Cholangiocarcinoma originally referred to intrahepatic bile duct cancer. However, the term currently includes intrahepatic, perihilar, and extrahepatic tumors of the bile tract such as hepatobiliary tract cancer. The gallbladder and ampulla of Vater are considered structures of the biliary tract system hence malignancies of those parts are usually included in research and publications involving cholangiocarcinoma. Cholangiocarcinoma is a rare and highly lethal malignancy due to the locally advanced, unresectable stage at diagnosis. 
Chronic inflammation is associated with the risk of developing biliary tract cancer. The strongest correlation to develop cholangiocarcinoma is primary sclerosing cholangitis (PSC), a feature characteristic of inflammatory bowel disease, particularly ulcerative colitis. In addition, choledochal cyst, hepatolithiasis, and liver fluke are well-known risk factors for cholangiocarcinoma. Other associations for intrahepatic cholangiocarcinoma are a chronic liver disease such as cirrhosis due to hepatitis C virus (HCV), hepatitis B virus (HBV), metabolic syndrome, and alcoholic and non-alcoholic fatty liver disease. Thorotrast, a radiological contrast, was banned due to its carcinogenic potential with a strong association with cholangiocarcinoma. Cholangiocarcinoma has been described with Lynch syndrome and multiple biliary papillomatosis.
Although cholangiocarcinoma represents 3% of all gastrointestinal malignancies, the United State Cancer Statistics estimate 52,450 new cases and 32,750 expected death cases by grouping liver, intrahepatic bile duct, gallbladder, and other biliary cancer. Collectively, this represents 6% of all new cancer sites, making it the fifth deadliest cancer. Intrahepatic, perihilar, and distal biliary tract cancers divided by anatomical site account for 5% to 10%, 50% to 60%, and 20% to 30% of cases, respectively. Cholangiocarcinoma incidence increases with age except in cases related to primary sclerosing cholangitis which manifests in younger patients and is slightly more common in males, excluding gallbladder cancer which has a female predominance.
The current hypothesis establishes that chronic inflammation of the bile duct tissue will accumulate successive genomic mutations that over the years will lead to malignant transformation similar to other gastrointestinal cancers. Intraductal papillary neoplasm and intraepithelial neoplasia are well-known cholangiocarcinoma precursors, which may progress from pre-neoplastic to a carcinoma in situ and then into invasive cancer while progressively harboring mutations in p53, SMAD4, CDK2A tumor suppressors and/or oncogenes RAS, BRAF, EGFR, and PIK3CA. Cholangiocarcinoma histopathology is adenocarcinoma in more than 90% of cases and, infrequently, squamous cell carcinoma. Intrahepatic carcinomas also may have a biphenotypic differentiation called hepatocholangiocarcinoma. 
Bile duct obstruction symptoms include jaundice; abdominal pain, particularly in the right upper quadrant; clay-colored stools; cola-colored urine; and skin pruritus which are common presentations of extrahepatic cholangiocarcinoma. Patients can present with unspecific symptoms of advanced malignancy including fever, night sweats, weight loss, and general malaise. Acute cholangitis is a rare presentation. Intrahepatic cholangiocarcinoma may present differently with a more obscure scenario, such as an abnormal laboratory finding or a lesion detected incidentally on imaging in an otherwise asymptomatic patient during hepatocellular carcinoma (HCC) screening for liver disease.
Physical examination may demonstrate jaundice, right upper quadrant pain, hepatomegaly, or Courvoisier sign with a palpable non-tender gallbladder which is more likely to develop due to a chronic progressive malignant obstruction rather than an intermittent benign obstruction.
Patients, particularly those with obstructive jaundice or right upper quadrant pain, will require complete blood count, basic chemistry panel, and liver function tests. Results may reveal an initial, unspecific cholestatic pattern caused by bile obstruction that may lead to hepatocellular injury.
Ultrasonography (US) and CT are the usual initial imaging for jaundiced patients and provide information on the location and anatomy of the lesion. CT scans performed for intrahepatic lesions have limitations in discriminating benign from malignant lesions, but dynamic magnetic resonance (MR) and MR cholangiopancreatography can provide the disease extent more accurately and better distinguish intrahepatic cholangiocarcinoma from hepatocellular carcinoma and biphenotypic carcinomas. Obtaining either intrahepatic or perihilar tissue for diagnosis may be challenging. Endoscopic ultrasound or endoscopic retrograde cholangiopancreatography are preferred modalities for extrahepatic obstruction because it allows direct bile duct visualization, diagnostic biopsy, and therapeutic interventions such as stent placement. Primary sclerosing cholangitis-associated cholangiocarcinoma can be challenging.
Tumor markers including carcinoembryonic antigen, alpha-fetoprotein, and carbohydrate antigen 19-9 are frequently collected to differentiate suspicious intrahepatic lesions. Elevated alpha-fetoprotein (AFP) may support hepatocellular carcinoma particularly those with liver disease and CA 19-9 for cholangiocarcinoma in the appropriate clinical scenario. Biphenotypic carcinomas may show AFP elevation. Ca 19-9 greater than 129 unit/mL, CEA greater than 5.2 ng/mL, and low IgG4 can support a cholangiocarcinoma diagnosis, particularly in patients with primary sclerosing cholangitis. A tumor markers baseline test is potentially useful for therapy monitoring and surveillance for recurrence of the disease. CA 19-9 on concentrations of hundreds of unit/mL are consistent with advanced disease and poor prognosis.
Initial staging workup may include CT chest, abdomen, and pelvis if not previously obtained. If no metastatic disease is evident and the patient is being considered for surgical resection, occasionally positron emission tomography/CT can be ordered to evaluate for an occult disease which can prevent a morbid surgery. Surgical candidates will proceed with diagnostic laparoscopy before resection.
An American Joint Committee on Cancer and Union for International Cancer Control 2017 group separated the staging systems of cholangiocarcinoma depending on whether the location of the bile duct cancer is perihilar, distal, or intrahepatic. Each was differentiated on tumor size (T) designation and 5-year overall survival prognosis accordingly. On a multi-institutional analysis of intrahepatic cholangiocarcinoma, the 5-year survival rate was higher for those patients without multiple tumors or vascular invasion and nodal disease on surgical pathology specimen evaluation. 
Neoadjuvant therapy is not considered a standard of care in cholangiocarcinoma. Rarely, locally advanced or borderline resectable cases may receive neoadjuvant chemotherapy or chemoradiation therapy based on low-powered studies. Orthotopic liver transplantation has been studied in selected populations with inconclusive results. Neoadjuvant therapy should be offered in a clinical trial setting.
Surgery is the only curative treatment for selected patients. The surgical procedure differs according to the anatomical location. Distal lesions are treated with pancreaticoduodenectomy, the Whipple procedure. Intrahepatic lesions will require hepatectomy, and lymphadenectomy is rarely performed. For hilar lesions, surgical resection will vary according to the Bismuth-Corlette anatomical classification.
Postoperative therapy should be offered within 8 to 12 weeks and requires baseline laboratory and imaging before therapy initiation.
Adjuvant therapy should be offered to patients with a resected pathological specimen and a report of vascular invasion, node positivity, and positive margins, and preferably, concurrent adjuvant chemoradiation or adjuvant chemotherapy alone should be offered. There is limited clinical trial data to define the standard of care, and enrollment in a clinical trial is encouraged.
The National Comprehensive Cancer Network (NCCN) consensus-based adjuvant guidelines recommend the following:
Extrahepatic Cholangiocarcinoma with Negative Margins and Negative Nodes
Chemotherapy alone for 6 months with gemcitabine (gem) [1000 mg/m2 weekly for 3 of every 4 weeks] or fluoropyrimidine (5-FU) [leucovorin 20 mg/m2 followed by FU 425 mg/m2 intravenous [IV] bolus days 1 through 5, every 28 days] published in the ESPAC-3 Trial which enrolled 96 patients with bile duct cancer, and the median overall survival (mOS) for the chemotherapy group was 43.1 months versus 35.2 months in the observation group, albeit not statistically significant. Alternatively, 5-FU [225 mg/m2 daily]-based adjuvant chemoradiation from other gastrointestinal malignancy extrapolation data from rectal cancer experience. 
Extrahepatic Cholangiocarcinoma with Positive Margins, Invasive Disease, or Carcinoma in Situ at the Margin
Four cycles of Capecitabine (Cap) [1500 mg/m(2) per day on days 1 to 14] plus Gemcitabine (Gem) [1000 mg/m(2) intravenously on days 1 and 8], every 21 days followed by 5-FU CRT [Cap 1330 mg/m2 per day divided into two daily doses and RT 45 Gy to regional lymphatics; 54 to 59.4 Gy to tumor bed] published in a single arm SWOG-S0809 trial enrolled 54 bile duct cancer and showed a mOS of 35 months without a comparison group.
Intrahepatic Cholangiocarcinoma with Negative Disease
Consider re-resection, ablation, 5-FU or Gemcitabine chemotherapy or chemoradiation therapy discussion with a multidisciplinary team.
At ASCO 2017, BILCAP study was presented as first phase 3 randomized adjuvant therapy for patients with no postsurgical complications and Eastern Cooperative Oncological Group of two or less (ECOG less than 2), 447 patients were randomized 1:1 Cap N 223[1250 mg/m2 D1-14, every 21 days, for eight cycles] or observation (Obs) N224 from 44 UK sites 2006 through 2014, it included 19% Intrahepatic, 28% hilar, 35% extrahepatic bile duct cancer and results showed an mOS for Cap 53mo when compared to Obs 36mo (HR 0.75 p0.028). Cap soon will be adopted as the new standard of care.
Surveillance by NCCN recommendations includes imaging every 6 months for 2 years if clinically indicated, then annually up to 5 years. The oncologist may monitor patients closely with liver function test and tumor markers (CEA and CA19-9) every 3 to 4 months for 2 years, then every 6 months up to 5 years. All above-mentioned tests can be performed when clinically indicated.
No single or combined therapy in unresectable, locally advanced, and metastatic cholangiocarcinoma will achieve a cure; rather the focus is on palliative intervention and extension of survival. All patients with the advanced and unresectable disease should be offered a clinical trial when feasible. Patients with good performance status (ECOG 0-1) for chemotherapy could consider first-line option Gem [1000 mg/m2] plus Cisplatin (Cis) [25 mg/m2] on days one and eight every three weeks with acceptable toxicity in low dose cis as published in ABC-02 randomized phase 2 study which included 242 metastatic bile duct cancer patients and showed a mOS of 11.7 months in the combination arm when compared to 8.3 months of Gem alone (HR, 0.70; p0.002). Other first-line, gem-based combinations are not randomized studies and have reported a mOS for GemCap 12.7 months and Gem with Oxaliplatin 14.3 months both on a selected population of patients. Alternative 5-FU-based combination plus Cis 11.5 months or Cap 11.3 months. Patients with poor performance may receive oral Cap which reported a mOS of 8.1 months when compared to the best supportive care of 4.5 months. Future clinical trials with targeted therapy, including FGFR, MEK, and other drugs tailored per the tumor molecular profile, are ongoing and preliminary reports are promising. 
Bile duct carcinoma is very difficult to diagnose as it may present with similar symptoms to gallstones including obstructive symptoms such as jaundice; abdominal pain; clay-colored stools; cola-colored urine; and skin pruritus. Patients can also present with unspecific symptoms of advanced malignancy including fever, night sweats, weight loss, and general malaise. The healthcare team needs to be diligent in considering the possibility of this deadly form of cancer and always include it as a possibility when evaluating patients with presentations of gallbladder disease. an interprofessional team approach of nurses, pharmacists, and physicians will provide the best possible results. [Level V]
|||Cancer Statistics, 2017., Siegel RL,Miller KD,Jemal A,, CA: a cancer journal for clinicians, 2017 Jan [PubMed PMID: 28055103]|
|||Biliary tract cancers., de Groen PC,Gores GJ,LaRusso NF,Gunderson LL,Nagorney DM,, The New England journal of medicine, 1999 Oct 28 [PubMed PMID: 10536130]|
|||Chapman RW, Risk factors for biliary tract carcinogenesis. Annals of oncology : official journal of the European Society for Medical Oncology. 1999; [PubMed PMID: 10436847]|
|||Cholangiocarcinoma: recent progress. Part 1: epidemiology and etiology., Okuda K,Nakanuma Y,Miyazaki M,, Journal of gastroenterology and hepatology, 2002 Oct [PubMed PMID: 12201863]|
|||Biliary intraepithelial neoplasia: an international interobserver agreement study and proposal for diagnostic criteria., Zen Y,Adsay NV,Bardadin K,Colombari R,Ferrell L,Haga H,Hong SM,Hytiroglou P,Klöppel G,Lauwers GY,van Leeuwen DJ,Notohara K,Oshima K,Quaglia A,Sasaki M,Sessa F,Suriawinata A,Tsui W,Atomi Y,Nakanuma Y,, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2007 Jun [PubMed PMID: 17431410]|
|||Peripheral cholangiocarcinoma (cholangiocellular carcinoma): clinical features, diagnosis and treatment., Chen MF,, Journal of gastroenterology and hepatology, 1999 Dec [PubMed PMID: 10634149]|
|||Serum and bile markers for cholangiocarcinoma., Nehls O,Gregor M,Klump B,, Seminars in liver disease, 2004 May [PubMed PMID: 15192787]|
|||Intrahepatic cholangiocarcinoma: an international multi-institutional analysis of prognostic factors and lymph node assessment., de Jong MC,Nathan H,Sotiropoulos GC,Paul A,Alexandrescu S,Marques H,Pulitano C,Barroso E,Clary BM,Aldrighetti L,Ferrone CR,Zhu AX,Bauer TW,Walters DM,Gamblin TC,Nguyen KT,Turley R,Popescu I,Hubert C,Meyer S,Schulick RD,Choti MA,Gigot JF,Mentha G,Pawlik TM,, Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011 Aug 10 [PubMed PMID: 21730269]|
|||Biliary tract neoplasms: diagnosis and staging., Gore RM,Shelhamer RP,, Cancer imaging : the official publication of the International Cancer Imaging Society, 2007 Oct 1 [PubMed PMID: 17921093]|
|||Serum markers of intrahepatic cholangiocarcinoma., Malaguarnera G,Paladina I,Giordano M,Malaguarnera M,Bertino G,Berretta M,, Disease markers, 2013 [PubMed PMID: 23396291]|
|||Benson AB 3rd,D'Angelica MI,Abbott DE,Abrams TA,Alberts SR,Saenz DA,Are C,Brown DB,Chang DT,Covey AM,Hawkins W,Iyer R,Jacob R,Karachristos A,Kelley RK,Kim R,Palta M,Park JO,Sahai V,Schefter T,Schmidt C,Sicklick JK,Singh G,Sohal D,Stein S,Tian GG,Vauthey JN,Venook AP,Zhu AX,Hoffmann KG,Darlow S, NCCN Guidelines Insights: Hepatobiliary Cancers, Version 1.2017. Journal of the National Comprehensive Cancer Network : JNCCN. 2017 May; [PubMed PMID: 28476736]|
|||Cisplatin plus gemcitabine versus gemcitabine for biliary tract cancer., Valle J,Wasan H,Palmer DH,Cunningham D,Anthoney A,Maraveyas A,Madhusudan S,Iveson T,Hughes S,Pereira SP,Roughton M,Bridgewater J,, The New England journal of medicine, 2010 Apr 8 [PubMed PMID: 20375404]|
|||SWOG S0809: A Phase II Intergroup Trial of Adjuvant Capecitabine and Gemcitabine Followed by Radiotherapy and Concurrent Capecitabine in Extrahepatic Cholangiocarcinoma and Gallbladder Carcinoma., Ben-Josef E,Guthrie KA,El-Khoueiry AB,Corless CL,Zalupski MM,Lowy AM,Thomas CR Jr,Alberts SR,Dawson LA,Micetich KC,Thomas MB,Siegel AB,Blanke CD,, Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2015 Aug 20 [PubMed PMID: 25964250]|
|||Effect of adjuvant chemotherapy with fluorouracil plus folinic acid or gemcitabine vs observation on survival in patients with resected periampullary adenocarcinoma: the ESPAC-3 periampullary cancer randomized trial., Neoptolemos JP,Moore MJ,Cox TF,Valle JW,Palmer DH,McDonald AC,Carter R,Tebbutt NC,Dervenis C,Smith D,Glimelius B,Charnley RM,Lacaine F,Scarfe AG,Middleton MR,Anthoney A,Ghaneh P,Halloran CM,Lerch MM,Oláh A,Rawcliffe CL,Verbeke CS,Campbell F,Büchler MW,, JAMA, 2012 Jul 11 [PubMed PMID: 22782416]|