Gefitinib Combined With Thalidomide to Treat NSCLC

NSCLC Clinical Trial

Official title:

A Phase III, Multi Center, Randomized, Placebo Controlled Study to Evaluate the Efficacy of the Combination Gefitinib With Thalidomide in Patients With Locally Advanced and Metastatic Non-Small-Cell-Lung-Cancer With EGFR Mutation

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02387086
• Other study ID #: GELI
• Status: Not yet recruiting
• Phase: Phase 2/Phase 3
• First received: March 3, 2015
• Last updated: March 11, 2015
• Start date: May 2015
• Est. completion date: May 2017

Study information

• Verified date: March 2015
• Source: Shaanxi Provincial People's Hospital
• Contact: Jun Bai
• Phone: +86-13186055863
• Email: baijun[@]yahoo.com
• Is FDA regulated: No
• Health authority: China: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether thalidomide can improve the effectiveness of the gefitinib in NSCLC patients with EGFR mutations.

Description:

Primary Objective:

To determine the 1 year progression-free survival(PFS) rate of the combination of thalidomide with gefitinib in patients who harbors EGFR mutations.

Secondary Objectives:

1. To evaluate the objective response rate and 2 years overall survival of this combination therapy;

2. To evaluate the safety and tolerability of this combination therapy;

3. To acquire preliminary data regarding the effects of thalidomide on interleukin-2 level in serum.

Treatment will be administered on an outpatient basis. Thalidomide starting at a dose of 50mg QD at night. After one week, increase the dose to 100mg QD at night.

Aspirin will be administered at 100mg QD continuously. Gefitinib will be administered at 250mg QD continuously. Maintenance Therapy patients responding to this therapy will be maintained with gefitinib、thalidomide and aspirin.

Duration of Therapy

In the absence of treatment delays due to adverse events, treatment may continue until one of the following criteria applies:

1. Disease progression,

2. Intercurrent illness that prevents further administration of treatment,

3. Unacceptable adverse events(s),

4. Patient decides to withdraw from the study, or

5. General or specific changes in the patient's condition render the patient unacceptable for further treatment in the judgment of the investigator.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 380
• Est. completion date: May 2017
• Est. primary completion date: May 2017
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients must be NSCLC confirmed by Histological or cytological;

• The NSCLC harbors EGFR-mutation and are previously untreated

• Patient must have measurable lesion and in stage IIIB or IV disease (includes M1a, M1b stages or recurrent disease) (according to the 7th edition of the tumor node metastasis (TNM) classification system).

• Patients be age >18 years and < 75 years.

• Patients must have a Life Expectancy of greater than 12 weeks.

• Patients must have an ECOG performance status 0 to 2.

• Patients must have normal organ and marrow function as defined below, within one week prior to randomization: absolute neutrophil count>1,500/mL platelets>100,000/mL total bilirubin: within normal institutional limits AST/ALT<2.5X institutional upper limit of normal creatinine=1.5X institutional upper limit of normal urine dipstick for proteinuria of < less than 1+. If urine dipstick is > 1+ then a 24 hour urine for protein must demonstrate <500mg of protein in 24 hours to allow participation in the study.

• Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.

• Patients must have an international normalized ratio (INR) < 1.5 and a partial thromboplastin time (PTT) no greater than upper limits of normal within 1 week prior to randomization.

• Patients with a history of hypertension must be well-controlled (<150 systolic/<100 diastolic) on a stable regimen of anti-hypertensive therapy.

• Patients must be able to swallow tablets.

• Patients must have the ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

• Patients with uncontrolled illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situation that would limit compliance with study requirements.

• Patients receiving therapeutic anticoagulation. Prophylactic anticoagulation of venous access devices is allowed provided Section 3.10 is met. Caution should be taken on treating patients with low dose heparin or low molecular weight heparin for DVT prophylaxis during treatment with bevacizumab as there may be an increased risk of bleeding.

• Patients cannot administer aspirin for the risk of bleeding or having stomach ulcers.

• Prior use of chemotherapy.

• Patients receiving immunotherapy, hormonal-therapy and or radiotherapy within 2 weeks prior to entering the study. Note: Those who have not recovered from adverse events due to these agents administered will be considered ineligible.

• Patients receiving any other investigational agents.

• Patients with uncontrolled brain metastasis. Note: Patients with brain metastases must have stable neurologic status following local therapy (surgery or radiation) for at least 2 weeks, and must be without neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.

• Patients with a history of allergic reactions attributed to compounds of similar chemical or biologic composition to thalidomide?gefitinib and aspirin or other agents used in the study are excluded.

• Women that are pregnant or breastfeeding Note: Pregnant women are excluded from this study because the agents used in this study may be teratogenic to a fetus. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with thalidomide, breastfeeding women are also excluded from this study.

• HIV-positive Patients that are on combination antiretroviral therapy due to the potential for lethal infections when treated with marrow-suppressive therapy.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• NSCLC

Intervention

Drug:
• Thalidomide

• placebo

• Gefitinib

• Aspirin

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Bai Jun

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	IL-2 level	IL-2 level in serum of patients	2 years	No
Primary	progression-free survival (PFS)	one year progression-free survival of the patients	1 year	No
Secondary	Objective Response Rate (ORR)	the Objective Response Rate	2 years	No
Secondary	Overall Survival (OS)	2 years Overall Survival	2 years	No