Inflammatory Scores: Comparison and Utility in HCC Patients Undergoing Transarterial Chemoembolization in a North American Cohort.

BACKGROUND: The purpose of this study is to determine and compare the ability of neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), aspartate-aminotransferase-to-lymphocyte ratio (ALRI), systemic-inflammation index (SII) and lymphocyte count to predict oncologic outcomes in hepatocellular carcinoma (HCC) patients undergoing transarterial chemoembolization (TACE).
MATERIALS AND METHODS: A single-center retrospective review of 296 patients who were treated for 457 HCCs was performed. Pre- and post-treatment laboratory and treatment outcome variables were collected. Objective radiologic response (ORR), progression-free survival (PFS), and overall survival (OS) were evaluated. Patients were categorized into above and below median scores and compared.
RESULTS: The median pretreatment NLR, PLR, ALRI, SII, and lymphocyte count were 2.7 (range: 0.4-55), 88.3 (range: 0.1-840), 71.8 (range: 0.1-910), 238.1 (range: 0.1-5150.8), and 1 (range: 0.1-5.2) 103/µL, respectively. Patients with above median ALRI scores were less likely to achieve an ORR as compared to those with below median ALRI values (132 (132/163, 81%) vs 150 (150/163, 92%), p = 0.004). On univariate analysis, patients with above median pretreatment NLR (HR 1.41, 95% CI: 1.09-1.83, p = 0.01) and below median lymphocyte count (HR 0.69, 95% CI: 0.53-0.92, p = 0.01) had significantly worse PFS. The relationship between PFS and NLR (p = 0.08) as well as lymphocytes (p = 0.20) no longer remained on multivariate analysis. On univariate analysis, below median pretreatment NLR (HR 1.72, 95% CI: 1.2-2.45, p = 0.003) and ALRI (HR 1.52, 95% CI: 1.05-2.2); p = 0.03) as well as above median lymphocyte count (HR 0.48, 95% CI: 0.34-0.7, p < 0.0001) were associated with improved OS. The significant relationship between lymphocytes and OS remained on multivariate analysis (HR 0.50, 95% CI: 0.28-0.9, p = 0.02), but the relationship with NLR (p = 0.94) did not persist.
CONCLUSION: NLR is predictive of PFS and OS in patients with HCC undergoing TACE and may be superior to other inflammatory scores (PLR, ALRI, and SII) in this setting. However, lymphocyte count may be most predictive of OS.

Introduction

Hepatocellular carcinoma (HCC) is the third most common cause of cancer death worldwide1, and since the publication of two ground-breaking clinical trials which demonstrated the superiority of transarterial chemoembolization (TACE) to best supportive care, TACE has been a mainstay of HCC treatment.2,3 As such, TACE is included in HCC treatment algorithms by virtually every major liver/HCC society, including the Barcelona Clinic Liver Cancer, American Association for the Study of Liver Disease, and European Association for the Study of the Liver (EASL).4–6 However, there have also been significant advances in the treatment options for patients with HCC over the last several years. This underlies the importance of identifying prognostic factors not only for patient education but also to select the best treatment strategy for each patient.

The tumor microenvironment and immune system have become increasingly recognized as integral components in cancer outcomes. At the same time, systemic inflammation has been recognized as an indicator of poorer outcomes. This has led to the investigation of neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) in the setting of TACE and HCC.7–29 While a number of papers have been written on the subject, there has been some disagreement over whether or not NLR and PLR are predictive of meaningful oncologic outcomes. This inconsistency may in part stem from the fact that the majority of studies have come from Asia, where the HCC patient population is not only significantly different from North America and Europe, but the included patients often have very advanced disease. While it is common for studies from Asia to treat patients with relatively large HCCs and those with aggressive features such as portal vein invasion with TACE, these patients are often treated with other means such as radioembolization in different parts of the world. Furthermore, we know that TACE techniques vary significantly between geographical regions.30,31 This raises the question as to whether or not PLR and NLR are useful for predicting oncologic outcomes in a North American cohort. The interest in this question is emphasized by the fact that some prior investigations of NLR in North America have failed to show its utility,9 while others have indicated it is of benefit, at least in terms of predicting radiologic response.29

In addition, other markers of systemic inflammation, such as aspartate aminotransferase-to-lymphocyte ratio (ALRI) and systemic-inflammation index (SII) which have shown promise in HCC patients treated by other means,31–33 have not been well studied in HCC patients undergoing TACE. To the authors’ knowledge, only 2 studies have investigated the utility of ALRI27,34 and 3 have investigated the utility of SII27,28,34 in this patient population. These papers all originate from Asia and have the same issues when being applied to North American and European patients as were described above.

Finally, lymphocytes, which are integral to all four inflammatory scores described above, have also not been well studied in HCC patients undergoing TACE, despite being shown to be of interest in other settings.35 In particular, little data is available which determines if NLR, PLR, ALRI, and SII are superior to simple lymphocyte count. This issue is emphasized by the fact that rarely have all four inflammatory scores and lymphocyte count been applied to the same cohort, making it difficult to compare the relative value of each in predicting outcomes.

Therefore, this study aims to evaluate and compare the ability of NLR, PLR, ALRI, and SII to predict oncologic outcomes in patients with HCC treated by TACE in a North American cohort and further investigate the role of lymphocyte count in these predictions.

Materials and Methods

After Internal Review Board approval, all consecutive patients treated with TACE at a single center between 1/1/2010 and 7/1/2018 were retrospectively reviewed. The patients’ electronic medical records were reviewed for pre- and post-treatment laboratory values, demographic data, and tumor characteristics. Radiologic response was evaluated utilizing the European Association for the Study of the Liver (EASL) criteria. An objective radiologic response (ORR) was considered to be a partial or complete response by EASL criteria. The initial response by EASL was recorded at 1 month post first TACE imaging, while maximal response was recorded in those patients who underwent more than one TACE treatment. The microcatheter position at delivery was then evaluated and recorded as super selective (sub segmental), selective (segmental), minimally selective (segmental), or non-selective (lobar). Overall survival (OS) was defined as the time between the initial treatment and time of death from any cause or the last clinical follow-up (at which time data were censored). Progression-free survival was defined as time from initial treatment to progression by EASL criteria or death.

NLR was calculated by dividing the neutrophil count by the lymphocyte count. PLR was calculated by dividing the platelet count divided by the lymphocyte count. ALRI was calculated by dividing the aspartate aminotransferase level by the lymphocyte count. Finally, SII was calculated by multiplying the neutrophil and platelet count and dividing that number by the lymphocyte count. Pre-treatment laboratory values were typically collected on the day of but prior to treatment; however, values collected within 2 weeks of treatment were included. If the patients’ HCC was treated multiple times with TACE, only the first treatment was included in the analysis.

Statistical Analysis

Demographic and clinical measures were summarized descriptively, either per tumor or per patient, as appropriate. Patients were categorized into above and below median groups for each inflammatory marker, consistent with prior studies.8,10,11 Chi-square and two sample t-tests were used to compare groups for categorical and numeric measures, respectively. Pearson correlation was calculated for the pre-treatment inflammatory scores vs the pre-treatment log alpha fetoprotein (AFP) and lesion size (cm). One-way ANOVA and Tukey’s post-hoc tests were used to determine significance in the relationship between cause of cirrhosis and pre-treatment inflammatory scores.

The OS and PFS curves were represented with the Kaplan–Meier method. Cox regression models were used to determine hazard ratios (HR) and statistical significance of the pre-treatment inflammatory above or below median groups. For OS models, only data from the first tumor per patient was included. For PFS models, all tumors per patient were included along with a cluster term to correct the standard errors using the grouped jackknife method that accounts for clustering due to multiple observations per patient. Both univariate models and models adjusting for the other pre-treatment inflammatory groups in addition to pre-treatment log AFP, lesion size (cm), and Child Pugh score were performed. These covariates were chosen a priori due to their clinical relevance. Due to missing data, there were 274 TACE treatments included in the PFS model with all adjustment factors and 170 in the adjusted OS model. p-values <0.05 were considered statistically significant. R (R Core Team, Version 3.6.0) was used for all statistical analyses.

Results

In total, 296 patients who were treated for 457 HCCs with TACE were included. Demographic data can be found in Table 1. The cohort consisted of 64 (64/296, 21.6%) women and 232 (232/296, 78.4%) men with a mean age of 61.4 ± 8.2 years. The most common cause of cirrhosis was hepatitis C (144/296 patients, 48.6%), and the mean size of treated HCC was 3.5 ± 3.4 cm.

Table 1

Demographic Data

Variable	Patients = 296, HCCs = 457
Age (years)	61.4 ± 8.2
Ethnicity
Caucasian/white non-hispanic	209 (209/296, 70.6%)
Black/African American	37 (37/296, 12.5%)
Asian	21 (21/296, 7.1%)
Hispanic	21 (21/296, 7.1%)
Native American	8 (8/296, 2.7%)
Cause of cirrhosis
Hepatitis C	144 (144/296, 48.6%)
Alcohol	39 (39/296, 13.2%)
Alcohol and hepatitis C	36 (36/296, 12.2%)
NASH	27 (27/296, 9.1%)
Hepatitis B	26 (26/296, 8.8%)
Cryptogenic	17 (17/296, 5.7%)
Other*	7 (7/296, 2.4%)
Sex
Female	64 (64/296, 21.6%)
Male	232 (232/296, 78.4%)
HCC size (cm)	3.5 ± 3.4
Number of TACE treatments	1.4 ± 0.7
Selectivity of TACE treatments
Lobar	31 (31/457, 6.8%)
<Lobar, >segmental	86 (86/457, 18.8%)
Segmental	200 (200/457, 43.8%)
Sub-segmental	140 (140/457, 30.6%)
WBC (109/L)	5.4 ± 2.2
Neutrophils (109/L)	3.3 ± 1.9
Lymphocytes (109/L)	1.2 ± 0.7
Hemoglobin (g/dL)	12.6 ± 2.6
INR	1.2 ± 0.2
Creatinine (mg/dL)	1 ± 1
Total bilirubin (mg/dL)	1.3 ± 0.7
Albumin (g/dL)	3.2 ± 0.6
MELD	10.5 ± 3.5
Child-Pugh score	6.5 ± 1.3
ECOG	0.3 ± 0.5
Alpha fetoprotein (ng/mL)	28.6 (0–363, 848.3)

Notes: *Other causes included hemochromatosis, primary biliary cirrhosis, autoimmune hepatitis, and cystic fibrosis. All numeric measures summarized as mean ± SD, except for AFP, which was summarized as median (range).

Abbreviations: HCC, hepatocellular carcinoma; NASH, non-alcoholic steatohepatitis; TACE, transarterial chemoembolization; cm, centimeter; ECOG, Eastern Cooperative Oncology Group; WBC, white blood cell count.

Table 2 provides summaries for the pretreatment NLR, PLR, ALRI, SII and lymphocyte count values. The median pretreatment NLR, PLR, ALRI, SII, and lymphocyte count were 2.7 (range: 0.4–55), 88.3 (range: 0.1–840), 71.8 (range: 0.1–910), 238.1 (range: 0.1–5150.8), and 1 (range: 0.1–5.2) 103/µL, respectively. evaluates the relationship between the pretreatment inflammatory scores and the pretreatment log AFP. However, log AFP did not correlate with inflammatory scores. evaluates the relationship between the pretreatment inflammatory scores and the pretreatment tumor size. While there was no correlation with tumor size in regard to NLR and ALRI, there was a modest correlation between PLR (r = 0.13, p < 0.001) and SII (r = 0.17, p < 0.001). evaluates the relationship between the cause of cirrhosis and inflammatory scores. Again, there was not a strong correlation between inflammatory scores and the underlying cause of cirrhosis. However, cryptogenic cirrhosis had significantly higher pre-treatment PLR and SII than all other causes (all p values < 0.025 after Tukey adjustment).

Table 2

Descriptive Summaries for the Pre- and Post-Treatment Inflammatory Values

Variable
Pretreatment NLR
Mean	4 ± 4.8
Median	2.7 (0.4, 55)
Pretreatment PLR
Mean	118.8 ± 110.3
Median	88.3 (0.1, 840.0)
Pretreatment ALRI
Mean	111.1 ± 133.5
Median	71.8 (0.1, 910.0)
Pretreatment SII
Mean	442.2 ± 606.1
Median	238.1 (0.1, 5150.8)
Pretreatment lymphocyte count (103/µL)
Mean	1.2 ± 0.7
Median	1 (0.1, 5.2)

Abbreviations: NLR, neutrophil-to-lymphocyte ratio; PLR, platelet-to-lymphocyte ratio; ALRI, aspartate-aminotransferase-to-lymphocyte ratio; SII, systemic-inflammatory index.

Radiologic Response

Data on the ability of inflammatory scores and lymphocyte count to predict the radiologic response can be found in Table 3. Of note patients with above median ALRI were less likely to achieve an ORR than those below the median (132 (132/163, 81%) vs 150 (150/163, 92%), p = 0.004).

Table 3

Radiologic Response by Inflammatory Markers. Comparison Between Treated Lesions with Above and Below Average (Log Mean and Median)

Variable	Above Median	Below Median	p value
Pretreatment NLR n = 357
Initial response
CR	102 (102/179, 57%)	90 (90/178, 50.6%)	0.43
PR	45 (45/179, 25.1%)	53 (53/178, 29.8%)
SD	24 (24/179, 13.4%)	30 (30/178, 16.8%)
PD	8 (8/179, 4.5%)	5 (5/178, 2.8%)
ORR	147 (147/179, 82.1%)	143 (143/178, 80.4%)	0.67
Maximal response
CR	112 (112/179, 62.6%)	113 (113/178, 63.5%)	0.95
PR	43 (43/179, 24%)	42 (42/178, 23.6%)
SD	17 (17/179, 9.5%)	18 (18/178, 10.1%)
PD	7 (7/179, 3.9%)	5 (5/178, 2.8%)
ORR	155 (155/179, 86.6%)	155 (155/178, 87.1%)	0.89
Pretreatment PLR n = 343
Initial response
CR	87 (87/171, 50.9%)	98 (98/172, 57%)	0.15
PR	54 (54/171, 31.6%)	40 (40/172, 23.3%)
SD	22 (22/171, 12.9%)	30 (30/172, 17.4%)
PD	8 (8/171, 4.6%)	4 (4/172, 2.3%)
ORR	141 (141/171, 82.5%)	138 (138/172, 80.3%)	0.60
Maximal response
CR	100 (100/171, 58.5%)	116 (116/172, 67.4%)	0.09
PR	49 (49/171, 28.7%)	33 (33/172, 19.2%)
SD	14 (14/171, 8.2%)	19 (19/172, 11%)
PD	8 (8/171, 4.7%)	4 (4/172, 2.4%)
ORR	149 (149/171, 87.2%)	149 (149/172, 86.6%)	0.89
Pretreatment ALRI n = 326
Initial response
CR	89 (89/163, 54.6%)	89 (89/163, 54.6%)	0.36
PR	38 (38/163, 23.3%)	48 (48/163, 29.4%)
SD	28 (28/163, 17.2%)	22 (22/163, 13.5%)
PD	8 (8/163, 4.9%)	4 (4/163, 2.5%)
ORR	127 (127/163, 77.9%)	137 (137/163, 84%)	0.14
Maximal response
CR	104 (104/163, 63.8%)	106 (106/163, 65%)	0.01
PR	28 (28/163, 17.2%)	44 (44/163, 27%)
SD	23 (23/163, 14.1%)	10 (10/163, 6.1%)
PD	8 (8/163, 4.9%)	3 (3/163, 1.9%)
ORR	132 (132/163, 81%)	150 (150/163, 92%)	0.004
Pretreatment SII n = 342
Initial response
CR	93 (93/171, 54.4%)	91 (91/171, 53.2%)	0.62
PR	49 (49/171, 28.7%)	45 (45/171, 26.3%)
SD	22 (22/171, 12.9%)	30 (30/171, 17.5%)
PD	7 (7/171, 4%)	5 (5/171, 3%)
ORR	142 (142/171, 83.1%)	136 (136/171, 79.5%)	0.41
Maximal response
CR	107 (107/171, 62.6%)	106 (106/171, 62%)	0.06
PR	47 (47/171, 27.5%)	36 (36/171, 21.1%)
SD	10 (10/171, 5.9%)	24 (24/171, 14%)
PD	7 (7/171, 4%)	5 (5/171, 2.9%)
ORR	154 (154/171, 90.1%)	142 (142/171, 83.1%)	0.06
Pretreatment lymphocytes n = 357
Initial response
CR	95 (95/186, 53.7%)	90 (90/171, 54.2%)	0.32
PR	54 (54/186, 30.5%)	40 (40/171, 24.1%)
SD	24 (24/186, 13.6%)	28 (28/171, 16.9%)
PD	4 (4/186, 2.3%)	8 (8/171, 4.8%)
ORR	149 (149/186, 84.2%)	130 (130/186, 78.3%)	0.16
Maximal response
CR	110 (110/186, 63.2%)	105 (105/171, 62.9%)	0.18
PR	47 (47/186, 27%)	34 (34/171, 20.4%)
SD	13 (13/186, 7.5%)	20 (20/171, 12%)
PD	4 (4/186, 2.3%)	8 (8/171, 4.8%)
ORR	157 (157/186, 90.2%)	139 (139/171, 83.2%)	0.06

Abbreviations: NLR, neutrophil-to-lymphocyte ratio; CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; ORR, objective radiologic response; PLR, platelet-to-lymphocyte ratio; ALRI, aspartate-aminotransferase-to lymphocyte ratio; SII, systemic-inflammatory index.

Progression-Free Survival

Progression-free survival Kaplan–Meier curves for median pretreatment NLR, PLR, ALRI, and SII can be found in Figure 1. This showed that patients with above median pretreatment NLR (HR 1.41, 95% CI: 1.09–1.83, p = 0.01) and below median lymphocyte count (HR 0.69, 95% CI: 0.53–0.92, p = 0.01) had significantly worse PFS. However, neither median pretreatment PLR (HR 1.12, 95% CI: 0.85–1.48, p = 0.43), ALRI (HR 1.11, 95% CI: 0.83–1.48, p = 0.47), nor SII (HR 1.13, 95% CI: 0.85–1.5, p = 0.41) predicted PFS.

Figure 1

Kaplan–Meier curves demonstrating progression-free survival (PFS) in patients with above or below median neutrophil-to-lymphocyte ratio (NLR) (A), platelet-to-lymphocyte ratio (PLR) (B), aspartate-aminotransferase-to-lymphocyte ratio (ALRI) (C) and systemic-inflammation index (SII) (D) Lymphocyte count (E) .

Cox Regression Analysis Using NLR, PLR, ALRI, and SII

In a Cox regression model which included all pretreatment inflammatory scores it was found that pretreatment NLR (HR 1.48, 95% CI: 1.10–1.99, p=0.009) was associated with PFS while PLR (HR 0.97, 95% CI: 0.68–1.37, p=0.86), ALRI (HR 0.95, 95% CI: 0.70–1.30, p=0.77) and SII (HR 0.99, 95% CI: 0.70–1.39, p=0.95) were not. If tumor size, log AFP, and Child-Pugh classification were added to this model, pretreatment NLR remained a significant predictor of PFS (HR 1.50, 95% CI: 1.08–2.10, p=0.017). While pretreatment PLR (HR 0.94, 95% CI: 0.62–1.44, p=0.79), ALRI (HR 0.79, 95% CI: 0.56–1.11, p=0.18), and SII (HR 1.0, 95% CI: 0.66–1.51, p=0.99) were not. Pretreatment AFP (HR 1.08, 95% CI: 1.01–1.16, p=0.034) was found to correlate with PFS, while tumor size (HR 0.98, 95% CI: 0.92–1.04, p=0.46) and Child-Pugh (HR 1.11, 95% CI: 0.97–1.28, p=0.14) did not.

Cox Regression Analysis Using NLR, PLR, ALRI, SII, and Lymphocyte Count

In a Cox regression model which included all pretreatment inflammatory scores as well as lymphocyte count, it was found that neither NLR (HR 1.28, 95% CI: 0.90–1.82, p = 0.17), PLR (HR 0.91, 95% CI: 0.64–1.3, p = 0.61), ALRI (HR 0.88, 95% CI: 0.65–1.2, p = 0.43), SII (HR 1.05, 95% CI: 0.75–1.48, p = 0.77), or lymphocyte count (HR 0.73, 95% CI: 0.49–1.09, p = 0.12) were correlated with PFS. If tumor size, log AFP, and Child-Pugh classification were added to this model, again neither pretreatment NLR (HR 1.27, 95% CI: 0.85–1.91, p = 0.25), PLR (HR 0.88, 95% CI: 0.58–1.32, p = 0.53), ALRI (HR 0.75, 95% CI: 0.53–1.05, p = 0.09), SII (HR 1.07, 95% CI: 0.71–1.61, p = 0.76) or lymphocyte count (HR 0.70, 95% CI: 0.47–1.06, p = 0.09) demonstrated significant association. While AFP (HR 1.08, 95% CI: 1.00–1.16, p = 0.05) nearly reached significance, neither tumor size (HR 0.98, 95% CI: 0.93–1.04, p = 0.55) nor Child-Pugh (HR 1.08, 95% CI: 0.94–1.24, p = 0.28) was associated with PFS.

Overall Survival

Overall survival Kaplan–Meier curves for median pretreatment NLR, PLR, ALRI, and SII can be found in Figure 2. Those with above median NLR (HR 1.72, 95% CI: 1.2–2.45); p = 0.003) and ALRI (HR 1.52, 95% CI: 1.05–2.2); p = 0.03) had a higher risk of death. Those patients with below median lymphocytes (HR 0.48, 95% CI: 0.34–0.7, p < 0.0001) also had a higher risk of death. There was no statistically significant difference seen in PLR (HR 1.19, 95% CI: 0.84–1.69, p = 0.33) or SII (HR 1.34, 95% CI: 0.94–1.91, p = 0.11).

Figure 2

Kaplan–Meier curves demonstrating overall survival (OS) in patients with above or below median neutrophil-to-lymphocyte ratio (NLR) (A), platelet-to-lymphocyte ratio (PLR) (B), aspartate-aminotransferase-to-lymphocyte ratio (ALRI) (C) and systemic-inflammation index (SII) (D) Lymphocyte count (E) .

In a Cox regression model which included all pretreatment inflammatory scores, it was found that neither pretreatment NLR (HR 1.50, 95% CI: 0.94–2.40, p = 0.09), PLR (HR 0.89, 95% CI: 0.53–1.51, p = 0.67), ALRI (HR 1.36, 95% CI: 0.90–2.06, p = 0.15) and SII (HR 1.23 95% CI: 0.70–2.16, p = 0.47) were significantly associated with OS. If tumor size, log AFP, and Child-Pugh classification were added to this model, pretreatment NLR (HR 1.31, 95% CI: 0.77–2.23, p = 0.32), PLR (HR 1.06, 95% CI: 0.59–1.89, p = 0.85), ALRI (HR 0.79, 95% CI: 0.48–1.31, p = 0.36), and SII (HR 1.06, 95% CI: 0.57–1.97, p = 0.84) were still not significant predictors of OS. Pretreatment AFP (HR 1.05, 95% CI: 0.98–1.16, p = 0.14) and tumor size (HR 1.02, 95% CI: 0.95–1.09, p = 0.62) were not found to be associated with OS; however, Child-Pugh (HR 1.51, 95% CI: 1.27–1.79, p < 0.001) did demonstrate an association.

In a Cox regression model which included all pretreatment inflammatory scores and lymphocyte count, it was found that only pretreatment lymphocytes (HR 0.51, 95% CI: 0.31–0.86, p = 0.010) was significantly associated with OS, while NLR (HR 1.13, 95% CI: 0.67–1.91, p = 0.64), PLR (HR 0.78, 95% CI: 0.46–1.32, p = 0.36), ALRI (HR 1.11, 95% CI: 0.71–1.73, p = 0.66), and SII (HR 1.47, 95% CI: 0.83–2.59, p = 0.19) were not. If tumor size, log AFP, and Child-Pugh classification were added to this model, again only pretreatment lymphocyte count (HR 0.50, 95% CI: 0.28–0.9, p = 0.02) was significantly associated. Pretreatment NLR (HR 0.98, 95% CI: 0.54–1.77, p = 0.94), PLR (HR 0.87, 95% CI: 0.48–1.56, p = 0.64), ALRI (HR 0.67, 95% CI: 0.40–1.13, p = 0.13), and SII (HR 1.32, 95% CI: 0.70–2.50, p = 0.39) were not associated. Pretreatment AFP (HR 1.08, 95% CI: 1.00–1.17, p = 0.06) and tumor size (HR 1.01, 95% CI: 0.95–1.08, p = 0.73) were not associated, while Child-Pugh (HR 1.41, 95% CI: 1.18–1.70, p < 0.001) was associated with OS.

Discussion

As the treatment options for patients with hepatocellular carcinoma (HCC) continue to expand, the importance of finding pre-treatment predictors of outcomes is emphasized. One area which has been investigated for these purposes is inflammatory scores. A number of inflammatory scores have been evaluated, and it is difficult to know which is best for a specific cancer and treatment method or if they provide more information than lymphocyte count alone. This study evaluated four of the commonly used inflammatory scores (NLR, PLR, ALRI, and SII) and pretreatment lymphocyte count in HCC patients undergoing TACE.

Of surprise, radiologic response was poorly predicted by the majority of the inflammatory scores and lymphocyte count. This seems to be in contradiction to Schobert et al who did find a correlation between higher NLR and PLR values and radiologic response when using qEASL.26 The results also differ from Cruz et al who showed that those patients with PD immediately after treatment had a significantly higher NLR.29 The reason for the discrepancies may be explained by the smaller cohorts in the prior studies as compared to this study. Similarly, of interest, the median of pre-treatment ALRI did show some promise in accurately predicting the maximal response of HCC lesions after TACE. While the reason for ALRI demonstrating promise while other markers did not is not evaluated in this study, it may be related to the fact that ALRI takes into account the aspartate aminotransferase, which may increase this marker’s sensitivity for the inflammatory environment of the liver, whereas NLR, PLR, SII, and lymphocyte count may be more tied to the systemic inflammatory environment.

This study also looked at PFS and found that patients with above or below median PLR, ALRI, or SII did not have significantly different PFS. However, those with above median NLR (HR 1.41, 95% CI: 1.09–1.83, p = 0.01) and below median lymphocyte count (HR 0.69, 95% CI: 0.53–0.92, p = 0.01) had significantly worse PFS on univariate analysis. When a multivariate model which did not include lymphocyte count was created, NLR remained significantly associated, even when adding in other factors such as tumor size, AFP, and Child-Pugh score. However, when lymphocyte count was added to these two multivariate modeling scenarios, neither NLR nor pretreatment lymphocyte count continued to be associated with PFS. When taken as a whole, the findings suggest that NLR and pretreatment lymphocyte count may be superior in terms of predicting those patients who will do poorly following TACE as compared to PLR, ALRI, and SII. The findings also suggest that the predictive ability of NLR may be heavily associated with lymphocyte count, perhaps more so than neutrophil count. The mechanism which connects an elevated NLR, lymphocyte count and poor outcomes in HCC patients is not well understood. However, high NLR and low lymphocyte counts can correlate with depleted lymphocytes, and lymphocytes play a role in cytotoxic cell death and the production of anti-tumor cytokines.36 Therefore, lymphopenia is associated with an impaired host immune response to the tumor and thus poor cancer-specific survival.37 Systemic neutrophilia has been associated with greater infiltration of tumor-associated macrophages (TAMs) as well as elevated pro-inflammatory cytokines, which promote angiogenesis and tumor growth.38,39 The measurement of the relative depletion of lymphocytes and/or neutrophilia likely explains NLR’s predictive values, while the lymphocyte role in anti-tumoral responses likely explains lymphocyte count predictive value. The findings of this study suggest that pretreatment NLR and lymphocyte count may allow providers to council patients more accurately on their prognosis.

This study also evaluated the ability of inflammatory scores to evaluate OS and showed that median NLR (HR 1.72, 95% CI: 1.2–2.45, p = 0.003), ALRI (HR 1.52, 95% CI: 1.05–2.2; p=0.03), and lymphocyte count (HR 0.48, 95% CI: 0.34–0.7, p<0.0001) were associated with OS on univariate Cox regression analysis. When multivariate analysis was performed and lymphocyte count was not included, NLR showed a trend toward association with OS in a model that did not include tumor size, AFP, or Child-Pugh score, but the trend no longer existed when these variables were included. When lymphocyte count was added to these models, NLR was not significant in either of them, but lymphocyte count was associated with OS in both models. The fact that when lymphocyte count was included as a variable in this study, the correlation between NRL and OS seemed to be negatively impacted is of interest. This would suggest that lymphocyte count was the driving force behind NLRs association with OS and perhaps it would be the best score for predicting OS. To the authors’ knowledge, this has not been studied in HCC patients undergoing TACE; however, lymphopenia is known to be associated with poorer outcomes in other settings.35

As discussed previously, the majority of studies that have evaluated inflammatory scores in this setting originate from Asia. These studies often differ from North American and European studies in the primary underlying cause of cirrhosis as well as the mean size of tumor. When looking at previous studies from North America and Europe, our findings are consistent with those of Rebonato et al who found that NLR was predictive of OS in their smaller study of 72 patients.14 However, they differ from the findings of Sullivan et al who reviewed outcomes in 75 HCC patients treated with surgical resection, liver transplant, or TACE which did not show NLR to be predictive of OS. Furthermore, the multivariate analysis in this relatively larger study would suggest that NLR has a higher association with OS than either PLR, ALRI, or SII while calling into question the importance of any inflammatory scores as compared to other well-established predictive factors such as Child-Pugh score. The question of importance of inflammatory scores is furthered by the fact that when lymphocyte count was added to the multivariate models, lymphocyte count remained associated with OS, while no inflammatory score did.

This study shares similarities with Yang et al who reviewed 189 patients treated with TACE for HCC and evaluated the prognostic value of NLR, PLR, ALRI, and SII.27 However, their study differed significantly in the demographics, with 53 patients (53/189, 28%) having tumors greater than 5 cm and 59 (59/189, 31.2%) having portal vein thrombosis. The Yang et al’s study found that while NLR, PLR, ALRI, and SII were all significantly associated with OS in univariate analysis, only ALRI and SII continued to be associated on multivariate analysis. They also found that there was a correlation between tumor size and portal vein thrombosis and elevated ALRI and SII.27 Of note, Yang et al did not evaluate the effect of lymphocyte count on outcomes, as was done here. Furthermore, the current study found that when separating patients by those with above and below median ALRI, those with lower ALRI scores had significantly longer survival on univariate analysis. However, SII had no significant association with OS in either evaluation. When performing multivariate analysis which included all inflammatory scores, neither ALRI nor SII was predictive of OS. These differences may result from the significantly smaller tumors without portal vein invasion which comprised this study's patient population. This theory is strengthened by the finding in the Yang et al’s study that SII and ALRI were correlated with tumor size and portal vein thrombosis, while this study did not find a similar association.

This study has a number of limitations, including its retrospective study design. While a fairly large cohort was included, it is still limited and this is furthered by the fact that not all values were available prior to all treatments. Additionally, the study represents a single quaternary referral center experience and therefore may not be applicable to all practice settings.

In conclusion, while NLR and ALRI are associated with OS in HCC patients undergoing TACE, this study would indicate that NLR has the highest correlation with both OS and PFS of the four inflammatory scores studied. However, these associations are weakened when lymphocyte count is considered and lymphocyte count may be the best predictor of OS. Therefore, NLR and lymphocyte count would likely be the best choice for further investigation in similar patient populations. Furthermore, those patients presenting with elevated NLRs or lymphopenia may benefit from counseling regarding the prognostic implications.