Intrahepatic cholangiocarcinoma in a transplant liver - selective internal radiation therapy followed by right hemihepatectomy: report of a case
© Sperling et al.; licensee BioMed Central Ltd. 2014
Received: 18 February 2014
Accepted: 12 June 2014
Published: 1 July 2014
Intra- or extrahepatic cholangiocarcinomas are the second most common primary liver malignancies behind hepatocellular carcinoma. Whereas the incidence for intrahepatic cholangiocarcinoma is rising, the occurrence of extrahepatic cholangiocarcinoma is trending downwards. The treatment of choice for intrahepatic cholangiocarcinoma remains liver resection. However, a case of liver resection after selective internal radiation therapy in order to treat a recurrent intrahepatic cholangiocarcinoma in a transplant liver is unknown in the literature so far. Herein, we present a case of a patient undergoing liver transplantation for Wilson’s disease with an accidental finding of an intrahepatic cholangiocarcinoma within the explanted liver. Due to a recurrent intrahepatic cholangiocarcinoma after liver transplantation, a selective internal radiation therapy with yttrium-90 microspheres was performed followed by right hemihepatectomy. Four years later, the patient is tumor-free and in a healthy condition.
KeywordsLiver transplantation Liver resection Intrahepatic cholangiocarcinoma Selective internal radiation therapy
Patients suffering from unresectable intrahepatic cholangiocarcinoma have an overall poor prognosis as demonstrated by a median survival of about three months in untreated patients . In the present case, the patient developed a recurrent intrahepatic cholangiocarcinoma (ICC) in a transplant liver that was initially classified as unresectable. Possible treatment modalities for unresectable ICC are systemic chemotherapy, loco-regional therapies and best supportive care . In selected patients and specialized centers, a neoadjuvant chemotherapy followed by liver transplantation is also feasible . At present, systemic chemotherapy may be seen as the treatment of choice for unresectable ICC . However, a standardized treatment strategy for patients with unresectable ICC has not yet been established. According to the recently updated and published guidelines for the management of ICC, loco-regional therapies can be considered as treatment options in such instances . Selective internal radiation therapy (SIRT) represents a promising loco-regional therapeutic modality for ICC although there are only few data on this issue and no randomized controlled trials until now [6–11]. However, the patient was treated with SIRT and showed good radiological response. In consequence, right hemihepatectomy was performed. Four years later, the patient is tumor free and in a healthy condition with sufficient liver function. The present case report describes the clinical course of the patient in detail and reviews the literature on the management of ICC with SIRT.
A 55-year-old patient with liver cirrhosis due to Wilson’s disease developed a tumor in segment VI of the liver. Whereas ultrasound-guided biopsy was not effective to achieve a definitive histological diagnosis, the tumor was highly suggestive of a hepatocellular carcinoma (HCC) on computed tomography (CT) and magnetic resonance imaging (MRI). The alpha-fetoprotein serum level was 13.5 IU/ml. The labMELD was 14. The tumor diameter was 18 mm. According to our department standards, HCC was the suspected diagnosis. This was in line with the diagnostic algorithm recently updated and published in the practice guidelines of the AASLD (American Association for the Study of Liver Diseases) .
At the time of the suspected diagnosis, the patients Child-Pugh Score was B. Due to the limited liver function combined with a restricted general condition, (ECOG (Eastern Cooperative Oncology Group) Performance Status: 1 to 2), we refrained from a surgical resection. Thus, in line with the BCLC (Barcelona Clinic Liver Cancer classification), the patient was considered for liver transplantation. Moreover, we decided to perform a transarterial chemoembolization (TACE) as a bridging therapy for tumor control. Therefore, the patient underwent four cycles of doxorubicin-based TACE resulting in a stable disease for one year. According to the Milan criteria, the patient was subsequently listed for liver transplantation (LTx).
Six months later, one and a half years after the initial tumor diagnosis, the patient underwent orthotopic LTx using a venovenous axillofemoral bypass. Initial immunosuppression consisted of cyclosporine, azathioprine and steroids. The peri- and postoperative course was uneventful and the patient was discharged from the hospital on the 15th postoperative day. The tumor in the explanted liver measured 17 × 15 × 14 mm. Surprisingly, the pathological result revealed an ICC (pT1, pN0, GII, R0) instead of the assumed HCC. Two lymph nodes next to the bile duct were free of malignancy. One month after LTx, the patient was admitted to the clinic with a complete fascial dehiscence requiring emergency surgical revision with direct suture. Immunosuppression was converted to tacrolimus monotherapy.
This case report is of interest for hepato-biliary and liver transplant surgeons, as it describes the first case of SIRT prior to right hemihepatectomy to treat an ICC within a transplant liver.
Intra- or extrahepatic cholangiocarcinomas are the second most common primary liver malignancies behind HCC . They are relatively rare, although with a rising incidence worldwide . In detail, several international studies have shown that the incidence of ICC is rising, whereas the occurrence of extrahepatic cholangiocarcinoma (ECC) is trending downwards . In case of an ICC, surgical resection remains the only therapy that offers long-term survival or even cure . However, due to bilobular tumor involvement or concomitant liver disease, curative surgery is feasible in only a few patients . In contrast to HCC, for which LTx or TACE are validated treatment options, little evidence of effective alternatives to liver resection exist in the literature for ICCs . TACE is not recommended for this type of tumor as ICCs are mainly fibrotic as well as non-hypervascular and, therefore, not the ideal target for this treatment modality. However, in the present case the tumor was primarily treated with four cycles of TACE assuming a HCC within the cirrhotic liver. Due to a limited liver function we decided against tumor resection. Although resection can be performed in patients with advanced liver disease, mortality is probably higher and patients might be better served by liver transplantation or ablation . However, we do not perform a radiofrequency ablation but TACE. This therapy form was chosen for tumor control in terms of a bridging therapy until liver transplantation. Of interest, the tumor remained stable for one year.
Whereas LTx is well established for HCC  it is far from being a well accepted indication for ICC or ECC. Regarding ECC, there are, beside careful patient selection, well defined neoadjuvant protocols prior to LTx which have led to encouraging results for this tumor entity [18–23]. However, the role of LTx in the management of ICC still remains controversial because of organ shortage, disease recurrence and the risk of accelerating tumor progression under immunosuppression after transplantation . Farges et al. even claim that there are only two exceptions where LTx for ICC lead to good results: first, LTx for very small ICCs that have been mistaken for HCC (like in our case) or incidentally discovered ICC within the explanted liver , and second, ECC from second order biliary branches, which can be viewed as ICC and treated by an aggressive neoadjuvant regimen . However, the key determinant identified for a promising outcome is a low tumor stage [24, 25]. ICCs with lymph node metastasis, vascular or bile duct invasion remain contraindications for LTx .
In the present case, the patient underwent LTx with an ICC in segment VI that was mistakenly diagnosed as HCC. Our patient developed recurrent disease four years after LTx, which is considered to be a very long time period of tumor free survival. The recurrent tumor was initially considered to be unresectable. Systemic chemotherapy may be seen as the treatment of choice in such instances with, however, palliative intent . To date, a treatment strategy for these patients has not been standardized. Beside systemic chemotherapy, loco-regional therapies can be performed in patients suffering from non-resectable disease . At present there are no established first-line loco-regional therapeutic options for patients with unresectable ICC .
SIRT is a radioembolization procedure which is considered to be an effective liver-directed therapy with a favorable therapeutic ratio that offers meaningful benefits for selected patients [26, 27]. SIRT is able to improve survival after intrahepatic recurrence of ICC . Of interest, the antitumor effect of SIRT is rather related to radiation than to embolization . Thereby, it provides a low toxicity profile and is able to deliver extremely high doses up to small target volumes while sparing the surrounding liver tissue . It remains debatable if the clinical situation in the present case is comparable to a recurrent ICC in a non-transplanted liver. However, after discussing the case in our interdisciplinary tumor board meetings, we decided to treat the patient with SIRT assuming that he was in an overall non-curative situation. SIRT can be conducted to downsize the intrahepatic tumor mass, because it is known that the use of yttrium-90 microspheres is useful for this purpose and might make the surgical resection easier . In the present case, SIRT led to relevant tumor necrosis as demonstrated by good radiological response. Thus, we decided to offer the patient surgical resection. However, due to relevant fibrosis combined with radiation-associated alteration induced by SIRT, right hemihepatectomy was needed while initially a limited resection may have been possible. To the best of our knowledge no similar case has been reported in the literature so far.
Another important issue in dealing with liver resection in a transplant liver is immunosuppression. The mTOR (mammalian target of rapamycin)-inhibitor rapamycin is known to inhibit tumor growth in vitro and in vivo[31–34]. Therefore, this drug provides the advantage of combining immunosuppression with anticancer therapy. The most important side effect of rapamycin is its negative influence on wound healing caused by its antiangiogenetic component . In the present case, the rapamycin-induced-immunosuppression was switched back to tacrolimus two weeks before liver resection to facilitate wound healing.
Nevertheless, the patient developed a biliary fistula combined with fascial necrosis. It may be that these complications might have been preventable if the mTOR-inhibitor had been stopped earlier. From our experiences it could, therefore, be recommended for repeated surgery in LTx-patients under mTOR-inhibition, that immunosuppression should be switched to tacrolimus or cyclosporine at least four weeks before surgery. After complete wound healing, the immunosuppression could then be reverted to mTOR-inhibition.
In addition, abdominal wall hernia is one of the most common surgical problems after LTx with an incidence ranging between 4.6 and 23% [36, 37]. Hernia repair with synthetic mesh graft showed good results, although these grafts have a high risk of infection leading to postoperative wound healing complications [38, 39]. In the present case, we successfully used a Permacol™ implant for the infected hernia side classified grade 3 to 4 according to the Ventral Hernia Working Group .
In conclusion, we demonstrated for the first time a multimodal treatment approach for ICC, including LTx for the primary ICC and SIRT prior to liver resection for recurrent/de novo ICC, with encouraging results. Furthermore, we were able to show that an abdominal wall hernia in an infected hernia site after LTx can be successfully repaired with a Permacol® biologic implant.
Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
American Association for the Study of Liver Diseases
Barcelona Clinic Liver Cancer classification
Eastern Cooperative Oncology Group
magnetic resonance imaging
mammalian target of rapamycin
selective internal radiation therapy
- Park J, Kim MH, Kim KP, Park do H, Moon SH, Song TJ, Eum J, Lee SS, Seo DW, Lee SK: Natural history and prognostic factors of advanced cholangiocarcinoma without surgery, chemotherapy, or radiotherapy: a large-scale observational study. Gut Liver. 2009, 3: 298-305.PubMed CentralView ArticlePubMed
- Kim YI, Park JW, Kim BH, Woo SM, Kim TH, Koh YH, Lee WJ, Kim CM: Outcomes of concurrent chemoradiotherapy versus chemotherapy alone for advanced-stage unresectable intrahepatic cholangiocarcinoma. Radiat Oncol. 2013, 21 (8): 292-298.View Article
- Rana A, Hong JC: Orthotopic liver transplantation in combination with neoadjuvant therapy: a new paradigm in the treatment of unresectable intrahepatic cholangiocarcinoma. Curr Opin Gastroenterol. 2012, 28 (3): 258-265.View ArticlePubMed
- Pracht M, Le Roux G, Sulpice L, Mesbah H, Manfredi S, Audrain O, Boudjema K, Raoul JL, Boucher E: Chemotherapy for inoperable advanced or metastatic cholangiocarcinoma: retrospective analysis of 78 cases in a single center over four years. Chemotherapy. 2012, 58 (2): 134-141.View ArticlePubMed
- Bridgewater J, Galle PR, Khan SA, Llovet JM, Park JW, Patel T, Pawlik TM, Gores GJ: Guidelines for the diagnosis and management of intrahepatic cholangiocarcinoma. J Hepatol. 2014, epub ahead of print
- Ibrahim SM, Mulcahy MF, Lewandowski RJ, Sato KT, Ryu RK, Masterson EJ, Newman SB, Benson A, Omary RA, Salem R: Treatment of unresectable cholangiocarcinoma using yttrium-90 microspheres: results from a pilot study. Cancer. 2008, 113 (8): 2119-2128.View ArticlePubMed
- Saxena A, Bester L, Chua TC, Chu FC, Morris DL: Yttrium-90 radiotherapy for unresectable intrahepatic cholangiocarcinoma: a preliminary assessment of this novel treatment option. Ann Surg Oncol. 2010, 17 (2): 484-491.View ArticlePubMed
- Wijlemans JW, Van Erpecum KJ, Lam MG, Seinstra BA, Smits ML, Zonnenberg BA, Van Den Bosch MA: Trans-arterial (90) yttrium radioembolization for patients with unresectable tumors originating from the biliary tree. Ann Hepatol. 2011, 10 (3): 349-354.PubMed
- Rafi S, Piduru SM, El-Rayes B, Kauh JS, Kooby DA, Sarmiento JM, Kim HS: Yttrium-90 radioembolization for unresectable standard-chemorefractory intrahepatic cholangiocarcinoma: survival, efficacy, and safety study. Cardiovasc Intervent Radiol. 2013, 36 (2): 440-448.View ArticlePubMed
- Sulpice L, Rayar M, Boucher E, Pracht M, Meunier B, Boudjema K: Treatment of recurrent intrahepatic cholangiocarcinoma. Br J Surg. 2012, 99 (12): 1711-1717.View ArticlePubMed
- Hyder O, Marsh JW, Salem R, Petre EN, Kalva S, Liapi E, Cosgrove D, Neal D, Kamel I, Zhu AX, Sofocleous CT, Geschwind JF, Pawlik TM: Intra-arterial therapy for advanced intrahepatic cholangiocarcinoma: a multi-institutional analysis. Ann Surg Oncol. 2013, 20 (12): 3779-3786.View ArticlePubMed
- Bruix J, Sherman M, American Association for the Study of Liver Diseases: Management of hepatocellular carcinoma: an update. Hepatology. 2011, 53 (3): 1020-1022.PubMed CentralView ArticlePubMed
- Petrowsky H, Hong JC: Current surgical management of hilar and intrahepatic cholangiocarcinoma: the role of resection and orthotopic liver transplantation. Transplant Proc. 2009, 41 (10): 4023-4035.View ArticlePubMed
- Aljiffry M, Walsh MJ, Molinari M: Advances in diagnosis, treatment and palliation of cholangiocarcinoma: 1990 to 2009. World J Gastroenterol. 2009, 15 (34): 4240-4262.PubMed CentralView ArticlePubMed
- Khan SA, Thomas HC, Davidson BR, Taylor-Robinson SD: Cholangiocarcinoma. Lancet. 2005, 366 (9493): 1303-1314.View ArticlePubMed
- Farges O, Fuks D: Clinical presentation and management of intrahepatic cholangiocarcinoma. Gastroenterol Clin Biol. 2010, 34 (3): 191-199.View ArticlePubMed
- Farinati F, Giacomin A, Vanin V, Sergio A, Burra P, Cillo U, Di Nolfo A, Del Poggio P, Benvegnu L, Zoli M, Borzio F, Giannini EG, Caturelli E, Cazzagon N, Rapaccini GL, Trevisani F, Italian Liver Cancer (ITA.LI.CA) group: Liver transplantation for hepatocellular carcinoma in clinical practice: the lesson from a 20-year multicentre experience in Italy. Eur J Gastroenterol Hepatol. 2012, 24 (2): 195-202.View ArticlePubMed
- Rosen CB, Heimbach JK, Gores GJ: Liver transplantation for cholangiocarcinoma. Transpl Int. 2010, 23 (7): 692-697.View ArticlePubMed
- 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 (1): 117-122.View ArticlePubMed
- Friman S, Foss A, Isoniemi H, Olausson M, Höckerstedt K, Yamamoto S, Karlsen TH, Rizell M, Ericzon BG: Liver transplantation for cholangiocarcinoma: selection is essential for acceptable results. Scand J Gastroenterol. 2011, 46 (3): 370-375.View ArticlePubMed
- Kaiser GM, Sotiropoulos GC, Jauch KW, Löhe F, Hirner A, Kalff JC, Königsrainer A, Steurer W, Senninger N, Brockmann JG, Schlitt HJ, Zülke C, Büchler MW, Schemmer P, Settmacher U, Hauss J, Lippert H, Hopt UT, Otto G, Heiss MM, Bechstein WO, Timm S, Klar E, Hölscher AH, Rogiers X, Stangl M, Hohenberger W, Müller V, Molmenti EP, Fouzas I: Liver transplantation for hilar cholangiocarcinoma: a German survey. Transplant Proc. 2008, 40 (9): 3191-3193.View ArticlePubMed
- Rea DJ, Rosen CB, Nagorney DM, Heimbach JK, Gores GJ: Transplantation for cholangiocarcinoma: when and for whom?. Surg Oncol Clin N Am. 2009, 18 (2): 325-337.View ArticlePubMed
- Sudan D, DeRoover A, Chinnakotla S, Fox I, Shaw B, McCashland T, Sorrell M, Tempero M, Langnas A: Radiochemotherapy and transplantation allow long-term survival for nonresectable hilar cholangiocarcinoma. Am J Transplant. 2002, 2 (8): 774-779.View ArticlePubMed
- Pascher A, Jonas S, Neuhaus P: Intrahepatic cholangiocarcinoma: indication for transplantation. J Hepatobiliary Pancreat Surg. 2003, 10 (4): 282-287.View ArticlePubMed
- Fu BS, Zhang T, Li H, Yi SH, Wang GS, Xu C, Yang Y, Cai CJ, Lu MQ, Chen GH: The role of liver transplantation for intrahepatic cholangiocarcinoma: a single-center experience. Eur Surg Res. 2011, 47 (4): 218-221.View ArticlePubMed
- Gulec SA, Pennington K, Hall M, Fong Y: Preoperative Y-90 microsphere selective internal radiation treatment for tumor downsizing and future liver remnant recruitment: a novel approach to improving the safety of major hepatic resections. World J Surg Oncol. 2009, 7: 6-PubMed CentralView ArticlePubMed
- Wang SC, Bester L, Burnes JP, Clouston JE, Hugh TJ, Little AF, Padbury RT, Price D: Clinical care and technical recommendations for 90 yttrium microsphere treatment of liver cancer. J Med Imaging Radiat Oncol. 2010, 54 (3): 178-187.View ArticlePubMed
- Ahmadzadehfar H, Biersack HJ, Ezziddin S: Radioembolization of liver tumors with yttrium-90 microspheres. Semin Nucl Med. 2010, 40 (2): 105-121.View ArticlePubMed
- Prompers L, Bucerius J, Brans B, Temur Y, Berger L, Mottaghy FM: Selective internal radiation therapy (SIRT) in primary or secondary liver cancer. Methods. 2011, 55 (3): 253-257.View ArticlePubMed
- Whitney R, Tatum C, Hahl M, Ellis S, Scoggins CR, McMasters K, Martin RC: Safety of hepatic resection in metastatic disease to the liver after yttrium-90 therapy. J Surg Res. 2011, 166 (2): 236-240.View ArticlePubMed
- Geissler EK, Schlitt HJ, Thomas G: mTOR, cancer and transplantation. Am J Transplant. 2008, 8 (11): 2212-2218.View ArticlePubMed
- Guba M, von Breitenbuch P, Steinbauer M, Koehl G, Flegel S, Hornung M, Bruns CJ, Zuelke C, Farkas S, Anthuber M, Jauch KW, Geissler EK: Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor. Nat Med. 2002, 8 (2): 128-135.View ArticlePubMed
- Koehl GE, Andrassy J, Guba M, Richter S, Kroemer A, Scherer MN, Steinbauer M, Graeb C, Schlitt HJ, Jauch KW, Geissler EK: Rapamycin protects allografts from rejection while simultaneously attacking tumors in immunosuppressed mice. Transplantation. 2004, 77 (9): 1319-1326.View ArticlePubMed
- Luan FL, Hojo M, Maluccio M, Yamaji K, Suthanthiran M: Rapamycin blocks tumor progression: unlinking immunosuppression from antitumor efficacy. Transplantation. 2002, 73 (10): 1565-1572.View ArticlePubMed
- Willems MC, van der Vliet JA, de Man BM, van der Laak JA, Lomme RM, Hendriks T: Persistent effects of everolimus on strength of experimental wounds in intestine and fascia. Wound Repair Regen. 2010, 18 (1): 98-104.View ArticlePubMed
- Kahn J, Müller H, Iberer F, Kniepeiss D, Duller D, Rehak P, Tscheliessnigg K: Incisional hernia following liver transplantation: incidence and predisposing factors. Clin Transplant. 2007, 21 (3): 423-426.View ArticlePubMed
- Vardanian AJ, Farmer DG, Ghobrial RM, Busuttil RW, Hiatt JR: Incisional hernia after liver transplantation. J Am Coll Surg. 2006, 203 (4): 421-425.View ArticlePubMed
- Brewer MB, Rada EM, Milburn ML, Goldberg NH, Singh DP, Cooper M, Silverman RP: Human acellular dermal matrix for ventral hernia repair reduces morbidity in transplant patients. Hernia. 2011, 15 (2): 141-145.View ArticlePubMed
- Piardi T, Audet M, Panaro F, Gheza F, Cag M, Portolani N, Cinqualbre J, Wolf P: Incisional hernia repair after liver transplantation: role of the mesh. Transplant Proc. 2010, 42 (4): 1244-1247.View ArticlePubMed
- Rosen MJ: Biologic mesh for abdominal wall reconstruction: a critical appraisal. Am Surg. 2010, 76 (1): 1-6.PubMed
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