Trial of BIBW 2992 (Afatinib) + Cetuximab in Non-Small Cell Lung Cancer

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim
ClinicalTrials.gov Identifier:
NCT01090011
First received: March 10, 2010
Last updated: December 10, 2013
Last verified: December 2013
  Purpose

The primary objective of this trial is to determine the maximum tolerated dose (MTD) and recommended Phase II doses for the combination of BIBW 2992 and cetuximab in patients with non-small cell lung cancer and acquired resistance to erlotinib or gefitinib.

Overall safety, pharmacokinetics and anti-tumor activity for the combination of BIBW 2992 and cetuximab in patients with non-small cell lung cancer and acquired resistance to erlotinib, gefitinib or BIBW 2992 will be evaluated as secondary objectives.

Initially a standard, 3+3 dose escalation will be performed to determine the MTD of BIBW 2992 when administered together with cetuximab in patients with advanced non small cell lung cancer and acquired resistance to erlotinib or gefitinib.

Subsequently, the preliminary efficacy and safety of the identified MTD of cetuximab administered with BIBW 2992 will be explored in a combo arm via a further expansion of MTD cohort up to a total of 140 EGFR mutation positive NSCLC with acquired resistance to erlotinib/gefitinib.

Furthermore, the safety and preliminary anti-tumor activity of the combination therapy in EGFR mutant NSCLC patients who developed acquired resistance (AR) to BIBW 2992, will be assessed in a sequential arm. The sequential arm will use a two-stage design with an early stopping rule after 12 patients with acquired resistance to BIBW 2992 have received up to 5 courses of BIBW 2992 plus cetuximab. If no responses are seen in 12 patients during 5 courses of combination therapy, accrual in the sequential arm will stop. If 1 or more responses are observed, the sequential arm will expand up to about 40 patients.


Condition Intervention Phase
Carcinoma, Non-Small-Cell Lung
Drug: Cetuximab
Drug: BIBW 2992
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Phase Ib Open-label Clinical Trial of Continuous Once Daily Oral Treatment Using BIBW 2992 Plus Cetuximab (Erbitux®) in Patients With Non-small Cell Lung Cancer With Progression Following Prior Erlotinib (Tarceva®) or Gefitinib (Iressa®)

Resource links provided by NLM:


Further study details as provided by Boehringer Ingelheim:

Primary Outcome Measures:
  • The primary endpoint is the occurrence of dose limiting toxicity (DLT). [ Time Frame: from day 1 treatment until first documented progression or undue toxicity ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Safety of BIBW 2992 when administered together with cetuximab as indicated by intensity and incidence of adverse events, graded according to NCI CTCAE Version 3 [ Time Frame: at least 4 weeks after end of treatment ] [ Designated as safety issue: No ]
  • Pharmacokinetic parameters of BIBW 2992 and cetuximab combination therapy [ Time Frame: from day 1 treatment until first documented progression or undue toxicity ] [ Designated as safety issue: No ]
  • Objective tumor response (Complete Response [CR] and Partial Response [PR]) determined by RECIST v1.1) [ Time Frame: screening, week 4, 8, 12 and every 8 weeks thereafter until progression or start of further treatment ] [ Designated as safety issue: No ]
  • Disease control (CR, PR and Stable Disease [SD] determined by RECIST v1.1) [ Time Frame: screening, week 4, 8, 12 and every 8 weeks thereafter until progression or start of further treatment ] [ Designated as safety issue: No ]
  • Duration of objective response (according to RECIST v1.1) [ Time Frame: screening, week 4, 8, 12 and every 8 weeks thereafter until progression or start of further treatment ] [ Designated as safety issue: No ]
  • Duration of disease control (according to RECIST v1.1) [ Time Frame: screening, week 4, 8, 12 and every 8 weeks thereafter until progression or start of further treatment ] [ Designated as safety issue: No ]
  • Progression-free survival (according to RECIST v1.1) [ Time Frame: screening, week 4, 8, 12 and every 8 weeks thereafter until progression or start of further treatment ] [ Designated as safety issue: No ]

Estimated Enrollment: 240
Study Start Date: March 2010
Estimated Study Completion Date: August 2014
Primary Completion Date: January 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: combination arm
patients to receive medium BIBW 2992 once daily plus biweekly cetuximab infusion at low, median and high dose level
Drug: Cetuximab
BIBW 2992 medium dose plus high dose level of cetuximab
Drug: BIBW 2992
BIBW 2992 medium dose plus high dose level of cetuximab
Experimental: sequential arm
patients to receive BIBW 2992 once daily, upon progression add biweekly cetuximab
Drug: Cetuximab
BIBW 2992 medium dose monotherapy, upon progression, cetuximab high dose is added
Drug: BIBW 2992
BIBW 2992 medium dose monotherapy, upon progression, cetuximab high dose is added

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  1. Pathologically or cytologically confirmed Stage IIIB/IV non-small cell lung cancer or recurrent disease following locoregional treatment
  2. Either or both of the following:

1) A tumor which harbors an Epidermal Growth Factor Receptor (EGFR) -mutation known to be associated with drug sensitivity (i.e., G719X, exon 19 deletion, L858R, L861Q) from previous tumor biopsy or surgery. A tumor which harbors exon 20 insertion or de novo T790M mutation is eligible for the treatment in the sequential arm 2) Objective clinical benefit from treatment with an Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR TKI) as defined by either

  1. Documented partial or complete response (Response Evaluation Criteria in Solid Tumors, RECIST), or
  2. Stable disease >=6 months as defined by RECIST in absence of radiographic progression after initiation of gefitinib or erlotinib; or stable disease/PR/CR >=12 weeks as defined by RECIST after initiation of BIBW 2992 3. Systemic progression of disease (RECIST v1.1) while on continuous treatment with erlotinib or gefitinib or BIBW 2992 within the last 30 days. Patients whose disease progresses only in the central nervous system (CNS) are not eligible 4. No intervening systemic therapy between cessation of gefitinib or erlotinib or BIBW 2992 and initiation of the treatment in the study 5. Adequate tumor-derived material such as fresh or archived tumor tissue or pleural fluid from malignant pleural effusion after disease progression on erlotinib/gefitinib/BIBW 2992 prior to the study entry must be made available for EGFR mutation analyses 6. Patients aged 18 years or older 7. Life expectancy of at least three (3) months 8. Eastern Cooperative Oncology Group (ECOG) performance score 0-2 9. Written informed consent that is consistent with ICH-GCP guidelines

Exclusion criteria:

  1. Prior treatment with EGFR targeting antibodies; prior severe infusion reaction to a monoclonal antibody
  2. Adverse events due to major surgery (at least 28 days after) or minor surgery not recovered to CTC grade 1 or less. Surgical wounds must be healing without clinical evidence of infection prior to study treatment to be eligible.
  3. Radiotherapy less than two weeks prior to the start of the study treatment
  4. Systemic chemotherapy, hormonal therapy, immunotherapy, or experimental or approved proteins/antibodies (except erlotinib/gefitinib/BIBW 2992) <=30 days before study treatment
  5. Less than three days from prior treatment with gefitinib or erlotinib. Patients with adverse events related to gefitinib or erlotinib must recover to CTC AE grade 1 or less to be eligible. No need to stop BIBW 2992 before start of the study treatment for patient who progressed on BIBW 2992 from a separate clinical trial/treatment setting
  6. Brain metastases, which are symptomatic. Patients with treated, asymptomatic brain metastases are eligible if there has been no change in brain disease status for at least four (4) weeks, no history of cerebral oedema or bleeding in the past four (4) weeks. Anticonvulsant therapy will be allowed if patient is stable on anticonvulsant treatment.
  7. Other malignancies diagnosed within the past five (5) years (other than non melanomatous skin cancer, ductal carcinoma in situ and in situ cervical cancer)
  8. Known pre-existing interstitial lung disease
  9. Significant or recent acute gastrointestinal disorders with diarrhea as a major symptom e.g., Crohns disease, malabsorption, or Common Toxicity Criteria for Adverse Events (CTCAE) grade >2 diarrhea of any etiology
  10. Women of childbearing potential (WOCBP), or men who are able to father a child, unwilling to use a medically acceptable method of contraception during the trial; pregnancy or breast-feeding
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01090011

Locations
United States, Colorado
1200.71.1004 Boehringer Ingelheim Investigational Site
Aurora, Colorado, United States
United States, Connecticut
1200.71.1003 Boehringer Ingelheim Investigational Site
New Haven, Connecticut, United States
United States, New York
1200.71.1001 Boehringer Ingelheim Investigational Site
New York, New York, United States
United States, Tennessee
1200.71.1002 Boehringer Ingelheim Investigational Site
Nashville, Tennessee, United States
Netherlands
1200.71.2002 Boehringer Ingelheim Investigational Site
Amsterdam, Netherlands
1200.71.2001 Boehringer Ingelheim Investigational Site
Groningen, Netherlands
Sponsors and Collaborators
Boehringer Ingelheim
Investigators
Study Chair: Boehringer Ingelheim Boehringer Ingelheim
  More Information

No publications provided

Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT01090011     History of Changes
Other Study ID Numbers: 1200.71, 2009-015911-42
Study First Received: March 10, 2010
Last Updated: December 10, 2013
Health Authority: Netherlands: Central Committee Research Involving Human Subjects
United States: Food and Drug Administration

Additional relevant MeSH terms:
Carcinoma
Carcinoma, Non-Small-Cell Lung
Lung Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Carcinoma, Bronchogenic
Bronchial Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Lung Diseases
Respiratory Tract Diseases
Cetuximab
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on April 17, 2014