An Exploratory Study of ABT-806, a Tumor-Specific Anti-EGFR Antibody, in Subjects with Recurrent or Metastatic Head and Neck and Other Squamous Cell Carcinomas

Introduction: Despite their benefit, current anti-EGFR therapies are limited by narrow efficacy profiles due to dose-limiting toxicities. This phase 2 open-label study evaluated the efficacy and safety of ABT-806, an EGFR-targeting antibody that is tumor specific, in patients with advanced EGFR-expressing tumors including head and neck cancers (H&NC) and squamous cell carcinoma (SCC) of other sites. Methods: Patients with advanced H&NC (cohort A) or SCC of other sites (cohort B) were enrolled in the study. ABT-806 was administered as monotherapy at a dose of 24 mg/kg intravenously using a twice weekly dosing schedule until unacceptable toxicity and/or evidence of disease progression. Adverse events (AEs) were graded using the National Cancer Institute Common Terminology Criteria for Adverse Events v4.0; tumor response was assessed using the Response Evaluation criteria in Solid Tumors v1.1. EGFR status was assessed with mAb806 and EGFRvIII immunohistochemistry and correlated with outcomes. Results: ABT-806 was well tolerated with no grade 3+ treatment-related AEs. Disease stabilization was observed in two patients (14%) and for a median duration of 19.5 weeks. This included one patient from cohort A and one patient from cohort B. Progression-free survival and overall survival was not significantly different between the two cohorts. Conclusions: Although clinical activity was limited in this small, heavily pre-treated, and biomarker-unselected population, ABT-806 demonstrated an excellent safety profile with minimal classical EGFR-related toxicity. These findings support the development of more tumor-specific EGFR antibodies for use, particularly in combinatorial regimens.

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Journal
Cancers
Published
2026-10-14
DOI
https://doi.org/10.3390/cancers18203313
Primary Topic
HER2/EGFR in Cancer Research
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article
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article

An Exploratory Study of ABT-806, a Tumor-Specific Anti-EGFR Antibody, in Subjects with Recurrent or Metastatic Head and Neck and Other Squamous Cell Carcinomas

Jodie Palmer, Hui Kong Gan, Malaka Ameratunga, Edward B. Reilly et al.
Cancers
HER2/EGFR in Cancer Research
article

An Exploratory Study of ABT-806, a Tumor-Specific Anti-EGFR Antibody, in Subjects with Recurrent or Metastatic Head and Neck and Other Squamous Cell Carcinomas

Jodie Palmer, Hui Kong Gan, Malaka Ameratunga, Edward B. Reilly, Kerryn T. Westcott, Jaren Caine, Fiona Elizabeth Scott, Andrew Mark Scott, Diana Cao, Sagun Parakh, Anis Hamid, Michelle Beecher, George Iatropoulos
article en

Abstract

Introduction: Despite their benefit, current anti-EGFR therapies are limited by narrow efficacy profiles due to dose-limiting toxicities. This phase 2 open-label study evaluated the efficacy and safety of ABT-806, an EGFR-targeting antibody that is tumor specific, in patients with advanced EGFR-expressing tumors including head and neck cancers (H&NC) and squamous cell carcinoma (SCC) of other sites. Methods: Patients with advanced H&NC (cohort A) or SCC of other sites (cohort B) were enrolled in the study. ABT-806 was administered as monotherapy at a dose of 24 mg/kg intravenously using a twice weekly dosing schedule until unacceptable toxicity and/or evidence of disease progression. Adverse events (AEs) were graded using the National Cancer Institute Common Terminology Criteria for Adverse Events v4.0; tumor response was assessed using the Response Evaluation criteria in Solid Tumors v1.1. EGFR status was assessed with mAb806 and EGFRvIII immunohistochemistry and correlated with outcomes. Results: ABT-806 was well tolerated with no grade 3+ treatment-related AEs. Disease stabilization was observed in two patients (14%) and for a median duration of 19.5 weeks. This included one patient from cohort A and one patient from cohort B. Progression-free survival and overall survival was not significantly different between the two cohorts. Conclusions: Although clinical activity was limited in this small, heavily pre-treated, and biomarker-unselected population, ABT-806 demonstrated an excellent safety profile with minimal classical EGFR-related toxicity. These findings support the development of more tumor-specific EGFR antibodies for use, particularly in combinatorial regimens.

CancersVol. 18(20)
The University of Melbourne (AU), La Trobe University (AU), Austin Hospital (AU), AbbVie (United States) (US), Olivia Newton-John Cancer Wellness & Research Centre (AU), Austin Health (AU)
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Openalex Percentile: Top 18%
HER2/EGFR in Cancer Research
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