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Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics
Published on: May 11, 2016
5T4-Targeted Therapy Ablates Cancer Stem Cells and Prevents Recurrence of Head and Neck Squamous Cell Carcinoma
Samuel A Kerk1, Kelsey A Finkel1, Alexander T Pearson1,2,3
1Department of Cariology, Restorative Sciences, Endodontics, University of Michigan School of Dentistry, Ann Arbor, Michigan.
Abstract:
Purpose: Locoregional recurrence is a frequent treatment outcome for patients with advanced head and neck squamous cell carcinoma (HNSCC). Emerging evidence suggests that tumor recurrence is mediated by a small subpopulation of uniquely tumorigenic cells, that is, cancer stem cells (CSC), that are resistant to conventional chemotherapy, endowed with self-renewal and multipotency.Experimental Design: Here, we evaluated the efficacy of MEDI0641, a novel antibody-drug conjugate targeted to 5T4 and carrying a DNA-damaging "payload" (pyrrolobenzodiazepine) in preclinical models of HNSCC.Results: Analysis of a tissue microarray containing 77 HNSCC with follow-up of up to 12 years revealed that patients with 5T4high tumors displayed lower overall survival than those with 5T4low tumors (P = 0.038). 5T4 is more highly expressed in head and neck CSC (ALDHhighCD44high) than in control cells (non-CSC). Treatment with MEDI0641 caused a significant reduction in the CSC fraction in HNSCC cells (UM-SCC-11B, UM-SCC-22B) in vitro Notably, a single intravenous dose of 1 mg/kg MEDI0641 caused long-lasting tumor regression in three patient-derived xenograft (PDX) models of HNSCC. MEDI0641 ablated CSC in the PDX-SCC-M0 model, reduced it by five-fold in the PDX-SCC-M1, and two-fold in the PDX-SCC-M11 model. Importantly, mice (n = 12) treated with neoadjuvant, single administration of MEDI0641 prior to surgical tumor removal showed no recurrence for more than 200 days, whereas the control group had 7 recurrences (in 12 mice; P = 0.0047).Conclusions: Collectively, these findings demonstrate that an anti-5T4 antibody-drug conjugate reduces the fraction of CSCs and prevents local recurrence and suggest a novel therapeutic approach for patients with HNSCC. Clin Cancer Res; 23(10); 2516-27. ©2016 AACR.
Insights
This study shows that MEDI0641, an antibody-drug conjugate targeting 5T4, effectively reduces cancer stem cells (CSCs) in head and neck squamous cell carcinoma (HNSCC). This approach prevents tumor recurrence, offering a new therapeutic strategy for HNSCC patients.
Area of Science:
- Oncology
- Cancer Biology
- Drug Development
Background:
- Locoregional recurrence is common in advanced head and neck squamous cell carcinoma (HNSCC).
- Cancer stem cells (CSCs) are implicated in tumor recurrence due to their resistance to chemotherapy and self-renewal capabilities.
- The 5T4 antigen is a potential therapeutic target in HNSCC.
Purpose of the Study:
- To evaluate the efficacy of MEDI0641, an antibody-drug conjugate targeting 5T4, in preclinical models of HNSCC.
- To determine if MEDI0641 can reduce the cancer stem cell (CSC) fraction in HNSCC.
- To assess the potential of MEDI0641 in preventing tumor recurrence.
Main Methods:
- Analysis of 77 HNSCC patient samples for 5T4 expression and correlation with overall survival.
- In vitro assessment of MEDI0641's effect on CSC fraction in HNSCC cell lines.
- In vivo evaluation of MEDI0641 in patient-derived xenograft (PDX) models of HNSCC, including neoadjuvant treatment prior to surgery.
Main Results:
- Patients with high 5T4 expression had significantly lower overall survival.
- MEDI0641 treatment significantly reduced the CSC fraction in HNSCC cells in vitro.
- A single dose of MEDI0641 induced long-lasting tumor regression in HNSCC PDX models and significantly prevented tumor recurrence after surgical resection.
Conclusions:
- The anti-5T4 antibody-drug conjugate MEDI0641 effectively reduces CSCs in HNSCC.
- MEDI0641 demonstrates potential in preventing local recurrence of HNSCC.
- Targeting 5T4 with antibody-drug conjugates represents a promising novel therapeutic strategy for HNSCC.
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