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GUIDELINE FOR THE MANAGEMENT OF BILE DUCT CANCERS BY THE BRAZILIAN GASTROINTESTINAL TUMOR GROUP

ABSTRACT

The Brazilian Gastrointestinal Tumor Group developed guidelines for the surgical and clinical management of patients with billiary cancers. The multidisciplinary panel was composed of experts in the field of radiology, medical oncology, surgical oncology, radiotherapy, endoscopy and pathology. The panel utilized the most recent literature to develop a series of evidence-based recommendations on different treatment and diagnostic strategies for cholangiocarcinomas and gallbladder cancers.

HEADINGS
Bile duct neoplasms; Cholangiocarcinoma; Therapeutics; Practice guidelines as topic; Consensus

RESUMO

O Grupo Brasileiro de Tumores Gastrointestinais desenvolveu diretrizes de tratamento cirúrgico e clínico de pacientes com tumores de vias biliares. O painel multidisciplinar foi composto de especialistas nas áreas radiologia, oncologia, cirurgia, radioterapia, endoscopia e anatomia patológica. O painel utilizou literatura atual para desenvolver recomendações baseadas em evidência científica para as diferentes estratégias terapêuticas e diagnósticas dos colangiocarcinomas e tumores de vesícula biliar.

DESCRITORES
Neoplasias dos ductos biliares; Colangiocarcinoma; Terapêutica; Guias de prática clínica como assunto; Consenso

INTRODUCTION

Malignant neoplasms of the biliary tract include gallbladder cancer, intrahepatic and extrahepatic (proximal and distal) cholangiocarcinoma and cancer of the duodenal papilla (ampulla of Vater). They form a relatively rare group of tumors with an estimated 10,310 new cases of gallbladder cancer or cholangiocarcinoma in the United States in 201438Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA Cancer J Clin. 2014;64:9-29..

The disease is usually diagnosed only in its late stages after the onset of related symptoms because of the absence of established preventive and/or screening programs. This explains the high levels of mortality associated with biliary tract cancer38Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA Cancer J Clin. 2014;64:9-29..

OBJECTIVE

This report is an initiative of the Brazilian Gastrointestinal Tumors Group (GTG) to bring together the opinion of Brazilian experts based on their extensive discussion of the current scientific evidence of the diagnosis, staging and treatment of biliary tract cancers.

METHODS

This article sets out the considerations of Brazilian experts from various specialties, including radiology, pathology, gastroenterology, digestive surgery, cancer surgery, radiation and medical oncology. The panel included experts from several regions of Brazil. All topics for discussion were previously selected and distributed among the panel members. The presentations and voting of experts occurred during face to face meetings and conference calls. A search of the medical literature related to selected subjects was performed using MEDLINE (National Library of Medicine). The scientific evidence and recommendations were classified according to Figures 1 and 2. In the absence of sufficient evidence to build a clear conclusion, final recommendations were based on the majority of panel experts' opinion.

FIGURE 1
Level of evidence (LE) - CDC Grading System

FIGURE 2
Strength of recommendations (SR) - Classification system CDC

All discussions and recommendations considered the TNM Staging of the AJCC 7th edition from 2010.

What tests have a diagnostic role in malignant neoplasms of the biliary tract?

Definitive diagnosis of biliary tract cancer occurs preferably after surgery as a result of pathology tests. However, diagnosis is equally necessary in situations where no such procedure is indicated, for example, in the cases of advanced disease where surgery is not indicated.

Endoscopic retrograde cholangiopancreatography (ERCP)

ERCP allows diagnosis by collecting material (bile or brushed) for cytology or biopsy and has a role in diagnosing cholangiocarcinoma, and identifying patients ineligible for surgery. LE: II - SR: B.

Upper GI Endoscopy (UGIE)

Endoscopy with biopsy also has a diagnostic indication for malignancies of the duodenal papilla. LE: II - SR: A.

Endoscopic ultrasound (EUS)

EUS guided biopsy can be used for diagnosis, especially of distal cholangiocarcinoma and duodenal bulb cancer. The technique allows access to primary tumors and regional lymph nodes. LE: III - SR: B.

There is no indication for EUS guided biopsy in either hilar or intrahepatic cholangiocarcinoma LE: III - SR: D.

Cholangioscopy

Cholangioscopy may help visualize suspicious lesions and perform biopsies of the distal bile duct. However, patient access to this test remains limited to a few centers. LE: V, R: C.

Which imaging tests should be used for the staging of biliary tract cancers?

Patients with an incidental finding of gallbladder adenocarcinoma after laparoscopic examination and who have pathologic stage T1a with negative margins do not require investigation with imaging. From stage T1a pathologic stage investigation with imaging should be carried out. LE: III - SR: B.

Total abdomen magnetic resonance imaging (MRI) with contrast associated with magnetic resonance cholangiopancreatography (MRCP) is considered the gold standard for the staging of malignant neoplasms of the biliary tract - LE: II - SR: A.

In cases where abdominal MRI associated with CPRM is not available, a total abdominal computed tomography (CT) scan with contrast is indicated. LE: II - SR: A

The abdominal imaging test for staging purposes should occur prior to biliary tract drainage to prevent post-drainage alterations obstructing the neoplastic assessments.

Chest CT should also be added for staging - LE: V - SR: B.

The EUS, if available, may be useful in staging the primary tumor and regional lymph nodes, especially in cases of distal cholangiocarcinoma, gallbladder adenocarcinoma - LE: III - SR: B, and ampullary malignancies - LE: III - SR: C.

The value of PET-CT in staging is still uncertain and therefore optional if available - LE: III - SR: C.

Which tumor markers can be used in biliary tract cancer?

The assessment of tumor markers such as carcinoembryonic antigen (CEA) and Ca 19.9 can be useful in the diagnosis of biliary tract cancer and is considered optional - LE: IV - SR: C.

Tumor markers should be assessed carefully prior to surgery because cholestasis may overestimate levels.

Assessment of Ca 19.9 is indicated for prognosis and response - LE: IV- SR: B but CEA assessment is optional - LE: IV - SR: C.

Should laparoscopy be used routinely in the staging of cancer of the biliary tract?

Laparoscopy is optional in the staging of biliary tract cancer, but may be considered for patients with signs of locally advanced disease in order to exclude metastatic disease - LE: III - SR: C.

What is the role of ERCP in the palliative treatment of cholangiocarcinoma?

ERCP for palliative treatment is indicated, allowing the unblocking of an obstructed biliary tract by using metal or plastic prostheses - LE: I - SR: A.

What are the minimum elements that should be described in the pathology report of cancer of the biliary tract?

The surgical specimen must contain information regarding resected segments, as well as size and weight.

For the description of a tumor, the pathological report must contain:

location;

size;

number of tumors (with special attention to the intrahepatic colangicarcinoma);

the growth pattern (mass-forming type, infiltrative periductal or mixed);

histological type and subtype (adenocarcinoma intestinal type, pancreatobiliary or papillary);

differentiation (well differentiated, moderately differentiated, poorly differentiated or undifferentiated);

tumor extension;

surgical margins;

angiolymphatic invasion (whether present or absent);

perineural invasion (whether present or absent);

associated diseases (cirrhosis, cholangitis, hepatitis, gallstones and others), and

TNM staging.

Negative surgical margins should mention the shortest distance; when positive, it must report which margins. Attention should also be given to the component of the margin, if invasive or in situ. Negative surgical margins are considered those with more than 1 cm, or if microscopic, larger than 0.1 cm.

Immunohistochemistry (IHC) is important in differentiating cancer of biliary lesions from benign or metastatic lesions. ICH also allows the differentiation of adenocarcinoma of the duodenal papilla in intestinal or pancreaticobiliary subtypes. The ICH panel must contain the following markers: CK7, CK20, CDX2, CK19, CEA and Ca19.9.

The assessment of microsatellite instability (MLH1, MSH2, MSH6 and PMS2) and prognostic factors (MUC, ciclinaD1, P16, P53, pRb and others) is optional.

Proper macroscopic processing of the surgical specimen is essential for adequate evaluation of margins. One of the most difficult and important margins is in the pancreatic duct. For processing purposes, the distal end of the main pancreatic duct margin should be dyed by making cuts longitudinal to the main pancreatic duct, and collecting samples for histological study of the duct and the dyed side. Thus, evaluation of the margin and its distance to the tumor or ductal epithelial dysplasia are easily measured.

What are the principles of surgical oncology in cancer of the biliary tract?

Complete surgical resection with negative margins is the only potentially curative treatment for patients with localized cancer of the biliary tract.

Clipping to facilitate adjuvant radiotherapy is optional and must be conducted in institutions that adopt this adjuvant treatment as routine - LE: V - SR: C.

Embolization techniques to increase the residual liver segment may be used if necessary.

Laparoscopic surgery allows surgical staging, hepatectomy, lymphadenectomy, and production of liver jejunal anastomosis. Thus it is optional - LE: V - SR: C.

Incidental finding of gallbladder cancer

The diagnosis of gallbladder cancer, as an incidental finding in post cholecystectomy, with the pathological Tis or T1a, does not require additional surgery and the patient should only be monitored - LE: III - SR: B.

Patients with pathologic stage T1b should be reoperated with hepatectomy of segments IVb and V and radical lymphadenectomy in order to have clear margins - LE: IV - SR: A.

Resection of the biliary tract is not indicated if it is not affected - LE: IV - SR: D.

Restaging with imaging tests may be necessary before reoperation in cases of gallbladder cancer with incidental finding in order to avoid surgery in cases of advanced disease. Reoperation is indicated in these cases, if the patient has completed the initial diagnostic intervention within 6 months - LE: V - SR: B.

Gallbladder

A patient diagnosed with T1a gallbladder cancer should be treated only with cholecystectomy - LE: III - SR: B25Lee SE, Jang JY, Lim CS, Kang MJ, Kim SW. Systematic review on the surgical treatment for T1 gallbladder cancer.. World J Gastroenterol 2011;17:174-80..

For other stages that have the possibility of curative surgery, the optimal procedure consists of cholecystectomy with limited hepatectomy (segments IVb and V) and portal lymphadenectomy - LE: III - SR: A10Downing SR, Cadogan KA, Ortega G, Oyetunji TA, Siram SM, Chang DC, et al. Early-stage gallbladder cancer in the Surveillance, Epidemiology, and End Results database: effect of extended surgical resection. Arch Surg. 2011;146:734-8. 17Jensen EH, Abraham A, Habermann EB, Al-Refaie WB, Vickers SM, Virnig BA, et al. A critical analysis of the surgical management of early-stage gallbladder cancer in the United States.. J Gastrointest Surg 2009;13:722-7. 37Shirai Y, Sakata J, Wakai T, Ohashi T, Hatakeyama K. "Extended" radical cholecystectomy for gallbladder cancer: long-term outcomes, indications and limitations.. World J Gastroenterol 2012;18:4736-43..

Other liver segments and bile duct resection may be required to obtain negative margins.

Hilar cholangiocarcinoma

The standard procedure is radical surgical resection, including withdrawal of the extrahepatic biliary tract, extended en bloc hepatectomy, lymphadenectomy and reconstruction of the vascular and biliary tree aiming to obtain negative margins - LE: III - SR: B5Cheng QB, Yi B, Wang JH, Jiang XQ, Luo XJ, Liu C, et al. Resection with total caudate lobectomy confers survival benefit in hilar cholangiocarcinoma of Bismuth type III and IV. Eur J Surg Oncol. 2012;38:1197-203. 6Cho JY, Paik YH, Chang YS, Lee SJ, Lee DK, Song SY, et al. Capecitabine combined with gemcitabine (CapGem) as first-line treatment in patients with advanced/metastatic biliary tract carcinoma. Cancer. 2005;104:2753-8. 41VanGulik TM, Kloek JJ, Ruys AT, Busch OR, vanTienhoven GJ, Lameris JS, et al. Multidisciplinary management of hilar cholangiocarcinoma (Klatskin tumor): extended resection is associated with improved survival.. Eur J Surg Oncol 2011;37:65-71. 42Wu XS, Dong P, Gu J, Li ML, Wu WG, Lu JH, et al. Combined portal vein resection for hilar cholangiocarcinoma: a meta-analysis of comparative studies.. J Gastrointest Surg 2013;17:1107-15..

Distal cholangiocarcinoma

The indicated surgical procedure is pancreaticoduodenectomy, aiming to obtain negative margins - LE: III - SR: B27Nagorney DM, Donohue JH, Farnell MB, Schleck CD, Ilstrup DM. Outcomes after curative resections of cholangiocarcinoma.. Arch Surg 1993;128:871-7..

Ampulla of Vater

Whipple surgery is the treatment of choice in cases of cancer of the duodenal papilla with localized disease considered resectable - LE: IV - SR: B.

Intrahepatic cholangiocarcinoma

The standard surgery for patients with intrahepatic cholangiocarcinoma is hepatectomy obtaining negative margins - LE: III - SR: B22Konstadoulakis MM, Roayaie S, Gomatos IP, Labow D, Fiel MI, Miller CM, et al. Fifteen-year, single-center experience with the surgical management of intrahepatic cholangiocarcinoma: operative results and long-term outcome. Surgery. 2008;143:366-74. 24Lang H, Sotiropoulos GC, Sgourakis G, Schmitz KJ, Paul A, Hilgard P, et al. Operations for intrahepatic cholangiocarcinoma: single-institution experience of 158 patients. J Am Coll Surg. 2009;208: 218-28. 33Ribero D, Pinna AD, Guglielmi A, Ponti A, Nuzzo G, Giulini SM, et al. Italian Intrahepatic Cholangiocarcinoma Study Group. Surgical Approach for Long-term Survival of Patients With Intrahepatic Cholangiocarcinoma: A Multi-institutional Analysis of 434 Patients.. Arch Surg 2012;147:1107-13.. Portal lymphadenectomy should be considered - LE: IV - SR: C7Clark CJ, Wood-Wentz CM, Reid-Lombardo KM, Kendrick ML, Huebner M, Que FG. Lymphadenectomy in the staging and treatment of intrahepatic cholangiocarcinoma: a population-based study using the National Cancer Institute SEER database. HPB (Oxford). 2011;13:612-20. 36Shimada M, Yamashita Y, Aishima S, Shirabe K, Takenaka K, Sugimachi K. Value of lymph node dissection during resection of intrahepatic cholangiocarcinoma. Br J Surg. 2001;88:1463-6..

Liver transplantation

Liver transplantation is indicated for hilar cholangiocarcinoma, although few centers worldwide would perform this procedure in this disease. Selected cases of hilar cholangiocarcinoma may be considered for liver transplantation if they meet the following criteria: localized disease, preferably sclerosing cholangitis with malignancy and negative lymph nodes - LE: IV - SR: B. In Brazil, this procedure is not yet approved for this indication by the Ministry of Health3Becker NS, Rodriguez JA, Barshes NR, O'Mahony CA, Goss JA, Aloia TA. Outcomes analysis for 280 patients with cholangiocarcinoma treated with liver transplantation over an 18-year period. J Gastrointest Surg. 2008;12:117-22. 8Darwish Murad S, Kim WR, Harnois DM, Douglas DD, Burton J, et al. Efficacy of neoadjuvant chemoradiation, followed by liver transplantation, for perihilar cholangiocarcinoma at 12 US centers. Gastroenterology. 2012;143:88-98. 12Duignan S, Maguire D, Ravichand CS, Geoghegan J, Hoti E, Fennelly D, et al. Neoadjuvant chemoradiotherapy followed by liver transplantation for unresectable cholangiocarcinoma: a single-centre national experience.. HPB (Oxford) 2014;16:91-8. 15Hong JC, Jones CM, Duffy JP, Petrowsky H, Farmer DG, French S, et al. Comparative analysis of resection and liver transplantation for intrahepatic and hilar cholangiocarcinoma: a 24-year experience in a single center.. Arch Surg 2011;146:683-9. 18Kaiser GM, Sotiropoulos GC, Jauch KW, Löhe F, Hirner A, Kalff JC, et al. Liver transplantation for hilar cholangiocarcinoma: a German survey. Transplant Proc. 2008;40:3191-3. 32Rea DJ, Heimbach JK, Rosen CB, Haddock MG, Alberts SR, Kremers WK, et al. Liver transplantation with neoadjuvant chemoradiation is more effective than resection for hilar cholangiocarcinoma. Ann Surg. 2005;242:451-8..

Adjuvant treatment

Adjuvant studies in biliary tract cancer are mostly based on small numbers of patients, retrospective, and involving heterogeneous populations which report conflicting results. However, due to the high risk of recurrence after surgery, patients diagnosed with cancer of the biliary tract may be considered for adjuvant treatment with chemotherapy and/or radiotherapy4Cereda S, Belli C, Reni M. Adjuvant treatment in biliary tract cancer: to treat or not to treat? World J Gastroenterol. 2012;18:2591-6.. LE: IV - SR: C.

Adjuvant treatment can be offered both for patients with positive surgical margins - LE: IV - SR: B and for patients with negative surgical margins - LE: IV - SR: C.

If used, chemotherapy and radiotherapy should be based on fluoropyrimidines. Adjuvant chemotherapy should use platinum-based regimens and gemcitabine (accepted due to extrapolation of metastatic disease).

Adjuvant chemotherapy with 5-fluorouracil (5FU) and radiotherapy has been shown to improve survival in a retrospective study conducted by the Mayo Clinic14Gold DG, Miller RC, Haddock MG, Gunderson LL, Quevedo F, Donohue JH, et al. Adjuvant therapy for gallbladder carcinoma: the Mayo Clinic Experience. Int J Radiat Oncol Biol Phys. 2009;75:150-5. .

A case-control study conducted in Korea with120 patients, offered chemotherapy combined with radiotherapy followed by chemotherapy or chemotherapy associated with isolated radiotherapy. The chemotherapy of choice was the 5FU. The progression-free survival (PFS) at 3 years was 26.6% versus 45.2% (P=0:04) and overall survival (OS) at 3 years was 30.8 versus 62.6 (P<0.01), with benefit for the group of chemotherapy associated with radiotherapy followed by chemotherapy26Lim KH, Oh DY, Chie EK, Jang JY, Im SA, Kim TY, et al. Adjuvant concurrent chemoradiation therapy (CCRT) alone versus CCRT followed by adjuvant chemotherapy: which is better in patients with radically resected extrahepatic biliary tract cancer?: a non-randomized, single center study. BMC Cancer. 2009;9:345..

The recent series of MDACC with 157 operated patients with gallbladder or cholangiocarcinoma cancer and free microscopic margins of cancer, showed no benefit in overall survival at 5 years in patients that received adjuvant chemotherapy or chemoradiotherapy13Glazer ES, Liu P, Abdalla EK, Vauthey JN, Curley SA. Neither neoadjuvant nor adjuvant therapy increases survival after biliary tract cancer resection with wide negative margins.. J Gastrointest Surg 2012;16:1666-71..

A phase III study conducted in Japan randomized 508 patients diagnosed with pancreatic or biliary tract cancer (cholangiocarcinoma 139 and 140 gallbladder cancer) surgically treated for adjuvant chemotherapy treatment with 5FU and mitomycin or observation. Subgroup analysis of patients with gallbladder cancer showed 26% overall survival at 5 years in the adjuvant chemotherapy group versus 14.4% for the observation group (P=0.0367), and 20.3% of PFS at 5 years in the chemotherapy group versus 11.6% in the control group (P=0.021)39Takada T, Amano H, Yasuda H, Nimura Y, Matsushiro T, Kato H, et al. Study Group of Surgical Adjuvant Therapy for Carcinomas of the Pancreas and Biliary Tract. Is postoperative adjuvant chemotherapy useful for gallbladder carcinoma? A phase III multicenter prospective randomized controlled trial in patients with resected pancreaticobiliary carcinoma. Cancer. 2002;95:1685-95.. This benefit was statistically significant only in patients with non-curative resection (positive margins). There was no benefit for adjuvant treatment in this study in other tumor sites (pancreas, ampulla of Vater and biliary duct).

A meta-analysis of published data, with 4915 patients treated with surgery alone versus 1797 treated with surgery followed by adjuvant treatment (chemotherapy and/or radiotherapy), suggested survival gain with adjuvant treatment (HR 0.74P 0:06)16Horgan AM, Amir E, Walter T, Knox JJ. Adjuvant therapy in the treatment of biliary tract cancer: a systematic review and meta-analysis. J Clin Oncol. 2012;30:1934-40.. Treatment with chemotherapy or chemoradiotherapy was better than adjuvant radiotherapy alone. The greatest benefits related to adjuvant therapy occurred in patients with margins or positive lymph nodes16Horgan AM, Amir E, Walter T, Knox JJ. Adjuvant therapy in the treatment of biliary tract cancer: a systematic review and meta-analysis. J Clin Oncol. 2012;30:1934-40..

For patients with tumors of the ampulla of Vater, the phase III study ESPAC-330Neoptolemos JP, Moore MJ, Cox TF, Valle JW, Palmer DH, McDonald AC, et al. European Study Group for Pancreatic Cancer. 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. JAMA. 2012;308:147-56. showed no significant gain in survival with the addition of adjuvant chemotherapy with 5FU and leucovorin (Lv) or gemcitabine.

What is the best systemic treatment in the first line for metastatic cancer of the biliary tract?

The first-line treatment for metastatic biliary tract cancer should be cisplatin and gemcitabine - LE: I - SR: A.

The replacement of cisplatin with oxaliplatin in combination with gemcitabine is a valid option - LE I-SR: C35Sharma A, Dwary AD, Mohanti BK, Deo SV, Pal S, Sreenivas V, et al. Best supportive care compared with chemotherapy for unresectable gall bladder cancer: a randomized controlled study.. J Clin Oncol 2010;28:4581-6..

In subsequent therapeutic lines, if the patients' performance allows, chemotherapy with fluoropirirmidinas, taxanes or irinotecan can be used - LE: III - SR: C (there was no consensus among the members of this multidisciplinary panel).

The use of targeted therapy in this setting is not indicated, except in the context of investigational protocols - LE: II - SR: E.

There are several phase II studies with different chemotherapy protocols, but with heterogeneous groups and limited numbers of patients1Alberts SR, Al-Khatib H, Mahoney MR, Burgart L, Cera PJ, Flynn PJ, et al. Gemcitabine, 5-fluorouracil, and leucovorin in advanced biliary tract and gallbladder carcinoma: a North Central Cancer Treatment Group phase II trial. Cancer. 2005;103:111-8. 2André T, Reyes-Vidal JM, Fartoux L, Ross P, Leslie M, Rosmorduc O, et al. Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study. Br J Cancer. 2008;99:862-7. 6Cho JY, Paik YH, Chang YS, Lee SJ, Lee DK, Song SY, et al. Capecitabine combined with gemcitabine (CapGem) as first-line treatment in patients with advanced/metastatic biliary tract carcinoma. Cancer. 2005;104:2753-8. 9Doval DC, Sekhon JS, Gupta SK, Fuloria J, Shukla VK, Gupta S, et al. A phase II study of gemcitabine and cisplatin in chemotherapy-naive, unresectable gall bladder cancer.. Br J Cancer 2004;90:1516-20. 11Ducreux M, Van Cutsem E, Van Laethem JL, Gress TM, Jeziorski K, Rougier P, et al. EORTC Gastro Intestinal Tract Cancer Group. A randomised phase II trial of weekly high-dose 5-fluorouracil with and without folinic acid and cisplatin in patients with advanced biliary tract carcinoma: results of the 40955 EORTC trial. Eur J Cancer. 2005;41:398-403. 19Kim HJ, Lee NS, Lee SC, Bae SB, Kim CK, Cheon YG, et al. A phase II study of gemcitabine in combination with oxaliplatin as first-line chemotherapy in patients with inoperable biliary tract cancer. Cancer Chemother Pharmacol. 2009;64:371-7. 20Kim TW, Chang HM, Kang HJ, Lee JR, Ryu MH, Ahn JH, et al. Phase II study of capecitabine plus cisplatin as first-line chemotherapy in advanced biliary cancer. Ann Oncol. 2003;14:1115-20. 21Knox JJ, Hedley D, Oza A, Feld R, Siu LL, Chen E, et al. Combining gemcitabine and capecitabine in patients with advanced biliary cancer: a phase II trial.. J Clin Oncol 2005;23:2332-8. 23Kornek GV, Schuell B, Laengle F, Gruenberger T, Penz M, Karall K, et al. Mitomycin C in combination with capecitabine or biweekly high-dose gemcitabine in patients with advanced biliary tract cancer: a randomised phase II trial.. Ann Oncol 2004;15:478-83. 28Nehls O, Klump B, Arkenau HT, Hass HG, Greschniok A, Gregor M, et al. Oxaliplatin, fluorouracil and leucovorin for advanced biliary system adenocarcinomas: a prospective phase II trial.. Br J Cancer 2002;87:702-4. 29Nehls O, Oettle H, Hartmann JT, Hofheinz RD, Hass HG, Horger MS, et al. Capecitabine plus oxaliplatin as first-line treatment in patients with advanced biliary system adenocarcinoma: a prospective multicentre phase II trial.. Br J Cancer 2008;98:309-15. 31Okusaka T, Nakachi K, Fukutomi A, Mizuno N, Ohkawa S, Funakoshi A, et al. Gemcitabine alone or in combination with cisplatin in patients with biliary tract cancer: a comparative multicentre study in Japan.. Br J Cancer 2010;103:469-74. 32Rea DJ, Heimbach JK, Rosen CB, Haddock MG, Alberts SR, Kremers WK, et al. Liver transplantation with neoadjuvant chemoradiation is more effective than resection for hilar cholangiocarcinoma. Ann Surg. 2005;242:451-8. 34Riechelmann RP, Townsley CA, Chin SN, Pond GR, Knox JJ. Expanded phase II trial of gemcitabine and capecitabine for advanced biliary cancer. Cancer. 2007;110: 1307-12. 35Sharma A, Dwary AD, Mohanti BK, Deo SV, Pal S, Sreenivas V, et al. Best supportive care compared with chemotherapy for unresectable gall bladder cancer: a randomized controlled study.. J Clin Oncol 2010;28:4581-6..

A study published in 2010 randomized patients with gallbladder adenocarcinoma in groups of palliative supportive care, chemotherapy with 5FU combined with leucovorin or gemcitabine associated with oxaliplatin (GEMOX). The group receiving chemotherapy with the GEMOX scheme had better overall survival (4.5 versus 4.6 versus 9.5 months respectively P=0.039)35Sharma A, Dwary AD, Mohanti BK, Deo SV, Pal S, Sreenivas V, et al. Best supportive care compared with chemotherapy for unresectable gall bladder cancer: a randomized controlled study.. J Clin Oncol 2010;28:4581-6..

The landmark ABC-02 phase III trial randomized 410 patients with inoperable biliary tract cancer to receive systemic treatment with gemcitabine with or without cisplatin. There was a benefit in overall survival favoring multidrug therapy (HR 0.64 - 8.1 vs 11.7 months P<0.001)40Valle J, Wasan H, Palmer DH, Cunningham D, Anthoney A, Maraveyas A, et al. ABC-02 Trial Investigators. Cisplatin plus gemcitabine versus gemcitabine for biliary tract cancer. N Engl J Med. 2010;362:1273-81..

Follow up after treatment with curative intent

Follow up should be clinical history and physical examination every 6 months for 2 years - LE: V - SR: B.

Performing abdominal imaging studies (CT or MRI) every 6 months for 2 years, and tumor markers CEA and CA19.9 with the same frequency are optional - LE: V - SR: C.

CONCLUSION

Malignant neoplasms of the biliary tract comprise a spectrum of different tumors with particular characteristics. The oncologic management of this entity should be based on the multidisciplinary assessment and on existing scientific evidence.

REFERENCES

  • Alberts SR, Al-Khatib H, Mahoney MR, Burgart L, Cera PJ, Flynn PJ, et al. Gemcitabine, 5-fluorouracil, and leucovorin in advanced biliary tract and gallbladder carcinoma: a North Central Cancer Treatment Group phase II trial. Cancer. 2005;103:111-8.
  • André T, Reyes-Vidal JM, Fartoux L, Ross P, Leslie M, Rosmorduc O, et al. Gemcitabine and oxaliplatin in advanced biliary tract carcinoma: a phase II study. Br J Cancer. 2008;99:862-7.
  • Becker NS, Rodriguez JA, Barshes NR, O'Mahony CA, Goss JA, Aloia TA. Outcomes analysis for 280 patients with cholangiocarcinoma treated with liver transplantation over an 18-year period. J Gastrointest Surg. 2008;12:117-22.
  • Cereda S, Belli C, Reni M. Adjuvant treatment in biliary tract cancer: to treat or not to treat? World J Gastroenterol. 2012;18:2591-6.
  • Cheng QB, Yi B, Wang JH, Jiang XQ, Luo XJ, Liu C, et al. Resection with total caudate lobectomy confers survival benefit in hilar cholangiocarcinoma of Bismuth type III and IV. Eur J Surg Oncol. 2012;38:1197-203.
  • Cho JY, Paik YH, Chang YS, Lee SJ, Lee DK, Song SY, et al. Capecitabine combined with gemcitabine (CapGem) as first-line treatment in patients with advanced/metastatic biliary tract carcinoma. Cancer. 2005;104:2753-8.
  • Clark CJ, Wood-Wentz CM, Reid-Lombardo KM, Kendrick ML, Huebner M, Que FG. Lymphadenectomy in the staging and treatment of intrahepatic cholangiocarcinoma: a population-based study using the National Cancer Institute SEER database. HPB (Oxford). 2011;13:612-20.
  • Darwish Murad S, Kim WR, Harnois DM, Douglas DD, Burton J, et al. Efficacy of neoadjuvant chemoradiation, followed by liver transplantation, for perihilar cholangiocarcinoma at 12 US centers. Gastroenterology. 2012;143:88-98.
  • Doval DC, Sekhon JS, Gupta SK, Fuloria J, Shukla VK, Gupta S, et al. A phase II study of gemcitabine and cisplatin in chemotherapy-naive, unresectable gall bladder cancer.. Br J Cancer 2004;90:1516-20.
  • Downing SR, Cadogan KA, Ortega G, Oyetunji TA, Siram SM, Chang DC, et al. Early-stage gallbladder cancer in the Surveillance, Epidemiology, and End Results database: effect of extended surgical resection. Arch Surg. 2011;146:734-8.
  • Ducreux M, Van Cutsem E, Van Laethem JL, Gress TM, Jeziorski K, Rougier P, et al. EORTC Gastro Intestinal Tract Cancer Group. A randomised phase II trial of weekly high-dose 5-fluorouracil with and without folinic acid and cisplatin in patients with advanced biliary tract carcinoma: results of the 40955 EORTC trial. Eur J Cancer. 2005;41:398-403.
  • Duignan S, Maguire D, Ravichand CS, Geoghegan J, Hoti E, Fennelly D, et al. Neoadjuvant chemoradiotherapy followed by liver transplantation for unresectable cholangiocarcinoma: a single-centre national experience.. HPB (Oxford) 2014;16:91-8.
  • Glazer ES, Liu P, Abdalla EK, Vauthey JN, Curley SA. Neither neoadjuvant nor adjuvant therapy increases survival after biliary tract cancer resection with wide negative margins.. J Gastrointest Surg 2012;16:1666-71.
  • Gold DG, Miller RC, Haddock MG, Gunderson LL, Quevedo F, Donohue JH, et al. Adjuvant therapy for gallbladder carcinoma: the Mayo Clinic Experience. Int J Radiat Oncol Biol Phys. 2009;75:150-5.
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    Disclosure of funding: no funding received

Publication Dates

  • Publication in this collection
    Jan-Mar 2016

History

  • Received
    18 June 2015
  • Accepted
    22 Sept 2015
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