A Study of Famitinib Plus Docetaxel in Patients With Advanced Non-squamous and Non-Small Cell Lung Cancer (NSCLC)

NCT ID: NCT02364362

Last Updated: 2019-01-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-01-31
• Study Completion Date: 2018-12-31

Brief Summary

Famitinib is a tyrosin-inhibitor agent targeting at c-Kit, VEGFR2, PDGFR, VEGFR3, Flt1 and Flt3. Phase I study has shown that the toxicity is manageable.

This study assessed the safety and maximum tolerated dose of continuous daily treatment with Famitinib plus docetaxel (60 mg/m^2, every 3 weeks) in patients with Advanced Non-squamous and Non-Small Cell Lung Cancer (NSCLC) to determine the recommended dose for the Phase II trial.

Conditions

Non-Small Cell Lung Cancer (NSCLC)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Famitinib + docetaxel

Low, medium and high dose of famitinib and 60 mg/m\^2 docetaxel every 3 weeks

Group Type: EXPERIMENTAL

famitinib L + docetaxel

Intervention Type: DRUG

famitinib 15mg qd + docetaxel 60 mg/m\^2

famitinib M + docetaxel

Intervention Type: DRUG

famitinib 20mg qd + docetaxel 60 mg/m\^2

famitinib H + docetaxel

Intervention Type: DRUG

famitinib 25mg qd + docetaxel 60 mg/m\^2

Interventions

famitinib L + docetaxel

famitinib 15mg qd + docetaxel 60 mg/m\^2

Intervention Type: DRUG

famitinib M + docetaxel

famitinib 20mg qd + docetaxel 60 mg/m\^2

Intervention Type: DRUG

famitinib H + docetaxel

famitinib 25mg qd + docetaxel 60 mg/m\^2

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Age:18-70 years;

2. ECOG PS (Eastern Cooperative Oncology Group Performance Status)of 0 or 1;

3. Life expectancy of at least 12 weeks;

4. Histologically or cytologically confirmed, locally advanced and/or metastatic NSCLC of stage IIIB or IV or recurrent NSCLC;

5. Relapse or failure of one first line prior platinum-based chemotherapy;EGFR mutation type previously treated with platinum-based chemotherapy and EGFR inhibitors;

6. At least one target tumour lesion that has not been irradiated within the past 3 months and that can accurately be measured ,according to RECIST 1.1;

7. Participants have adequate organ and marrow function as defined below:

• Hemoglobin ≥ 90g/L ( no blood transfusion in 2 weeks)
• Absolute neutrophil count (ANC) ≥ 1.5×10^9/L
• Platelets(PLT)≥ 100×10^9/L
• Bilirubin < 1.25×ULN(Upper Limit Of Normal)
• ALT < 2.5×ULN; ALT < 5×ULN ( If have liver metastases)
• AST < 2.5×ULN; AST < 5×ULN ( If have liver metastases)
• Serum creatinine < 1.25×ULN, and endogenous Cr clearance > 45 ml/min(Cockcroft-Gault Formula)
• Cholesterol ≤ 1.5×ULN and triglyceride≤ 2.5×ULN
• Left ventricular ejection fraction(LVEF): ≥ LLN(Lower Limit Of Normal) by Color Doppler Ultrasonography

8. Female: Child bearing potential, a negative urine or serum pregnancy test result 7 days before initiating famitinib.All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 8 weeks after the last dose of test article. Male: All subjects who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 8 weeks after the last dose of test article;

9. Patient has given written informed consent.

Exclusion Criteria

1. More than one chemotherapy treatment regimen (except,either neoadjuvant or adjuvant or neoadjuvant plus adjuvant) for advanced and/or metastatic or recurrent NSCLC;

2. Previous therapy with other VEGFR inhibitors (including sunitinib,sorafenib,pazopanib,axitinib,other than bevacizumab) or docetaxel for treatment of NSCLC;

3. Radiographical evidence of cavitary or necrotic tumours;

4. Centrally located tumours with radiographical evidence (CT or MRI) of local invasion of major blood vessels;

5. Pre-existing ascites and/or clinically significant pleural effusion;

6. Pulmonary hemorrhage/ bleeding event ≥ CTCAE gr. 2 before initiating investigational drugs;

7. History of clinically significant haemoptysis within the past 3 months（24h >half teaspoon）;

8. Current peripheral neuropathy greater than CTCAE grade 2;

9. Other malignancy within the past 3 years other than basal cell skin cancer, or carcinoma in situ of the cervix;

10. Active brain metastases (such as stable time ≤ 4 weeks,no radiotherapy treatment,any symptoms,or seizures treatment needing) or leptomeningeal disease.;

11. Treatment with other investigational drugs or other anti-cancer therapy, or treatment in another clinical trial within the past 4 weeks before start of therapy or concomitantly with this trial;

12. Persistence of clinically relevant therapy related toxicities from previous chemotherapy and/or radiotherapy;

13. Treatment with cytotoxic drugs, radiotherapy(except extremities and brain) , immunotherapy , monoclonal antibody, or TKI inhibitor therapy within the past 4 weeks, being previous anti-cancer treatment interval ≤ 4 weeks.;

14. Patients with hypertension using combination therapy (systolic blood pressure>140 mmHg, diastolic blood pressure>90 mmHg). Patients with unstable angina, myocardial ischemia or myocardial infarction in the past 6 months, congestive heart failure>NYHA II,and arrhythmia (including QTcF interval ≥ 450ms for male and 470ms for female);

15. Urine protein ≥ + + and confirmed the 24-hour urinary protein>1.0 g;

16. History of major thrombotic or clinically relevant major bleeding event in the past 6 months，and known inherited predisposition to bleeding or thrombosis;

17. PT or APTT bias from normal range≥50%;

18. Application of anticoagulants or vitamin K antagonists such as warfarin, heparin or its analogues;If the prothrombin time international normalized ratio (INR) ≤ 1.5, with the purpose of prevention, the use of small doses of warfarin (1mg orally, once daily) ， low-dose aspirin (less than 100mg daily) is allowed;

19. Preexisting thyroid dysfunction, even using medical therapy, thyroid function cannot maintain in the normal range;

20. Diabetes mellitus can not controlled with hypoglycemic agent;

21. Active or chronic hepatitis C and/or B infection with liver dysfunction;

22. History of immunodeficiency disease, concurrent acquired or congenital immunodeficiency,or history of organ transplantation;

23. Serious infections requiring systemic antibiotic therapy;

24. Variety of factors that affect the oral medication (such as inability to swallow, gastrointestinal resection, chronic diarrhea and intestinal obstruction);

25. Significant weight loss (>10 %) within the past 6 months;

26. Pregnancy , breast feeding or child bearing potential, a positive urine or serum pregnancy test result 7 days before initiating famitinib;

27. Active alcohol or drug abuse;

28. Any contraindications for therapy with docetaxel；History of severe hypersensitivity reactions to docetaxel or other drugs formulated with polysorbate 80 (Tween 80)；Hypersensitivity to famitinib and/or the excipients of the trial drugs；Hypersensitivity to contrast media;

29. Psychological, familial, sociological, or geographical factors potentially hampering compliance with the study protocol and follow-up schedule;

30. Patients unable to comply with the protocol;

31. 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shanghai Pulmonary Hospital, Shanghai, China

OTHER

Sponsor Role: collaborator

Jiangsu HengRui Medicine Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Shanghai Pulmonary Hospital

Shanghai, , China

Countries

China

Other Identifiers

HR-FMTN- Ⅱ-NSCLC-COM

Identifier Type: -

Identifier Source: org_study_id