Targeting Epidermal Growth Factor Receptor (EGFR) and Human Epidermal Growth Factor Receptor 2 (HER2) Expressing

Mohammad R Siddiqui1,2, Reema Railkar1, Thomas Sanford1

  • 1Urologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD - 20892, USA.

Scientific Reports
|February 16, 2019
PubMed

Insights

This study introduces a combination photoimmunotherapy (PIT) approach for bladder cancer (BC) targeting both EGFR and HER2. This combinatorial therapy shows improved efficacy over single-target treatments, offering a promising strategy for heterogeneous BC.

Area of Science:

  • Oncology
  • Immunotherapy
  • Biotechnology

Background:

  • Bladder cancer (BC) is molecularly heterogeneous, expressing diverse cell surface targets.
  • Photoimmunotherapy (PIT) utilizes antibody-photoabsorber conjugates activated by near-infrared light (NIR) for targeted tumor destruction.
  • Current PIT efficacy may be limited in tumors with low or heterogeneous target expression.

Purpose of the Study:

  • To evaluate a combinatorial PIT strategy for bladder cancer targeting both EGFR and HER2.
  • To assess the efficacy of combining panitumumab-IR700 and trastuzumab-IR700 in preclinical models of BC.
  • To investigate the potential of dual-receptor targeting for overcoming limitations of single-target PIT.

Main Methods:

  • Analysis of EGFR and HER2 expression in human BC tissues and cell lines.
  • In vitro efficacy assessment of single and combination PA-labeled MAb treatments with NIR activation.
  • In vivo evaluation of combination PIT efficacy in BC tumor xenografts.

Main Results:

  • Approximately 45% of BC tissues co-expressed EGFR and HER2.
  • Combination therapy (panitumumab-IR700 + trastuzumab-IR700 + NIR) demonstrated superior in vitro efficacy compared to individual agents.
  • Combination PIT significantly inhibited tumor growth in xenograft models.

Conclusions:

  • Combinatorial PIT targeting EGFR and HER2 is effective for bladder cancer, particularly in tumors with low or moderate receptor expression.
  • Dual-receptor targeting enhances cell death and offers a more robust therapeutic approach for molecularly diverse bladder tumors.
  • This strategy holds promise for improving treatment outcomes in heterogeneous bladder cancer.

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