DOI: https://doi.org/10.21203/rs.3.rs-228801/v1
Background: Stereotactic body radiation therapy (SBRT) has high efficacy for early-stage hepatocellular carcinoma (HCC) and is expected as an accepted alternative to radiofrequency ablation (RFA). However, SBRT for HCC may cause subacute liver injury leading to negative clinical outcomes. In this study, we compared changes of liver function and prognosis after SBRT or RFA in patients with single, small HCC by using a propensity-score matching analysis.
Methods: We reviewed medical records of 140 patients with single ≤3 cm HCC treated with SBRT or RFA at Kurashiki Central Hospital between January 2014 and February 2019. Changes of albumin-bilirubin (ALBI) score, local recurrence, and overall survival were compared between the propensity-score matched groups (31 patients treated with SBRT and 62 treated with RFA).
Results: The ALBI score increased modestly but significantly after SBRT, while it was unchanged in the RFA group; the intergroup difference was statistically significant (p = 0.004). No local recurrence of tumor was identified in the SBRT group, whereas the cumulative recurrence incidence was 9.7% in the RFA group (p = 0.023). Overall survival was not significantly different between the two groups (hazard ratio 1.32, 95% confidence interval 0.60–2.89, p = 0.401).
Conclusions: SBRT had modestly negative impact on liver function but better local control of HCC than did RFA. Although long-term follow-up of liver function is necessary with SBRT treatment especially in patients with impaired liver function, SBRT is a satisfactory alternative to RFA for treatment of single, small HCC.
Hepatocellular carcinoma (HCC) is the fourth most common cause of cancer-related death worldwide [1]. Curative treatment at an early stage is a cornerstone for improving the outcome of HCC [2]. In the current guidelines, surgical resection, radiofrequency ablation (RFA), or liver transplantation is recommended for treatment of early-stage HCC [3]. However, each treatment has drawbacks: Surgical resection is invasive and may cause postoperative morbidity and liver failure [4]; the curability with RFA may be limited by tumor size and its location [5, 6]; and, because of the scarcity of donor organs, liver transplantation is rarely performed in Asian countries [7].
Remarkable technological advances in radiotherapy for HCC have been made in recent years [8]. Stereotactic body radiation therapy (SBRT) uses hypo-fractionated irradiation with a very high dose per fraction, which enables satisfactory therapeutic effects with lower toxicity [8]. The local control rate of SBRT for early-stage HCC has been reported to be 87–100% [9–11]. SBRT is expected to overcome the drawbacks of surgical resection and RFA because it is less invasive than resection, and it is less influenced by tumor size and location than is RFA [6].
However, important issues with SBRT remain to be clarified. First, SBRT can cause radiation-induced liver disease (RILD) [12, 13]. Thanks to modern radiotherapy techniques, classic RILD (i.e., hepatomegaly, ascites, and elevated liver enzymes) is rare in the current era [14]. Nonetheless, non-classic RILD, which also is associated with worse prognosis, sometimes occurs [13], and the long-term impact of SBRT on liver function is uncertain. Second, survival outcomes with SBRT are variable; a multi-center study reported better overall survival with SBRT than with RFA [6, 15], whereas an analysis using the National Cancer Database reported an opposite result [16, 17]. In this study, using a propensity-score matching analysis, we compared the long-term impact on liver function and clinical outcomes of patients with single, small HCC treated with SBRT or RFA.
We conducted a retrospective study by reviewing medical records of 641 patients with HCC treated at Kurashiki Central Hospital between January 2014 and February 2019. The inclusion criteria for this study were 1) a single HCC of 3 cm or smaller; 2) diagnosis established by histology or contrast-enhanced imaging; 3) treatment with SBRT or RFA; and 4) patients age 20 years old or older. The exclusion criteria were 1) macrovascular invasion or extrahepatic metastasis; 2) Child–Pugh score 10 or higher; and 3) refusal to join in the study. One hundred forty patients were included in this study; 44 were treated with SBRT and 96 with RFA. In our institution, RFA was the first-choice therapy for single, small HCC, and SBRT was chosen when RFA was considered inappropriate (e.g., local recurrence after RFA and tumors adjacent to the vessels or liver surface). All procedures were performed in accordance with the Helsinki Declaration of 1975, as revised in 2008.This study was approved by the Medical Ethics Committee of Kurashiki Central Hospital (no. 2948). Informed consent was obtained from all patients included in the study in an opt-out protocol.
Patients were immobilized with use of an individually shaped vacuum pillow and underwent a 4-dimensional (4D) computed tomography (CT) scan. The gross tumor volume was delineated with the assistance of contrast-enhanced CT scans and MRI (magnetic resonance imaging). The 4D CT was used to help create an internal target volume to compensate for respiratory motion. The planning target volume included the internal target volume plus a 3- to 5-mm expansion. A stereotactic, multiarc, dynamic, conformal radiation procedure or volumetric modulated arc therapy was performed by use of TrueBeam or Clinac IX (Varian Medical Systems, Palo Alto, CA), with respiratory gating or breath hold. Target alignment and setup accuracy were ensured through use of implanted fiducial markers (Gold Anchor™ (Naslund Medical AB, Huddinge, Sweden) or VISICOIL™ (IZI Medical Products, Baltimore, USA)). A total dose of 40 Gy was delivered in five fractions over 5–9 days on either an inpatient or outpatient basis.
RFA was performed with real-time ultrasonographic guidance on an inpatient basis. We used Cool-tip™ RF Ablation System E Series (Covidien, Mansfield, USA) and tried to create an ablative margin of at least 5 mm surrounding the tumor. Contrast-enhanced CT or nonenhanced MRI was performed on the day after RFA; if ablation was incomplete, an additional session was conducted during the same hospital stay.
After treatment, patients were assessed every 3 months with laboratory and radiological examination. Contrast-enhanced CT or MRI was performed at least every 6 months unless patients had contraindications to contrast administration. Post-treatment response was assessed according to the Response Evaluation Criteria in Cancer of the Liver [18]. If HCC recurred, appropriate treatment was provided based on the clinical guideline [3].
Categorical variables were expressed as numbers (percentages) and continuous variables were expressed as median [interquartile range] or mean ± standard deviation. To compare differences in patients’ characteristics between the two groups, Fisher's exact test and the Mann–Whitney U test were used for categorical values and continuous values, respectively. Longitudinal changes of albumin-bilirubin (ALBI) score, local recurrence, and overall survival were compared between the propensity-score matched groups. Time to local recurrence was defined as the time from SBRT or RFA to radiologic diagnosis of local recurrence. Overall survival was defined as the time from SBRT or RFA to all-cause death, with living patients censored on the date of last follow-up. Patients in the SBRT group were matched at a 1:2 ratio with patients treated with RFA. The variables included in the propensity-score model were age, tumor size, performance status, baseline ALBI score, baseline Child–Pugh score, and the number of previous treatments for HCC. In each treatment group, ALBI scores at 12 months after treatment were compared with the baseline values by using the Wilcoxon rank sum test. To analyze the intergroup difference of the longitudinal change of ALBI scores, repeated analysis of variance was employed. Kaplan–Meier analysis, the log-rank test, and the Cox proportional hazards models were used for analysis of local recurrence and overall survival. A two-tailed p value of < 0.05 was considered statistically significant. All statistical analyses were performed with R (version 3.5.1, R Foundation) and JMP (version 12.2, SAS Institute Japan).
Among the 140 patients, 101 (72.1%) were male, and the median age was 75 [67.3–81] years. Most patients (80.7%) had well-compensated liver function (Child–Pugh class A). Median tumor size was 13 mm [10–20 mm]. Before propensity-score matching (Table 1), patients in the SBRT group had significantly higher age, worse performance status, higher proportion of stage A tumors, and more patients having had previous treatment than did those in the RFA group. In addition, SBRT was more frequently performed as salvage therapy for recurrence after RFA or transcatheter arterial chemoembolization (TACE). After the matching (Table 2), 31 patients treated with SBRT were compared with 62 patients treated with RFA. ALBI scores and other baseline characteristics were well balanced between the two groups, but patients with HCV infection were more numerous in the RFA group (41/62, 66.1% vs. 13/62, 41.9%; p = 0.044), and the frequency of salvage therapy was significantly higher in the SBRT group (8/23, 25.8% vs. 1/16, 1.6%, p < 0.001).
| SBRT group (n = 44) | RFA group (n = 96) | p value | |
|---|---|---|---|
| Age (years) | 78 [70–82] | 73 [67–79] | 0.020 |
| Sex (male/female) | 32 / 12 | 69 / 27 | 1.000 |
| Etiology | 0.170 | ||
| HBV | 8 (18.2%) | 12 (12.5%) | |
| HCV | 22 (50.0%) | 64 (66.7%) | |
| Others | 14 (31.8%) | 20 (20.8%) | |
| Tumor size (mm) | 14 [10–23] | 13 [10–17] | 0.189 |
| Tumor location, segment | 0.222 | ||
| 1/2/3/4 | 0 / 1 / 2 / 7 | 1 / 3 / 6 / 16 | |
| 5/6/7/8 | 4 / 7 / 10 / 13 | 17 / 16 / 6 / 31 | |
| BCLC staging (0/A) | 27 / 17 | 76 / 20 | 0.044 |
| Total bilirubin (mg/dL) | 0.6 [0.4–0.9] | 0.6 [0.5–0.9] | 0.637 |
| Albumin (g/dL) | 3.5 [3.2–3.8] | 3.5 [3.1–3.9] | 0.597 |
| ALBI score | -2.40 [-2.51– -1.93] | -2.33 [-2.65– -1.97] | 0.760 |
| Child–Pugh score (5/6/7/8/9) | 19 / 18 / 6 / 1 / 0 | 43 / 33 / 12 / 5 / 3 | 0.666 |
| Performance status (0/1) | 32 / 12 | 85 / 11 | 0.036 |
| Prior treatment | |||
| Surgery | 21 (47.7%) | 37 (38.5%) | 0.401 |
| RFA | 28 (63.6%) | 55 (57.3%) | 0.600 |
| TACE | 32 (72.7%) | 44 (45.8%) | 0.005 |
| Others | 10 (22.7%) | 3 (3.1%) | < 0.001 |
| Number of prior treatments | 3.5 [2–6] | 2 [0–4] | 0.006 |
| Treatment setting (salvage*/not salvage) | 11 / 33 | 1 / 95 | < 0.001 |
| SBRT, stereotactic body radiation therapy; RFA, radiofrequency ablation; HBV, hepatitis B virus; HCV, hepatitis C virus; BCLC, Barcelona Clinic liver cancer; ALBI, albumin-bilirubin; TACE, transcatheter arterial chemoembolization. | |||
| *recurrence after RFA or TACE. | |||
| SBRT group (n = 31) | RFA group (n = 62) | SMD | p value | |
|---|---|---|---|---|
| Age*, years | 75.2 ± 9.1 | 75.0 ± 7.5 | 0.025 | 0.907 |
| Sex (male/female) | 24 / 7 | 43 / 19 | 0.183 | 0.471 |
| Etiology | ||||
| HBV | 8 / 23 | 7 / 55 | 0.380 | 0.132 |
| HCV | 13 / 18 | 41 / 21 | 0.500 | 0.044 |
| Tumor size* (mm) | 14.7 ± 6.4 | 15.0 ± 5.5 | 0.043 | 0.842 |
| Tumor location (right lobe/left lobe) | 25 / 6 | 48 / 14 | 0.079 | 0.795 |
| BCLC staging (0/A) | 22 / 9 | 46 / 16 | 0.072 | 0.806 |
| ALBI score* | -2.32 ± 0.45 | -2.28 ± 0.46 | 0.088 | 0.692 |
| Child–Pugh score* | 5.74 ± 0.81 | 5.82 ± 1.05 | 0.086 | 0.709 |
| Performance status (0/1) | 26 / 5 | 51 / 11 | 0.043 | 1.000 |
| Number of prior treatments* | 3.9 ± 3.1 | 3.7 ± 3.4 | 0.065 | 0.774 |
| Surgery | 0.52 ± 0.63 | 0.55 ± 0.69 | 0.049 | 0.828 |
| RFA | 1.39 ± 1.63 | 1.55 ± 1.60 | 0.100 | 0.649 |
| TACE | 1.68 ± 1.47 | 1.40 ± 1.58 | 0.180 | 0.422 |
| Treatment setting (salvage/ not salvage) | 8 / 23 | 1 / 61 | 0.751 | < 0.001 |
| SBRT, stereotactic body radiation therapy; RFA, radiofrequency ablation; SMD, standardized mean difference; HBV, hepatitis B virus; HCV, hepatitis C virus; BCLC, Barcelona Clinic liver cancer; ALBI, albumin-bilirubin; TACE, transcatheter arterial chemoembolization | ||||
| *variables included in the propensity score model | ||||
Figure 1 illustrates the longitudinal ALBI scores in the two treatment groups. In the SBRT group, the ALBI score gradually increased (i.e., liver function got worse) between the baseline and 12 months after treatment (-2.32 ± 0.45 vs. -2.17 ± 0.61, p < 0.001) (Fig. 1A). In contrast, the ALBI score was unchanged in the RFA group (-2.28 ± 0.46 at the baseline vs. -2.30 ± 0.55 at 12 months after treatment, p = 0.839) (Fig. 1B). Table 3 presents the numerical values for the longitudinal changes in ALBI values for the SBRT and RFA groups; the intergroup difference of the longitudinal changes of ALBI scores was statistically significant in the propensity-score matched cohort (p = 0.004) and in the whole cohort (p = 0.034). Figure 2 illustrates the subgroup analysis stratified by baseline modified ALBI (mALBI) grade [19]; whereas ALBI scores increased after SBRT in patients who had reduced liver function (mALBI grade 2a, p = 0.007; and 2b, p = 0.041) at baseline, scores did not increase in the patients who had good ALBI score (mALBI grade 1, p = 0.285) at baseline. During the 12 months after therapy, intrahepatic recurrence of HCC including local recurrence was identified in 9 patients in the SBRT group (29.0%) and 19 patients in the RFA group (30.6%), a statistically insignificant difference (p = 1.000). This result is evident that recurrence of HCC was not responsible for differences in longitudinal changes of ALBI scores in the two groups.
| SBRT group | RFA group | Pinteraction* | |
|---|---|---|---|
| Matched cohort (n = 93) | 0.004 | ||
| Baseline | -2.32 ± 0.45 | -2.28 ± 0.46 | |
| 3 months | -2.33 ± 0.48 | -2.29 ± 0.43 | |
| 6 months | -2.28 ± 0.47 | -2.31 ± 0.57 | |
| 9 months | -2.15 ± 0.56 | -2.36 ± 0.48 | |
| 12 months | -2.17 ± 0.61 | -2.30 ± 0.55 | |
| Cohort before the matching (n = 140) | 0.034 | ||
| Baseline | -2.26 ± 0.52 | -2.29 ± 0.49 | |
| 3 months | -2.28 ± 0.55 | -2.30 ± 0.47 | |
| 6 months | -2.17 ± 0.65 | -2.32 ± 0.57 | |
| 9 months | -2.13 ± 0.65 | -2.34 ± 0.54 | |
| 12 months | -2.16 ± 0.68 | -2.30 ± 0.56 | |
| SBRT, stereotactic body radiation therapy; RFA, radiofrequency ablation; HCC, hepatocellular carcinoma | |||
| *Repeated measures analysis of variance | |||
Figure 3A illustrates that during the follow-up periods of up to 63.3 months (median, 23.4 months) in the SBRT group and up to 76.6 months (median, 27.1 months) in the RFA group, no local recurrence of HCC was identified in the SBRT group, whereas 6 cases were identified in the RFA group, a cumulative incidence of 9.7% (p = 0.024). Figure 3B illustrates that during the follow-up periods, 10 (32.3%) patients in the SBRT group and 17 (27.4%) patients in the RFA group died, a statistically insignificant difference (hazard ratio 1.32, 95% confidence interval 0.60–2.89, p = 0.401).
In this study of therapy for single, small HCC, SBRT had significantly worse impact on liver function, assessed by ALBI score, but achieved better local control than did RFA. Despite these differences, overall survival was similar between patients treated with the two procedures. To our best knowledge, this is the first study that compared, with propensity-score matching analysis, the long-term effects of SBRT and RFA on liver function.
In studies that have used Child–Pugh score for assessment of liver toxicity, the changes of liver function after treatment were not significantly different between SBRT- and RFA-treated patients [15, 20]. We used ALBI score for assessment of liver function -- which is reportedly a better predictor of the prognosis of HCC than is Child–Pugh score [21] -- to analyze the liver function as a continuous variable. Thus, we could analyze the delicate changes of liver function, which disclosed the differences between SBRT and RFA treatment.
The increases in ALBI score became noticeable more than 6 months after SBRT. This long interlude can be explained by the fact that, after SBRT, blood flow decreases and the necrotic parenchyma expands over several months [22, 23]. We also found that increase of ALBI scores was associated with abnormal liver function (mALBI grade 2a and 2b) at baseline. This observation is in accordance with reports that worse liver function at baseline was associated with higher risk of RILD [24–26]. Thus, careful follow-up of liver function should be continued for at least 1 year after SBRT, especially in patients with known impaired liver function.
Although liver toxicity, defined by increased ALBI score, was associated with SBRT more than with RFA, the degree was mild and not critical. Moreover, it should be appreciated that the excellent local control rate and the similar overall survival with SBRT was achieved despite the procedure being mostly performed for tumors that were difficult to completely ablate with RFA. Other studies also have found better local control of HCC with SBRT than with RFA, especially for perivascular tumors [6, 15, 20]. Since complete ablation is associated with better prognosis [2], the excellent local control with SBRT may also be beneficial.In contrast to our findings, an analysis of the National Cancer Database in the United State found SBRT inferior to RFA in survival benefit [14]. However, that study did not include important variables, such as liver function, performance status, and treatment history for HCC, as matching factors. Other studies that balanced baseline liver function and previous treatment history found that survival outcomes with SBRT were similar to [15, 28] or even superior to outcomes with RFA [6]. We also included the numbers of previous treatment and liver function in the propensity-score model and found that overall survival with SBRT was like that with RFA. Taken together, our findings suggest that SBRT is a promising treatment for early-stage HCC, especially for HCCs that are difficult to treat with RFA, despite its modest adverse effect on liver function.
The adverse effect on liver function in our patients treated with SBRT occurred despite our cautious use of that modality. Patients were treated with a total dose of 40Gy, TACE was not combined, and fiducial gold marker was used to compensate for respiratory liver motion. In other institution, doses higher than 40Gy together with TACE have been used [29, 30]. The results of our subgroup analysis stratified by baseline liver function suggest that lower radiation dose (35Gy) may be appropriate for patients with impaired liver function [15].
Limitations of our study are these: 1) It is a retrospective study, thus inherently flawed by selection and indication bias; though we performed propensity-score matching, unidentified confounding factors could have existed. A prospective study (UMIN000036081) is ongoing in our institution to reassess the present results. 2) Dose and fractions of radiation used for HCC may not have been optimal. Although giving 40 Gy in five fractions is a commonly accepted protocol for treating HCC [15, 30], the issue needs further study.
SBRT is a promising alternative to RFA for treatment of single, small HCC despite need for long-term monitoring of liver function, especially in patients with pretreatment impaired liver function.
This study was approved by the Medical Ethics Committee of Kurashiki Central Hospital (no. 2948). Informed consent was obtained from all patients included in the study in an opt-out protocol.
Not applicable
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
The authors declare that they have no competing interests.
None
MUand HT designed the study. MU collected the data. All authors analyzed and interpreted the data. MU and SI wrote the draft of the manuscript and all other authors revised it. Final version of the manuscript was approved by all authors. All authors agreed to be accountable for all aspects of the work.
We are grateful to A. Takeda for helpful discussions and comments on the manuscript. We also thank W. R. Brown for the English language review.