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Prospective clinical study of intensity-modulated radiation therapy plus 3D-image-guided HDR-brachytherapy boost based on 3D printed nasopharyngeal intracavitary applicator for early T-stage nasopharyngeal carcinoma

Prospective clinical study of intensity-modulated radiation therapy plus 3D-image-guided HDR-brachytherapy boost based on 3D printed nasopharyngeal intracavitary applicator for early T-stage nasopharyngeal carcinoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015995
Enrollment
Unknown
Registered
2018-05-05
Start date
2018-05-01
Completion date
Unknown
Last updated
2019-07-15

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:individualized 3D-image-guided brachytherapy plan after the intensity-modulated radiation

Sponsors

Jiangxi Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. WHO II/III patients with initial diagnosis of nasopharyngeal cancer; 2. The clinical phase is T1-2N0-3M0(I-IVa, UICC/AJCC 8th edition), and T2 phase pharynx violations = 1.5 cm; 3. Receive strong radiation therapy and post-installation radiotherapy; 4. ECOG PS 0-2 points; 5. Aged between 18 and 70 years; 6. Male or non-pregnant or lactating female; 7) Hematology examination: white blood cells >4×10^9/L, neutrophils >2×10^9/L, hemoglobin >90g/L, platelet>100×10^9/L; 8. Liver function: ALT, AST60 ml/min; 10. The patient has signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. WHO pathological classification is keratinized squamous carcinoma or basal cell-like carcinoma; 2. palliative care; 3. History of other malignant neoplasms(basal cell carcinoma of the skin / squamous carcinoma, except cervical carcinoma in situ); 4. Pregnant or lactating women(women of childbearing age are considering pregnancy tests and patients are required to use effective contraception during treatment); 5. Past history of radiotherapy(except for non-melanoma of the skin outside the target area of the planned exposure); 6. Chemotherapy or surgery has been performed on primary focal or lymph nodes(except for diagnostic operations); 7. Any serious disease that may pose a risk to the test or affect the compliance of the test, such as unstable heart disease, kidney disease, chronic hepatitis, diabetes with poor blood sugar control that requires treatment(fasting blood sugar > 1.5 × ULN) and emotional illness; 8. Past history of radiation therapy of the head and neck; 9. Past history of cancer.

Design outcomes

Primary

MeasureTime frame
Local free-recurrence period;

Secondary

MeasureTime frame
Acute reactions and late adverse complications;overall survival rate;

Countries

China

Contacts

Public ContactTang Yiqiang

Jiangxi Cancer Hospital

johnytangyq@hotmail.com+86 13607916372

Outcome results

None listed

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