Abstract
Purpose
Radioembolisation is part of the multimodal treatment of hepatocellular carcinoma (HCC) at specialist liver centres. This study analysed the impact of prior treatment on tolerability and survival following radioembolisation.
Methods
This was a retrospective analysis of 325 consecutive patients with a confirmed diagnosis of HCC, who received radioembolisation with yttrium-90 resin microspheres at eight European centres between September 2003 and December 2009. The decision to treat was based on the clinical judgement of multidisciplinary teams. Patients were followed from the date of radioembolisation to last contact or death and the nature and severity of all adverse events (AEs) recorded from medical records.
Results
Most radioembolisation candidates were Child-Pugh class A (82.5%) with multinodular HCC (75.9%) invading both lobes (53.1%); 56.3% were advanced stage. Radioembolisation was used first-line in 57.5% of patients and second-line in 34.2%. Common prior procedures were transarterial (chemo)embolisation therapies (27.1%), surgical resection/transplantation (17.2%) and ablation (8.6%). There was no difference in AE incidence and severity between prior treatment subgroups. Median (95% confidence interval [CI]) survival following radioembolisation was similar between procedure-naive and prior treatment groups for Barcelona Clinic Liver Cancer (BCLC) stage A: 22.1 months (15.1–45.9) versus 30.9 months (19.6–46.8); p = 0.243); stage B: 18.4 months (11.2–19.4) versus 22.8 months (10.9–34.2); p = 0.815; and stage C: 8.8 months (7.1–10.8) versus 10.8 months (7.7–12.6); p = 0.976.
Conclusions
Radioembolisation is a valuable treatment option for patients who relapse following surgical, ablative or vascular procedures and remain suitable candidates for this treatment.
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Introduction
Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and a leading cause of cancer death worldwide [1, 2]. Curative treatment is feasible by resection or transplantation in early stage HCC (Barcelona Clinic Liver Cancer [BCLC] stage 0 or BCLC stage A) [1]. However, a high proportion of patients are not diagnosed until they are at an advanced stage (BCLC stage C) of the disease where curative interventions are not feasible. Tumour recurrence, or development of new tumour occurs in 70–80% of patients by 5 years after resection [3]. Percutaneous ablation, either radiofrequency ablation (RFA) or percutaneous ethanol injection, are options for BCLC stage 0-A HCC unsuitable for surgery. Locoregional therapy with transarterial chemoembolisation (TACE) is the preferred first-line treatment option for patients with intermediate stage (BCLC stage B) HCC [4, 5]. Sorafenib is an oral multi-tyrosine kinase and angiogenesis inhibitor that is the only approved systemic treatment for advanced stage (BCLC stage C) HCC, but while sorafenib has been shown to improve overall survival, its adverse event profile is an important limitation to its use [6, 7].
Radioembolisation—or selective internal radiation therapy (SIRT)—is a form of brachytherapy by the intra-arterial delivery of small (30–35 μm) biocompatible glass or resin microspheres loaded with the radionuclide yttrium-90 (90Y) to tumour sites in the liver. The 90Y microspheres lodge in the tumour capillaries plexus where they deliver a localised high-energy (0.93 MeV) dose of beta-radiation. Due to the limited tissue penetration of the beta-radiation, its tumouricidal activity is confined to the immediate proximity of the tumour, largely sparing normal liver parenchyma.
SIRT with 90Y microspheres, is used in specialist liver centres as part of the multimodal treatment of hepatocellular carcinoma (HCC) [8, 9]. However, the impact of prior treatment on tolerability and survival after radioembolisation has not been analysed.
Methods
This study was a retrospective analysis of the data from the European Network on Radioembolisation with 90Y resin microspheres (ENRY) [8] to evaluate the impact of prior procedures on the safety and efficacy of radioembolisation in HCC. The patient population was identical to that reported in the original 2011 publication.
Consecutive patients with a confirmed diagnosis of HCC (either histologically proven or based on non-invasive European Association for the Study of the Liver criteria) and who had at least one follow-up visit after treatment were included in the analysis. Candidates for radioembolisation were considered from a population of patients who were not suitable for surgery (resection, liver transplantation), local ablation (percutaneous ethanol injection [PEI], radiofrequency ablation [RFA], cryoablation) or vascular (transarterial embolisation [TAE] or chemoembolisation [TACE]). Radioembolisation was performed with 90Y resin microspheres (SIR-Spheres; Sirtex Medical Limited, North Sydney, Australia). Patients may have received radioembolisation as a first-line therapy or after having progressed on previous surgical or non-surgical treatments (ablation, TAE or TACE). The decision to treat using radioembolisation was based on the clinical judgement of multidisciplinary teams at each centre. All patients provided informed consent for radioembolisation prior to treatment planning.
As part of a detailed pre-treatment work-up, patients underwent a thorough angiographic analysis and therapy simulation using 99mTc-MAA to detect and occlude all collateral vessels that may carry microspheres to extrahepatic organs, and to rule out a high lung shunt, respectively. Depending upon the extent of tumour burden, patients were treated by either a segmental, lobar or whole-liver treatment approach. Further details of the treatment procedure are published elsewhere [10, 11].
Patients were followed from the date of radioembolisation to last contact or date of death. The nature and severity of all adverse events (AEs) were accessed from the medical records and graded using the Common Terminology Criteria for Adverse Events version 3.0 (CTCAE v3). An analysis of clinical and laboratory AEs was performed from baseline to the end of month 3 and the highest grade recorded from any one of the two analysis periods (from day 0 to 7 or from day 8 to month 3).
All statistical algorithms were conducted using SAS (Cary, North Carolina) analytical software. P-values for continuous variables were compared by one-way ANOVA, for nominal categorical variables by chi-square general association test, and for ordinal variables by Cochran-Mantel-Haenszel row mean scores. The change in CTCAE grade from baseline to 3 months (month 3 minus baseline) was calculated and compared among five subgroups by the Kruskal-Wallis test. Transitions in laboratory CTCAE grade 3–4 (yes/no) at month 0 to CTCAE grade 3–4 (yes/no) at month 3 was compared by the exact McNemar test. Kaplan-Meier analyses were used to estimate overall survivals with stratification by prior treatment group and by Barcelona Clinic Liver Cancer (BCLC) stage.
Results
Patient and treatment characteristics
Overall, 325 patients who were recruited from eight European centres in Germany, Italy and Spain between September 2003 and December 2009 were included in the analyses.
Candidates for radioembolisation were mostly cirrhotic (78.5%) and had a Child-Pugh class A (82.5%). Many had multinodular HCC (75.9%) invading both lobes (53.1%) and/or the portal vein (13.5% branch; 9.8% main), and had an altered Eastern Cooperative Oncology Group (ECOG) performance status (ECOG ≥1: 45.8%). According to the BCLC staging system, 56.3% of patients were classified as advanced (stage C).
Just over half (187 patients; 57.5%) received radioembolisation as a first-line therapy, approximately one-third (111 patients; 34.2%) as second-line therapy and 27 patients (8.3%) as third or fourth-line treatment. Details of prior treatment and sequence are listed in Fig. 1 with baseline characteristics described in Table 1. The most common prior procedures overall were TACE or TAE in 88 patients (27.1%), followed by surgical resection or liver transplantation in 56 patients (17.2%) and ablation in 28 patients (8.6%).
As shown in Table 1, baseline characteristics varied little between the no-prior procedure and any-prior procedure groups, with a similar ECOG performance status and BCLC stage across all groups. There were, however, a few notable between- and intra-group differences. The incidence of cirrhosis at baseline was lower among second-line post-surgical patients than in the other subgroups (p = 0.002) and mean baseline total bilirubin and INR were lowest in the post-surgical group (p = 0.003 and 0.049, respectively). Not surprisingly, treatment was most likely to be delivered as a whole-liver (or whole-remnant) procedure in second-line post-surgical patients and in those treated at third-line or beyond (p = 0.010), and occlusion of the non-target arteries prior to administration was more likely to be performed in the second-line post-surgical cohort (p = 0.006). A significantly higher activity was administered to treatment-naïve patients (median 1.7 versus 1.5 GBq; p = 0.003).
Patients that had undergone a prior procedure tended to have a smaller tumour burden (14.1% versus 11.2%; p = 0.060), were less likely to have an elevated baseline total bilirubin compared with patients who were procedure-naïve (mean ± SD: 1.0 ± 0.48 versus 1.2 ± 0.63 mg/dL; p < 0.001), and were less likely to receive a whole-liver treatment than a lobar/segmental approach (whole-liver: 40.8% versus 58.2%, respectively; p = 0.017).
Patients with any prior surgical procedure were less likely to have an elevated total bilirubin (mean ± SD: 0.8 ± 0.38 versus 1.1 ± 0.52; p = 0.014), cirrhosis (64.3% versus 84.6%; p = 0.008), portal vein occlusion (8.9% versus 26.9%; p = 0.035) or hepatitis C aetiology (35.7% versus 55.1%; p = 0.035) at baseline compared with those receiving other prior procedures. Nearly three-quarters (73.2%) of these post-surgical patients received whole-liver radioembolisation of the remnant liver (a statistically higher proportion than in the remaining cohorts [47.4%]; p = 0.030). By contrast, patients with any prior ablation were older (mean ± SD: 68.5 ± 9.9 versus 63.2 ± 11.3 years; p = 0.025), and appeared more likely to have cirrhosis (89.7% versus 72.6%; p = 0.082), compared to those receiving other prior procedures. Finally, patients who had had any prior TAE or TACE were less likely to have non-target arteries occluded (54.5% versus 78.3%; p = 0.008) compared with those receiving other prior procedures.
Safety and tolerability
There were no significant differences between subgroups according to prior procedures in the reporting of clinical AEs (Table 2) or changes in CTCAE grade from baseline to 3 months (Table 3). The incidence of commonly reported mild-to-moderate procedure-related events in the first 7 days after radioembolisation (including fatigue, nausea, and vomiting, pain and fever) was numerically higher in the prior-ablative subgroup but not statistically different from the remainder of patients. This is likely to be linked to a higher, but not significantly different, proportion of patients with more advanced, symptomatic disease reflected by higher rates of ECOG performance status ≥1, tumour burden, cirrhosis, and Child B class (Table 1). In this setting, the prior ablative subgroup, not surprisingly, also had higher (but not significantly different) pre- and post-radioembolisation grades of total bilirubin, albumin, ALT, INR and platelets, although there did not appear to be any additional increase in post-treatment grades in this subgroup as a consequence of the existing dysfunction (Table 1).
Overall survival
Overall survival following radioembolization was similar in the procedure-naive group to those who had received any prior procedure (Fig. 2a). Similarly, stratification of patients by BCLC stage showed that median (95% CI) survivals were not statistically different in the procedure-naive group and those who received radioembolisation second line in patients with BCLC stage A: 22.1 months (15.1–45.9) versus 30.9 months (19.6–46.8; p = 0.243); BCLC stage B: 18.4 months (11.2–19.4) versus 22.8 months (10.9–34.2, p = 0.815); or BCLC stage C: 8.8 months (7.1–10.8) versus 10.8 months (7.7–12.6, p = 0.976). Furthermore, stratifying patients by prior procedure, whether surgical (Fig. 2b), vascular (Fig. 2c), or ablative (Fig. 2d) showed that survival differed little by prior treatment type.
Discussion
Our analysis of 325 patients showed that patients with HCC who have failed prior procedures can be treated effectively with radioembolisation and have outcomes similar to those who had no prior procedures. This is perhaps analogous to the observation that patients with progression or intolerance to sorafenib had a better-than-expected outcome when treated with systemic agents, showing that later lines of therapy can still be effective after earlier lines of treatment have failed [12, 13]. These data may be indicative of the tumours in patients with good functional reserve, who are eligible for additional treatment, having a less aggressive nature upon progression.
It is quite reassuring to observe that prior treatment did not significantly increase the rate of severe AEs post-radioembolisation, particularly after resection where liver functional reserve is diminished, and following vascular procedures where the liver vascular network is altered. Minor differences in adverse event rates post-radioembolisation (e.g. fatigue and abdominal pain) tended to reflect existing dysfunction recorded at baseline. Survival was particularly promising for a small subset of patients (34/325 patients; 10.5% of the overall cohort) with early or intermediate-stage disease who received radioembolisation after failing prior surgery (with or without TACE or embolisation). These data suggest that the hypothesis that radioembolisation may be an alternative to TACE earlier in the treatment paradigm is worth further study. Due to the small patient numbers, we were unable to draw any conclusions on the safety or efficacy of radioembolisation in patients who had received prior systemic therapy.
Often the sequential use of locoregional therapies is key in optimising outcomes for patients with localised disease. The nature and duration of prior treatment often determines subsequent treatment options. There are, however, few published data on the relative value of conducting TACE before radioembolisation, or vice versa. Our study has shown that in patients who are eligible for radioembolisation, prior failure of TACE does not affect the subsequent outcomes of treatment using 90Y resin microspheres. However, we emphasise that patients who are suitable candidates for radioembolisation after TACE are necessarily expected to have a more favourable prognosis (i.e., no or less extrahepatic progression, and less rapid progression) than patients who are unsuitable for radioembolization after TACE. With the availability of effective alternatives to conventional TACE, an individualised approach to treatment is needed that is appropriate both to the intention of treatment (i.e. palliation or down-sizing) and the patient’s health status. Such decisions should be based on the collective experiences of the multidisciplinary team.
While there is evidence to suggest that repeating TACE prolongs survival, it can be a difficult decision to know when to stop TACE and consider alternative treatment. In the opinion of some experts, patients should receive no more than two sessions of TACE in the presence of persistent tumoural activity on imaging [14, 15]. This is supported by two recent papers from researchers in Vienna, who used Assessment for Retreatment with TACE (ART) scoring to show that patients with deteriorating liver function, defined by rising aspartate aminotransferase (AST) and Child-Pugh score in the absence of radiologic tumour response, are poor candidates for ongoing TACE [16, 17]. Furthermore, although SIRT is an effective salvage therapy in patients after TACE, the feasibility of SIRT tends to decrease in patients who have undergone more than four previous TACE sessions [18]. Finally, better tumour control has been documented with SIRT, albeit with 90Y glass microspheres (TheraSphere®; MDS Nordion, Ottawa, ON, Canada), when compared with conventional TACE in a randomised prospective trial [19]. This study showed a significantly longer median time to progression (>26 months) in the SIRT group than in the TACE group (6.8 months; p = 0.0012). Such evidence may strengthen the argument for the potential use of SIRT earlier in the disease course.
Personalised dosimetry was not conducted in this study, nor was it performed in either of the large randomised controlled trials on the use of SIRT in locally advanced HCC [20, 21]. However, two earlier trials have indicated that a delivered dose calculated based on 99mTc-MAA quantification may affect treatment outcome. A study with 90Y resin microspheres reported that survival was significantly better in patients whose tumours received >120 Gy (median survival 55.9 weeks) than those who received lower doses (median survival 26.2 weeks; p = 0.005) [22]. In another study with 90Y glass microspheres, median OS was 4.4 months in patients whose dose was <205 Gy versus 15.7 months in patients whose dose was ≥205 Gy (p = 0.0004) [23]. These studies indicate a that personalised dosimetry according to the finding of 99mTc-MAA angiography may optimise the outcome of SIRT. When individualised dosimetry is used in clinical practice, the benefit of SIRT may be greater than that seen in the large randomised controlled trials.
On the whole, survival following radioembolisation was not statistically significantly different between treatment naïve patients and patients who had received at least one prior procedure (13.6 months and 12.8 months). These data are strikingly similar to the results from the SHARP study, which found that median overall survival with sorafenib was 11.9 months in both subgroups of patients who had received prior curative treatment (resection or ablation) or TACE [24]. In conclusion, this analysis shows that radioembolisation is a valuable treatment option for patients who relapse following surgical, ablative or vascular procedures and who remain suitable candidates for this treatment.
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Acknowledgements
We wish to thank Rae Hobbs (of Scribe Medical) for her editorial/writing assistance in the development of this paper funded by Sirtex Medical Ltd. Also thanks to ESP Bioscience Ltd. for editorial assistance funded by Sirtex Medical Ltd.
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Dr. Sangro and Dr. Van Buskirk are consultants for Sirtex Medical. The remaining authors have no relevant affiliations or financial involvement with any organisation or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript.
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Sangro, B., Maini, C.L., Ettorre, G.M. et al. Radioembolisation in patients with hepatocellular carcinoma that have previously received liver-directed therapies. Eur J Nucl Med Mol Imaging 45, 1721–1730 (2018). https://doi.org/10.1007/s00259-018-3968-5
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DOI: https://doi.org/10.1007/s00259-018-3968-5