Risk of malignancy in Caroli disease and syndrome: A systematic review.

BACKGROUND: Congenital intrahepatic bile duct dilatation without fibrosis is called Caroli disease (CD), and is called Caroli syndrome (CS) when it has fibrotic and cirrhotic liver morphology. The development of intrahepatic carcinoma is described in both conditions, but the reported incidence varies extensively. Potential risk factors for the malignant transformation were not described. Furthermore, conservative or surgical treatment is performed depending on the extent of cystic malformation, hepatic dysfunction and structural hepatic changes, but little is known about which treatment should be offered to patients with CD or CS and cancer. AIM: To further investigate the malignant transformation in these conditions.
METHODS: A systematic review of the current literature until January 2019 was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement. A search using Medline (PubMed) was performed using a combination of Medical Subject Headings terms "caroli disease", "caroli syndrome", "tumor", "malignant", and "cholangiocarcinoma". Only human studies published in English were used for this systematic review. The following parameters were extracted from each article: year of publication, type of study, number of patients, incidence of malignant tumor, duration of symptoms, age, sex, diagnostics, identification of tumor, surgical therapy, survival and tumor recurrence.
RESULTS: Twelve retrospective studies reporting the courses of 561 patients (53% females) were included in this systematic review. With a mean age of 41.6 years old (range 23 to 56 years old), patients were younger than other populations undergoing liver surgery. Depending on the size of the study population the incidence of cholangiocarcinoma varied from 2.7% to 37.5% with an overall incidence of 6.6%. There were only few detailed reports about preoperative diagnostic work-up, but a multimodal work-up including ultrasound of the liver, computed tomography, magnetic resonance imaging and endoscopic retrograde cholangiopancreatography was used in most studies. Disease duration was variable with up to several years. Most patients had episodes of cholangitis, sepsis, fever or abdominal pain. Tumor detection was an incidental finding of the surgical specimen in most cases because it is currently often impossible to detect tumor manifestation during preoperative diagnostics. Liver resection or liver transplantation was performed depending on the extent of the biliary pathology and additional alterations of the liver structure or function. No postoperative adjuvant chemotherapy was reported, but chemotherapy was administered in selected cases of tumor recurrence. Overall survival rates after one year were low at 36% and a high recurrence rate of up to 75% during the observation period.
CONCLUSION: Only few retrospective studies reported a low tumor incidence. Despite the high rate of mortality and tumor recurrence, definite surgical treatment should be offered as soon as possible. ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.

Core tip: Congenital intrahepatic bile duct dilatation with or without fibrosis is called Caroli syndrome or Caroli disease, respectively. We performed a systematic review of the current literature to investigate the incidence of malignant transformation, risk factors, and surgical treatment options. There were only 12 retrospective cohort studies reporting 561 patients, including 37 patients with malignancy, so an exact preoperative diagnostic work-up, risk factors and preferred surgical treatment were impossible to conclude due to lack of data. Overall survival rates after one year were low (36%), and recurrence rate was high (75%) during the observation period.

INTRODUCTION

Vachell first described Caroli disease (CD) in 1906[1]. The segmental dilatation of the intrahepatic biliary ducts in combination with renal cystic disease and liver fibrosis is named Caroli syndrome (CS)[2,3]. Due to focal inflammation, likely initiated by an intrauterine malformation of the bile ductal plate, the biliary tract is continuously destroyed over decades[4,5]. Consequently, the further progression of this destructive inflammatory state leads to recurrent episodes of cholangitis, the development of biliary stones and malignant transformation in some cases, and cholangiocarcinoma is described, but is rare overall with reports up to 14%[5-7]. However, the risk of developing intrahepatic cholangiocellular carcinoma in CD or CS is increased 100-fold compared to healthy individuals[8]. The association between intrahepatic cystic lesions in CS or CD and cholangiocarcinoma was first published in 1968[9]. The distinct etiology of this association and malformation is not clear[8], but several theories are postulated: Carcinogenic component of the bile with prolonged effect during biliary stasis[8]; permanent stone irritation and formation of carcinogens[10]; and cellular predisposition for neoplastic change of the congenital cystic malformation of the biliary tract[8]. Unfortunately, the preoperative diagnosis of malignant transformation is difficult, and final diagnosis of the cholangiocarcinoma is typically made during pathological examination of the surgical specimen and less common in preoperative liver biopsies[6,11,12]. Furthermore, malignancy in CS or CD is suggested to be more likely in older patients[11], insufficient bile drainage[8] and long disease duration[8,10,12]. Therefore, the time span between the onset of first symptoms and definitive treatment is up to 60 mo in many cases[13,14]. The complaint symptoms may be unspecific and vary from pain, pruritus, fever, sepsis, recurrent cholangitis, abscesses, pancreatitis, weight loss, and adynamia[3,5,15-22]. Besides biliary drainage operations or interventions[7,22-24], liver resection[7,12,25] or orthotopic liver transplantation (OLT)[7] are performed. The decision to perform a specific intervention depends on the extent of biliary pathology and hepatic fibrosis and portal hypertension consecutively.

The present systematic review (1) analyzed the existing literature on the current incidence of malignancy in CS or CD; (2) the potential risk factors for the development of malignancy in patients with CS or CD; (3) the postoperative outcome of CS or CD after liver resection or OLT; and (4) the best treatment options for patients with CS or CD and suspected malignancy.

MATERIALS AND METHODS

A systematic review of the literature until January 2019 was performed according the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement[26] to identify studies reporting the incidence of tumors in patients with CS and CD underwent resection or liver transplantation. Therefore, a literature search was performed using Medline (PubMed) from January 1993 to January 2019. During screening process, non-English articles were excluded. Reports with less than five patients and review articles were excluded. The search was performed using a combination of Medical Subject Headings terms “caroli disease”, “caroli syndrome”, “tumor”, “malignant”, and “cholangiocarcinoma”. Only human studies were used for this systematic review. The titles and abstracts of the articles were screened first for scientific relevance of this review. The full article was reviewed for potential eligibility and reported incidence of malignancy in the next step. The flow-chart show the process of identification, screening and final inclusion of articles in Figure 1.

Figure 1

Flow-chart of the identification, screening and final inclusion of articles.

The following parameters were extracted from each article: Year of publication, type of study, number of patients with CD or CS, incidence of malignant tumor, duration of symptoms (months), age in years, sex (females vs males), used diagnostics (ultrasound, computed tomography (CT), magnetic resonance imaging (MRI), endoscopic retrograde cholangiopancreatography (ERCP), and percutaneous cholangiography), identification of tumor (preoperative biopsy or incidental finding), surgical therapy (liver resection, OLT), survival and tumor recurrence.

RESULTS

Included studies

Twelve manuscripts were included in this systematic review (Table 1). All studies were of a retrospective nature. Most studies were single-center studies (n = 8), and four studies included data of an official registry (n = 2) or multicenter (n = 2) analysis. The study populations of each study were small, with only three studies including more than 100 patients and 75% of the studies included less than 45 patients, with a total of 561 patients. The reported incidence of cholangiocarcinoma in patients treated for CS or CD varied from 2.7% to 37.5%, depending on the size of the study population. The overall incidence of cholangiocarcinoma in all included patients was 6.6% (n = 37).

Table 1

Literature search results and analyzed manuscripts

Ref.	Country	Year of publication	Type of study	n of reported patients	n of cancer (%)
Ammori et al[27]	United Kingdom	2002	Single-center, retrospective	8	3 (37.5)
De Kerckhove et al[19]	Belgium	2005	ELTR registry, retrospective	113	3 (2.7)
Kassahun et al[21]	Germany	2005	Single-center, retrospective	33	3 (9)
Habib et al[17]	United States	2006	Single-center, retrospective	33	1 (3)
Bockhorn et al[30]	Germany	2006	Single-center, retrospective	12	3 (25)
Millwala et al[5]	United States	2008	UNOS registry, retrospective	104	3 (2.9)
Ulrich et al[3]	Germany	2008	Single-center, retrospective	44	4 (9)
Hori et al[24]	Japan	2010	Single-center, retrospective	5	1 (20)
Lendoire et al[13]	Argentina	2011	Multicenter, retrospective	24	1 (4.2)
Mabrut et al[20]	France	2013	Multicenter, retrospective	155	8 (5)
Moslim et al[12]	United States	2015	Single-center, retrospective	9	3 (33.3)
Fahrner et al[25]	Germany	2018	Single-center, retrospective	21	4 (19)

ELTR: European Liver Transplant Registry; UNOS: United Network of Organ Sharing.

Diagnostic preoperative work-up

Only few studies reported a detailed preoperative diagnostic work-up for patients with CS and CD in general, and no study presented a work-up to identify cholangiocarcinoma within CS and CD (Table 2). Ultrasound of the liver, CT, MRI, and ERCP revealed the standard of preoperative diagnostics in most of the studies. Three studies reported percutaneous cholangiography to estimate the extent of biliary pathology.

Table 2

Diagnostic work flow prior to surgery

Ref.	CT	MRI	ERCP	Ultrasound	Others
Ammori et al[27]	Yes	Yes	100%	Yes	No data
De Kerckhove et al[19]	Yes	Yes	Yes	Yes	Percutaneous cholangiography
Kassahun et al[21]	100%	16.2%	83.9%	100%	No data
Habib et al[17]	No data	No data	No data	No data	No data
Bockhorn et al[30]	100%	No data	92%	100%	No data
Millwala et al[5]	No data	No data	No data	No data	No data
Ulrich et al[3]	Yes	Yes	Yes	Yes	Percutaneous cholangiography
Hori et al[24]	No data	No data	No data	No data	No data
Lendoire et al[13]	Yes	Yes	Yes	Yes	Percutaneous cholangiography
Mabrut et al[20]	No data	74.7%	27.7%	No data	No data
Moslim et al[12]	No data	No data	No data	No data	No data
Fahrner et al[25]	No data	No data	No data	No data	No data

Percentages given indicate frequency of diagnostic tool within the study. CT: Computed tomography; MRI: Magnetic resonance imaging; ERCP: Endoscopic retrograde cholangiopancreatography.

Patient demographics

There was a slight predominance of female sex in all patients (53% females, Table 3). Patients suffering from CS or CD are younger than other populations undergoing liver resection, for e.g., liver cancer, the mean patient age ranged from 23 to 56 years old, with a total mean of 41.6 years old at the time point of surgery. Only five studies reported data on the duration of disease or symptoms. Patients reported at least 7 mo of mean duration of symptoms, but the most patients suffered from cholangitis, fever or abdominal pain for several years (Table 3). In most cases (89%), tumor identification was finally made in definitive histological assessment as an incidental finding. The diagnosis was suspected prior surgery or proven by preoperative biopsy only in less than five patients (14%).

Table 3

Patient demographics, duration of disease and tumor identification

Ref.	Age (yr)	Female sex (%)	Duration of disease	Tumor identification
Ammori et al[27]	35	75	No data	No data
De Kerckhove et al[19]	39.7	52	No data	No data
Kassahun et al[21]	51.5	55	< 1 yr 51%, 1-5 yr 13%, > 5 yr 35%	No data
Habib et al[17]	26	50	No data	No data
Bockhorn et al[30]	39	42	No data	67% incidental finding
Millwala et al[5]	35	55	No data	No data
Ulrich et al[3]	49	55	< 1 yr 55%, > 5 yr 2.5%	100% incidental finding
Hori et al[24]	23.74	No data	6.4 yr	100% puncture of nodule prior surgery
Lendoire et al[13]	48.7	70	2.6 yr	100% incidental finding
Mabrut et al[20]	55.7	43	7 mo	No data
Moslim et al[12]	40	22	No data	100% incidental finding
Fahrner et al[25]	56	74	No data	75% incidental finding 25% suspicious nodules in diagnostics

Tumor treatment and survival

Patients with CS or CD were treated via liver resection or OLT (Table 4). The indication for the onco-surgical treatment (liver resection or OLT) was primarly based on the extent of the biliary pathology and an additional alteration of the liver structure or function. Most of the tumors were incidental findings, and no exact proposal of liver resection or liver transplantation was possible on the basis of the data, but the proposed treatment of cholangiocarcinomas without CS or CD is likely applicable in these patients. In cases of tumor identification in histological assessment of the surgical specimen, no postoperative adjuvant chemotherapy was reported. Chemotherapy was administered in selected cases of tumor recurrence. Unfortunately, few data were available on the tumor-node-metastasis (TNM) classification or grading of the tumors. Most tumors were localized within in the liver (pT1 or pT2), but local lymph node involvement or peritoneal seeding was described (Table 4). However, overall survival rates after one year were low at 36% in total. It was impossible to distinguish the effect of liver resection or liver transplantation due to the retrospective reports of both different surgical treatments. The reported recurrence rate during the observation period in 7 studies was high, at up to 75%.

Table 4

Surgical treatment, tumor characteristics and survival

Ref.	Surgery for all patients (LR vs OLT)1	TNM	1-yr survival cancer patients	Recurrence
Ammori et al[27]	50% vs 50%	No data	33%	0%
De Kerckhove et al[19]	0% vs 100%	No data	66%	33%
Kassahun et al[21]	87% vs 0%	No data	0%	33%
Habib et al[17]	0% vs 100%	No data	0%	No data
Bockhorn et al[30]	83% vs 17%	n = 1 pT1, n = 1 pT2	66%	0%
Millwala et al[5]	0% vs 100%	No data	0%	No data
Ulrich et al[3]	90% vs 10%	No data	0%	No data
Hori et al[24]	0% vs 100%	No data	No data	No data
Lendoire et al[13]	91.6% vs 0%	No data	100%	No data
Mabrut et al[20]	75% vs 18.9%	n = 6 R0, n = 1 peritoneal seeding	33%	50%
Moslim et al[12]	22% vs 78%	No data	0%	33%, 66% tumor progression
Fahrner et al[25]	90% vs 10%	n = 1 pT1N1, n = 2 pT2, n = 1 pT3	100%	75%

Besides liver resection and orthotopic liver transplantation, other surgical interventions performed, so that the sum of the percentages does not equal 100%. LR: Liver resection; OLT: Orthotopic liver transplantation; TNM: Tumor-nodes-metastases.

DISCUSSION

Only a few reports investigated CS and CD and the development of cancer, and there was no suitable explanation for this fact in most of the publications. The present review analyzed the data of 561 patients included in 12 studies who were treated either with liver resection or OLT. Unfortunately, most of the studies were reports of less than 45 patients, and retrospective single or multicenter experiences were reported over several years in all cases. In addition, various case reports were not included in this systematic review.

The total incidence of cancerous transformation or simultaneous cancer in CS and CD is approximately 7%, but it ranged from approximately 3% to almost 40% in the beginning of the 2000s depending on the cohort[19,27]. Over time this incidence did not change, and the latest publications during the last six years reported incidences between 5% to 33%[12,20,25]. There were no new aspects reported on the development of cancerous transformation, and biliary stasis[8], stone irritation[10], a cellular predisposition of the cystic congenital malformation[8] and a combination of these factors are possible pathways[28]. Most cases of cancer are cholangiocarcinoma or adenocarcinoma, and the biliary epithelium is propagated as the origin of the cancerous transformation[6]. As one trigger for the malignant transformation, chronic inflammation of the biliary epithelium during cholangitis with consecutive dysplasia and carcinogenesis is postulated[29]. Unfortunately, due to little data, the hypothesis of an increased incidence for malignant transformation in large bile ducts rather than in small peripheral ducts could not be proven in this review[14].

There are only few data on the structured preoperative work-up of patients with CS and CD regarding the used method. Ultrasound was used in most studies to identify cystic lesions within the liver and potential altered liver structure, such as liver cirrhosis[21,30]. To further evaluate the biliary tract, ERCP or percutaneous cholan-giography was used in selected cases in some of the studies[3,13,19,27]. However, the use of invasive biliary diagnostics should be avoided and performed only in selected patients because they are often associated with an increased risk for infections[19]. If reported, CT or MRI scans were used to investigate the nature of the cysts, identify possible malignant transformation, and plan and assess the surgical resectability[20,21,27]. The tumor markers Ca-19-9 is often elevated in cases of benign biliary obstruction or cholangitis, and higher levels may mislead the correct diagnosis[7]. Overall, the diagnosis of malignancy in CS and CD is difficult, and the tumor identification was an incidental finding in most of the reports in this review, which was made during the final histological assessment of the surgical specimen, because the preoperative identification of a tumor within a dilated cystic bile tract is almost impossible[3,8,11,13,25]. Therefore, the value of screening patients with CS and CD for malignancy is quite inaccurate, and definite treatment should be sought, because delayed diagnosis and widespread tumor are associated with a poor prognosis[18]. In the future, a more aggressive diagnostic work-up including endoscopic ultrasound, puncture of suspected segments within the biliary tract, cholangioscopy (percutaneously) should be used, with the goal to detect more frequently patients with malignant trans-formation and therefore avoiding delay of definite surgical treatment.

The initial treatment of CS and CD is often nonsurgical and supportive therapy using analgesia, antibiotics in case of biliary infections and ursodeoxycholic acid[31,32]. Surgical or interventional drainage procedures may be performed to remove biliary tract obstructions and improve biliary passage to decrease the risk and burden of cholangitis[33,34]. Beside this conservative treatment, the final diagnosis of CS or CD often takes months or years until the patient is referred for definite surgical treatment. During that time, patients suffer recurrent infections, sepsis, hepatic abscesses, portal hypertension, and the risk of malignant transformation without solving the problem of the dilated and cystic biliary tract[30,35-38]. There are reports that malignant transformation does not depend on the disease duration, because cancer occurred in patients with symptomatic CS or CD of two months to two decades. Therefore, it has been postulated that there are likely more aggressive subgroups in CS or CD with increased potential for malignancy[30]. Due to a lack of data, there is no explanation or postulated pathway for this fact.

As a conclusion for this observation, surgical treatment with liver resection or OLT should be offered to patients with CS or CD as soon as possible to avoid recurrent sepsis and primarily malignant transformation[3,25,30]. In cases of conservative treatment, even asymptomatic patients should be regularly screened clinically and radiologically for malignancy[30]. To obtain the best treatment and surveillance, an interdisciplinary management team, including surgeons, gastroenterologists, hepatologists, radiologists, pediatrician and specialists in infectious diseases, is needed. Therefore, these patients are often treated in transplant centers. Overall, a high suspicion for potential malignant transformation is needed, and early treatment should be intended.

After one year, the survival rate of all tumor patients was 35%, which is low and much lower than in hepatocellular carcinoma patients[39-41] or selected surgical treated cholangiocarcinoma patients[42-45]. At least 32% had tumor recurrence during the observation period, but five studies did not report any data about recurrence. Therefore, the incidence may be even higher, and some patients likely died before the detection of any tumor recurrence probably due to the high mortality rate. In some studies, a high morbidity and in-house mortality was reported after OLT due to infectious complications and therapy-resistant sepsis[17,21]. The general treatment suggestion is to perform liver resection in defined and localized cystic degeneration and evaluate OLT in diffuse cystic affection with structural hepatic changes[3,25,27,30].

On the basis of the data, no adjuvant chemotherapy was administered in cases of cholangiocarcinoma or adenocarcinoma. There were only a few reports of chemotherapy in cases of recurrence when surgery was no longer an option. This result is comparable to patients with cholangiocarcinoma without CS or CD, where chemotherapy is used only in nonresectable and extended tumors or recurrence[46].

The studies were not comparable. For example, TNM staging was available only in a few studies. The extent of cystic degeneration and underlying structural liver changes greatly influences the choice of treatment as mentioned previously. In cases of cancer in CS patients treated with OLT, the long-term survival rate was 0%[17,27], and recurrence rates were high, which are comparable to studies of OLT and cholangiocarcinoma without CS or CD[47]. Patients with localized and small cholangiocarcinoma likely benefit from OLT, although little current data exist[7].

The following limitations of this systematic review must be addressed. Overall, there were predominantly small, retrospective cohort studies with nonhomogeneous patient collectives treated with liver resection or OLT. Therefore, it was not possible to identify specific risk factors indicating the risk for malignant transformation in CS or CD, because these two entities were not reported separately. Another aspect was that most of the tumors were incidental findings, so a specific work-up algorithm is likely not possible to define. Further prospective and multicenter studies or databases with the specific goal to identify risk factors for malignant transformation are needed.

In conclusion, there were only few retrospective studies of patients treated with surgery in cases of CS and CD. Therefore, it was not possible to identify valuable risk factors for the malignant transformation in these patients. On the other hand, the previously postulated factors for the development of malignancy could neither be proven nor rebutted. Overall, the incidence of simultaneous malignancy in CS or CD is low, but high tumor rates to almost 40% were reported depending on the investigated cohort. Because a high proportion of malignant tumors were incidental findings, the definite surgical treatment should be offered as soon as possible to avoid septic complications and the development of carcinoma. Surgical treatment should include liver resection in localized affection (primarily CD) and OLT in diffuse affection and structural liver changes, such as liver fibrosis (CS). In proven malignant transformation, small tumors may be treated with OLT successfully, but extensive tumors are mostly associated with an inferior outcome, e.g., due to tumor recurrence. Overall, the postoperative results are associated with a high rate of mortality and tumor recurrence. Therefore, patient selection and the timing of surgery are of high importance. On the basis of the current literature, there are no optimal screening methods described to identify patients with malignant transformation early and safely. Therefore, a high suspicion of malignancy is needed to find the exact time point for surgery and avoid delay in definite surgical treatment. Finally, new screening tools are needed to increase the rate of tumor identification during long-term surveillance of patients with CS or CD.

ARTICLE HIGHLIGHTS

Research background

Congenital intrahepatic bile duct dilatation without fibrosis is called Caroli disease (CD), and is called Caroli syndrome (CS) when it has fibrotic and cirrhotic liver morphology. The development of intrahepatic carcinoma is described in both conditions, but the reported incidence varies extensively. Furthermore, there are no valid guidelines how to treat and diagnose malignant transformation in these patients.

Research motivation

So far no valid potential risk factors for the malignant transformation were described. Furthermore, conservative or surgical treatment is performed depending on the extent of cystic malformation, hepatic dysfunction and structural hepatic changes, but little is known about which treatment should be offered to patients with CD or CS and especially cancer.

Research objectives

We performed a systematic review of the current literature to investigate specific conditions for malignant transformation in patients with CD and CS and to identify potential risk factors and recommendations regarding diagnosis and surgical treatment.

Research methods

A systematic review of the current literature until January 2019 was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement. During screening process, non-English articles and reports with less than five patients were excluded. The search was performed using a combination of Medical Subject Headings terms “caroli disease”, “caroli syndrome”, “tumor”, “malignant”, and “cholangiocarcinoma”. Only human studies were used for this systematic review.

Research results

Twelve retrospective studies reporting the courses of 561 patients (53% females) were included in this systematic review. The patients’ mean age was 41.6 years old (range 23 to 56 years old), therefore patients were younger than other populations undergoing liver surgery. The incidence of cholangiocarcinoma varied from 2.7% to 37.5% with an overall incidence of 6.6%. There were only few detailed reports about preoperative diagnostic work-up. Disease duration was variable with up to several years. In most cases tumor detection was an incidental finding of the surgical specimen as tumor detection in preoperative diagnostics was often impossible. Surgical treatment depended on the extent of the biliary pathology and additional alterations of the liver structure or function. No adjuvant chemotherapy was reported. Overall survival rates after one year were low at 36% and a high recurrence rate of up to 75% during the observation period was seen.

Research conclusions

Only few retrospective studies are available and reported a low tumor incidence. On the basis of these studies distinct suggestions regarding diagnosis and treatment are impossible to define. Despite the high rate of mortality and tumor recurrence, definite surgical treatment should be offered as soon as possible.

Research perspectives

Further prospective multicenter investigations regarding patient surveillance, diagnostic tools, time point of surgery and risk factors of malignant transformation are needed.