Maintenance Treatment of Apatinib in Nasopharyngeal Carcinoma

NCT03130270 | Unknown Phase 2

• 1 other identifier: GLMU-02
• Study Type: interventional
• Target: 29
• Locations: 1 country
• Sites: 4

Brief Summary

The study is to evaluate the efficacy and safety of Apatinib for later treatment of patients(after second-line treatment for locally recurrent or metastatic nasopharyngeal carcinoma), including overall survival (OS), distant metastasis-free survival (DMFS) and locoregional relapse-free survival (LRRFS); the relationship between EBV DNA copy number and survival after radiotherapy or radiochemotherapy; Quality of life score (QoL); evaluation of drug safety.

Conditions

Nasopharyngeal Carcinoma

Keywords

nasopharyngeal carcinoma; disease-free survival; adverse reaction

Outcome Measures

Primary Outcomes (1)

• Objective Response Rate (ORR) after Second-Line Treatment for Locally Recurrent or Metastatic Nasopharyngeal Carcinoma

  To evaluate ORR every 6-8 weeks after initiation of apatinib.

  up to 24 months

Secondary Outcomes (3)

• Disease-free survival (DFS)

  up to 24 months

• Overall survival (OS)

  up to 24 months

• Toxicity evaluation

  up to 24 months

Study Arms (1)

Apatinib group

EXPERIMENTAL

Apatinib mesylate tablet：the starting dose was 500 mg, orally, qd; tolerance assessment for a cycle, patients with poorly tolerance were treated with low dose (500 mg, qd), and patients with well tolerance were treated with high dose (750 mg, qd).

Drug: Apatinib mesylate tablet

Interventions

Apatinib mesylate tablet DRUG

Patients with locally recurrent or metastatic nasopharyngeal carcinoma (NPC) after second-line treatment are assigned to receive apatinib mesylate tablet. A treatment cycle was defined as 28 days (4 weeks). The starting dose was 500 mg, orally, qd; tolerance assessment for a cycle, patients with poorly tolerance were treated with low dose (500 mg, qd), and patients with well tolerance were treated with high dose (750 mg, qd). All patients continuous treatment until progression disease or non-tolerated toxicity. Note: good tolerance was defined that no grade 3/4 hematology or/and non hematologic side effects occurred within 4 weeks after initiation treatment; poor tolerance was defined that grade 3/4 hematology or/and non hematologic side effects appeared within 4 weeks after initiation treatment.

Also known as: No.

Apatinib group

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male and female patients aged ranging from 18 to 70 years old.
• Patients with newly histologically proven nasopharyngeal carcinoma (NPC).
• Local recurrent NPC patients after comprehensive treatment, including clinical examination found a clear local area residue: electronic nasopharyngoscope found clear residual or enlarged cervical lymph nodes.
• Distant metastatic NPC patients after comprehensive treatment, including liver B ultrasound, chest X-ray, bone scan or other clinicians consider appropriate tests such as CT, MRI or PET/CT found distant metastases.
• Comprehensive treatment of local recurrence or distant metastasis after line or second-line therapy found progressive disease.
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 1.
• Patient who has the expected survival time more than 3 months.
• Adequate hematological function: hemoglobin \>80 g/L (no transfusion within 14 days), neutrophil count \> 1.5×109/L, platelet count 80×109/L.
• Adequate liver function (serum total bilirubin ≤ 1.5 mg/dL, serum transminase ≤ 2.5 times higher than upper limit).
• Adequate renal function (creatinine clearance ≥ 50 mL/min).
• Participants volunteered to participate in this study, signed informed consent, good compliance and cooperated with us to complete the follow-up.

You may not qualify if:

• Before treatment, MRI showed that the tumor might be an important risk factor (for example, wrapping around the internal carotid artery / vein); or researchers judged that the tumor is a high risk of serious blood vessel bleeding during the treatment.
• Patient who has serious hemorrhages, any serious bleeding events classification at 3 degree or more (according to CTCAE4.0) within the last 4 weeks.
• Patient who has high blood pressure can not be controlled by a single antihypertensive drug treatment (Systolic pressure \> 140 mmHg, diastolic pressure \> 90 mmHg); any unstable angina pectoris; with a history of angina pectoris were newly diagnosed with angina pectoris within 3 months before screening; any myocardial infarction events occurred within 6 months before screening; arrhythmia (including QTcF: male ≥ 450ms, female ≥ 470 ms) need long time use of antiarrhythmic drugs and heart function insufficiency ≥II according to New York Heart Association class.
• Patient who has positive urine protein.
• Patient who has abnormal coagulation and bleeding tendency (signed informed consent before 14 days, and must be satisfied: INR is in the normal range without the use of anticoagulants); Application of anticoagulants or vitamin K antagonists such as Hua Falin, heparin or its analogues, with international normalized ratio (INR) is less than 1.5, allows the use of small dose Hua Falin (1 mg orally, once daily) or small dose aspirin (total dose ≤ 100 mg daily).
• Medical history of arteriovenous thrombosis event within the past year, such as cerebral vascular accident (including transient ischemic attack) and deep venous thrombosis (venous catheter thrombosis caused by chemotherapy and investigator judged that the patient had recovered, these patients should be except) and pulmonary embolism.
• A healed wound for long time or incomplete fracture.
• Any factors that affect the oral drug, such as the inability to swallow, diarrhea and intestinal obstruction.
• For females: patients should be surgical sterilization or postmenopausal patients, or willing to receive a medical approved contraception during treatment and 6 months after the end of the treatment; serum or urine pregnancy test must be negative, and must be non lactating period within 7 days before study; for males: patients should be treated with surgical sterilization or willing to receive a medical approved contraception during treatment and 6 months after the end of the treatment.
• History of psychotropic substance abuse and can not be removed or psychiatric disorders.
• Medical history of immunodeficiency, or other acquired, congenital immunodeficiency disease, or history of organ transplantation.
• Any serious harm to the subject's safety or evidence of significant medical illness that in the investigator's judgment will substantially increase the risk associated with the subject's participation in and completion of the study.

Sponsors & Collaborators

• Guilin Medical University, China: lead
• Wuzhou Red Cross Hospital: collaborator
• Guangxi Naxishan Hospital: collaborator
• People's Hospital of Guangxi Zhuang Autonomous Region: collaborator

Study Sites (4)

Guilin Medical University

Guilin, Guangxi, 541001, China

Location

Nanxishan hospital

Guilin, Guangxi, China

Location

National Hospital of Guangxi Zhuang Autonomous Region

Nanning, Guangxi, China

Location

Wuzhou Red Cross Hospital

Wuzhou, Guangxi, China

Location

Related Publications (1)

• Ruan X, Liang JH, Pan Y, Cai R, Zhang RJ, He Z, Yang X, Niu Z, Jiang W. Apatinib for the treatment of metastatic or locoregionally recurrent nasopharyngeal carcinoma after failure of chemotherapy: A multicenter, single-arm, prospective phase 2 study. Cancer. 2021 Sep 1;127(17):3163-3171. doi: 10.1002/cncr.33626. Epub 2021 May 27.

  PMID: 34043812 DERIVED

MeSH Terms

Conditions

Nasopharyngeal Carcinoma

Interventions

apatinib

Condition Hierarchy (Ancestors)

Carcinoma; Neoplasms, Glandular and Epithelial; Neoplasms by Histologic Type; Neoplasms; Nasopharyngeal Neoplasms; Pharyngeal Neoplasms; Otorhinolaryngologic Neoplasms; Head and Neck Neoplasms; Neoplasms by Site; Nasopharyngeal Diseases; Pharyngeal Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases

Study Officials

• Wei Jiang

  Guilin Medical University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Guilin Medical University

Study Record Dates

• First Submitted: April 21, 2017
• First Posted: April 26, 2017
• Study Start: January 1, 2017
• Primary Completion: April 8, 2019
• Study Completion: December 8, 2019
• Last Updated: May 16, 2018

Record last verified: 2018-05

Data Sharing

• IPD Sharing: Will not share

Locations

CN (4)