Cholangiocarcinoma natural history, complications and prognosis: Difference between revisions
Jump to navigation
Jump to search
Farima Kahe (talk | contribs) |
Farima Kahe (talk | contribs) |
||
| Line 14: | Line 14: | ||
===Prognosis=== | ===Prognosis=== | ||
The most important factor in prognosis of cholangiocarcinoma is whether or not the tumor is able to be resected. Even with resection, prognosis is poor with 5-year survival of only 10-44%.<ref name=radio>Cholangiocarcinoma. Radiopaedia. http://radiopaedia.org/articles/cholangiocarcinoma</ref> The [[prognosis]] may be worse for patients with [[primary sclerosing cholangitis]] who develop cholangiocarcinoma, likely because the cancer is not detected until it is advanced.<ref>{{cite journal |author=Kaya M, de Groen P, Angulo P, Nagorney D, Gunderson L, Gores G, Haddock M, Lindor K |title=Treatment of cholangiocarcinoma complicating primary sclerosing cholangitis: the Mayo Clinic experience |journal=Am J Gastroenterol |volume=96 |issue=4 |pages=1164–9 |year=2001 |pmid=11316165}}</ref> Some evidence suggests that outcomes may be improving with more aggressive surgical approaches and [[adjuvant#oncology|adjuvant therapy]].<ref>{{cite journal |author=Nakeeb A, Tran K, Black M, Erickson B, Ritch P, Quebbeman E, Wilson S, Demeure M, Rilling W, Dua K, Pitt H |title=Improved survival in resected biliary malignancies |journal=Surgery |volume=132 |issue=4 |pages=555–63; discission 563-4 |year=2002 |pmid=12407338}}</ref> Surgical resection offers the only potential chance of cure in cholangiocarcinoma. | The most important factor in prognosis of cholangiocarcinoma is whether or not the tumor is able to be resected. Even with resection, prognosis is poor with 5-year survival of only 10-44%.<ref name=radio>Cholangiocarcinoma. Radiopaedia. http://radiopaedia.org/articles/cholangiocarcinoma</ref> The [[prognosis]] may be worse for patients with [[primary sclerosing cholangitis]] who develop cholangiocarcinoma, likely because the cancer is not detected until it is advanced.<ref>{{cite journal |author=Kaya M, de Groen P, Angulo P, Nagorney D, Gunderson L, Gores G, Haddock M, Lindor K |title=Treatment of cholangiocarcinoma complicating primary sclerosing cholangitis: the Mayo Clinic experience |journal=Am J Gastroenterol |volume=96 |issue=4 |pages=1164–9 |year=2001 |pmid=11316165}}</ref> Some evidence suggests that outcomes may be improving with more aggressive surgical approaches and [[adjuvant#oncology|adjuvant therapy]].<ref>{{cite journal |author=Nakeeb A, Tran K, Black M, Erickson B, Ritch P, Quebbeman E, Wilson S, Demeure M, Rilling W, Dua K, Pitt H |title=Improved survival in resected biliary malignancies |journal=Surgery |volume=132 |issue=4 |pages=555–63; discission 563-4 |year=2002 |pmid=12407338}}</ref> Surgical resection offers the only potential chance of cure in cholangiocarcinoma. | ||
*Depending on the extent of the cholangiocarcinoma at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor. | |||
===Extent of the tumor=== | ===Extent of the tumor=== | ||
Revision as of 15:28, 5 February 2018
|
Cholangiocarcinoma Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Cholangiocarcinoma natural history, complications and prognosis On the Web |
|
American Roentgen Ray Society Images of Cholangiocarcinoma natural history, complications and prognosis |
|
FDA on Cholangiocarcinoma natural history, complications and prognosis |
|
CDC on Cholangiocarcinoma natural history, complications and prognosis |
|
Cholangiocarcinoma natural history, complications and prognosis in the news |
|
Blogs on Cholangiocarcinoma natural history, complications and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Suveenkrishna Pothuru, M.B,B.S. [2]
Overview
Common complications of cholangiocarcinoma include infection, liver failure, and tumor metastasis. Prognosis is generally poor, and the survival rate of patients with cholangiocarcinoma mainly depends on extent of the tumor and resectability. Even with resection, prognosis is poor with 5-year survival of only 10-44%.[1] The presence of primary sclerosing cholangitis is associated with a particularly poor prognosis among patients with cholangiocarcinoma.
Complications
Common complications of cholangiocarcinoma include:
Prognosis
The most important factor in prognosis of cholangiocarcinoma is whether or not the tumor is able to be resected. Even with resection, prognosis is poor with 5-year survival of only 10-44%.[1] The prognosis may be worse for patients with primary sclerosing cholangitis who develop cholangiocarcinoma, likely because the cancer is not detected until it is advanced.[2] Some evidence suggests that outcomes may be improving with more aggressive surgical approaches and adjuvant therapy.[3] Surgical resection offers the only potential chance of cure in cholangiocarcinoma.
- Depending on the extent of the cholangiocarcinoma at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor.
Extent of the tumor
- Prognosis is somewhat better for people with early stage cancer than for people with advanced stage cancer.
- Patients with multiple tumors, larger tumors and tumors that have spread to nearby blood vessels or lymph nodes tend to have a poor outcome.
Resectability
Tumors that can be completely removed by surgery (resectable) have a more favorable prognosis than tumors that cannot be removed by surgery (unresectable). Palliative chemotherapy, radiotherapy, and photodynamic therapy have been relatively ineffective in treating non-operable cholangiocarcinomas, with a 5 yr survival <5% without resection, due to the refractoriness of these tumors:[4]
- Distal cholangiocarcinomas (those arising from the common bile duct) are generally treated with a Whipple procedure. Long-term survival rates range from 15%–25%, although one series reported a five year survival of 54% for patients with no involvement of the lymph nodes.[5]
- Intrahepatic cholangiocarcinomas (those arising from the bile ducts within the liver) are usually treated with partial hepatectomy. Various series have reported survival estimates after surgery ranging from 22%–66%. The outcome may depend on involvement of lymph nodes and completeness of the surgery.[6]
- Perihilar cholangiocarcinomas (those occurring near where the bile ducts exit the liver) are least likely to be operable. When surgery is possible, they are generally treated with an aggressive approach often including cholecystectomy and potentially part of the liver. In patients with operable perihilar tumors, reported 5 yr survival rates range from 20%–50%.[7]
Surgical margins
- The best prognostic factors are resection of tumor-free surgical margin without lymph node invasion, while tumor diameter, histology, and differentiation are poor predictors of good outcome with 5-year survival rates varying from 20 to 60%.[4]
- The 5 yr survival for resection of tumor-free surgical margins of extrahepatic cholangiocarcinomas is about 30%, with recurrence observed in the majority of patients due to disseminated tumors or the de novo formation of tumors in the already oncogenic liver tissue.
Liver transplantation performed after neoadjuvant chemoradiation in selected patients, due to organ shortage, has afforded a very good disease-free 5-year survival (>80%), providing a better outcome and fewer recurrences than conventional resection.
References
- ↑ 1.0 1.1 Cholangiocarcinoma. Radiopaedia. http://radiopaedia.org/articles/cholangiocarcinoma
- ↑ Kaya M, de Groen P, Angulo P, Nagorney D, Gunderson L, Gores G, Haddock M, Lindor K (2001). "Treatment of cholangiocarcinoma complicating primary sclerosing cholangitis: the Mayo Clinic experience". Am J Gastroenterol. 96 (4): 1164–9. PMID 11316165.
- ↑ Nakeeb A, Tran K, Black M, Erickson B, Ritch P, Quebbeman E, Wilson S, Demeure M, Rilling W, Dua K, Pitt H (2002). "Improved survival in resected biliary malignancies". Surgery. 132 (4): 555–63, discission 563-4. PMID 12407338.
- ↑ 4.0 4.1 Macias, Rocio I. R. (2014). "Cholangiocarcinoma: Biology, Clinical Management, and Pharmacological Perspectives". ISRN Hepatology. 2014: 1–13. doi:10.1155/2014/828074. ISSN 2314-4041.
- ↑ Studies of surgical outcomes in distal cholangiocarcinoma include:
- Nakeeb A, Pitt H, Sohn T, Coleman J, Abrams R, Piantadosi S, Hruban R, Lillemoe K, Yeo C, Cameron J (1996). "Cholangiocarcinoma. A spectrum of intrahepatic, perihilar, and distal tumors". Ann Surg. 224 (4): 463–73, discussion 473-5. PMID 8857851.
- Nagorney D, Donohue J, Farnell M, Schleck C, Ilstrup D (1993). "Outcomes after curative resections of cholangiocarcinoma". Arch Surg. 128 (8): 871–7, discussion 877-9. PMID 8393652.
- Jang J, Kim S, Park D, Ahn Y, Yoon Y, Choi M, Suh K, Lee K, Park Y (2005). "Actual long-term outcome of extrahepatic bile duct cancer after surgical resection". Ann Surg. 241 (1): 77–84. PMID 15621994.
- Bortolasi L, Burgart L, Tsiotos G, Luque-De León E, Sarr M (2000). "Adenocarcinoma of the distal bile duct. A clinicopathologic outcome analysis after curative resection". Dig Surg. 17 (1): 36–41. PMID 10720830.
- Fong Y, Blumgart L, Lin E, Fortner J, Brennan M (1996). "Outcome of treatment for distal bile duct cancer". Br J Surg. 83 (12): 1712–5. PMID 9038548.
- ↑ Studies of outcome in intrahepatic cholangiocarcinoma include:
- Nakeeb A, Pitt H, Sohn T, Coleman J, Abrams R, Piantadosi S, Hruban R, Lillemoe K, Yeo C, Cameron J (1996). "Cholangiocarcinoma. A spectrum of intrahepatic, perihilar, and distal tumors". Ann Surg. 224 (4): 463–73, discussion 473-5. PMID 8857851.
- Lieser M, Barry M, Rowland C, Ilstrup D, Nagorney D (1998). "Surgical management of intrahepatic cholangiocarcinoma: a 31-year experience". J Hepatobiliary Pancreat Surg. 5 (1): 41–7. PMID 9683753.
- Valverde A, Bonhomme N, Farges O, Sauvanet A, Flejou J, Belghiti J (1999). "Resection of intrahepatic cholangiocarcinoma: a Western experience". J Hepatobiliary Pancreat Surg. 6 (2): 122–7. PMID 10398898.
- Nakagohri T, Asano T, Kinoshita H, Kenmochi T, Urashima T, Miura F, Ochiai T (2003). "Aggressive surgical resection for hilar-invasive and peripheral intrahepatic cholangiocarcinoma". World J Surg. 27 (3): 289–93. PMID 12607053.
- Weber S, Jarnagin W, Klimstra D, DeMatteo R, Fong Y, Blumgart L (2001). "Intrahepatic cholangiocarcinoma: resectability, recurrence pattern, and outcomes". J Am Coll Surg. 193 (4): 384–91. PMID 11584966.
- ↑ Estimates of survival after surgery for perihilar cholangiocarcinoma include:
- Burke E, Jarnagin W, Hochwald S, Pisters P, Fong Y, Blumgart L (1998). "Hilar Cholangiocarcinoma: patterns of spread, the importance of hepatic resection for curative operation, and a presurgical clinical staging system". Ann Surg. 228 (3): 385–94. PMID 9742921.
- Tsao J, Nimura Y, Kamiya J, Hayakawa N, Kondo S, Nagino M, Miyachi M, Kanai M, Uesaka K, Oda K, Rossi R, Braasch J, Dugan J (2000). "Management of hilar cholangiocarcinoma: comparison of an American and a Japanese experience". Ann Surg. 232 (2): 166–74. PMID 10903592.
- Chamberlain R, Blumgart L. "Hilar cholangiocarcinoma: a review and commentary". Ann Surg Oncol. 7 (1): 55–66. PMID 10674450.
- Washburn W, Lewis W, Jenkins R (1995). "Aggressive surgical resection for cholangiocarcinoma". Arch Surg. 130 (3): 270–6. PMID 7534059.
- Nagino M, Nimura Y, Kamiya J, Kanai M, Uesaka K, Hayakawa N, Yamamoto H, Kondo S, Nishio H. "Segmental liver resections for hilar cholangiocarcinoma". Hepatogastroenterology. 45 (19): 7–13. PMID 9496478.
- Rea D, Munoz-Juarez M, Farnell M, Donohue J, Que F, Crownhart B, Larson D, Nagorney D (2004). "Major hepatic resection for hilar cholangiocarcinoma: analysis of 46 patients". Arch Surg. 139 (5): 514–23, discussion 523-5. PMID 15136352.
- Launois B, Reding R, Lebeau G, Buard J (2000). "Surgery for hilar cholangiocarcinoma: French experience in a collective survey of 552 extrahepatic bile duct cancers". J Hepatobiliary Pancreat Surg. 7 (2): 128–34. PMID 10982604.