As for the management of hilar cholangiocarcinoma (HCCA), the curative-intent surgery, including an extra-hepatic bile duct resection combined with partial hepatectomy and a regional or more extended lymphadenectomy, has always been regarded as the gold standard therapeutic modality.1–3 However, such invasive surgical procedure often takes a high risk of early mortalities, especially in those who developed post-hepatectomy liver failure (PHLF). One recently-published meta-analysis revealed a 12% 90-day mortality rate and a 40% major morbidity rate in patients with HCCA who have received a radical resection.4 A higher mortality rate reaching 18% was even observed in some experienced centers.4
Accumulating evidence has suggested that the preoperatively-estimated functional liver remnant volume (FLRV) had the most intensive relationship with PHLF among resected HCCA patients who received a combined partial hepatectomy at the same time.5–11 A better-preserved functional liver remnant after partial hepatectomy can be extremely vital due to its key role in patients' postoperative rehabilitation, accelerating anastomotic growth and the further prevention of early occurrence of anastomotic leakage. Currently, the classical and acceptable criteria of FLRV is larger than 40%, which has been validated in previous studies.8,12 However, this standard has its limitations that FLRV is only defined broadly but not specifically. For example, for patients with cirrhosis or obstructive jaundice who shared a relatively worse liver health status, whether FLRV should be modified accordingly remains unexplored. Patients with HCCA were often presented with obstructive jaundice preoperatively and suffered chronic injuries resulted from the elevated serum bilirubin level-mediated hepatocytotoxicity. Compared with those without obstructive jaundice who were about to receive curative surgery, jaundiced patients generally shared an impaired liver function reserve. Therefore, in such a circumstance, a modified FLRV in jaundiced patients with HCCA who were about to receive curative surgery might be more appropriate and feasible. However, having screened all relevant studies, corresponding studies focused on the optimal FLRV in jaundiced HCCA patients who were about to receive a standard surgical procedure were still lacking.
Therefore, current study was performed to evaluate the predictive value of FLRV for postoperative liver failure among resected HCCA patients who have received a combined partial hepatectomy at the same time. Moreover, an optimal cut off value would also been furtherly identified. The predictive accuracy of newly-acquired predictive criteria of FLRV versus the classical FLRV (40%) would also be compared.
METHODS PatientsWe retrospective reviewed resected HCCA patients between June, 2000 and June, 2018 at our hospital. Only patients received a standard radical resection were included, including an extra-hepatic bile duct resection, combined with partial hepatectomy and lymphadenectomy. A right or left hemi-hepatectomy or more extended hepatectomy would be performed in patients with Bismuth III or IV disease with an obvious liver invasion. For patients with Bismuth I or II disease, when an obvious caudate lobe invasion was detected, combined partial hepatectomy would also be performed. Moreover, a wedge resection would also be performed in order to achieve cholangioplasty and the subsequent high position biliary-enteric anastomosis. This study was approved by institutional ethics review board of West China Hospital.
Preoperative evaluation, preparation, and surgeryThe perioperative management were consistent with our previous studies.13–16 Upon admission, a systemic body examination, including peripheral blood-based examination such as tumor-specific biomarkers CA199, or radiological examinations such as computed tomography (CT) or magnetic resonance imaging (MRI), would be applied in all patients to have an initial evaluation on tumor stage and tumor load. Patients who were considered to have developed distant metastatic disease would be excluded. A preoperative percutaneous trans-hepatic cholangial drainage or endoscopic biliary drainage, combined with hepatoprotective therapy, would be applied in those with obstructive jaundice (TB level >200 μmol/L) so as to relieve the high bilirubin-mediated hepatotoxicity as well as prevent the occurrence of PHLF. After drainage, patients with preoperative bilirubin level lower than 200 μmol/L were considered eligible for curative surgery. The liver volumetry has been regularly performed in our center since the first hepatectomy in the general surgery department. If the estimated FLRV indicated a relative compensable liver volume after partial hepatectomy, PVE would be avoided and more aggressive surgical procedures would be acquired, especially a wider resection margin would be performed in order to ensure tumor clearance. However, for patients whose FLRV were less than 40% or remnant liver volume seemed to be un-compensable after surgery, the potential risk of PHLF, ICU admission with an extremely increased hospital expense, or even perioperative mortalities would be informed in detail to patients and their families. If they still insisted on performing curative surgery, they were required to sign an informed consent form that they were willing to undertake the relevant risk. The FLRV was mainly assessed and calculated via computed tomography-volumetric evaluation. Moreover, a preoperative Child A or B degree of liver function was also required. The specific exact inclusion and exclusion criteria were consistent with our previous series.16 All surgical candidates have experienced a multi-disciplinary discussion to find the most applicable surgical regime.
The definition ofRegarding the criteria of PHLF, current study adopted the criteria proposed by the International Hepatic Surgery Research Group (ISGLS) in 2011.17 As is illustrated in Figure S2, for cases with preoperative normal INR level (≤1.5), a higher or abnormal INR level (>1.5) combined with hyper-bilirubinemia level (>17.1 μmol/L) were diagnosed with PHLF.17 However, for cases with obstructive jaundice derived from various postoperative factors, such as cholangitis, the criteria mentioned above would be not feasible. For cases with preoperatively-detected abnormal INR level (>1.5), an increased INR level than preoperative INR level combined with hyper-bilirubinemia level (>17.1 μmol/L) were diagnosed with PHLF. Additionally, for cases with a normal INR on or after post-surgical Day 5, patients with a hyperbilirubinemia combined with coagulation disfunction, such as the requirement of continuous infusion of fresh frozen plasma for the stability of coagulation function, would also be considered. The severity of PHLF is classified as three categories: Grade A: only with laboratory parameters abnormalities and requires no special clinical care; Grade B: with laboratory parameters abnormalities but requires special clinical care or non-invasive intervention; Grade C: with laboratory parameters abnormalities but requires invasive intervention, such as artificial liver, or liver transplantation.17
Follow upAll surgically-treated patients were informed to monitor their disease status at the outpatient of our hospital every 1–2 months in the first year and every six months thereafter. Our researchers would renew their survival data once a year via telephone or any other social media. The most-recently follow-up was performed on October 1 2023.
Statistical analysisIBM SPSS version 25.0 (IBM SPSS, Chicago, IL, USA), Graph-Pad Prism 7, and R software (version 4.2.2) (R package pROC) were used for statistical analysis. All data were recorded as categorical data, which were presented as numbers (percentages) and compared via chi squared and Fisher's exact tests. Overall survival (OS) was defined as the survival period from the date of receiving radical surgery to the date of death or last follow-up. Disease-free survival (DFS) was defined as the survival period from the date of receiving surgery to the date of recurrence or disease progression. Kaplan–Meier curves were used for evaluating survival differences. Cox-proportional hazards model was used to create multivariate model for independent prognostic factors for survival, which were presented with hazard ratio (HR) with its 95% confidence interval (CI). The binary logistic regression was used for the selection of predictors as well as independent predictors on PHLF, which were presented with odds ratio (OR) and its 95% CI. p values lower than 0.05 indicated the existence of statistical significance.
RESULTS Comparative analyses between patients withBased our own cancer database, a total of 380 HCCA patients received curative surgery in our hospital and 90 patients did not receive a combined hepatectomy. Among the remaining 290 patients who received a combined hepatectomy, 54 patients were presented without jaundice and were therefore excluded. Moreover, owing to the inadequate original data, 12 patients were furtherly excluded. Finally, a total of 224 jaundiced patients who received the standard curative surgery with adequate clinical data were finally identified. As is recorded in Table 1, patients who developed PHLF and those who did not develop PHLF were comparable in age (≥70 vs. <70) (p = 0.1630) and sex (male vs. female) (p = 0.2650). However, patients in the former group were more frequently detected with Bismuth III-IV disease (79.1% vs. 54.1%, p = 0.0420). Moreover, patients with PHLF shared a higher but not statistically significant incidence of receiving preoperative biliary drainage (95.3% vs. 88.4%, p = 0.1630). Pre-surgery PVE was more frequently performed in patients with PHLF (18.6% vs. 3.9%, p = 0.0010). Major hepatectomy (48.8% vs. 17.1%, p < 0.0001) and major vascular resection and reconstruction (41.9% vs. 26%, p = 0.0320) were more frequently performed in patients with PHLF. Patients who developed PHLF were generally in a more advanced TNM stage (III–IV disease: 90.7% vs. 74.6%, p = 0.0140). The proportion of patients with FLRV <40% was significantly higher in patients with PHLF (32.6% vs. 13.3%, p = 0.0040). The incidence of concurrent other postoperative major morbidities (Clavien-Dindo grade III–IV) was significantly higher in patients with PHLF (52.1% vs. 12.2%, p < 0.0001). Comparable incidence of mortalities within 90 days after surgery (p = 0.1570) and overall recurrence rate (p = 0.2180) were acquired between two group.
TABLE 1 Baseline characteristics of the entire cohort based on liver failure.
Abbreviations: AJCC, American Joint on Cancer; AJCC, American Joint Committee on Cancer; C–D grade, Clavien-Dindo grade; FLRV, functional liver remnant volume; PVE, portal vein embolization.
aResected more than three segments.
In the survival analyses, as is illustrated in Figure 1, patients with PHLF shared comparable OS (median survival period: 17.9 vs. 22.02 months, p = 0.2078) and DFS (median survival period: 37.44 vs. 47.33 months, p = 0.1863) versus those without PHLF.
FIGURE 1. KM curves between patients who developed PHLD and those without PHLD. (A) OS; (B) DFS. The inconsistent distribution of FLRV between patients with PHLD and those without PHLD as well as the predictive accuracy of FLRV (continuous data) was also presented. (C) Box plot showing the inconsistent distribution of FLRV; (D) ROC curve reflecting the predictive accuracy of FLRV.
As is presented in Figure 1C, the level of FLRV in patients with PHLF and those without PHLF varied a lot (p < 0.0500). We subsequently performed a ROC curve evaluating the predictive accuracy of FLRV in predicting the occurrence of PHLF among jaundiced post-hepatectomy HCCA patients. The result indicated a high predictive accuracy (AUC: 0.81, p < 0.0001) (Figure 1D). Moreover, we also acquired the optimal cut off value of FLRV in jaundiced HCCA patients with favorable specificity and sensitivity. The results indicated that the optimal cut off value of FLRV was 53.5%, with a sensitivity of 81.2% and a specificity of 81.4% (Figure 1D). At the same time, we evaluated the predictive value of FLRV (continuous data) in PHLF. The results suggested that FLRV (continuous data) was an independent predictor of PHLF (p < 0.0001) (Table S1). We furtherly evaluated the predictive accuracy of FLRV in PHLF among jaundiced HCCA patients based on the performance of major hepatectomy. For patients who received major hepatectomy, FLRV failed to show a significant predictive accuracy (AUC: 0.52) (Figure S1A). However, for patients who received partial hepatectomy but not major hepatectomy, FLRV revealed a significant predictive accuracy (AUC: 0.86) (Figure S1B).
Comparative analyses regarding clinic-pathological features and long-term survival based on differentAs is recorded in Table 2, we furtherly evaluated the impact of newly-acquired FLRV cut off value in terms of clinic-pathological features and long-term survival. Patients with FLRV <53.5% were comparable versus patients with FLRV ≥53.5% in terms of age (p = 0.3730) and sex (p = 0.9560). The proportion of patients with Bismuth III-IV disease was significantly higher in patients with FLRV <53.5% (p = 0.0070). Concurrent hepato-atrophy was more frequently detected in patients with FLRV<53.5% (p = 0.0420). Preoperative PVE was more frequently performed in patients with FLRV <53.5% (p < 0.0001). Major hepatectomy (p < 0.0001) and major vascular resection and reconstruction (p = 0.0010) were also more frequently performed among patients in the former group. Comparable surgical margin status (p = 0.2560), resected margin width (p = 0.2550) and resected tumor size (p = 0.3410) were acquired. Comparable pathological features, such as perineural invasion, were also acquired between two groups. Patients with FRLV <53.5% were generally in a more advanced stage. Moreover, higher frequencies of postoperative any morbidity (p = 0.0010), major morbidities (p < 0.0001), and PHLF (p < 0.0001) were detected among patients with FLRV <53.5%. Comparable incidence of mortalities within 90 days after surgery (p = 0.1390) and overall recurrence rate (p = 0.6110) were acquired between two group. In the survival analyses, FLRV of 53.5% could furtherly stratify patients with different survival outcomes that jaundiced HCCA patients with FLRV <53.5% shared a much worse OS (median survival period: 14.97 vs. 26.19 months, p = 0.0038) (Figure 3A) but similar DFS (median survival period: 37.44 vs. 47.33 months, p = 0.3194) (Figure 3B) than those with FLRV ≥53.5%.
TABLE 2 Basic characteristics of patients according to cut off values of FLRV.
Abbreviations: AJCC, American Joint Committee on Cancer; C–D grade, Clavien-Dindo grade; FLRV, functional liver remnant liver volume; PVE, portal vein embolization.
aResected more than three segments.
As for the other conventional FLRV cut off value of 40%, similar observations were also detected. Patients with FLRV <40% and those with FLRV ≥40% were comparable in terms of Bismuth type (p = 0.0850), concurrent hepato-atrophy (p = 0.1890), and preoperative PVE (p = 0.0560). Comparable incidence of major vascular resection and reconstruction (p = 0.2440) were also acquired between two groups. The overall tumor stage was also comparable between two groups (p = 0.8370). Moreover, comparable incidence of postoperative any complication (p = 0.2320) and major complication (p = 0.1330) were detected between two groups. FLRV of 40% had no impact on the overall prognosis that comparable OS (median survival period: 17.07 vs. 22 months, p = 0.3194) (Figure 3C) and DFS (median survival period: 37.44 vs. 46.73 months, p = 0.3315) (Figure 3D) were acquired between two groups.
Comparison of the predictive accuracy ofWe furtherly compared the predictive accuracy of newly-acquired FLRV criteria (53.5%) versus conventional FLRV criteria (40%) in PHLF. The result indicated a significantly higher predictive accuracy of our new criteria (AUC: 0.81 vs. 0.60, p < 0.0500) (Figure 2).
FIGURE 2. ROC curve comparing the predictive accuracy of PHLF among jaundiced HCCA patients based on different cut off value of FLRV.
FIGURE 3. KM curves reflecting the survival difference based on different cut off values of FLRV. (A) OS based on FLRV of 53.5%; (B) DFS based on FLRV of 53.5%; (C) OS based on FLRV of 40%; (D) DFS based on FLRV of 40%.
Final results indicated that major hepatectomy (performed vs. not performed) (p < 0.0001), major vascular reconstruction (performed vs. not performed) (p = 0.0410), FLRV (≥53.5% vs. <53.5%) (p < 0.0001), FLRV (≥40% vs. <40%) (p = 0.003), PVE (Performed vs. not performed) (p = 0.0020), and TNM stage (I/II vs. III/IV) (p = 0.0300) were predictors of PHLF in resected HCCA patients with obstructive jaundice. Multi-variate analysis indicated that FLRV (>53.5% vs. ≤53.5%) (p < 0.0001) was an independent predictor of PHLF. Moreover, major hepatectomy (performed vs. not performed) (p = 0.0610) was also a potential independent predictor of PHLF with a borderline p value 0.061 (Table 3).
TABLE 3 Univariate and multivariate logistic regression of predictors for postoperative liver failure.
Variables | Univariate p-value | Multivariate analysis | ||
OR | 95%CI | Multivariate p-value | ||
Age (≥70 vs. <70) | 0.2230 | |||
Concurrent hepato-atrophy (yes vs. no) | 0.4190 | |||
Major hepatectomy (performed vs. not performed) | <0.0001 | 0.156 | 0.022–1.093 | 0.0610 |
Major vascular reconstruction (performed vs. not performed) | 0.0410 | 1.124 | 0.453–2.792 | 0.8010 |
FLRV (≥40% vs. <40%) | 0.0030 | 0.697 | 0.107–4.535 | 0.7060 |
FLRV (≥53.5% vs. <53.5%) | <0.0001 | 83.124 | 18.601–371.456 | <0.0001 |
Preoperative PVE (performed vs. not performed) | 0.0020 | 1.636 | 0.205–13.091 | 0.6420 |
Preoperative biliary drainage (performed vs. not performed) | 0.2200 | |||
Preoperative cholangitis (yes vs. no) | 0.5240 | |||
Preoperative liver function (child A vs. child B) | 0.5430 | |||
TNM stage (I/II vs. III/IV) | 0.0300 | 2.065 | 0.587–7.267 | 0.2590 |
Abbreviations: CI: confidence interval; FLRV: functional liver remnant volume; OR: odds ratio; PVE: portal vein embolization.
Univariate and multi-variate cox regression of prognostic factors forAs is recorded in Table 4, the results of univariate analyses indicated that Bismuth Type (I/II vs. III/IV) (p < 0.0001), FLRV (≥53.5% vs. <53.5%) (p = 0.0040), Surgical margin (positive vs. negative) (p = 0.002), Surgical margin width (<5 mm vs. ≥5 mm) (p = 0.050), T stage (T1–2 vs. T3–4, 8th AJCC) (p < 0.0001), Lymph node status (N− vs. N+, 8th AJCC) (p < 0.0001), perineural invasion (yes vs. no) (p = 0.0240) were all prognostic factors for OS of the entire cohort. Multi-variate analysis indicated that Surgical margin (positive vs. negative) (p = 0.046), FLRV (≥53.5% vs. <53.5%) (p = 0.0470), T stage (T1–2 vs. T3–4, 8th AJCC) (p < 0.0001), and lymph node status (N− vs. N+, 8th AJCC) (p = 0.0020), and perineural invasion (yes vs. no) (p = 0.0330) were independent prognostic factors for OS of the entire cohort.
TABLE 4 Univariate and multivariate cox regression of prognostic factors for OS of the entire cohort.
Variables | Univariate p value | Multivariate analysis | ||
HR | 95%CI | Multivariate p value | ||
Age (≥70 vs. <70) | 0.6820 | |||
Sex (male vs. female) | 0.8010 | |||
CA199 (<150 U/mL vs. ≥150 U/mL) | 0.3080 | |||
Bismuth type (I/II vs. III/IV) | <0.0001 | 1.286 | 0.898–1.843 | 0.1700 |
FLRV (≥53.5% vs. <53.5%) | 0.0040 | 1.379 | 1.005–1.892 | 0.0470 |
Surgical margin (positive vs. negative) | 0.0020 | 1.416 | 1.006–1.991 | 0.0460 |
Surgical margin width (<5 mm vs. ≥5 mm) | 0.0050 | 0.782 | 0.560–1.093 | 0.1500 |
T stage (T1–2 vs. T3–4, 8th AJCC) | <0.0001 | 2.381 | 1.640–3.458 | <0.0001 |
Lymph node status (N− vs. N+, 8th AJCC) | <0.0001 | 1.613 | 1.197–2.174 | 0.0020 |
Perineural invasion (yes vs. no) | 0.0240 | 1.397 | 1.028–1.897 | 0.0330 |
Lymph-vascular invasion (yes vs. no) | 0.2050 |
Abbreviations: AJCC, American Joint Committee on Cancer; CI, confidence interval; FLRV, functional liver remnant volume; HR, hazard ratio.
DISCUSSIONOur previous meta-analysis has indicated that preoperative jaundice in in patients with gallbladder carcinoma was correlated with a significantly lower resectability rate and a higher incidence of perioperative mortalities.18 Similarly, in the surgical management of patients with HCCA, the majority of cases were presented with obstructive jaundice upon admission or surgery. Moreover, according to the latest NCCN guidelines, in order to acquire a clear margin, once the tumor invaded beyond the confluence of the right and left hepatic bile duct and involved the liver, the corresponding hemi-hepatectomy would be unavoidable. In such a circumstance, owing to the hepatotoxicity resulted from high bilirubin level, HCCA patients who were about to receive curative surgery often took a high risk of PHLF and other severe postoperative morbidities, as well as perioperative mortalities. Therefore, it's quite necessary for clinicians to find optimal predictors in predicting PHLF.
Either for patients with hepatic malignancies or biliary malignancies, combined partial hepatectomy has always been performed in a high frequency and the potential predictors of PHLF has been widely discussed. Numerous studies have indicated that preoperative selective PVE could lead to a significantly decreased incidence of PHLF as well as early mortalities among surgically-treated HCCA patients.6,9 Others have revealed the predictive value of concurrent cholangitis in post-hepatectomy liver insufficiency.7 Preoperative ICG R15 has been reported to be closely-associated with PHLF and any other moderate-to-severe morbidities.19 External biliary drainage has been demonstrated to increase the risk of PHLF.10 Additionally, intraoperative major vascular resection and reconstruction has also been demonstrated to be closely-associated with liver disfunction.11 The incidence of major vascular reconstruction of our cohort in jaundiced patients was 29% and patients with obstructive jaundice shared a significantly higher incidence of major vascular reconstruction than those without it (p = 0.0320). Intraoperative major vascular (portal vein, hepatic artery, or major hepatic veins) resections and reconstructions are generally performed in patients with an obvious outflow obstruction. The venous wall was often thin and fragile and it is often difficult to reconstruct and re-anastomosis the broken ends of venous vessels, which would lead to an uncontrolled intraoperative bleeding as well as warm ischemia time, causing severe ischemia-resulted injury to our liver.20–23 The massive intraoperative bleeding would furtherly increase the difficulty of surgery, which would significantly prolong operative time and increase intraoperative blood loss. Besides, intraoperative long-time hepatic inflow occlusion is often required in the process of major vascular reconstruction, which would furtherly aggravate ischemia-mediated liver injury furtherly. Moreover, many other postoperative risk factors, such as severe abdominal infectious disease, would also contribute a lot to the development of secondary PHLF. However, this issue has been rarely explored.
Although various invasive or non-invasive predictors have been reported and discussed, FLRV has always been the most applicable modality in evaluating PHLF for patients who were about to receive a combined radical resection. Lee JW et al indicated a high predictive accuracy in PHLF when it combined with volume-to-body weight.8 FLRV has also been reported as independent predictor of PHLD in patients with cirrhotic HCC.24 The defects of FLRV have also been discussed and previous studies have showed its inferiority versus Future liver remnant function (FLRF).25,26 However, we cannot deny the fact that FLRV still served as the corner stone in predicting PHLF that FLRF was calculated from FRL: FLRF = FLRV% × total liver function. To date, few researchers have paid attention on the more specific criteria of FLRV in different situations, especially in jaundiced patients with HCCA. Considering the more complex and severe burden to liver among jaundiced HCCA patients as mentioned above, the classical and conventional criteria of FLRV <40% might be not applicable to some extent. Consequently, based on our single-center experience, we focused on jaundiced HCCA patients and have put forward a new standard of FLRV. The newly-detected FLRV level was correlated with a much higher predictive accuracy in PHLF versus the old standard (FLRV: 40%) and has been demonstrated as an independent predictor of PHLF. Further analyses regarding its impact on the clinic-pathological features and long-term survival has been performed. The final results indicated that the newly-acquired FLRV (53.5%) could better help clinicians to stratify patients with different postoperative outcomes, especially the occurrence of postoperative major morbidities versus conventional FLRV (40%) (p < 0.0001 vs. p = 0.133, Table 2). Moreover, in the subsequent survival analysis, patients with an estimated FLRV lower than 53.5% even shared a worse OS than those with FLRV higher than 53.5% while the phenomenon was not obvious for FLRV of 40%. These promising findings might help clinicians to choose more favorable therapeutic regimes for HCCA patients who were about to receive curative surgery with more satisfying postoperative and survival outcomes. More deeply, we furtherly evaluated the predictive accuracy of FLRV in jaundiced HCCA patients based on the perform of major hepatectomy. As is illustrated in Figure S1, among patients who received major hepatectomy, FLRV showed an extremely lower predictive accuracy versus those who did not receive major hepatectomy (AUC 0.52 vs. AUC 0.86). One of the reasons might be that major hepatectomy also served as an independent predictor of PHLF with a borderline p value (p = 0.061) and the effect of FLRV was confounded.
Current study should be interpreted with several limitations. Firstly, our study is a single-center study and only reflected general condition of Asian populations. Secondly, our cohort came across nearly two decades and the development in perioperative management would also impact a lot on the occurrence of PHLF. Thirdly, if various geographical and genetic characteristics could be incorporated, the results would be more validating. However, the inadequate original data hindered us from further exploration. In such a case, a multi-center studies with geographical, racial and genetic data included, accompanied with training group and validation group, would be furtherly required. Fourth, the correlation between tumor diameter and FLRV or PHLF should also be furtherly evaluated. The larger the tumor volume, the higher the likelihood of tumor invasion into the liver or the tumor extending beyond the hilar bile duct confluence, resulting in a greater extent of liver resection needed to achieve R0 resection. However, in our tumor database, only a small portion of patients have clear tumor diameter information. Therefore, the above analysis is not feasible in our single-center study. This issue requires further exploration in future larger sample size, multicenter studies. Finally, many other potential influencing factors, such as preoperative comorbidities, still need to be analyzed furtherly. However, the inadequate original date hindered us from further exploration.
CONCLUSIONFLRV (continuous data) had a high predictive accuracy in jaundiced patients in predicting PHLF and the newly-acquired cut off value (FLRV: 53.5%) showed an extremely high predictive accuracy (AUC: 0.81) than conventional FLRV <40% (AUC: 0.60) (p < 0.05). Moreover, its impact on various postoperative outcomes, especially the occurrence of major morbidities, as well as long-term survival has also been revealed, which might help clinicians to stratify patients with different therapeutic modalities and outcomes. Future multi-center studies with more parameters included, such as geographical, racial and genetic data, for training and validation are required for further validation.
AUTHOR CONTRIBUTIONSTian-Run Lv: Conceptualization (lead); data curation (lead); formal analysis (lead); resources (lead); software (lead); supervision (lead); validation (lead); visualization (lead); writing – original draft (lead); writing – review and editing (lead). Wen-Jie Ma: Conceptualization (equal); data curation (equal); formal analysis (equal); writing – original draft (equal); writing – review and editing (equal). Fei Liu: Conceptualization (equal); data curation (equal); formal analysis (equal); visualization (equal); writing – review and editing (equal). Hai-Jie Hu: Funding acquisition (lead). Yan-Wen Jin: Resources (equal); software (equal); supervision (equal); validation (equal); visualization (equal); writing – review and editing (equal). Fu-Yu Li: Methodology (equal); project administration (lead); writing – review and editing (equal).
FUNDING INFORMATIONThis study was supported by 1.3.5 project for disciplines of excellence, West China Hospital, Sichuan University (ZYJC21046); 1.3.5 project for disciplines of excellence-Clinical Research Incubation Project, West China Hospital, Sichuan University (2021HXFH001); China Telecom Sichuan Company Biliary Tract Tumor Big Data Platform and Application Phase I R&D Project (312230752). National Natural Science Foundation of China for Young Scientists Fund (82203650, 82203782); Sichuan Natural Science Foundation (2024NSFSC0742, 2024NSFSC1949); Sichuan University-Sui Ning School-local Cooperation project (2022CDSN-18).
CONFLICT OF INTEREST STATEMENTAll authors declare have no conflicts of interest to disclose.
DATA AVAILABILITY STATEMENTAll original data were extracted from cancer database of our hospital and can be provided if required.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Objective
Our study aims to evaluate the predictive accuracy of functional liver remnant volume (FLRV) in post-hepatectomy liver failure (PHLF) among surgically-treated jaundiced patients with hilar cholangiocarcinoma (HCCA).
Methods
We retrospectively reviewed surgically-treated jaundiced patients with HCCA between June, 2000 and June, 2018. The correlation between FRLV and PHLF were analyzed. The optimal cut off value of FLRV in jaundiced HCCA patients was also identified and its impact was furtherly evaluated.
Results
A total of 224 jaundiced HCCA patients who received a standard curative resection (43 patients developed PHLF) were identified. Patients with PHLF shared more aggressive clinic-pathological features and were generally in a more advanced stage than those without PHLF. An obvious inconsistent distribution of FLRV in patients with PHLF and those without PHLF were detected. FLRV (continuous data) had a high predictive accuracy in PHLF. The newly-acquired cut off value (FLRV = 53.5%, sensitivity = 81.22%, specificity = 81.4%) showed a significantly higher predictive accuracy than conventional FLRV cut off value (AUC: 0.81 vs. 0.60,
Conclusion
For jaundiced patients with HCCA, a modified FLRV of 53.5% is recommended due to its great impact on PHLF, as well as its correlation with postoperative major morbidities as well as overall prognosis, which might help clinicians to stratify patients with different therapeutic regimes and outcomes. Future multi-center studies for training and validation are required for further validation.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details

1 Department of Biliary Tract Surgery, General Surgery, West China Hospital of Sichuan University, Chengdu, Sichuan, China; Research Center for Biliary Diseases, West China Hospital of Sichuan university, Chengdu, Sichuan, China