http://orcid.org/0000-0002-7631-4124
Figures
Abstract
Background
Combined hepatocellular-cholangiocarcinoma (cHCC-CC) can present as a hypervascular or peripherally enhancing tumor in dynamic imaging. We evaluated the effect of transarterial chemoembolization (TACE) on prognosis according to post-operative recurrence imaging patterns.
Methods
We retrospectively analyzed 42 cHCC-CC and 59 hepatocellular carcinoma (HCC-control) patients at the Asan Medical Center. We classified recurrent cHCC-CC according to enhancement pattern (globally enhancing: GE cHCC-CC, peripherally enhancing: PE cHCC-CC) and evaluated tumor response, time-to-local progression (TTPlocal), and overall survival (OS).
Results
The GE cHCC-CC group had a significantly higher best objective response rate (complete remission + partial response) than the PE cHCC-CC group (36% vs 0%, P = 0.005), and it was comparable to that of the HCC-control group (35.6%, P = 0.97). TTPlocal in the GE cHCC-CC group was significantly shorter than in the HCC-control group (6.6 vs 27.1 months, P < 0.001), and was not significantly different from that in the PE cHCC-CC group (5.3 months, P = 0.12). OS was 12.4 months, 52.8 months, and 67.5 months in the PE cHCC-CC, GE cHCC-CC, and HCC-control groups, respectively (Ps < 0.05). The adjusted hazard ratios (HRs) for TTPlocal and OS revealed an independent association with enhancement pattern of recurrent cHCC-CC (TTPlocal: HR 2.46; 95% CI 1.10–5.46; P = 0.03; OS: HR 5.97; 95% CI 2.38–14.96; P < 0.001).
Citation: Na SK, Choi GH, Lee HC, Shin YM, An J, Lee D, et al. (2018) The effectiveness of transarterial chemoembolization in recurrent hepatocellular-cholangiocarcinoma after resection. PLoS ONE 13(6): e0198138. https://doi.org/10.1371/journal.pone.0198138
Editor: Heather Francis, Digestive Disease Research Center, Scott & White Healthcare, UNITED STATES
Received: February 19, 2018; Accepted: May 14, 2018; Published: June 7, 2018
Copyright: © 2018 Na et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: CC, Cholangiocarcinoma; cHCC-CC, combined hepatocellular-cholangiocarcinoma; CI, confidence interval; CR, complete remission; CT, computed tomography; GE, globally enhancing; HCC, hepatocellular carcinoma; HR, hazard ratio; MRI, magnetic resonance imaging; OS, overall survival; PD, progressive disease; PE, peripherally enhancing; PFS, progression-free-survival; PR, partial response; RECIST, Response Evaluation Criteria in Solid Tumors; SD, stable disease; TACE, transarterial chemoembolization; TTP, time-to-progression; TTPlocal, time-to-local-progression
Introduction
Combined hepatocellular-cholangiocarcinoma (cHCC-CC) accounts for 0.4%–14.2% of primary liver malignancies [1, 2], and contains pathological components of both hepatocellular carcinoma (HCC) and cholangiocarcinoma (CC) [3]. Pre-operative diagnosis of cHCC-CC is sometimes challenging due to its heterogeneous imaging characteristics with overlapping features of both HCC and CC [4–7]. It can present predominantly as a hypervascular lesion resembling HCC or a peripherally enhancing lesion resembling CC, according to the predominant histologic component within the tumor. The enhancement patterns of cHCC-CC on dynamic computed tomography (CT) or magnetic resonance imaging (MRI) are known to be in good agreement with the dominant pathologic component [3, 8].
Surgical resection and liver transplantation are considered curative treatments for cHCC-CC. However, post-operative recurrence is frequent, and the 5-year survival rate after surgical resection is around 30% [9–13]. The prognosis after liver transplantation for cHCC-CC is poorer than that of HCC and confers a survival rate similar to that of selected patients with CC [14, 15].
Transarterial chemoembolization (TACE) has been used as a mainstay of palliative treatment for HCC [16, 17]. Tumor vascularity is a significant prognostic factor for TACE because chemotherapeutic agents and embolic material can be delivered much more effectively in hypervascular tumors. Many cHCC-CC tumors are less vascular and more fibrotic than HCC [2]; hence, the effectiveness of TACE for cHCC-CC is questionable. There have been no established treatments for recurrent cHCC-CC, although TACE can be considered as a palliative treatment. A previous study suggested that TACE response was highly related to tumor vascularity in patients with primary non-resectable cHCC-CC [18]. However, as far as we know, the therapeutic efficacy of TACE has not been systematically evaluated in recurrent cHCC-CC, especially according to enhancement patterns, although several studies have reported their relationship with patient prognosis [3, 18, 19].
The aim of the present study was to evaluate the therapeutic efficacy of TACE and patient prognosis according to the post-operative recurrence patterns of cHCC-CC in comparison with HCC.
Patients and methods
The present study was reviewed and approved by the Institutional Review Board of the Asan Medical Center (IRB No. 2016–1125). Patient records and information were anonymized and de-identified prior to analysis.
Patients
Between January 2000 and May 2016, 287 patients who had undergone curative surgical resection at the Asan Medical Center were pathologically diagnosed as having cHCC-CC. Among these patients, recurrences occurred in 135 patients, and 93 patients were excluded for the following reasons: 11 patients had concurrent other malignancies; 3 patients were lost to follow-up; and 79 patients received treatments other than TACE for the first recurrence (surgical resection: 9, liver transplantation: 1, radiofrequency ablation: 11, percutaneous ethanol injection: 1, cytotoxic chemotherapy: 11, sorafenib: 20, radiation treatment: 8, and supportive treatment: 18). After exclusion, a total of 42 patients were analyzed retrospectively (Fig 1).
cHCC-CC, combined hepatocellular-cholangiocarcinoma; GE, globally enhancing; PE, peripherally enhancing; TACE, transarterial chemoembolization; HCC, hepatocellular carcinoma.
To compare treatment responses and prognosis, we also analyzed a total of 59 HCC patients treated with TACE for their first post-operative recurrence after curative surgical resection between January 2008 and June 2008. All patients received follow-up appointments every 2–3 months until death or 31 October 2016.
Radiological evaluation
The dynamic CT/MRI findings, from diagnosis to end of follow-up, were analyzed by a radiologist (Y.M.S.) with 25 years of experience in imaging of the liver. We classified the tumors according to the enhancement patterns at the time of first recurrence after surgical resection. Tumors with global arterial enhancement (more than 50% of tumor volume) on CT/MRI were arbitrarily classified as recurrent globally enhancing (GE) cHCC-CC, while those that showed only peripheral/rim enhancement or iso-enhancement were classified as recurrent peripherally enhancing (PE) cHCC-CC.
Tumor response to TACE was evaluated with follow-up CT performed 4–6 weeks after TACE according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria [20], since the viability of PE cHCC-CC after TACE could not be determined by enhancement criteria such as modified RECIST or the European Association for the Study of the Liver criteria [21, 22]. According to the RECIST criteria, complete remission (CR) was defined as the total disappearance of the lesion; partial response (PR) and progressive disease (PD) as a greater than 30% decrease and a greater than 20% increase, respectively, of the sum of the longest diameters of the target lesions; and stable disease (SD) as neither PR nor PD. The appearance of new lesions ≥ 1 cm in maximum diameter was defined as PD. A maximum of two index lesions in the liver were evaluated for time-to-progression (TTP) according to the RECIST 1.1 criteria [20]. To evaluate the therapeutic effectiveness of TACE, we also assessed the time-to-local progression (TTPlocal) during the follow-up period. TTPlocal was defined as the time from the start of TACE to objective local progression of the initial recurrent hepatic mass, regardless of the appearance of a new lesion. We also assessed progression-free survival (PFS) and overall survival (OS) after recurrence.
TACE protocol
The TACE protocol used in our institution has been described elsewhere [23]. All TACE sessions were performed by experienced radiologists. Both superior mesenteric and common hepatic arteriography were performed to assess overall anatomy, tumor burden, and portal vein patency. Cisplatin (Dong-A Pharmaceutical, Seosan, Korea) at 2 mg/kg was administered into the lobar hepatic artery for 15 minutes. After selective vascular catheterization of the tumor-feeding artery, an emulsion of 2–20 mL of iodized oil (Lipiodol Ultra-Fluide; Laboratoire Guerbet, Aulnay-Sous-Bois, France) and cisplatin in a 1:1 ratio was infused into the target arteries. The embolization of the arterial tumor feeders was then performed using 1-mm-diameter absorbable gelatin sponge particles (Gelfoam; Upjohn, Kalamazoo, MI, USA) until arterial flow stasis was achieved.
TACE was repeated every 2–3 months if residual viable tumor tissue was evident without the appearance of clinically significant extrahepatic metastases, main portal vein invasion, or deterioration in liver function. Though we applied the RECIST criteria for the evaluation of tumor response in this study, TACE was delayed until definite viable tumors were evident or new lesions appeared if there was dense lipiodol deposition and no definite tumor enhancement on dynamic CT scan.
Statistical analysis
Statistical analysis was performed using the Student’s t-test or Mann-Whitney test for continuous variables, and the chi-square test or Fisher’s exact test for categorical variables. TTP, TTPlocal, PFS, and OS were calculated and plotted using the Kaplan-Meier method, and differences between the groups were analyzed using a log-rank test. Univariable and multivariable Cox proportional-hazard regression models were performed to identify prognostic factors in relation to tumor progression and survival. For the multivariable Cox proportional-hazard regression model, we included factors that were significant or that showed a trend toward significance (P < 0.1) in a univariable model and performed backward elimination (P < 0.05) using the “standard method” of removing the variable with the largest P-value. Potential for risk was expressed as a hazard ratio (HR) with corresponding 95% confidence interval (CI), and P-values less than 0.05 were considered to be statistically significant. All statistical analyzes were performed using the Statistical Package for the Social Sciences statistical software (version 21; SPSS-IBM, Chicago, IL, USA) or R version 3.02 (R Foundation for Statistical Computing, Vienna, Austria).
Results
Pre-operative baseline characteristics according to recurrence pattern
The baseline clinical and pathologic characteristics of GE cHCC-CC, PE cHCC-CC, and recurrent HCC control (HCC-control) patients before surgery are shown in Table 1. The mean ages of the GE cHCC-CC, PE cHCC-CC, and HCC-control groups were 54.2 ± 10.1, 52.6 ± 8.9, and 56.2 ± 9.8 years, respectively. All groups had a higher portion of male patients (GE cHCC-CC, 84%; PE cHCC-CC, 94.1%; and HCC-control, 89.8%). Chronic hepatitis B virus infection was the major etiologic factor (92%, 100%, and 84.7% in the GE cHCC-CC, PE cHCC-CC, and HCC-control groups, respectively), and about half of the patients had liver cirrhosis (56%, 47.1%, and 54.2%, respectively). Most of the patients had Child-Turcotte-Pugh class A (100%, 100% and 94.9% in the GE cHCC-CC, PE cHCC-CC, and HCC-control groups, respectively) and a single tumor at initial diagnosis (84%, 76.5%, and 76.3%, respectively). The median values of maximum tumor diameter were 3.5 (interquartile range [IQR], 2.2–9.3) cm in the GE cHCC-CC group, 5.5 (IQR, 3.6–7.5) cm in the PE cHCC-CC group, and 5.0 (IQR, 3.5–7.5) cm in the HCC-control group. Gross vascular invasion was observed in 12%, 5.9%, and 11.9% of the GE cHCC-CC, PE cHCC-CC, and HCC-control groups, respectively, and metastases to the lymph nodes or distant sites were not observed. Before operation, a GE pattern was observed in 14 of 25 (56%) patients in the GE cHCC-CC group and 4 of 17 (23.5%) patients in the PE cHCC-CC. Therefore, the agreement of enhancement patterns between the initial and recurrent tumor was 77.8% in the GE cHCC-CC group and 54.2% in the PE cHCC-CC group.
The major pathologic type of both GE cHCC-CC and PE cHCC-CC was combined (96% vs 82.4%, P = 0.29). Tumor staging according to the 7th American Joint Committee on Cancer system identified 17 (68%) stage I and 8 (32%) stage II cases in the GE cHCC-CC group and 12 (70.6%) stage I and 5 (29.4%) stage II cases in the PE cHCC-CC group.
Clinical characteristics of the GE cHCC-CC, PE cHCC-CC, and HCC Groups at first recurrence
At the time of first recurrence, the mean ages of the GE cHCC-CC, PE cHCC-CC, and HCC-control groups were 55.1 ± 10.2, 53.2 ± 8.8, and 58.3 ± 9.6 years, respectively (Table 2). The median interval from resection to recurrence was significantly shorter in the GE cHCC-CC group than in the HCC-control group (5.2 vs. 16.4 months, P < 0.001), and was not significantly different between the GE cHCC-CC and PE cHCC-CC groups (5.2 vs. 5.9 months, P = 0.67). There was no significant difference in age, time to recurrence, proportion of single recurrence, tumor size, or the presence of portal vein invasion or metastasis between the GE cHCC-CC and PE cHCC-CC groups. Multiple recurrence and vascular invasion were significantly more frequent in the GE cHCC-CC group than in the HCC-control group (68% vs 32.2%, P = 0.002 and 16% vs 1.7%, P = 0.03, respectively), and there was no significant difference in distant metastasis (20% vs 6.8%, P = 0.12).
Tumor response outcome to TACE
A median of 2 (range, 1–4) cycles of TACE were performed in the cHCC-CC group and 5 (range, 2–8) cycles were performed in the HCC-control group (P = 0.002). Tumor response was evaluated 4–6 weeks after the first cycle of TACE by RECIST criteria. At the first evaluation, 41.2% of patients in the PE cHCC-CC group had PD, while 20% and 15.3% in the GE cHCC-CC and HCC-control groups had PD, respectively (Table 3). The objective response rate (CR plus PR) and the disease control rate (CR plus PR plus SD) in the GE cHCC-CC and PE cHCC-CC groups were not significantly different (12% vs. 0%, P = 0.26 and 80% vs. 58.8%, P = 0.17, respectively). Moreover, the objective response rate and disease control rate in the GE cHCC-CC and HCC-control groups were comparable (12% vs. 8.5%, P = 0.69 and 80% vs. 84.7%, P = 0.75, respectively). However, the disease control rate in the PE cHCC-CC and HCC-control groups was significantly different (58.8% vs. 84.7%, P = 0.02).
The best tumor response was significantly different according to enhancing pattern at recurrence. The objective response rates were 0% in the PE cHCC-CC group, 36.0% in the GE cHCC-CC group, and 35.6% in the HCC-control group (P = 0.005 for PE cHCC-CC vs. GE cHCC-CC; P = 0.97 for GE cHCC-CC vs. HCC-control). The disease control rate was significantly lower in the PE cHCC-CC group (58.8%) than in the HCC-control group (86.4%; P = 0.01), but the difference was not significant between the GE cHCC-CC (80%) and PE cHCC-CC (58.8%) groups (P = 0.17).
During the follow-up period, tumor progression was confirmed in 37 (88.1%) patients in the cHCC-CC groups. Among these, 13 (30.9%) patients showed progression of the index lesion, 18 (42.9%) patients showed a new hepatic or extrahepatic lesion without progression of the hepatic index lesion, and 6 (14.3%) patients showed a new hepatic or extrahepatic lesion with progression of the hepatic index lesion. To evaluate the effectiveness of TACE on target lesions, the median TTPlocal was calculated. It was significantly shorter in both the GE cHCC-CC (6.6 months) and PE cHCC-CC groups (5.3 months) than in the HCC-control group (27.1 months, P < 0.001; Table 4 and Fig 2A). However, it was not different between the GE cHCC-CC and PE cHCC-CC groups (6.6 vs. 5.3 months, P = 0.12). The TTP was also marginally shorter in the PE cHCC-CC group than in the GE cHCC-CC group (2.1 vs 4.7 months, P = 0.06) and significantly shorter in the GE cHCC-CC group than in the HCC-control group (10.1 months, P = 0.01; Fig 2B).
(A) Time-to-local progression, (B) time-to-progression, (C) progression-free-survival and (D) overall survival. cHCC-CC, combined hepatocellular-cholangiocarcinoma; GE, globally enhancing; PE, peripherally enhancing; HCC, hepatocellular carcinoma.
Survival outcome after TACE
The median follow-up duration was 2.0 (IQR, 1.3–3.7) years in the cHCC-CC group and 7.9 (IQR, 3.5–9.1) years in the HCC-control group. During follow-up, 56 (55.4%) patients died (69.0% in the cHCC-CC group and 45.8% in the HCC-control group), mostly as a result of cancer progression. The PFS of the PE cHCC-CC, GE cHCC-CC, and HCC-control groups was significantly different (2.1 vs 4.7 vs 9.7 months; P = 0.04 for GE cHCC-CC vs PE cHCC-CC, P = 0.02 for GE cHCC-CC vs HCC-control group, and P < 0.001 for PE cHCC-CC vs HCC-control; Table 3 and Fig 2C).
As shown in Table 4 and Fig 2D, there were significant differences in OS between the three groups (12.4 months in the PE cHCC-CC group, 52.8 months in the GE cHCC-CC group, and 67.5 months in the HCC-control group; P < 0.001 for GE cHCC-CC vs PE cHCC-CC and P = 0.04 for GE cHCC-CC vs HCC-control).
Predictive factors for poor outcomes after TACE in patients with recurrent cHCC-CC after surgical resection
We performed Cox regression analyzes for TTPlocal and OS. Through univariable analysis, PE cHCC-CC at the time of initial diagnosis, PE cHCC-CC at the time of recurrence, multiple recurrences, and maximum diameter of the recurrent tumor were selected as variables for multivariable analysis. After subsequent multivariable Cox analysis using the backward elimination method, the adjusted HRs for TTPlocal revealed an independent association with the enhancement pattern of recurrent cHCC-CC at the time of recurrence (HR 2.46; 95% CI 1.10–5.46; P = 0.03; Table 5). Other predictors related to short TTPlocal were multiple recurrences and maximum tumor diameter (HRs 5.13 and 1.04, respectively; P < 0.05 for each).
Likewise, the enhancement pattern of cHCC-CC at the time of recurrence was independently related to OS. Through univariable analysis, PE cHCC-CC at the time of initial diagnosis, PE cHCC-CC at the time of recurrence, age at the time of recurrence, Child-Pugh class B, multiple recurrences, maximum diameter of the recurrent tumor, and distant metastasis were selected as variables for multivariable analysis. Unadjusted and adjusted HRs of PE cHCC-CC on OS were respectively 3.77 (95% CI 1.71–8.30; P = 0.001) and 5.97 (95% CI 2.38–14.96; P < 0.001; Table 5). Other covariates independently associated with OS were age, Child-Turcott-Pugh class, maximum tumor diameter, and presence of distant metastasis (HRs 0.95, 45.92, 1.04, and 7.93, respectively; Ps < 0.05).
Discussion
In the present study, we evaluated the response and prognosis of post-operative recurrent cHCC-CC treated with TACE. We found that the GE cHCC-CC group showed better prognosis and response to TACE than the PE cHCC-CC group, but poorer response and prognosis than the HCC-control group. Interestingly, the enhancement pattern of recurrent cHCC-CC was an independent prognostic factor for both PFS and OS after TACE, but that of pre-operative cHCC-CC was not.
This is the first study to systematically evaluate the therapeutic efficacy of TACE and prognosis for recurrent cHCC-CC compared to those for HCC. There is one report examining TACE in cHCC-CC. Kim et al. reported that vascularity was highly associated with tumor response and survival outcome (HR 4.19) [18]. Recent studies have observed different prognoses according to image patterns of cHCC-CC patients treated with surgery. Mao et al. reported better prognosis of GE cHCC-CC patients [19]. Park at el. also revealed that the enhancement patterns reflect the proportion of tumor components and amount of fibrotic stroma, and demonstrated better prognosis of hypervascular cHCC-CC on gadoxetic acid-enhancement MRI [8]. However, these studies examined patients upon diagnosis and did not describe post-surgical recurrence pattern or treatment efficacy.
Two factors might have influenced the different tumor response and survival among the three groups. First, tumor vascularity may be a determining factor for the response to TACE. In concordance with this scenario, the best objective response to TACE, which reflects the size reduction of the tumor after TACE, was significantly better in the GE cHCC-CC and HCC-control groups than in the PE cHCC-CC group, but was not different between the GE cHCC-CC and HCC-control groups. However, different tumor biology among the three groups might also be an important factor affecting tumor progression and OS. TTP was significantly shorter in the cHCC-CC groups, especially the PE cHCC-CC group, than in the HCC-control group, and 48.6% (18/37) of patients in the cHCC-CC groups had new intrahepatic and/or extrahepatic lesions prior to progression of the index hepatic lesion, suggesting a more aggressive metastatic potential in cHCC-CC.
However, the tumor response to TACE per se also seemed to be poorer in the cHCC-CC groups, since the TTPlocal of the GE cHCC-CC group was significantly shorter than that of the HCC-control group, despite the similar objective response rate. These findings imply that local tumor progression was more rapid in non-responders and/or the response was not durable even in responders in the GE cHCC-CC group. In fact, at the time of recurrence, the cHCC-CC groups showed more multiple recurrences and vascular invasion than the HCC-control group. Moreover, time-to-recurrence after resection in the cHCC-CC groups was shorter than that in the HCC-control group. All these findings suggest that cHCC-CC, especially PE cHCC-CC, has more aggressive tumor biology than HCC.
It should be noted that, in interpreting these results, this study did not reflect the prognosis of all cHCC-CC patients who underwent surgery. To evaluate the efficacy of TACE in patients with recurrent cHCC-CC, this study included only cHCC-CC patients who received TACE after recurrence. However, the 1-, 3-, and 5-year survival rates in this study were 88.1%, 41.2% and 30.9%, respectively, which are comparable to the results of a previous study conducted in a more inclusive cohort (73.3%, 35.6% and 30.5%, respectively) [13].
In our study, agreement of image patterns between the primary and recurrent tumors was over 50% in the cHCC-CC groups, and primary hypervascular tumors were more likely to have the same image patterns in the recurrent tumor than PE tumors (77.8% vs. 54.2%). This is concordant with a previous study which also showed over 50% agreement in image patterns [3]. Interestingly, in the GE cHCC-CC group, patients with initial GE and subsequent recurrent GE cHCC-CC showed significantly longer TTPlocal than patients with initial PE and recurrent GE cHCC-CC (median TTPlocal, 19.0 ± 9.8 vs. 5.4 ± 0.4 months, P = 0.01, data not shown).
In our study, a quite number (10/42, 23.8%) of patients with cHCC-CC underwent TACE even in the presence of metastasis. Five patients had lung metastasis, 4 had lymph node metastasis, and one had bone metastasis. Three of these patients had less than 1 cm of lung metastasis and 3 of the lymph node metastases were difficult to diagnose as definite metastasis at the time of TACE.
Our study suggest that TACE is considered to be ineffective in recurred PE cHCC-CC patients and other treatment strategies are needed for these patients. However, there is no established treatment for primary cHCC-CC as well as recurred cHCC-CC because of rarity of patients. We suggest to treat PE cHCC-CC according to cholangiocarcinoma guideline[24]. If recurred PE-cHCC is localized disease, re-operation or radiation therapy could be considered first [25, 26]. If these local modality is difficult, systemic therapy could be considered such as gemcitabine or fluoropyrimidine-based chemotherapy. Combination therapy with immunotherapy and chemotherapy or radiation therapy could be an alternative to the disease with a dismal prognosis.
The present study has some limitations. First, this is a single centre retrospective study with a small population. The rarity of cHCC-CC has been an obstacle in previous studies and will make a larger prospective study difficult. Second, only recurrent cHCC-CCs after surgical resection were included. This was because the diagnosis of cHCC-CC is often difficult with needle biopsy only. As cases proven with needle biopsy only might not represent the general cHCC-CC population, we decided to include recurrent cases only after surgical resection. Third, although we discovered that the enhancement pattern at the time of recurrence was more strongly related to the response to TACE and overall survival than that before surgery, the pathology of recurrent tumors was not confirmed. Moreover, this study did not use the 2010 WHO classification system that categorized cHCC-CCs into classical type and subtypes with stem cell features [27], but the traditional classification system described by Allen and Lisa that categorizes cHCC-CC into double tumor, combined type, and mixed type [28]. Our institution used the traditional classification until 2012, and most of the enrolled patients underwent surgery before 2012. Additionally, the clinical and prognostic implications of the 2010 WHO classification system are still controversial [29–32].
In conclusion, the PE cHCC-CC group showed poorer response and prognosis than the GE cHCC-CC group after TACE. The GE cHCC-CC group showed comparable response to the HCC-control group, although the GE cHCC-CC group had poorer prognosis. Our results suggest that different treatment plans are needed according to enhancement patterns of recurrent cHCC-CC.
References
- 1. Wang AQ, Zheng YC, Du J, Zhu CP, Huang HC, Wang SS, et al. Combined hepatocellular cholangiocarcinoma: Controversies to be addressed. World journal of gastroenterology. 2016;22(18):4459–65. Epub 2016/05/18. pmid:27182157; PubMed Central PMCID: PMCPMC4858629.
- 2. Kassahun WT, Hauss J. Management of combined hepatocellular and cholangiocarcinoma. International journal of clinical practice. 2008;62(8):1271–8. Epub 2008/02/21. pmid:18284443.
- 3. Shin CI, Lee JM, Kim SH, Choi JY, Lee JY, Han JK, et al. Recurrence patterns of combined hepatocellular-cholangiocarcinoma on enhanced computed tomography. Journal of computer assisted tomography. 2007;31(1):109–15. Epub 2007/01/30. pmid:17259842.
- 4. Ebied O, Federle MP, Blachar A, Brancatelli G, Grazioli L, Cazals-Hatem D, et al. Hepatocellular-cholangiocarcinoma: helical computed tomography findings in 30 patients. Journal of computer assisted tomography. 2003;27(2):117–24. Epub 2003/04/19. pmid:12702999.
- 5. Hwang J, Kim YK, Park MJ, Lee MH, Kim SH, Lee WJ, et al. Differentiating combined hepatocellular and cholangiocarcinoma from mass-forming intrahepatic cholangiocarcinoma using gadoxetic acid-enhanced MRI. Journal of magnetic resonance imaging: JMRI. 2012;36(4):881–9. Epub 2012/06/26. pmid:22730271.
- 6. Fowler KJ, Sheybani A, Parker RA, 3rd, Doherty S, E MB, Chapman WC, et al. Combined hepatocellular and cholangiocarcinoma (biphenotypic) tumors: imaging features and diagnostic accuracy of contrast-enhanced CT and MRI. AJR American journal of roentgenology. 2013;201(2):332–9. Epub 2013/07/26. pmid:23883213.
- 7. Li R, Yang D, Tang CL, Cai P, Ma KS, Ding SY, et al. Combined hepatocellular carcinoma and cholangiocarcinoma (biphenotypic) tumors: clinical characteristics, imaging features of contrast-enhanced ultrasound and computed tomography. BMC cancer. 2016;16(1):158. Epub 2016/02/27. pmid:26917546; PubMed Central PMCID: PMCPMC4768404.
- 8. Park SH, Lee SS, Yu E, Kang HJ, Park Y, Kim SY, et al. Combined hepatocellular-cholangiocarcinoma: Gadoxetic acid-enhanced MRI findings correlated with pathologic features and prognosis. Journal of magnetic resonance imaging: JMRI. 2016. Epub 2016/11/23. pmid:27875000.
- 9.
Edge SB BD, Compton CC, Fritz AG, Greene FL, Trotti A. American Joint Committee on Cancer: AJCC Cancer Staging Manual. 7th ed. New York: Springer; 2010.
- 10. Aishima S, Kuroda Y, Asayama Y, Taguchi K, Nishihara Y, Taketomi A, et al. Prognostic impact of cholangiocellular and sarcomatous components in combined hepatocellular and cholangiocarcinoma. Human pathology. 2006;37(3):283–91. Epub 2006/04/15. pmid:16613323.
- 11. Yin X, Zhang BH, Qiu SJ, Ren ZG, Zhou J, Chen XH, et al. Combined hepatocellular carcinoma and cholangiocarcinoma: clinical features, treatment modalities, and prognosis. Annals of surgical oncology. 2012;19(9):2869–76. Epub 2012/03/28. pmid:22451237.
- 12. Chu KJ, Lu CD, Dong H, Fu XH, Zhang HW, Yao XP. Hepatitis B virus-related combined hepatocellular-cholangiocarcinoma: clinicopathological and prognostic analysis of 390 cases. European journal of gastroenterology & hepatology. 2014;26(2):192–9. Epub 2013/12/29. pmid:24370644.
- 13. Yoon YI, Hwang S, Lee YJ, Kim KH, Ahn CS, Moon DB, et al. Postresection Outcomes of Combined Hepatocellular Carcinoma-Cholangiocarcinoma, Hepatocellular Carcinoma and Intrahepatic Cholangiocarcinoma. Journal of gastrointestinal surgery: official journal of the Society for Surgery of the Alimentary Tract. 2016;20(2):411–20. Epub 2015/12/03. pmid:26628072.
- 14. Park YH, Hwang S, Ahn CS, Kim KH, Moon DB, Ha TY, et al. Long-term outcome of liver transplantation for combined hepatocellular carcinoma and cholangiocarcinoma. Transplantation proceedings. 2013;45(8):3038–40. Epub 2013/10/26. pmid:24157031.
- 15. Vilchez V, Shah MB, Daily MF, Pena L, Tzeng CW, Davenport D, et al. Long-term outcome of patients undergoing liver transplantation for mixed hepatocellular carcinoma and cholangiocarcinoma: an analysis of the UNOS database. HPB: the official journal of the International Hepato Pancreato Biliary Association. 2016;18(1):29–34. Epub 2016/01/19. pmid:26776848; PubMed Central PMCID: PMCPMC4750226.
- 16. Llovet JM, Real MI, Montana X, Planas R, Coll S, Aponte J, et al. Arterial embolisation or chemoembolisation versus symptomatic treatment in patients with unresectable hepatocellular carcinoma: a randomised controlled trial. Lancet (London, England). 2002;359(9319):1734–9. Epub 2002/06/07. pmid:12049862.
- 17. Llovet JM, Bruix J. Systematic review of randomized trials for unresectable hepatocellular carcinoma: Chemoembolization improves survival. Hepatology (Baltimore, Md). 2003;37(2):429–42. Epub 2003/01/24. pmid:12540794.
- 18. Kim JH, Yoon HK, Ko GY, Gwon DI, Jang CS, Song HY, et al. Nonresectable combined hepatocellular carcinoma and cholangiocarcinoma: analysis of the response and prognostic factors after transcatheter arterial chemoembolization. Radiology. 2010;255(1):270–7. Epub 2010/03/24. pmid:20308463.
- 19. Mao Y, Xu S, Hu W, Huang J, Wang J, Zhang R, et al. Imaging features predict prognosis of patients with combined hepatocellular-cholangiocarcinoma. Clinical radiology. 2017;72(2):129–35. Epub 2016/12/06. pmid:27916195.
- 20. Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). European journal of cancer (Oxford, England: 1990). 2009;45(2):228–47. Epub 2008/12/23. pmid:19097774.
- 21. Bruix J, Sherman M, Llovet JM, Beaugrand M, Lencioni R, Burroughs AK, et al. Clinical management of hepatocellular carcinoma. Conclusions of the Barcelona-2000 EASL conference. European Association for the Study of the Liver. Journal of hepatology. 2001;35(3):421–30. Epub 2001/10/11. pmid:11592607.
- 22. Lencioni R, Llovet JM. Modified RECIST (mRECIST) assessment for hepatocellular carcinoma. Seminars in liver disease. 2010;30(1):52–60. Epub 2010/02/23. pmid:20175033.
- 23. Shim JH, Lee HC, Kim SO, Shin YM, Kim KM, Lim YS, et al. Which response criteria best help predict survival of patients with hepatocellular carcinoma following chemoembolization? A validation study of old and new models. Radiology. 2012;262(2):708–18. Epub 2011/12/22. pmid:22187634.
- 24.
Network NCC. Hepatobiliary Cancers (Version 1.2018) [updated February 14, 2018April 5, 2018]. Available from: https://www.nccn.org/professionals/physician_gls/PDF/hepatobiliary.pdf.
- 25. Zeng ZC, Tang ZY, Fan J, Zhou J, Qin LX, Ye SL, et al. Consideration of the role of radiotherapy for unresectable intrahepatic cholangiocarcinoma: a retrospective analysis of 75 patients. Cancer journal (Sudbury, Mass). 2006;12(2):113–22. Epub 2006/04/25. pmid:16630402.
- 26. Kopek N, Holt MI, Hansen AT, Hoyer M. Stereotactic body radiotherapy for unresectable cholangiocarcinoma. Radiotherapy and oncology: journal of the European Society for Therapeutic Radiology and Oncology. 2010;94(1):47–52. Epub 2009/12/08. pmid:19963295.
- 27.
Theise ND PY, Nakanuma Y. WHO Classification of Tumours of the Digestive System. 4th ed. ed. Lyon, France: IARC; 2010. 225 p.
- 28. Allen RA, Lisa JR. Combined liver cell and bile duct carcinoma. The American journal of pathology. 1949;25(4):647–55. Epub 1949/07/01. PubMed Central PMCID: PMCPMC1942823. pmid:18152860
- 29. Akiba J, Nakashima O, Hattori S, Tanikawa K, Takenaka M, Nakayama M, et al. Clinicopathologic analysis of combined hepatocellular-cholangiocarcinoma according to the latest WHO classification. The American journal of surgical pathology. 2013;37(4):496–505. Epub 2013/02/08. pmid:23388123.
- 30. Ikeda H, Harada K, Sato Y, Sasaki M, Yoneda N, Kitamura S, et al. Clinicopathologic significance of combined hepatocellular-cholangiocarcinoma with stem cell subtype components with reference to the expression of putative stem cell markers. American journal of clinical pathology. 2013;140(3):329–40. Epub 2013/08/21. pmid:23955451.
- 31. Sasaki M, Sato H, Kakuda Y, Sato Y, Choi JH, Nakanuma Y. Clinicopathological significance of 'subtypes with stem-cell feature' in combined hepatocellular-cholangiocarcinoma. Liver international: official journal of the International Association for the Study of the Liver. 2015;35(3):1024–35. Epub 2014/04/10. pmid:24712771.
- 32. Shibahara J, Hayashi A, Misumi K, Sakamoto Y, Arita J, Hasegawa K, et al. Clinicopathologic Characteristics of Hepatocellular Carcinoma With Reactive Ductule-like Components, a Subset of Liver Cancer Currently Classified as Combined Hepatocellular-Cholangiocarcinoma With Stem-Cell Features, Typical Subtype. The American journal of surgical pathology. 2016;40(5):608–16. Epub 2016/01/07. pmid:26735856.