BIBW 2992 (Afatinib) in Head & Neck Cancer

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim
ClinicalTrials.gov Identifier:
NCT00514943
First received: August 9, 2007
Last updated: June 3, 2014
Last verified: November 2013
  Purpose

The primary objective of this study is to explore the efficacy of BIBW 2992 compared with cetuximab (Erbitux) in patients with metastatic or recurrent head and neck cancer after failure of platinum-containing therapy. In addition, the trial aims to clarify the influence of EGFR genotype on tumor response to the treatment regimens.


Condition Intervention Phase
Head and Neck Neoplasms
Carcinoma, Squamous Cell
Drug: BIBW 2992
Drug: Cetuximab
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Randomized, Open-label Phase II Study of BIBW 2992 Versus Cetuximab (Erbitux) in Patients With Metastatic or Recurrent Head and Neck Squamous Cell Carcinoma (HNSCC) After Failure of Platinum-containing Therapy With a Cross-over Period for Progressing Patients

Resource links provided by NLM:


Further study details as provided by Boehringer Ingelheim:

Primary Outcome Measures:
  • Tumor Shrinkage Before Crossover Per Investigator Assessment [ Time Frame: From randomization until start of Stage 2 treatment, or within 28 days after the termination of Stage 1. ] [ Designated as safety issue: No ]
    Tumor shrinkage before crossover was defined as the change from baseline in the smallest post-randomisation sum of the longest diameters of target lesions (SLD), calculated as the smallest SLD after randomisation but before crossover minus SLD at baseline. Baseline was the SLD measured before randomisation. A negative value means the smallest post-randomisation SLD was smaller than baseline (decreased since baseline); a positive value means tumor size increased since baseline.


Secondary Outcome Measures:
  • Tumor Shrinkage After Crossover (Stage 2) Per Investigator Assessments [ Time Frame: From baseline assessed prior to first dose of Stage 2 study medication to 28 days after termination of Stage 2 treatment. ] [ Designated as safety issue: No ]
    Tumor shrinkage after crossover was defined as the change from baseline in the smallest post-crossover sum of the longest diameters of target lesions (SLD), calculated as the smallest SLD after crossover minus SLD at baseline. Baseline was the SLD measured at the time of crossover, or the closest measurement before the patient started stage 2 treatment. A negative value means the smallest post-crossover SLD was smaller than baseline (decreased after crossover), a positive value means tumor size increased after crossover.

  • Best Overall Response Per Investigator Assessment for Stage 1 [ Time Frame: Response determined from randomization until patient started Stage 2 or within 28 days after termination of Stage 1 treatment ] [ Designated as safety issue: No ]
    Overall response is assessed by the investigator according to the RECIST 1.0.

  • Best Overall Response Per ICR for Stage 1 [ Time Frame: Response determined from randomization until patient started Stage 2 or within 28 days after termination of Stage 1 treatment ] [ Designated as safety issue: No ]
    Overall response is assessed by independent central review (ICR) according to the RECIST 1.0.

  • Best Overall Response Per Investigator Assessment for Stage 2 [ Time Frame: Response determined during Stage 2 or within 28 days after termination of Stage 2 treatment ] [ Designated as safety issue: No ]
    Overall response is assessed by the investigator according to the RECIST 1.0.

  • Best Overall Response Per ICR for Stage 2 [ Time Frame: Response determined during Stage 2 or within 28 days after termination of Stage 2 treatment ] [ Designated as safety issue: No ]
    Overall response is assessed by independent central review (ICR) according to the RECIST 1.0.

  • Overall Survival (OS) Time [ Time Frame: From randomisation to data cut-off date. ] [ Designated as safety issue: No ]
    OS is defined as time from randomisation to death.

  • Progression Free Survival (PFS) Before Crossover Based on Investigator Assessment [ Time Frame: From randomisation to disease progression in Stage 1 or death whichever came first before crossover. ] [ Designated as safety issue: No ]
    PFS is defined as time from randomisation to until the occurrence of tumor progression or death, whichever came first, during Stage 1 of the trial.

  • Progression Free Survival (PFS) After Crossover Based on Investigator Assessment [ Time Frame: From first administration of study medication after cross over to disease progression in Stage 2 or death whichever came first after crossover. ] [ Designated as safety issue: No ]
    PFS is defined as time from first administration study medication after cross over until the occurrence of tumor progression or death, whichever came first, during Stage 2 of the trial.

  • Time to Deterioration in HRQoL - Stage 1 [ Time Frame: From randomisation to deterioration in HRQoL scores before crossover. ] [ Designated as safety issue: No ]

    Health related Quality of Life (HRQoL) was assessed with the questionnaires EORTC QLQ-C30 and EORTC QLQ-H&N35.

    Time to deterioration in HRQoL (defined as a 10-point change towards worsening from the baseline score on a 0-100 point scale) was determined for:

    • global health status (QLQ−C30 items 29 and 30)
    • pain (QLQ−HN35 items 31 to 34)
    • swallowing (QLQ−HN35 items 35 to 38)

  • Pre-dose Concentration of Afatinib in Plasma at Steady State on Day 15 (Cpre,ss,15) [ Time Frame: Day 15 ] [ Designated as safety issue: No ]
    Cpre,ss,15 represents the pre-dose concentration of afatinib in plasma at steady state on day 15.

  • Patients With AEs Resulting in Diarrhea and Skin Rash [ Time Frame: First administration of trial medication until 28 days after last ] [ Designated as safety issue: Yes ]
    Patients with adverse events (AEs) resulting in Diarrhea and skin rash.


Enrollment: 124
Study Start Date: August 2007
Primary Completion Date: June 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: BIBW 2992
once daily taken orally
Drug: BIBW 2992
experimental drug taken once daily orally
Active Comparator: Cetuximab
once every week by intravenous injection
Drug: Cetuximab
active comparator administered weekly intravenously

  Eligibility

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

Inclusion criteria:

1. Metastatic (stage IVc) or recurrent HNSCC 2. Histologically or cytologically confirmed diagnosis of squamous cell of the head and neck. Patients with well-differentiated (keratinizing) nasopharyngeal carcinomas and patients with squamous cell carcinomas metastatic to the neck from an unknown head and neck primary are eligible. 3. Patients must have documented progressive disease (PD) following receipt of prior platinum-based therapy (either as neoadjuvant, adjuvant, concomitant with radiotherapy, or for recurrent/ metastatic disease). 4. Patients must have measurable disease as defined by RECIST criteria. 5. Patients must have recovered from any therapy-related toxicities from previous chemo-, immuno-, or radiotherapies to CTC smaller or equal to Grade 1. 6. Patients must have recovered from previous surgery. 7. Life expectancy of at least three (3) months. 8. Eastern Cooperative Oncology Group (ECOG, R01-0787) performance score 0 or 1.

9. Patients must be eighteen (18) years of age or older. 10. Willingness and ability to give written informed consent consistent with ICH-GCP guidelines.

Exclusion criteria:

  1. Progressive disease within 3 months after completion of curative intent treatment for localized/locoregionally advanced disease.
  2. Prior use of an EGFR or erbB2 inhibitor in the recurrent/metastatic disease setting (treatment with cetuximab (Erbitux®) or other EGFR inhibitor during radiotherapy or chemoradiotherapy is permissible).
  3. More than 2 chemotherapeutic regimens given for recurrent/metastatic disease.
  4. Treatment with other investigational drugs, other anti-cancer-therapy (e.g., chemotherapy, immunotherapy, radiotherapy), concomitantly with therapy on this study and/or during the last four weeks, prior to the first treatment with the trial drug
  5. eliminated per Amendment #1
  6. Patients with history of other malignancy (except for appropriately treated superficial basal cell skin cancer and surgically cured cervical cancer in situ) unless free of disease for at least 3 years.
  7. Patients with history of decompensated heart failure.
  8. Cardiac left ventricular function with resting ejection fraction <50% or less than the institutional lower limit of normal by MUGA or echocardiogram.
  9. Active infectious disease.
  10. Gastrointestinal disorders that may interfere with the absorption of the study drug or chronic diarrhea.
  11. Serious illness, concomitant non-oncological disease or mental problems considered by the investigator to be incompatible with the protocol.
  12. Use of alcohol or drugs incompatible with patient participation in the study in the investigator's opinion.
  13. Patients unable to comply with the protocol.
  14. Patients with active/symptomatic brain metastases. Patients with a history of treated brain metastases must have stable or normal cerebral MRI scan at screening and be at least three months post-radiation or surgery.
  15. Absolute neutrophile count (ANC) less than 1000/mm3.
  16. Platelet count less than 75,000/mm3.
  17. Bilirubin greater than 1.5 mg/dl/ Higher bilirubin values are acceptable for patients with known Gilbert's disease, approval by the PI and sponsor necessary.
  18. Asparate amino transferase (AST) or alanine amino transferase (ALT) greater than 3 times the upper limit of normal.
  19. Serum creatinine greater than 1.5 X upper limit of normal for the institution.
  20. Patients who are sexually active and unwilling to use a medically acceptable method of contraception.
  21. Pregnancy or breast-feeding.
  22. Patients with known pre-existing interstitial lung disease.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00514943

  Show 36 Study Locations
Sponsors and Collaborators
Boehringer Ingelheim
Investigators
Study Chair: Boehringer Ingelheim Boehringer Ingelheim
  More Information

Additional Information:
No publications provided

Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT00514943     History of Changes
Other Study ID Numbers: 1200.28, 2008-007097-38
Study First Received: August 9, 2007
Results First Received: August 8, 2013
Last Updated: June 3, 2014
Health Authority: Belgium: Federal Service Public Health, Food Chain Safety and Environment
France: Agence Francaise de Securite Sanitaire des Produits de Sante
Spain: Spanish Agency of Medicines
United States: Food and Drug Administration

Additional relevant MeSH terms:
Neoplasms
Carcinoma
Carcinoma, Squamous Cell
Head and Neck Neoplasms
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms, Squamous Cell
Neoplasms by Site
Cetuximab
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on July 22, 2014