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Retrospective real-world study of the radiotherapy efficiency effect and safety evaluation of patients with locally advanced nasopharyngeal cancer: Simena combined with concurrent chemoradiotherapy versus concurrent chemoradiotherapy

Retrospective real-world study of the radiotherapy efficiency effect and safety evaluation of patients with locally advanced nasopharyngeal cancer: Simena combined with concurrent chemoradiotherapy versus concurrent chemoradiotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055708
Enrollment
Unknown
Registered
2022-01-16
Start date
2003-01-01
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

Himena combined with concurrent radiotherapy and chemotherapy vs. concurrent chemoradiotherapy and chemotherapy: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. Newly diagnosed patients with stage III~IV nasopharyngeal carcinoma confirmed by histopathology and imaging (see Appendix1); 2. Aged from 18 to 70; 3. KPS >= 70 (see Appendix 2); 4. Patients' lung, liver and kidney function, cardiac function, haematological indicators and urinary routine within normal limits. 5.no other radiotherapy sensitizer was used except ximena. 6.The use of sodium glyci-didazole has ended; 7.No other tumors, except cured cervical carcinoma in situ and basal skin carcinoma; 8.No AIDS, active tuberculosis and other serious immune disorders; 9. Treated with IMRT; 10.No chemotherapy drugs were used during the treatment. 11.Treatment and follow-up data were complete.

Exclusion criteria

Exclusion criteria: 1.Serious and uncontrolled diseases and infections; 2.Serious diseases of the heart, liver, kidney and other organs; 3.Previous or concurrent malignancy. 4.History of active hepatitis; 5.Treated with conventional radiotherapy techniques; 6.Obvious diseases that the investigator felt should be excluded from the study; 7.Other patients considered unsuitable for inclusion in the 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 ContactYun-fei 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