CURE: The Rare Cancer Initiative

CURE: The Rare Cancer Initiative will bring new hope to cancer patients.

Case Comprehensive Cancer Center's Rare Cancer Initiative is a comprehensive, innovative effort that will transform rare cancer research and save lives around the world.

The Jedi Rare Cancer Foundation has committed to raise $5 Million over 5 years for Case Comprehensive Cancer Centers’s CURE: The Rare Cancer Initiative, a comprehensive, innovative effort that will transform rare cancer research and save lives around the world.

CURE Breaking News (9/29/2023)

Better together:
Vision meets opportunity

While each CURE collaborator is capable of impressive scientific achievement on its own, the Case CCC is built upon a belief that together everyone can achieve more. CURE will allow unprecedented understanding and targeting of rare cancers using groundbreaking scientific approaches developed by Dr. Schwartz and his collaborators to:

Bring rare cancer research to scale through a dedicated network of tissue sample biobanks.
Generate and analyze data to identify druggable targets in rare cancers, using machine learning and AI when applicable.
Partner across the consortium to create avatar cell models of specific cancers to advance testing and understanding.
Develop clinical trials, giving new hope to patients and families facing a rare cancer diagnosis and catalyzing new research to enhance effectiveness.

Innovative perspective, novel approach

CURE and Case CCC Director Dr. Schwartz’s groundbreaking science are built on the understanding that tumors are complex ecosystems composed of not only cancer cells, but also “healthy” cells that can be co-opted by cancer to fuel its growth, or immune cells that actively attempt to kill cancer cells. Within each of the cellular compartments of a tumor, there exists further heterogeneity, such that cancer cells differ among each other, and immune cells have varying functions and cell-to-cell interactions. Novel cutting-edge technologies, called single-cell genomics, enable deep molecular characterization of tens of thousands of cells, one cell at a time, thus providing the required resolution to dissect the complex tumor ecosystem. Linking single-cell genomics analyses with drug predictions and response data offers a unique opportunity for informing therapies in patients.

Philanthropic support: a critical resource

The Jed Ian Taxel Foundation for Rare Cancer Research is the key supporter of this effort and will serve as the primary foundation among several foundations the consortium hopes to engage. Additional philanthropic support is critical for transforming CURE from concept to reality and collecting vitally important early-stage research results that will position it for large-scale funding from the National Institutes of Health, National Cancer Institute and more, which will accelerate our progress toward our ultimate and shared goal of lifesaving cures.

More healthy survivors, less family heartbreak.

Your generous donation has the power to save lives.

Together, we will END rare cancer.

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Subscribe to our e-News Updates

Learn about lifesaving rare cancer research, foundation news, events, and discoveries that make a real, measurable difference in the lives of rare cancer patients and their families.