CFCF       

2012 E-Update Number 5

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In this Issue
2012 CFCF-AACR Grant Recipient
What's New in PNETs?
LX 1032 Receives Orphan Drug Status
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CFCF is pleased to announce that this E-Update is supported by Novartis Pharmaceuticals Corporation
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Survivor Story Photo  
 Sandra Becham
(submitted 3/26/12)
  
CFCF is honored to present Survivor Stories. They reflect remarkable courage and determination. Thank you to our Survivors for sharing their courage and words of hope with other patients.

Read our newest survivor stories:
Candye Kane, Pamela Ter Gast,
 Ivan StarrJoy Hasty
Give hope and a future to  neuroendocrine tumor patients: donate to CFCF where 100% of all individual donations go to carcinoid and related neuroendocrine tumor research.

CFCF is a 501(c)(3) organization-all contributions are tax-deductible.  We want our donors to know that we are allocating their donations responsibly and wisely to achieve a carcinoid cure as quickly as possible. 


To learn more, view CFCF's:
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IRS Form 990

Caring for Carcinoid Foundation
198 Tremont Street, Box 456
Boston, MA 02116
617.948.2514
www.caringforcarcinoid.org
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CFCF meets all 20 Wise Giving Alliance standards for charity accountability established by the Better Business Bureau. Click here to check out the CFCF Wise Giving Report.
Announcing 2012 CFCF-AACR Grant Recipient

Ron Hollander, Judy Garber, Renata Pasqualini

The Caring for Carcinoid Foundation is pleased to announce the newest research grant awarded through its partnership with the American Association for Cancer Research. This two-year grant of $250,000 ($125,000 per year) will support a research team headed by Renata Pasqualini, Ph.D., of the University of Texas MD Anderson Cancer Center. Dr. Pasqualini's collaborators include Wadih Arap, M.D., Ph.D, of MD Anderson and Steven K. Libutti, M.D., of Albert Einstein College of Medicine. The team will explore a new, targeted strategy for treating patients with pancreatic neuroendocrine tumors.

 

Specifically, Dr. Pasqualini and her team will develop components of a virus that will be designed to kill neuroendocrine cancer cells. The virus will be modified to attach to somatostatin receptors on pancreatic neuroendocrine tumor cells, limiting negative effects on healthy tissues. The researchers will then test the effectiveness of the virus in the lab and in mouse models.

 

In 2011, CFCF and the AACR awarded grants to two innovative studies. The first, from Charles Rudin, M.D., Ph.D., examines how the Seneca Valley Virus targets neuroendocrine tumor cells. Meanwhile, Xianxin Hua, M.D., Ph.D., is developing novel modalities useful for treating pancreatic neuroendocrine tumors. Dr. Hua was recently published in the prestigious journal, Nature.

 

"We are excited to welcome Dr. Renata Pasqualini into our expanding community of carcinoid and neuroendocrine cancer researchers," said CFCF Executive Director Ron Hollander. "CFCF's partnership with AACR is a critical component of our strategy to develop effective targeted therapies and eventual cures."

What's New in Pancreatic Neuroendocrine Tumors?
Medical Oncologist Dr. Diane Reidy-Lagunes recently published a review article in Current Oncology Reports focusing on treatment strategies for pancreatic and other neuroendocrine tumors (pNETs, NETs). The piece provides an overview of the commonly used treatments for pNETs and NETs, including liver-directed therapies, tumor growth-pathway-targeting drugs, and conventional chemotherapy regimens. Both traditional and newer therapies are discussed within each category, with a focus on "what's different" about the new innovative therapies currently in development.
 
Dr. Reidy stresses that seeking to identify particular biomarkers for pancreatic neuroendocrine tumors may be able to help clinicians decide which treatments are best for individual patients with neuroendocrine cancers. Click here to learn more about Dr. Reidy and her current CFCF-funded research project on Personalized Medicine for Neuroendocrine Cancer Patients.
LX 1032 Receives Orphan Drug Status

FDALexicon Pharmaceuticals has received orphan drug designation for LX1032 (telotristat etiprate) for the treatment of carcinoid syndrome. Telotristat etiprate is currently being developed under "Fast Track" status in the United States and Orphan Designation in the European Union.

  

Orphan Drug designation is granted by the Food and Drug Administration (FDA) to drugs intended for the treatment of rare diseases. This designation affords various incentives from the Federal Government, such as tax benefits and enhanced patent protection.

 

Telotristat etiprate was developed to inhibit serotonin production. Excessive levels of serotonin have been implicated in symptoms associated with carcinoid syndrome, especially diarrhea and carcinoid heart disease.

 

To learn more about clinical trials of telotristat etiprate and other treatments for carcinoid, please visit CFCF's Clinical Trials Finder.