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NCT Number: NCT02444949

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

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.

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Key information

Conditions

Nasopharyngeal Neoplasms Head and Neck Neoplasms Nasopharyngeal Diseases Neoplasms Neoplasms by Site Otorhinolaryngologic Diseases Otorhinolaryngologic Neoplasms Pharyngeal Diseases Pharyngeal Neoplasms Stomatognathic Diseases

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age from 18 to 70 ears ;
  • Eastern Cooperative Oncology Group performance status of 0-1;
  • diagnosed with first-treated NPC (Ⅲ/Ⅳa 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.

Treatment and study plan

Endostar

Drug

Other names: Human recombinant vascular endothelial inhibitor

Intensity modulated radiation

Radiation

Cisplatin

Drug

Other names: DDP

Primary outcomes

  1. Progression-free Survival

    Time frame: 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.

  2. Overall response rate

    Time frame: 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 outcomes

  1. Adverse effects as assessed by adverse events

    Time frame: It is the time from the start of treatment to 20 weeks

  2. Overall survival

    Time frame: 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.

  3. Quality of Life measured by the ECDG score

    Time frame: Firstly, Patients will be assessed before the start of periodicity treatment, then they will be assessed 20 weeks and 24 weeks after the treatment.

Sponsors and collaborators

Lead sponsor

China Three Gorges University, Yichang, China

Other

Registry information

Important dates

Study start
2014
Primary completion
2016
Study completion
2019
First posted
May 15, 2015
Registry last updated
Jun 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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