Page 130 - Read Online
P. 130

Fatourou et al. Hepatoma Res 2018;4:63  I  http://dx.doi.org/10.20517/2394-5079.2018.62                                          Page 3 of 11

                                                                          [6]
               similar prognostic outcomes was addressed in a study by Merani et al. . This retrospective analysis included
               6817 patients that were listed with a diagnosis of HCC in the Scientific Registry of Transplant Recipients
               (SRTR) in the United States and showed that downstaging to an AFP level ≤ 400 ng/mL was associated with
               good survival rates and prognosis, regardless of the initial AFP level. More specifically, patients who were
               successfully downstaged to AFP ≤ 400 ng/mL had a similar dropout rate (10% in both groups) and post-
               transplant survival rates (89% vs. 78% at 3 years, P = 0.11) to patients with AFP levels persistently ≤ 400 ng/mL.

               A strong dose-response relationship between AFP level and post-transplant outcomes was demonstrated in
               a study that utilised data from the UNOS registry, that included patients (n = 45,267) who were transplanted
                                           [15]
               in the US between 2002 and 2011 . Although patients with an AFP < 15 ng/mL prior to transplantation had
               similar survival rates to patients without HCC, there was a significant decrease in survival as AFP increased;
               16-65 ng/mL [adjusted hazard ratio (AHR) = 1.38, 95% CI : 1.23-1.54], 66-320 ng/mL (AHR = 1.65, 95% CI : 1.45-
               1.88), and greater than 320 ng/mL (AHR = 2.37, 95% CI : 2.06-2.73). In addition, patients with tumours beyond
               the Milan criteria at listing had excellent post-transplant survival if serum AFP level was ≤ 15 ng/mL (AHR =
               0.97, 95% CI : 0.66-1.43). This study also showed that downstaging of AFP following locoregional treatment was
                                                                    [15]
               associated with improved post-transplant survival and prognosis .
                                             [12]
               In a prospective study by Lai et al. , mRESIST (modified Response Evaluation criteria in Solid Tumours)
               progression following locoregional treatment and AFP slope > 15 ng/mL/month, as defined by the difference
               between the initial and the last pre-LT AFP value divided by the time span between the two values, were
               independent risk factors of recurrence and survival. Patients within and beyond radiological Milan criteria had
               similar recurrence-free and overall survival rates if they had stable disease post locoregional treatment and/
               or an AFP slope < 15 ng/mL/month. Similarly, patients within the Milan criteria but with either progressive
               disease or AFP slope > 15 ng/mL/month were shown to have increased recurrence rates compared to patients
                                                          [12]
               within or beyond Milan criteria with no risk factors . Another retrospective study from the same group, has
               shown that AFP > 400 ng/mL can result in an 8-fold increase in the risk of recurrence and a combination with
               a total tumour diameter < 8 cm can result comparable 5 year survival and recurrence rates .
                                                                                         [16]
               The predictive value of AFP slope, rather than an AFP single value alone, was also examined in a study by
                          [17]
               Vibert et al. , which included 252 patients transplanted between 1985 and 2005, in a single centre. AFP
               progression, as defined by an increase greater than 15 ng/mL monthly, was significantly associated with
               reduced 5 year recurrence-free (47% vs. 74%, P = 0.01) and overall survival (54% vs. 77%, P = 0.02). In the
               multivariate analysis, progression of AFP was independently associated with recurrence-free and overall
               survival. Interestingly, all examined static values of AFP prior to transplantation were not correlated with
               overall or recurrence-free survival. AFP progression was also significantly associated with the presence of
               vascular invasion and poor histological differentiation, which suggests that it can be a valuable surrogate pre-
               operative marker of unfavourable histological findings .
                                                            [17]
                                           [11]
               Another study by Hameed et al.  has shown that setting a cut-off value of 1000 ng/mL as an exclusion
               criteria for transplantation, would have resulted in a 20% reduction in the rate of HCC recurrence at the cost
               of excluding only 4.7% of patients listed. Following this observation, our own national (United Kingdom)
               Transplant guidelines have applied this cut-off level as an exclusion criterion for LT. This study has also
               demonstrated a strong correlation between AFP and micro-vascular invasion, especially in patients with AFP
                                                [11]
               values varying between 300-1000 ng/mL .
               A large retrospective European multicentre study intended to identify variables for selecting patients that
               would have the best benefit from transplantation . AFP ≥ 1000 ng/mL, MELD ≤ 13, mRESIST progressive
                                                        [18]
               or complete response and within Milan criteria were associated with a poor intention to treat (ITT) benefit
               from LT. Based on these risk factors, four benefit groups were identified. Patients that met three out of four
   125   126   127   128   129   130   131   132   133   134   135