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Creating Matched In vivo/In vitro Patient-Derived Model Pairs of PDX and PDX-Derived Organoids for Cancer Pharmacology Research
Published on: May 5, 2021
Establishment of a Large-Scale PDX Library of Head and Neck Cancers for Functional Precision Oncology
Hisano Yanagi1,2, Tomoki Kuki3, Tetsuya Takimoto2
1Department of Medical Oncology, Fujita Health University School of Medicine, Toyoake, Japan.
Background:
Precision oncology leverages the molecular and genetic characteristics of tumors to enable accurate diagnosis and effective treatment selection. However, recent clinical trials have highlighted the limitations of current approaches and underscored the need to integrate static molecular profiling with functional analyses using patient-derived xenograft (PDX) models-particularly for cancers such as head and neck cancer (HNC), where driver mutations are rare and prognosis remains poor.
Methods:
Here, we aimed to establish a large-scale PDX library for HNC, termed the Fujita Xenograft Library (FXeL), annotated with detailed clinical information. Since 2022, tumor specimens from over 100 surgical cases at Fujita Health University Hospital have been transplanted into immunodeficient mice, resulting in the successful establishment of 62 PDX models.
Results:
Advanced clinical stage was significantly associated with successful engraftment, and serial passaging led to progressively accelerated tumor growth. Comparative analyses of genomic profiles between patient tumors and PDXs demonstrated that major cancer-related mutations were largely preserved in PDXs, while clonal selection and evolution occurred during engraftment. Histopathological features, including keratinization and nuclear atypia, were retained, whereas stromal components such as cancer-associated fibroblasts exhibited compositional shifts. Furthermore, drug sensitivity assays revealed that PDX responses to cisplatin (CDDP) closely mirrored the clinical outcomes of the corresponding patients.
Conclusions:
The FXeL represents a robust and scalable platform for investigating HNC biology and therapeutic response. Despite limitations such as stromal remodeling and the absence of an immune microenvironment, these models provide valuable translational insights and support the advancement of functional precision oncology.
Insights
A new patient-derived xenograft (PDX) library for head and neck cancer (HNC) models was established, showing preserved mutations and mirroring patient drug responses for precision oncology. This FXeL platform aids HNC research and treatment development.
Area of Science:
- Oncology
- Genomics
- Translational Research
Background:
- Precision oncology aims to tailor treatments based on tumor molecular profiles.
- Current methods face limitations, especially for head and neck cancer (HNC), necessitating integrated functional analyses.
- Patient-derived xenograft (PDX) models offer a platform for functional studies.
Purpose of the Study:
- To establish a comprehensive patient-derived xenograft (PDX) library for head and neck cancer (HNC).
- To annotate the Fujita Xenograft Library (FXeL) with detailed clinical data.
- To evaluate the utility of PDX models for HNC research and therapeutic development.
Main Methods:
- Tumor specimens from over 100 surgical HNC cases were used to create PDX models.
- Successful engraftment was correlated with advanced clinical stage.
- Genomic, histopathological, and drug sensitivity analyses were performed on established PDX models.
Main Results:
- 62 PDX models were successfully established, with accelerated tumor growth upon serial passaging.
- PDX models largely preserved major cancer-related mutations but showed clonal evolution.
- Histopathological features were retained, while stromal composition shifted; drug sensitivity assays (cisplatin) correlated with patient outcomes.
Conclusions:
- The Fujita Xenograft Library (FXeL) provides a scalable platform for HNC research.
- PDX models offer valuable translational insights despite limitations like stromal remodeling and lack of immune microenvironment.
- FXeL supports the advancement of functional precision oncology for HNC.
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