A Trial of Endostar in Combination With Chemotherapy of DF and Sequential Intensity Modulated Radiation Therapy for Patients With Advanced Nasopharyngeal Carcinoma

Nasopharyngeal Neoplasms Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02444949
• Other study ID #: CTGU001
• Status: Completed
• Phase: Phase 2
• Start date: June 2014
• Est. completion date: December 2019

Study information

• Verified date: June 2020
• Source: China Three Gorges University, Yichang, China
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Among all the head and neck tumors, nasopharyngeal carcinoma (NPC) has a high tendency of recurrence and metastasis. For the advanced NPC patients, chemoradiotherapy is the main way of treatment. Currently, chemotherapy with cisplatin (DDP) combines with 5-fluorouracil (5-FU) is the classic front line therapy for NPC. However, the abnormal richness of angiogenesis of tumor and blood supply in tissue caused by radiation therapy often decrease the effects of radiochemotherapy. Human recombinant vascular endothelial inhibitor (endostar) can improve the sensitivity to chemoradiation via selectively inhibiting the migration of endothelial cells and the formation of tumor vessels. Moreover, it would induce vascular remodeling and normalization of the tumor vasculature, which will effectively aid the delivery of oxygen and anticancer drugs. In sum, antiangiogenesis in combination with chemoradiotherapy will be a promising way of treatment for NPC. In this study, the first-treated patients with NPC (stage Ⅲ or Ⅳa) confirmed by pathology, and patients with recurrent and metastatic NPC will be randomly assigned to two groups (1:1): a trial group (DDP, 5-FU, endostar and sequential intensity modulated radiation therapy (IMRT)), and a control group (DDP，5-FU and sequential IMRT). Evaluations will be developed including progression-free survival (PFS), Overall response rate（ORR）, overall survival (OS), adverse effects rate and quality of life. This research will provide more evidences of evidence-based medicine for the safety and tolerability of endostar and the clinical application of endostar in NPC treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 75
• Est. completion date: December 2019
• Est. primary completion date: December 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Age from 18 to 70 ears ;

• Eastern Cooperative Oncology Group performance status of 0-1;

• diagnosed with first-treated NPC (?/?a stage) confirmed by pathology;

• ecurrent and metastatic NPC with indication of chemoradiotherapy;

• one measurable lesion at least (according to the RECIST guidelines, the lesion iameter=20 mm with MRI);

• life expectancy of = 12 weeks;

• adequate hematologic, renal, cardiac and liver function;

• hemameba=4.0×109/L;

• neutrophil=2.0×109/L;

• platelet=100×109/L;

• hemoglobin=95g/L;

• Serum bilirubin, ALT and AST =1.5 times of maximum criteria;

• sufficiently understand this study situation and signed the informed consent.

Exclusion Criteria:

• allergy or intolerance to study drugs;

• receiving other anti-cancer therapy;

• uncontrolled central nervous system lesions;

• dysfunction of important organs;

• history of cardiovascular disease(including congestive heart-failure, uncontrolled arrhythmia, angina pectoris which require long-term drug treatment, lular heart disease, myocardial infarction and resistant hypertension);

• pregnancy or lactation in women;

• protracted Infective wound;

• history of mental illness which is not easy controlled.

Related Conditions & MeSH terms

• Nasopharyngeal Neoplasms

Intervention

Drug:
• endostar

Radiation:
• intensity modulated radiation

Drug:
• cisplatin

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
China Three Gorges University, Yichang, China

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free Survival		Patients will be followed from the day in which patients are enrolled the clinical trial and end up one year later, during the one year the patients will be observed whether they have disease progress or die from any cause.
Primary	Overall response rate		After the second periodicity chemotherapy, an expected average of 12 weeks, the rate of patients with complete response and partial response accounted for the total number of assessable cases .
Secondary	Adverse effects as assessed by adverse events		It is the time from the start of treatment to 20 weeks
Secondary	Overall survival		Patients will be followed from the day in which patients are enrolled the clinical trial and end up two years later, during the two years the patients will be observed whether they die from any cause.
Secondary	Quality of Life measured by the ECDG score		Firstly, Patients will be assessed before the start of periodicity treatment, then they will be assessed 20 weeks and 24 weeks after the treatment.