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Gefitinib With or Without Chemotherapy in Brain Metastases From Non-small Cell Lung Cancer

Primary Purpose

Non-small Cell Lung Cancer, Brain Metastases, EGFR Mutation

Status
Recruiting
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Gefitinib and Pemetrexed/platinum
Gefitinib mono-therapy
Sponsored by
Sun Yat-sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-small Cell Lung Cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patient who was confirmed stage IV NSCLC with EGFR activating mutation and brain metastases by pathologic histology or cytology
  2. Patients who had never received therapy (including chemotherapy,WBRT,EGFR-TKI and EGFR monoclonal antibody) after diagnosed brain metastases
  3. Patients had at least three metastatic lesions in brain, or patients with 1-2 intracranial lesions who were not suitable for brain radiotherapy, or patients with 1-2 intracranial lesions who refused brain radiotherapy, at least one intracranial lesion with the longest diameter of >5 mm
  4. Adult patients (≥ 18 years and ≤75 years). ECOG Performance Status 0 or 1 Life expectancy of at least 12 weeks.,Haemoglobin ³ 10.0 g/dl, Absolute neutrophil count (ANC) ³1.5 x 109/L, platelets ³ 100 x 109/L. Total bilirubin £ 1.5 x upper limit of normal (ULN). ALT and AST < 2.5 x ULN in the absence of liver metastases, or < 5 x ULN in case of liver metastases. Creatinine clearance ³ 60ml/min (calculated according to Cockcroft-gault formula).
  5. Patients should be contraceptive during the period of the trial until 8 weeks after the last administration of icotinib.
  6. Able to comply with the required protocol and follow-up procedures, and able to receive oral medications.

Exclusion Criteria:

  1. Patient was received irradiation of brain. Patient with meningeal metastases were confirmed by MRI or cytology test of cerebrospinal fluid.
  2. Patient is received the treatment of Phenytoin, carbamazepine, rifampicin, phenobarbital, or St. John's Wort.
  3. Patient was received EGFR Tyrosine Kinase Inhibitor or EGFR monoclonal antibody.
  4. Interstitial pneumonia.Pericardial effusion, pleural effusion is uncontrolled .
  5. Any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, myocardial infarction within the previous year, serious cardiac arrhythmia requiring medication, hepatic, renal, or metabolic disease).
  6. Any significant ophthalmologic abnormality ,especially severe dry eye syndrome ,keratoconjunctivitis sicca,Sjogren syndrome,severe exposure keratitis or any other disorder likely to increase the risk of corneal epithelial lesions.
  7. Lack of physical integrity of the upper gastrointestinal tract, or malabsorption syndrome, or inability to take oral medication, or have active peptic ulcer disease.
  8. The symptoms of increased intracranial pressure are uncontrolled after dehydration and cortisone treatment

Sites / Locations

  • Sun Yat-sen University of Cancer CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Gefitinib and Pemetrexed/platinum

Gefitinib mono-therapy

Arm Description

Gefitinib 250mg is Taken Orally on day 1-28,combined Pemetrexed (D1)+cisplatin (D1-3) chemotherapy or Pemetrexed (D1)+nedaplatin (D1) chemotherapy, every 28 days

Gefitinib 250mg is Taken Orally everyday

Outcomes

Primary Outcome Measures

iPFS(intracranial progression free survival
defined as time from randomization to intracranial progressive disease or death.

Secondary Outcome Measures

ORR
proportion of patients with complete or partial response of overall lesions
intracranial objective response rate (iORR)
proportion of patients with complete or partial response of intracranial lesions
PFS(Progression Free Survival)
time from randomization to overall disease progression or death
OS(Overall Survival)
time from randomization to death from any cause
adverse events
adverse events were evaluated according to NCI-CTCAE 4.0.

Full Information

First Posted
September 16, 2013
Last Updated
February 19, 2022
Sponsor
Sun Yat-sen University
Collaborators
Wu Jieping Medical Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01951469
Brief Title
Gefitinib With or Without Chemotherapy in Brain Metastases From Non-small Cell Lung Cancer
Official Title
Multicenter Phase III Study of Gefitinib Mono-therapy or Gefitinib Combined With Chemotherapy in Patients With Brain Metastases From Non-small Cell Lung Cancer Harboring EGFR Mutation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 2016 (Actual)
Primary Completion Date
June 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University
Collaborators
Wu Jieping Medical Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a multi-center phase III randomized controlled study to assess the efficacy of Gefitinib alone and Gefitinib combination with Pemetrexed/platinum on patients with brain metastasis from non-small cell lung cancer(NSCLC) harboring EGFR mutation type by intracranial PFS(iPFS),also PFS ,DCR and OS.The side effect is evaluated as well.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-small Cell Lung Cancer, Brain Metastases, EGFR Mutation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gefitinib and Pemetrexed/platinum
Arm Type
Experimental
Arm Description
Gefitinib 250mg is Taken Orally on day 1-28,combined Pemetrexed (D1)+cisplatin (D1-3) chemotherapy or Pemetrexed (D1)+nedaplatin (D1) chemotherapy, every 28 days
Arm Title
Gefitinib mono-therapy
Arm Type
Active Comparator
Arm Description
Gefitinib 250mg is Taken Orally everyday
Intervention Type
Drug
Intervention Name(s)
Gefitinib and Pemetrexed/platinum
Intervention Description
Gefitinib 250mg is Taken Orally on day 1-28,combined Pemetrexed (D1)+cisplatin (D1-3) or Pemetrexed (D1) + nedaplatin (D1) chemotherapy, every 28 days
Intervention Type
Drug
Intervention Name(s)
Gefitinib mono-therapy
Intervention Description
Gefitinib 250mg is Taken Orally everyday
Primary Outcome Measure Information:
Title
iPFS(intracranial progression free survival
Description
defined as time from randomization to intracranial progressive disease or death.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
ORR
Description
proportion of patients with complete or partial response of overall lesions
Time Frame
2 years
Title
intracranial objective response rate (iORR)
Description
proportion of patients with complete or partial response of intracranial lesions
Time Frame
2 years
Title
PFS(Progression Free Survival)
Description
time from randomization to overall disease progression or death
Time Frame
2 years
Title
OS(Overall Survival)
Description
time from randomization to death from any cause
Time Frame
3 years
Title
adverse events
Description
adverse events were evaluated according to NCI-CTCAE 4.0.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient who was confirmed stage IV NSCLC with EGFR activating mutation and brain metastases by pathologic histology or cytology Patients who had never received therapy (including chemotherapy,WBRT,EGFR-TKI and EGFR monoclonal antibody) after diagnosed brain metastases Patients had at least three metastatic lesions in brain, or patients with 1-2 intracranial lesions who were not suitable for brain radiotherapy, or patients with 1-2 intracranial lesions who refused brain radiotherapy, at least one intracranial lesion with the longest diameter of >5 mm Adult patients (≥ 18 years and ≤75 years). ECOG Performance Status 0 or 1 Life expectancy of at least 12 weeks.,Haemoglobin ³ 10.0 g/dl, Absolute neutrophil count (ANC) ³1.5 x 109/L, platelets ³ 100 x 109/L. Total bilirubin £ 1.5 x upper limit of normal (ULN). ALT and AST < 2.5 x ULN in the absence of liver metastases, or < 5 x ULN in case of liver metastases. Creatinine clearance ³ 60ml/min (calculated according to Cockcroft-gault formula). Patients should be contraceptive during the period of the trial until 8 weeks after the last administration of icotinib. Able to comply with the required protocol and follow-up procedures, and able to receive oral medications. Exclusion Criteria: Patient was received irradiation of brain. Patient with meningeal metastases were confirmed by MRI or cytology test of cerebrospinal fluid. Patient is received the treatment of Phenytoin, carbamazepine, rifampicin, phenobarbital, or St. John's Wort. Patient was received EGFR Tyrosine Kinase Inhibitor or EGFR monoclonal antibody. Interstitial pneumonia.Pericardial effusion, pleural effusion is uncontrolled . Any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, myocardial infarction within the previous year, serious cardiac arrhythmia requiring medication, hepatic, renal, or metabolic disease). Any significant ophthalmologic abnormality ,especially severe dry eye syndrome ,keratoconjunctivitis sicca,Sjogren syndrome,severe exposure keratitis or any other disorder likely to increase the risk of corneal epithelial lesions. Lack of physical integrity of the upper gastrointestinal tract, or malabsorption syndrome, or inability to take oral medication, or have active peptic ulcer disease. The symptoms of increased intracranial pressure are uncontrolled after dehydration and cortisone treatment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
li-kun Chen, MD
Phone
13798019964
Email
chenlk@sysucc.org.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Xue Hou
Phone
13570569436
Email
houxue@sysucc.org.cn
Facility Information:
Facility Name
Sun Yat-sen University of Cancer Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
li-kun Chen, doctor
Phone
13798019964
Email
chenlk@sysucc.org.cn
First Name & Middle Initial & Last Name & Degree
li-kun Chen, doctor

12. IPD Sharing Statement

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Gefitinib With or Without Chemotherapy in Brain Metastases From Non-small Cell Lung Cancer

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