival;No local recurrence of the survival period;Total irradiation dose at total and partial remission;

Countries

China

Contacts

Public ContactYunfei Xia

Sun Yat-sen University Cancer Center

xiayf@sysucc.org.cn+86 13602805461

Outcome results

None listed

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