Trial Search Results

BIBW 2992 (Afatinib) in Head & Neck Cancer

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.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Boehringer Ingelheim

Stanford Investigator(s):

Intervention(s):

  • Drug: BIBW 2992
  • Drug: Cetuximab

Phase:

Phase 2

Eligibility


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.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Ruth Lira
6507231367
Not Recruiting