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Comparator-Controlled Study for EGFR(+) Patients With Multiple BMs From NSCLC (BROKE) (EGFR-epidermal Growth Factor Receptor;BM-brain Metastases) (EGFR)

Primary Purpose

Non-Small Cell Lung Cancer, Brain Metastases, EGFR Gene Mutation

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Gefitinib
WBRT
Sponsored by
Shanghai Chest Hospital
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 - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • years of age or older
  • ECOG score ≤ 2
  • Recursive Partitioning Analysis(RPA) Class I-II;
  • The pathological diagnosis of primary non-small cell lung cancer and detection of pulmonary primary ARMs;
  • Sequencing EGFR mutation(primary lesion or metastases,exon 19 deletions or exon 21 L858R (EGFR mutation in exon 21, L858R point mutation) mutations;
  • Enhanced MRI showed brain metastases ≥ 4;
  • 1 or 2 line treatment revealed failure;

    • No use of EGFR-TKIs(Tyrosine kinase inhibitors) previously;
    • No treatment for BM previously,including WBRT、SRS、surgery or experimental therapy;
    • Expected survival period over 3 months;
    • Two weeks before randomization, organs function in patients with meet the following criteria:

      • bone marrow:HB(hemoglobin) ≥ 90g/L, neutrophil≥ 1.5 × 109/L and platelet ≥ 100 × 109/L;
      • liver function:total bilirubin ≤ 1.5 times the upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 times the upper limit of normal;
      • renal function:more than 1.5 times the upper limit of normal serum creatinine or creatinine clearance rate ≥ 60 ml/min;
      • Urine dipstick testing the proteinuria < 1+; if the urine dipstick test value, 1+, is 24 hours total urine protein must < 500mg;
      • blood glucose:normal range,DM(diabetes mellitus) patients are under treatment and have a stable state;
    • Can understand and consent

Exclusion Criteria:

  • Patients have been treated with brain radiation or surgery of BM;
  • Prior of EGFR-TKIs;
  • Mixed with small cell lung cancer patients with components;
  • Wild-type of EGFR;
  • Unable to tolerate MRI scanning;
  • Post 2 line treated patients;
  • Brain meninges metastases or incorporate with brain meninges metastases;
  • 5 years before other cancers except NSCLC treatment in patients with the start of the study (except for simple operation resection and there are at least 5 consecutive years disease free survival, has been cured of cervical carcinoma in situ, has cured the base cell cancer and bladder epithelial tumor);
  • Before entering the group 4 weeks received any other investigational drugs;
  • Incorporate with local symptoms(hemiplegic paralysis、anepia、nystagmus、ataxia.et);
  • Pregnancy or lactation female;
  • Allergic to EGFR-TKIs or any components;
  • Patients were not permitted to receive the following drugs: phenytoin, carbamazepine, rifampicin, phenobarbital or itraconazole because of their potential to affect the metabolism of EGFR-TKIs and reduce its plasma concentration. Patients were not permitted to receive oral medicine such as CoumadinTM、Warfarin. If anticoagulant therapy is needed,low molecular heparin is suggested to instead of Coumarin drugs;
  • Organs function in patients with meet the following criteria:

    • Diagnose with interstitial lung disease、drug induced interstitial disease、hormone dependent radiation pneumonia previously,et al;
    • Any unstable system diseases: including active infection, moderate to severe chronic obstructive pulmonary disease, uncontrolled hypertension, unstable angina pectoris, congestive heart failure, within the last 6 months of the onset of myocardial infarction, need serious mental disorder drug treatment, liver, kidney or metabolic diseases; mental / spiritual diseases such as Alzheimer's disease;
    • Gastrointestinal tract disease resulting in an inability to take oral medication or a requirement for intravenous (IV) alimentation, prior surgical procedures affecting absorption or active peptic ulcer;
    • With immunodeficiency disease, or suffer from other acquired, congenital immunodeficiency disease, or a history of organ transplantation;
    • Known human immunodeficiency virus (HIV) infection;
    • Without full control of ocular inflammation or eye infections, or any may cause the eye disease situation;
  • Any disease, metabolic disorders, or physical examination or laboratory suspicion or treatment of complications in patients at high risk of drug.

Sites / Locations

  • Varian linear acceleratoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Gefitinib alone

Gefitinib concurrent WBRT

Arm Description

Patients harboring an EGFR mutation with multiple BM from NSCLC will receive Gefitinib 250mg per day until progression of disease.

Patients harboring an EGFR mutation with multiple BM from NSCLC will receive Gefitinib concurrent WBRT until progression of disease.Gefitinib was given 250mg per day. WBRT was delivered in 3.0 Gy fractions once per day 5 days per week to a total dose of 30Gy (10 fractions).

Outcomes

Primary Outcome Measures

Time to progression
Compare the progression free survival(PFS) and safety in two arms,including intracranial PFS、extracranial PFS and overall PFS.

Secondary Outcome Measures

Overall survival
Disease Progression Classification
intracranial or extracranial site
Health-related quality of life
measured by ECGO(Eastern Cooperative Oncology Group) PS (Performance Status)
Mental Status
measured by scale of MMSE( Mini Mental Status Examination)

Full Information

First Posted
December 23, 2014
Last Updated
January 23, 2015
Sponsor
Shanghai Chest Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02338011
Brief Title
Comparator-Controlled Study for EGFR(+) Patients With Multiple BMs From NSCLC (BROKE) (EGFR-epidermal Growth Factor Receptor;BM-brain Metastases)
Acronym
EGFR
Official Title
Gefitinib Alone or With Concomitant Whole Brain Radiotherapy for Patients Harboring an EGFR Mutation With Multiple Brain Metastases From Non-Small-cell Lung Cancer: a Phase II/III Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
November 2014 (undefined)
Primary Completion Date
November 2017 (Anticipated)
Study Completion Date
November 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Chest Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Compare the effect and safety of gefitinib alone with gefitinib plus concomitant WBRT(whole-brain radiotherapy ) in treatment of NSCLC patients harboring an EGFR mutation with multiple BM. Verify the failure pattern of NSCLC patients harboring an EGFR mutation with multiple BM. Explore the rescuable therapy after progression of disease.
Detailed Description
All patients will be randomized to receive gefitinib or gefitinib concurrent WBRT until progression of disease. Gefitinib concurrent WBRT, patients were given gefitinib 250mg per day concurrently with WBRT(whole-brain radiotherapy ). Dose reduction was allowed for intolerable adverse effects such as rash(grade 4)、diarrhea(grade 3-4) or non hematological toxicity(grade 3-4) from 250mg per day to 250mg every other day then to 250mg every three days if needed. WBRT was delivered in 3.0 Gy(Gray)fractions once per day 5 days per week to a total dose of 30Gy (10 fractions). Radiation was delivered as opposed lateral 6-MV(Micro Voltage) beams with Varian linear accelerator.

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 Gene Mutation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
210 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gefitinib alone
Arm Type
Experimental
Arm Description
Patients harboring an EGFR mutation with multiple BM from NSCLC will receive Gefitinib 250mg per day until progression of disease.
Arm Title
Gefitinib concurrent WBRT
Arm Type
Experimental
Arm Description
Patients harboring an EGFR mutation with multiple BM from NSCLC will receive Gefitinib concurrent WBRT until progression of disease.Gefitinib was given 250mg per day. WBRT was delivered in 3.0 Gy fractions once per day 5 days per week to a total dose of 30Gy (10 fractions).
Intervention Type
Drug
Intervention Name(s)
Gefitinib
Other Intervention Name(s)
Iressa
Intervention Description
Gefitinib was given 250mg per day. Dose reduction was allowed for intolerable adverse effects such as rash(grade 4)、diarrhea(grade 3-4) or non hematological toxicity(grade 3-4) from 250mg per day to 250mg every other day then to 250mg every three days if needed.
Intervention Type
Radiation
Intervention Name(s)
WBRT
Intervention Description
WBRT was delivered in 3.0 Gy fractions once per day 5 days per week to a total dose of 30Gy (10 fractions).
Primary Outcome Measure Information:
Title
Time to progression
Description
Compare the progression free survival(PFS) and safety in two arms,including intracranial PFS、extracranial PFS and overall PFS.
Time Frame
12-14 months
Secondary Outcome Measure Information:
Title
Overall survival
Time Frame
3 years
Title
Disease Progression Classification
Description
intracranial or extracranial site
Time Frame
3 years
Title
Health-related quality of life
Description
measured by ECGO(Eastern Cooperative Oncology Group) PS (Performance Status)
Time Frame
3 years
Title
Mental Status
Description
measured by scale of MMSE( Mini Mental Status Examination)
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: years of age or older ECOG score ≤ 2 Recursive Partitioning Analysis(RPA) Class I-II; The pathological diagnosis of primary non-small cell lung cancer and detection of pulmonary primary ARMs; Sequencing EGFR mutation(primary lesion or metastases,exon 19 deletions or exon 21 L858R (EGFR mutation in exon 21, L858R point mutation) mutations; Enhanced MRI showed brain metastases ≥ 4; 1 or 2 line treatment revealed failure; No use of EGFR-TKIs(Tyrosine kinase inhibitors) previously; No treatment for BM previously,including WBRT、SRS、surgery or experimental therapy; Expected survival period over 3 months; Two weeks before randomization, organs function in patients with meet the following criteria: bone marrow:HB(hemoglobin) ≥ 90g/L, neutrophil≥ 1.5 × 109/L and platelet ≥ 100 × 109/L; liver function:total bilirubin ≤ 1.5 times the upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 times the upper limit of normal; renal function:more than 1.5 times the upper limit of normal serum creatinine or creatinine clearance rate ≥ 60 ml/min; Urine dipstick testing the proteinuria < 1+; if the urine dipstick test value, 1+, is 24 hours total urine protein must < 500mg; blood glucose:normal range,DM(diabetes mellitus) patients are under treatment and have a stable state; Can understand and consent Exclusion Criteria: Patients have been treated with brain radiation or surgery of BM; Prior of EGFR-TKIs; Mixed with small cell lung cancer patients with components; Wild-type of EGFR; Unable to tolerate MRI scanning; Post 2 line treated patients; Brain meninges metastases or incorporate with brain meninges metastases; 5 years before other cancers except NSCLC treatment in patients with the start of the study (except for simple operation resection and there are at least 5 consecutive years disease free survival, has been cured of cervical carcinoma in situ, has cured the base cell cancer and bladder epithelial tumor); Before entering the group 4 weeks received any other investigational drugs; Incorporate with local symptoms(hemiplegic paralysis、anepia、nystagmus、ataxia.et); Pregnancy or lactation female; Allergic to EGFR-TKIs or any components; Patients were not permitted to receive the following drugs: phenytoin, carbamazepine, rifampicin, phenobarbital or itraconazole because of their potential to affect the metabolism of EGFR-TKIs and reduce its plasma concentration. Patients were not permitted to receive oral medicine such as CoumadinTM、Warfarin. If anticoagulant therapy is needed,low molecular heparin is suggested to instead of Coumarin drugs; Organs function in patients with meet the following criteria: Diagnose with interstitial lung disease、drug induced interstitial disease、hormone dependent radiation pneumonia previously,et al; Any unstable system diseases: including active infection, moderate to severe chronic obstructive pulmonary disease, uncontrolled hypertension, unstable angina pectoris, congestive heart failure, within the last 6 months of the onset of myocardial infarction, need serious mental disorder drug treatment, liver, kidney or metabolic diseases; mental / spiritual diseases such as Alzheimer's disease; Gastrointestinal tract disease resulting in an inability to take oral medication or a requirement for intravenous (IV) alimentation, prior surgical procedures affecting absorption or active peptic ulcer; With immunodeficiency disease, or suffer from other acquired, congenital immunodeficiency disease, or a history of organ transplantation; Known human immunodeficiency virus (HIV) infection; Without full control of ocular inflammation or eye infections, or any may cause the eye disease situation; Any disease, metabolic disorders, or physical examination or laboratory suspicion or treatment of complications in patients at high risk of drug.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liyan JIang, M.D,Ph.D.
Phone
18017321302
Email
liyanjiangxkyy@sina.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaolong FU, M.D,Ph.D.
Phone
13651635103
Email
xlfu1964@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Liyan JIang, M.D,Ph.D.
Organizational Affiliation
Department of Respiratory, Shanghai Chest Hospital,Shanghai JIaotong University
Official's Role
Study Director
Facility Information:
Facility Name
Varian linear accelerato
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Liyan Jiang, M.D,Ph.D
Phone
18017321302
Email
jiang_liyan2000@126.com

12. IPD Sharing Statement

Learn more about this trial

Comparator-Controlled Study for EGFR(+) Patients With Multiple BMs From NSCLC (BROKE) (EGFR-epidermal Growth Factor Receptor;BM-brain Metastases)

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