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Completed

NCT Number: NCT03180476

Maintenance Therapy of Apatinib After Chemoradiotherapy in Metastatic Nasopharyngeal Carcinoma

The study is to evaluate the efficacy and safety of Apatinib as maintenace therapy for Nasopharyngeal Carcinoma With Metastasis after Chemoradiotherapy, including progress free survival(PFS)、overall survival (OS)、Quality of life score (QoL) and evaluation of drug safety.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Sichuan Cancer Hospital

Chengdu, Sichuan, 600000, China

About this study

In locally advanced nasopharyngeal carcinoma(NPC), although radiotherapy and chemotherapy has been given, patients still locally recurrence and distant metastasis. There is no standard treatment recommendation for metastatic NPC who failed to chemoradiotherapy therapy. Apatinib has been approved as a second-line treatment for advanced gastric cancer. Several phase III studies of liver cancer, non small cell lung cancer and other tumors also showed apatinib has less toxicities and better tolerance. However, the clinical application of apatinib in nasopharyngeal carcinoma is still lack of evidence-based medicine. And this trial is designed to investigate the efficacy and safety of apatinib as maintenance therapy after chemoradiotherapy in nasopharyngeal carcinoma with metastasis.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male and female patients aged ranging from 18 to 75 years old.
  • Naive or recurrent Nasopharyngeal Carcinoma with metastasis after chemotherapy or radiotherapy.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2.
  • Adequate hematologic (neutrophil count>=1.5×109/L, hemoglobin>=80g/L, platelets>=80×109/L), hepatic function (aspartate transaminase (AST) & alanine transaminase(ALT) =<upper normal limit(UNL) x2, bilirubin level =< UNL x 1.5).
  • Adequate renal function (creatinine clearance ≥ 60 mL/min).
  • Patients have the ability to understand and voluntarily sign the informed consent, and allow adequate follow-up.

Exclusion criteria

  • Previously, patients did receive the therapy of Apatinib or other VEGFR inhibitor, such as Sorafenib, Sunitinib.
  • Difficulties in taking pills (inability to swallow tablets,GI tract resection, chronic bacillary diarrhea and intestinal obstruction).
  • Bleeding tendency or coagulation disorders.
  • with brain metastases.
  • Uncontrolled hypertension (systolic pressure>150 mmHg , or diastolic pressure> 90 mmHg).
  • Urine protein≥++, or urine protein in 24 hours≥1.0g
  • Severe uncured wounds, ulcers or fracture.
  • Pregnant or breast-feeding.
  • Patients with epilepsy who need to take medicine (such as steroids or anti epilepsy agents).
  • Patients have these symptoms, such as neurological diseases, mental illness, serious infection.
  • The researcher believe that the Patient is not suitable to participate in the study.

Treatment and study plan

apatinib

Drug

Apatinib, also known as YN968D1, is a tyrosine kinase inhibitor that selectively inhibits the vascular endothelial growth factor receptor-2 (VEGFR2, also known as KDR). It is an orally bioavailable, small molecule agent which is thought to inhibit angiogenesis in cancer cells; specifically apatinib inhibits VEGF-mediated endothelial cell migration and proliferation thus blocking new blood vessel formation in tumor tissue. This agent also mildly inhibits c-Kit and c-SRC tyrosine kinases.

Other names: YN968D1, apatinib mesylate tablets

Primary outcomes

  1. Progression-free survival

    Time frame: 12 months

    The first day of treatment to the date that disease progression is reported

Secondary outcomes

  1. Overall survival

    Time frame: up to 24 months

    the first day of treatment to death or last survival confirm date.

  2. Quality of Life (QoL) questionnaire

    Time frame: up to 24 months

    in cancer patients and survivors with dermatologic conditions. This is a nontherapeutic and nondiagnostic protocol to obtain quality of life assessments from cancer patients and survivors who have dermatologic conditions, whether related to cancer therapies, or directly related to the primary cancer diagnosis. Data will be collected by using one or more dermatology-specific QoL instruments based on the underlying skin condition/s.

Sponsors and collaborators

Lead sponsor

Sichuan Cancer Hospital and Research Institute

Other

Collaborators

  • Jiangsu HengRui Medicine Co., Ltd.

Registry information

Important dates

Study start
2017
Primary completion
2020
Study completion
2020
First posted
Jun 8, 2017
Registry last updated
Apr 14, 2023

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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