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ET Retreat 2009 T Meiller DDS, PhD
Head and Neck Squamous  Cell Carcinoma ,[object Object],[object Object],[object Object],[object Object]
Premalignant Lesions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Premalignant Development ,[object Object],[object Object],[object Object],[object Object],[object Object]
Mixed Results Historically Some Efficacy but Unacceptable Toxicities ,[object Object]
Prevention of Oral Squamous Cell Carcinoma ,[object Object],[object Object]
Pre-malignant and malignant epithelial lesions Oral Pathology Acquisitions DS SCC CIS Severe Dysplasia Moderate Dysplasia Mild Dysplasia Hyperkeratosis Hyperortho-keratosis Hyperpara-keratosis Acanthosis Years 41 2 9 13 23 15 103 80 109 1997 52 10 15 10 18 6 90 80 95 1998 69 4 9 12 17 7 85 74 103 1999 64 3 7 8 12 3 80 78 75 2000 97 6 8 10 19 12 90 89 129 2001 91 6 12 11 20 10 107 112 178 2002 87 8 9 25 16 4 98 88 138 2003 56 7 12 8 9 3 94 95 133 2004 71 12 13 12 26 5 78 117 132 2005 65 2 11 18 16 2 97 84 139 2006 69 4 14 19 26 7 105 118 170 2007 83 6 10 14 32 0 102 120 130 2008 36 1 8 7 19 3 51 78 86 2009*
Patient Accrual Assumptions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Erlotinib Prevention of Oral Cancer (EPOC) NCI P01 CA106451 IEN alone Proportion of cases not developing SOM (%) IEN plus cancer history
Microdissection DNA extraction PCR Patient eligibility determined   within 7 business days Data entered in Web-based database for automatic calculations Determining Protocol Eligibility by LOH DNA fragment separation and quantification
Erlotinib as an EGFR inhibitor  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object]
Primary objective To determine the clinical and histologic response of oral premalignant lesions to 24 weeks of therapy with pioglitazone, 45 mg qd, defined as 50% or greater reduction in the measured product of perpendicular dimensions of the target lesion. ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Erlotinib Prevention of Oral Cancer Trial

  • 1. ET Retreat 2009 T Meiller DDS, PhD
  • 2.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7. Pre-malignant and malignant epithelial lesions Oral Pathology Acquisitions DS SCC CIS Severe Dysplasia Moderate Dysplasia Mild Dysplasia Hyperkeratosis Hyperortho-keratosis Hyperpara-keratosis Acanthosis Years 41 2 9 13 23 15 103 80 109 1997 52 10 15 10 18 6 90 80 95 1998 69 4 9 12 17 7 85 74 103 1999 64 3 7 8 12 3 80 78 75 2000 97 6 8 10 19 12 90 89 129 2001 91 6 12 11 20 10 107 112 178 2002 87 8 9 25 16 4 98 88 138 2003 56 7 12 8 9 3 94 95 133 2004 71 12 13 12 26 5 78 117 132 2005 65 2 11 18 16 2 97 84 139 2006 69 4 14 19 26 7 105 118 170 2007 83 6 10 14 32 0 102 120 130 2008 36 1 8 7 19 3 51 78 86 2009*
  • 8.
  • 9. Erlotinib Prevention of Oral Cancer (EPOC) NCI P01 CA106451 IEN alone Proportion of cases not developing SOM (%) IEN plus cancer history
  • 10. Microdissection DNA extraction PCR Patient eligibility determined within 7 business days Data entered in Web-based database for automatic calculations Determining Protocol Eligibility by LOH DNA fragment separation and quantification
  • 11.
  • 12.
  • 13.