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| | HR0716 | | LRB101 20252 MST 69792 r |
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| 1 | | HOUSE RESOLUTION
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| 2 | | WHEREAS, Cholangiocarcinoma (bile duct cancer) is a rare |
| 3 | | form of cancer that originates
from the cells lining the bile |
| 4 | | ducts that play a key role in digestion; there are three types, |
| 5 | | Intrahepatic,
extrahepatic, and perihilar; and
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| 6 | | WHEREAS, There are approximately 12,000 Americans |
| 7 | | diagnosed each year in the United States, with numbers
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| 8 | | increasing yearly; the mortality rate has increased |
| 9 | | dramatically in the last decade; and
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| 10 | | WHEREAS, Patients are typically diagnosed at a late stage |
| 11 | | due to no validated early method of detection; symptoms of |
| 12 | | jaundice, abdominal pain, itchy skin, and weight loss are |
| 13 | | symptoms that do not usually present till
advanced disease |
| 14 | | progression; and
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| 15 | | WHEREAS, Cholangiocarcinoma is a rare cancer; of the top |
| 16 | | eight deadliest cancers, seven are rare; rare cancers
have a |
| 17 | | five-year survival rate under 50%, with the cholangiocarcinoma |
| 18 | | five-year survival rate being approximately
20%; and |
| 19 | | WHEREAS, There is currently no cure for |
| 20 | | cholangiocarcinoma/bile duct cancer; and |