LUX-Lung 5: Afatinib Plus Weekly Paclitaxel Versus Investigator's Choice of Single Agent Chemotherapy Following Afatinib Monotherapy in Non-small Cell Lung Cancer Patients Failing Erlotinib or Gefitinib

February 15, 2017 updated by: Boehringer Ingelheim

Phase III Randomized Trial of BIBW 2992 Plus Weekly Paclitaxel Versus Investigator's Choice of Chemotherapy Following BIBW 2992 Monotherapy in Non-small Cell Lung Cancer Patients Failing Previous Erlotinib or Gefitinib Treatment (LUX Lung 5)

The primary objective of this randomized, open-label, active-controlled, multi-center trial is to determine the efficacy of BIBW 2992 given as an add-on to chemotherapy in patients with NSCLC Stage IIIb or IV progressing after BIBW 2992 monotherapy compared to chemotherapy alone in this patient population. Patients on both treatment arms will receive best supportive care in addition to study treatment. Patients enrolled into the trial will be treated and followed until death or lost to follow-up. Additional information on the health-related quality of life (HRQOL) will be collected.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

1154

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Argentina
      • Ciudad Autonoma de Buenos Aires, Argentina
        • Boehringer Ingelheim Investigational Site
  • Australia
    • New South Wales
      • Kingswood, New South Wales, Australia
        • Boehringer Ingelheim Investigational Site
    • Queensland
      • South Brisbane, Queensland, Australia
        • Boehringer Ingelheim Investigational Site
    • Victoria
      • Box Hill, Victoria, Australia
        • Boehringer Ingelheim Investigational Site
      • Fitzroy, Victoria, Australia
        • Boehringer Ingelheim Investigational Site
      • Wodonga, Victoria, Australia
        • Boehringer Ingelheim Investigational Site
  • Austria
      • Salzburg, Austria
        • Boehringer Ingelheim Investigational Site
  • Belgium
      • Aalst, Belgium
        • Boehringer Ingelheim Investigational Site
      • Bruxelles, Belgium
        • Boehringer Ingelheim Investigational Site
      • Duffel, Belgium
        • Boehringer Ingelheim Investigational Site
      • La Louvière, Belgium
        • Boehringer Ingelheim Investigational Site
      • Liège, Belgium
        • Boehringer Ingelheim Investigational Site
      • Middelheim, Belgium
        • Boehringer Ingelheim Investigational Site
      • Ottignies, Belgium
        • Boehringer Ingelheim Investigational Site
  • Brazil
      • Porto Alegre, Brazil
        • Boehringer Ingelheim Investigational Site
  • China
      • Beijing, China
        • Boehringer Ingelheim Investigational Site
      • Changchun, China
        • Boehringer Ingelheim Investigational Site
      • Chengdu, China
        • Boehringer Ingelheim Investigational Site
      • Fuzhou, China
        • Boehringer Ingelheim Investigational Site
      • Guangzhou, China
        • Boehringer Ingelheim Investigational Site
      • Hangzhou, China
        • Boehringer Ingelheim Investigational Site
      • Nanjing, China
        • Boehringer Ingelheim Investigational Site
      • Shanghai, China
        • Boehringer Ingelheim Investigational Site
  • Finland
      • Helsinki, Finland
        • Boehringer Ingelheim Investigational Site
  • France
      • Bayonne, France
        • Boehringer Ingelheim Investigational Site
      • Caen Cedex 5, France
        • Boehringer Ingelheim Investigational Site
      • Dijon, France
        • Boehringer Ingelheim Investigational Site
      • La Tronche, France
        • Boehringer Ingelheim Investigational Site
      • Lyon Cedex 08, France
        • Boehringer Ingelheim Investigational Site
      • Paris, France
        • Boehringer Ingelheim Investigational Site
      • Paris cedex 20, France
        • Boehringer Ingelheim Investigational Site
      • Saint-Herblain cedex, France
        • Boehringer Ingelheim Investigational Site
      • Villejuif Cedex, France
        • Boehringer Ingelheim Investigational Site
  • Germany
      • Berlin, Germany
        • Boehringer Ingelheim Investigational Site
      • Essen, Germany
        • Boehringer Ingelheim Investigational Site
      • Esslingen, Germany
        • Boehringer Ingelheim Investigational Site
      • Gauting, Germany
        • Boehringer Ingelheim Investigational Site
      • Hamburg, Germany
        • Boehringer Ingelheim Investigational Site
      • Hannover, Germany
        • Boehringer Ingelheim Investigational Site
      • Heidelberg, Germany
        • Boehringer Ingelheim Investigational Site
      • Mainz, Germany
        • Boehringer Ingelheim Investigational Site
      • Münster, Germany
        • Boehringer Ingelheim Investigational Site
  • Hungary
      • Budapest, Hungary
        • Boehringer Ingelheim Investigational Site
      • Pecs, Hungary
        • Boehringer Ingelheim Investigational Site
      • Törökbálint, Hungary
        • Boehringer Ingelheim Investigational Site
  • India
      • Chennai, India
        • Boehringer Ingelheim Investigational Site
      • Jaipur, India
        • Boehringer Ingelheim Investigational Site
      • Maharashtra, India
        • Boehringer Ingelheim Investigational Site
      • Mumbai, India
        • Boehringer Ingelheim Investigational Site
      • Nashik, Maharashtra, India
        • Boehringer Ingelheim Investigational Site
  • Israel
      • Kfar Saba, Israel
        • Boehringer Ingelheim Investigational Site
      • Petach Tikva, Israel
        • Boehringer Ingelheim Investigational Site
      • Tel Hashomer, Israel
        • Boehringer Ingelheim Investigational Site
  • Italy
      • Avellino, Italy
        • Boehringer Ingelheim Investigational Site
      • Aviano (PN), Italy
        • Boehringer Ingelheim Investigational Site
      • Bergamo, Italy
        • Boehringer Ingelheim Investigational Site
      • Genova, Italy
        • Boehringer Ingelheim Investigational Site
      • Milano, Italy
        • Boehringer Ingelheim Investigational Site
      • Monza (mi), Italy
        • Boehringer Ingelheim Investigational Site
      • Ravenna, Italy
        • Boehringer Ingelheim Investigational Site
      • Roma, Italy
        • Boehringer Ingelheim Investigational Site
  • Korea, Republic of
      • Goyang, Korea, Republic of
        • Boehringer Ingelheim Investigational Site
      • Hwasun, Korea, Republic of
        • Boehringer Ingelheim Investigational Site
      • Seoul, Korea, Republic of
        • Boehringer Ingelheim Investigational Site
  • Mexico
      • Distrito Federal, Mexico
        • Boehringer Ingelheim Investigational Site
  • Netherlands
      • Maastricht, Netherlands
        • Boehringer Ingelheim Investigational Site
      • Nieuwegein, Netherlands
        • Boehringer Ingelheim Investigational Site
  • Peru
      • Arequipa, Peru
        • Boehringer Ingelheim Investigational Site
      • La Victoria, Peru
        • Boehringer Ingelheim Investigational Site
  • Poland
      • Gdansk, Poland
        • Boehringer Ingelheim Investigational Site
      • Olsztyn, Poland
        • Boehringer Ingelheim Investigational Site
      • Otwock, Poland
        • Boehringer Ingelheim Investigational Site
      • Warszawa, Poland
        • Boehringer Ingelheim Investigational Site
  • Russian Federation
      • Obninsk, Russian Federation
        • Boehringer Ingelheim Investigational Site
      • St. Petersburg, Russian Federation
        • Boehringer Ingelheim Investigational Site
  • Spain
      • A Coruña, Spain
        • Boehringer Ingelheim Investigational Site
      • Barcelona, Spain
        • Boehringer Ingelheim Investigational Site
      • Madrid, Spain
        • Boehringer Ingelheim Investigational Site
      • Mataró, Spain
        • Boehringer Ingelheim Investigational Site
      • Málaga, Spain
        • Boehringer Ingelheim Investigational Site
      • Valencia, Spain
        • Boehringer Ingelheim Investigational Site
  • Taiwan
      • Kaohsiung, Taiwan
        • Boehringer Ingelheim Investigational Site
      • Taichung, Taiwan
        • Boehringer Ingelheim Investigational Site
      • Tainan, Taiwan
        • Boehringer Ingelheim Investigational Site
      • Taipei, Taiwan
        • Boehringer Ingelheim Investigational Site
      • Taoyuan, Taiwan
        • Boehringer Ingelheim Investigational Site
  • Ukraine
      • Dnipropetrovks, Ukraine
        • Boehringer Ingelheim Investigational Site
      • Donetsk, Ukraine
        • Boehringer Ingelheim Investigational Site
      • Kharkiv, Ukraine
        • Boehringer Ingelheim Investigational Site
      • Kyiv, Ukraine
        • Boehringer Ingelheim Investigational Site
  • United Kingdom
      • Brighton, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • Dundee, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • Exeter, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • London, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • Maidstone, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • Manchester, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • Sutton, Surrey, United Kingdom
        • Boehringer Ingelheim Investigational Site
      • Truro, Cornwall, United Kingdom
        • Boehringer Ingelheim Investigational Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion criteria:

Part A

  1. Patients with pathologically confirmed diagnosis of NSCLC Stage IIIB (with cytologically proven pleural effusion or pericardial effusion) or Stage IV who have failed treatment with erlotinib (Tarceva) or gefitinib (Iressa).
  2. Patients should have received and failed at least one line of cytotoxic chemotherapy including a platinum-based regimen in patients eligible for platinum-based therapy and pemetrexed in pemetrexed eligible patients (unless pemetrexed is not considered a regulatory or clinical standard of care e.g. no label indication, no availability or no coverage by 3rd party payer(s)) for advanced or metastatic disease and have progressive disease following at least 12 weeks of treatment with erlotinib or gefitinib
  3. Patients pretreated with taxane-based chemotherapy for advanced or metastatic disease must have experienced stable disease, partial or complete response as best response
  4. Eastern Cooperative Oncology Group performance Score 0 or 1.
  5. Patients with at least one tumor lesion that can accurately be measured by magnetic resonance imaging (MRI), or computed tomography (CT) in at least one dimension with longest diameter to be recorded as 10 mm but no less than double the slice thickness according to RESIST 1.1.
  6. Male and female patients no less than 18 years of age.
  7. Life expectancy of at least three (3) months.
  8. Written informed consent that is consistent with ICH-GCP guidelines. Part B 1) Clinical benefit (disease stabilization or antitumor response) of 12 weeks duration in Part A of the trial determined on the second tumour assessment.

2.) Patients should have progressed in Part A according to RECIST 1.1 3.) New informed consent, including consent to biomarker sampling, must be signed before patients enter Part B of the trial

Exclusion criteria:

  1. Previous treatment with BIBW 2992
  2. Chemo-, hormone- (other than megestrol acetate, steroids required for maintenance non-cancer therapy or as premedication before chemotherapy) or immunotherapy within the past 4 weeks; except for TKI pretreatment (2 weeks only)
  3. Active/symptomatic brain metastases including leptomeningeal disease. Patients with a history of treated brain metastasis must have a stable or normal brain MRT/CT scan at screening and be at least 4 weeks post-radiation or surgery for brain metastasis. Dexamethasone therapy will be allowed if administered as a stable dose for at least one month before randomization.
  4. Significant or recent acute gastrointestinal disorders with diarrhea as a major symptom e.g., Crohn's disease, mal-absorption, or CTCAE Grade >2 diarrhea of any etiology at baseline
  5. Patients who have any other life-threatening illness or organ system dysfunction, which in the opinion of the Investigator, would either compromise patient safety or interfere with the evaluation of the safety of the test drug
  6. Other malignancies diagnosed within the past five (5) years (other than non-melanomatous skin cancer and in situ cervical cancer)
  7. Radiotherapy within the past 2 weeks prior to treatment with the trial drug
  8. History or presence of clinically relevant cardiovascular abnormalities such as uncontrolled hypertension, congestive heart failure New york Heart Association (NYHA) functional classification of 3, unstable angina, or poorly controlled arrhythmia. Myocardial infarction within 6 months prior to entering the trial.
  9. Cardiac left ventricular function with resting ejection fraction of less than 50% measured by multigated blood pool imaging of the heart (MUGA scan) or echocardiogram .
  10. Prior treatment with anthracyclines with a cumulative dose of doxorubicin (or equivalent) at or greater than 400 mg/m2
  11. Absolute neutrophil count (ANC) at or less than 1500 / mm3
  12. Platelet count at or less than 100,000 / mm3
  13. Bilirubin at or greater than 1.5 mg / dL (>26 mol / L, SI unit equivalent)
  14. Aspartate amino transferase (AST) or alanine amino transferase (ALT) at or greater than three times the upper limit of normal (if related to liver metastases at or greater than five times the upper limit of normal)
  15. Serum creatinine at or greater 1.5 times the upper normal limit or calculated/measured creatinine clearance at or less than 45 mL/min
  16. Women of child-bearing potential or men who are able to father a child unwilling to use a medically acceptable method of contraception during the trial
  17. Pregnancy or breast feeding
  18. Patients unable to comply with the protocol
  19. Patients with any serious active infection including known human immunodeficiency virus (HIV), active hepatitis B or active hepatitis C
  20. Known or suspected active drug or alcohol abuse
  21. Pre-existing or current Interstitial lung disease (ILD) 22.)
  22. Peripheral polyneuropathy of > Grade 2
  23. Requirement for treatment with any of the pohibited concomitant medication listed in section 4.2.2.1.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Investigator's choice of chemotherapy
Patients will be treated with investigator's choice of chemotherapy
Drug: Investigator´s choice of chemotherapy
BIBW 2992 in a medium dose in combination with Paclitaxel to explore safety and efficacy versus investigator´s choice of chemotherapy
Experimental: BIBW 2992 and Paclitaxel
Patients will be treated with BIBW 2992daily with a medium dose and weekly administration of Paclitaxel at a dose of 80 mg/m2
Drug: BIBW 2992
BIBW 2992 will be given in a medium dose in combination with Paclitaxel to explore safety and efficacy versus investigator´s choice of chemotherapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Progression Free Survival (Part B)
Time Frame: From randomization until disease progression or death; Up to 32 months

Progression free survival (PFS) time as determined by Response Evaluation Criteria in Solid Tumors (RECIST), Version 1.1 from day of randomization until disease progression or death for patients randomised to combination therapy with afatinib plus paclitaxel or to investigator's choice of chemotherapy.

Median was calculated from the Kaplan-Meier curve.
From randomization until disease progression or death; Up to 32 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Progression Free Survival (Part A)
Time Frame: From first dose administration until disease progression or death; Up to 51 months

Progression free survival (PFS) as determined by Response Evaluation Criteria in Solid Tumours (RECIST) 1.1 for Part A.

Median was calculated from the Kaplan-Meier curve.
From first dose administration until disease progression or death; Up to 51 months
Overall Survival (Part B)
Time Frame: From randomization until death; Up to 32 months

Overall survival (OS) as determined by the time from randomization to death in part B.

Median was calculated from the Kaplan-Meier curve.
From randomization until death; Up to 32 months
Objective Response (Part A)
Time Frame: Post baseline tumour-imaging was performed at every 6 weeks thereafter until disease progression; upto 51 months
Objective response defined as the best overall response of complete response [CR]: disappearance of all target lesion & partial response [PR]: ≥30% decrease in the sum of the longest diameter of target lesions , taking as reference the baseline sum longest diameter of Afatinib monotherapy according to RECIST 1.1 for Part A.
Post baseline tumour-imaging was performed at every 6 weeks thereafter until disease progression; upto 51 months
Objective Response (Part B)
Time Frame: Post baseline tumour-imaging was performed at every 8 weeks thereafter until disease progression; up to 32 Months
Objective response (CR, PR) of Afatinib/paclitaxel combination therapy and comparator chemotherapy in Part B after progression in Part A according to RECIST 1.1 .
Post baseline tumour-imaging was performed at every 8 weeks thereafter until disease progression; up to 32 Months
Intensity and Incidence of Adverse Events (AEs) for Part A & Part B.
Time Frame: From first administration of treatment until 28 days after last drug administration, up to 51 Months (Part A) and from randomization until 28 days after last drug administration of Trial medication, up to 32 Months (Part B)
Safety of Afatinib as indicated by intensity and incidence of adverse events, graded according to United States National Cancer Institute Common terminology Criteria for Adverse Events (US NCI CTCAE) Version 3.0 both for Part A and Part B. The CTCAE grades are: 1 (mild AE), 2 (moderate AE), 3 (severe AE), 4 (life-threatening or disabling AE), 5 (death related to AE).
From first administration of treatment until 28 days after last drug administration, up to 51 Months (Part A) and from randomization until 28 days after last drug administration of Trial medication, up to 32 Months (Part B)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Boehringer Ingelheim

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2010

Primary Completion (Actual)

October 1, 2013

Study Completion (Actual)

January 1, 2016

Study Registration Dates

First Submitted

March 10, 2010

First Submitted That Met QC Criteria

March 10, 2010

First Posted (Estimate)

March 11, 2010

Study Record Updates

Last Update Posted (Actual)

April 4, 2017

Last Update Submitted That Met QC Criteria

February 15, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1200.42
  • 2009-014563-39 (EudraCT Number: EudraCT)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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