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GP-induced Chemotherapy Combined With IMRT and TPF-induced Chemotherapy Combined With IMRT in the Treatment of Distant Metastatic Nasopharyngeal Carcinoma

G

Guiyang Medical University

Status

Unknown

Conditions

Advanced Nasopharyngeal Carcinoma

Treatments

Drug: TPF+IMRT
Drug: GP+IMRT

Study type

Observational

Funder types

Other

Identifiers

NCT03723343
201805045

Details and patient eligibility

About

Mainly compared with GP induction chemotherapy combined with IMRT and TPF induction chemotherapy combined with IMRT in the treatment of nasopharyngeal carcinoma, the cure rate, remission rate, treatment of distant metastases and lymph node metastasis, quality of life improvement rate, etc.

Full description

  1. The main purpose: Whether the GP program can improve the efficiency of patients with nasopharyngeal carcinoma, especially overall survival (OS), in the TPF program. 2. Secondary purpose: To compare the progression-free survival (PFS) local failure-free survival (LR-FFS), the short-term remission rate of the tumor, the adverse chemotherapy response, and the treatment compliance Sex, as well as quality of life. 3. Significance of the research project Nasopharyngeal carcinoma is sensitive to radiotherapy and chemotherapy. Platinum-based chemotherapy is used in the treatment of distant metastasis and metastasis. It can effectively alleviate local symptoms and reduce local symptoms. The tumor volume thereby reduces the high dose area of the target area. Primary lesions and lymphatic drainage area radiotherapy can reduce tumor burden, relieve symptoms, and improve quality of life.

Enrollment

146 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. The pathological type is non-keratinized cancer (according to the pathological classification of the World Health Organization, WHO).

  2. The stage is TxNxM1 (according to the eighth edition of the AJCC staging standard) (Appendix I).

  3. There is evidence of distant transfer (M1).

  4. functional status: Karnofsky scale (KPS) > 70 (Appendix II).

  5. normal bone marrow function: white blood cell count > 4 × 109 / L, hemoglobin > 90g / L and platelet count > 100 × 109 / L.

  6. normal liver function: alanine aminotransferase (ALT), aspartate aminotransferase (AST) <1.5 times the upper limit of normal (ULN), and alkaline phosphatase (alkaline phosphatase, ALP) < 2.5 x ULN and bilirubin < ULN.

  7. normal renal function: creatinine clearance (creatinine clearance) > 60 ml / min.

  8. The patient must be informed of the basic content of the study and sign an informed consent form.

Exclusion criteria

  1. the pathological type is WHO keratinized squamous cell carcinoma or basal squamous cell carcinoma.

  2. age > 65 years old or < 18 years old.

  3. a history of malignant tumors, except for adequately treated basal cell carcinoma or squamous cell carcinoma and cervical carcinoma in situ.

  4. Women during pregnancy or lactation (pregnancy tests should be considered for women of childbearing age; effective contraception should be emphasized during treatment).

  5. has received radiation therapy (if it is non-melanoma skin cancer and the previous lesion is placed

    Except for the target area of treatment.

  6. primary lesions and cervical metastases have received chemotherapy or surgery (except for diagnostic treatment).

  7. accompanied by other serious diseases, may bring greater risk or affect the compliance of the test. For example: unstable heart disease, kidney disease, chronic hepatitis, uncontrolled diabetes (fasting blood glucose > 1.5 x ULN), and mental illness. -

Trial design

146 participants in 2 patient groups

Experimental: GP+IMRT
Description:
Test group: GP-induced chemotherapy (Gemcitabine 1000 mg/m2 d1, 8+Cisplatin 80 mg/m2 d1, once every 3 weeks, 4/6 course) + IMRT radiotherapy alone
Treatment:
Drug: GP+IMRT
Active Comparator: TPF+IMRT
Description:
Control group: TPF-induced chemotherapy (Docetaxel: 75 mg/m2d1, Cisplatin 75 mg/m2, d1\~d5, 5-fluorouracil 750 mg/m2/dd1\~d5, 4/6 course) + IMRT radiotherapy alone
Treatment:
Drug: TPF+IMRT

Trial contacts and locations

1

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Central trial contact

Feng Jin, Bachelor; Jinhua Long, Master

Data sourced from clinicaltrials.gov

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