Apatinib Plus Docetaxel in Advanced Non-squamous Non-small Cell Lung Cancer(NSCLC)

• Sponsor: Affiliated Hospital of North Sichuan Medical College (Other)
• Overall Status: Unknown status
• CT.gov ID: NCT03416231
• Collaborator: Jiangsu HengRui Medicine Co., Ltd. (Industry)
• Enrollment: 20
• Location: 1
• Arm: 1
• Anticipated Duration (Months): 37
• Patients Per Site Per Month: 0.5

Study Details

Study Description

Brief Summary

The purpose of this study was to evaluate the effectiveness and safety of apatinib combined with docetaxel in NSCLC.

Condition or Disease	Intervention/Treatment	Phase
NSCLC	Drug: Apatinib; Drug: Docetaxel	Phase 2

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 20 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Study of Combined Treatment of Apatinib With Docetaxel as Post Second-line Therapy in Advanced Non-squamous Non-small Cell Lung Cancer(NSCLC)
• Actual Study Start Date: Nov 30, 2016
• Anticipated Primary Completion Date: Jan 1, 2019
• Anticipated Study Completion Date: Jan 1, 2020

Arms and Interventions

Arm	Intervention/Treatment
Experimental: apatinib plus docetaxel apatinib combine with docetaxel， 4~6 cycles	Drug: Apatinib; apatinib, at a dose of 250 mg daily,Treatment was continued until disease progression.; Other Names: Aitan ; Drug: Docetaxel; Docetaxel, at a dose of 75mg/m2 on days 1 and 22, repeat every 4 weeks for 4~6 cycles.

Outcome Measures

Primary Outcome Measures

1. objective response rate (ORR) [6 month]

   Proportion of patients with reduction in tumor burden of a predefined amount

Secondary Outcome Measures

1. progression free survival (PFS) [12 month]

   The length of time during and after the treatment of a disease, such as cancer, that a patient lives with the disease but it does not get worse.

2. disease control rate (DCR) [6 month]

   Disease Control Rate (DCR) and Clinical Benefit Rate (CBR) are defined as the percentage of patients with advanced or metastatic cancer who have achieved complete response, partial response and stable disease to a therapeutic intervention in clinical trials of anticancer agents.

3. 6-month overall survival rate [6 month]

   6-month overall survival rate

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• 1. Male or female patients, age: ≥ 18 years of age;
• 1. Pathologically diagnosed late (stage IIIB, stage IV, see Annex 1) non-squamous non-small cell lung cancer with measurable lesions (CT scan of tumor lesion longer than 10 mm in diameter, shorter than 15 CT scan of lymph nodes mm, the scanning layer thickness is not more than 5 mm;
• 1. Previous drug treatment consisted of a platinum-based chemotherapy regimen (> 1 chemotherapy regimen) for relapse or failure of treatment.
• 1. The main organs function properly, that is, within 14 days prior to the relevant indicators meet the following requirements:(1) a. Hemoglobin (HB) ≥90 g / L; (no blood transfusion within 14 days):b. neutrophil count (ANC) ≥ 1.5 × 109 / L; c. Platelet count (PLT) ≥80 × 109 / L;(2) biochemical tests to meet the following criteria:a. Total bilirubin (TBIL) <1.5?ULN (upper limit of normal);b. Blood alanine aminotransferase (ALT) and aspartate aminotransferase (AST).

1. Sign the inform consent form with good compliance.

Exclusion Criteria:

• 1. Squamous cell carcinoma (including adenosquamous carcinoma); Small cell lung carcinoma (including small cell carcinoma and non-small cell mixed lung carcinoma)
• 1. Patients who had previously received docetaxel treatment were excluded
• 1. Patients with active brain metastasis, carcinomatous meningitis, or spinal compression, or disease of brain or pia mater according to the screening test, imaging, CT or MRI tests (patients who have completed the treatment and in a stable condition 21 days before screening could be included, but brain MRI, CT or venography is required to confirm that there are no brain hemorrhage symptoms).
• 1. Patients with uncontrollable hypertension (systolic blood pressure> 140 mmHg, diastolic blood pressure> 90 mmHg, despite optimal drug therapy).
• 1. Patients with with grade Ⅱ myocardial ischemia or myocardial infarction, poor control of arrhythmias (including QTc interval male ≥ 450 ms, female ≥470 ms).
• 1. According to NYHA standard, grade Ⅲ ~ Ⅳ heart failure, or cardiac color Doppler ultrasound examination showed left ventricular ejection fraction (LVEF) <50%.
• 1. Coagulation dysfunction (INR> 1.5, PT> ULN +4s or APTT> 1.5 ULN), with bleeding tendency or ongoing thrombolysis or anti-blood coagulation treatment.
• 1. Patients treated with anticoagulation agents or Vitamin K antagonist such as Warfarin, heparin, or other similar drugs.
• 1. Patients who had obvious hemoptysis within 2 months before screening, or experienced daily hemoptysis with a volume more than half a tea spoon (2.5ml) or above.
• 1. Patients who experienced bleeding symptoms of clinical significance within 3 months before screening, or with confirmed bleeding tendency such as hemorrhage of digestive tract, hemorrhagic gastric ulcer, baseline occult blood in stool ++ and above, or vasculitis, etc.
• 1. Patients who manifested arterial/venous thrombus events, e.g. cerebrovascular accident (including transient ischemic attack), deep venous thrombosis and pulmonary embolism, etc., within 12 months before screening.
• 1. Known genetic or acquired bleeding or bleeding tendency (such as hemophilia, blood coagulation dysfunction, thrombocytopenia, and hypersplenism, etc.).
• 1. Patients who have unhealed wounds or fractures for a long time.
• 1. Patients who received major surgical operations or experienced severe traumatic injuries, bone fracture, or ulcers within 4 weeks before screening.
• 1. Patients with obvious factors affecting absorption of oral drugs, such as difficulties in swallowing, chronic diarrhea and intestinal obstruction, etc.
• 1. Occurrence of abdominal fistula, gastrointestinal perforation, or intraperitoneal abscess within 6 months before screening.
• 1. Patients whose routine urine tests indicate that urine protein ≥ ++ or verifies that the 24-h urine protein quantitation ≥ 1.0 g.
• 1. Patients with active hepatitis B virus or hepatitis c virus infection.
• 1. Active infection requiring antimicrobial treatment, such as antibacterial, antifungal, or antiviral therapy.
• 1. Patients with clinical symptoms, or dropsy of serous cavity requiring surgical treatment (including hydrothorax, ascites, and hydropericardium).
• 1. Patients who have a history of psychotropic drug abuse and are unable to break the habit, or who have a psychogeny.
• 1. Patients who have taken part in other drug clinical tests within 4 weeks before screening.
• 1. Prior VEGFR inhibitor treatment.
• 1. Patients who formerly suffered from or currently are complicated with other uncured malignant tumors, except basal cell carcinoma, carcinoma in situ of cervix and superficial bladder cancer that have been cured.
• 1. Patients who received the treatment with potent CYP3A4 inhibitors within 7 days before screening, or potent CYP3A4 inducers within 12 days before being included.
• 1. Pregnant or lactating women, fertile patients who are unwilling or unable to take effective contraceptive measures.
• 1. Conditions determined by investigators to possibly affect the clinical study or determination of the study results.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Affiliated Hospital of North Sichuan Medical College	Nanchong	Sichuan	China	600000

Sponsors and Collaborators

• Affiliated Hospital of North Sichuan Medical College
• Jiangsu HengRui Medicine Co., Ltd.

Investigators

• Principal Investigator: Daiyuan Ma, M.D, Affiliated Hospital of North Sichuan Medical College
• Study Director: xin hu, M.D., Nanchong Central Hospital
• Study Director: xiangdong fang, M.d., Dazhou Central Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Affiliated Hospital of North Sichuan Medical College
• ClinicalTrials.gov Identifier: NCT03416231
• Other Study ID Numbers: APTN-ANSCLC-2017-001
• First Posted: Jan 31, 2018
• Last Update Posted: Jan 31, 2018
• Last Verified: Jan 1, 2018

• Individual Participant Data (IPD) Sharing Statement: Undecided
• Plan to Share IPD: Undecided
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Affiliated Hospital of North Sichuan Medical College: apatinib; Docetaxel
• Additional relevant MeSH terms: Carcinoma, Non-Small-Cell Lung; Docetaxel; Apatinib

Study Results

No Results Posted as of Jan 31, 2018