Rare cancers collectively account for ∼25% of all cancer diagnoses yet remain underserved due to limited biological understanding, a lack of preclinical models, and challenges associated with conducting clinical trials. Overcoming these barriers requires both the development of rare cancer research resources and new approaches for identifying therapeutic vulnerabilities from limited patient samples. This presentation will highlight how rare cancer biorepositories, patient-derived tumor models, large-scale polypharmacology datasets, and machine learning approaches can be integrated to accelerate therapeutic discovery and functional precision oncology. A rare cancer biorepository containing cryopreserved patient specimens, molecular profiling data, patient-derived microtumors, and xenograft models provides a foundation for studying tumor biology across diverse rare malignancies and generating clinically relevant experimental systems. To enable systematic therapeutic discovery, we developed KIRHub, a comprehensive functional atlas of FDA-approved kinase inhibitors and oncogenic kinase variants that supports characterization of kinase inhibitor polypharmacology, drug repurposing, and mechanism discovery. This approach identified Polo-like kinase 1 (PLK1) as a therapeutic vulnerability in fibrolamellar carcinoma, an ultra-rare liver cancer driven by the DNAJB1-PRKACA fusion, illustrating how functional and computational approaches can uncover actionable dependencies in rare cancers. Patient-derived microtumor models that preserve key features of the native tumor microenvironment further enable rapid ex vivo drug testing and identification of therapeutic vulnerabilities that may not be captured in conventional cancer cell lines. Building on these models, SmartMatch integrates microtumor screening with machine learning-based prediction of therapeutic response. By leveraging responses to a focused set of compounds, SmartMatch prioritizes treatment options across thousands of drugs while delivering clinically actionable results within seven days. Together, these examples demonstrate how experimental and computational modeling approaches can be combined to accelerate therapeutic discovery, identify actionable vulnerabilities, and expand treatment opportunities for patients with rare and treatment-refractory cancers.
Taran Gujral. Functional Precision Oncology in Rare Cancers: From Biobank to Drug Discovery [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Breaking Barriers in the Fight against Rare Cancers; 2026 Jul 18-20; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(14_Suppl):Abstract nr IA004.
Rare cancers collectively account for ∼25% of all cancer diagnoses, yet they remain disproportionately understudied due to limited patient numbers, biological heterogeneity, and a lack of robust preclinical models. This gap has constrained mechanistic understanding and slowed the development of effective therapies, leaving many patients with limited treatment options. To address these challenges, we established a living biobank of 247 rare tumor specimens with banked materials (e.g., RNA, DNA, FFPE tissue) and associated molecular data, including RNAseq profiles. The collection also includes 112 cryopreserved microtumor or tissue fragments and 11 patient-derived xenograft (PDX) models, complemented by integrated multi-omic datasets from over 1000 additional rare tumors curated from public repositories. Building on this foundation, we developed patient-derived microtumor cultures as a central functional platform. These three-dimensional tissues preserve native tumor architecture and key components of the tumor microenvironment (TME), including stromal and immune elements, enabling more physiologically relevant modeling than conventional systems. This approach bridges ex vivo and in vivo models, supporting rapid drug sensitivity testing, efficient generation of PDX models, and capturing therapeutic responses often missed in standard cell culture. Using this integrated platform, we have identified novel and potentially actionable therapeutic vulnerabilities across multiple rare cancers, including sensitivity to CDK4/6 inhibition in rare bladder cancer, PLK1 inhibition in fibrolamellar carcinoma, and synergistic targeting of MEK and YAP signaling in solitary fibrous tumors. Together, this combined biobanking and functional precision oncology framework provides a scalable and translationally relevant approach to accelerate therapeutic discovery and expand treatment opportunities for patients with rare cancers.
Songli Zhu, Joel Vaz, Deanna Mische, Marina Chan, Taran Gujral. A Living Biobank and Functional Precision Oncology Platform for Rare Cancers [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Breaking Barriers in the Fight against Rare Cancers; 2026 Jul 18-20; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(14_Suppl):Abstract nr B022.
Songli Zhu, Joel M Vaz, Deanna F Mische et al.· Cancer Research· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.