Efficacy of combined modality therapy with sorafenib following hepatic arterial injection chemotherapy and three-dimensional conformal radiotherapy for advanced hepatocellular carcinoma with major vascular invasion.

The prognosis of hepatocellular carcinoma (HCC) patients exhibiting macroscopic vascular invasion (MVI) is poor, and the most appropriate treatment approach remains unclear. The current study aimed to investigate the efficacy and safety of sorafenib treatment following chemoradiotherapy for advanced HCC exhibiting MVI. A newly reported regimen, including 5-fluorouracil and cisplatin therapy (NewFP), plus three-dimensional conformal radiotherapy (3D-CRT) for MVI was used as the initial treatment. Additionally, sorafenib, as a secondary treatment, was administered after NewFP plus 3D-CRT for MVI. The present retrospective study enrolled patients with unresectable advanced HCC that was treated with NewFP plus 3D-CRT for MVI between January 2009 and December 2017. In total, 32 HCC patients with MVI were registered. Of these 32 patients, 18 were treated with NewFP plus 3D-CRT for MVI (NewFP + 3D-CRT group) and 14 were treated with sorafenib following NewFP plus 3D-CRT for MVI (sorafenib after NewFP + 3D-CRT group). The study endpoints were overall survival, overall response rate and disease control rate. Clinical factors influencing overall survival were identified using univariate and multivariate analyses. The median survival time in the NewFP + 3D-CRT group and sorafenib following NewFP + 3D-CRT group was 6.7 and 49.2 months, respectively (P=0.0003). For patients with advanced HCC exhibiting MVI, the initial treatment with NewFP plus 3D-CRT for MVI was well tolerated. The administration of sorafenib as the secondary treatment following NewFP plus 3D-CRT for MVI was associated with a significantly higher overall response rate, disease control rate and increased overall survival as compared with the NewFP plus 3D-CRT treatment. Copyright: © Nomura et al.

Introduction

Hepatocellular carcinoma (HCC) is the most common type of liver cancer, and is the third leading cause of cancer deaths worldwide, causing nearly 745,000 deaths each year (1). HCC tends to invade vessels as it progresses and is often associated with macroscopic vascular invasion (MVI). Recent studies found that MVI including portal vein tumor thrombosis (PVTT) and inferior vena cava tumor thrombosis (IVCTT) were found in 12.5 to 39.7% of cases at the time of diagnosis, respectively (2,3). The prognosis of HCC patients showing MVI is extremely poor, and the median survival time (MST) of these patients has been reported to be 2–3 months (2,4). Sorafenib is the only evidence-based treatment option for patients classified to be at an Advanced stage (C) in the Barcelona Clinic Liver Cancer Staging System (BCLC) (5–7). However, in a pooled analysis of 2 pivotal phase 3 trials, sorafenib prolonged the median survival of these patients by only 47 days compared with placebo (7–9).

Prognosis improvement of advanced HCC is obtained by combined modality therapy according to liver residual function and progress (10,11). With recent technological advances, external beam radiotherapy (RT) could be considered an alternative treatment option for patients with HCC (12). Regarding the role of RT, the effectiveness of three-dimensional conformal radiotherapy (3D-CRT) has been recognized for treating PVTT/IVCTT (13). RT is a better initial therapy option than sorafenib for patients who have advanced unresectable HCC with PVTT (14). A combined treatment consisting of transarterial chemoembolization (TACE) and RT has shown promising radiologic response rates and improved overall survival of HCC with MVI in observational studies (15,16).

Hepatic arterial infusion chemotherapy (HAIC) is used more commonly than systemic chemotherapy, although no survival advantage has been demonstrated. Randomized controlled studies are currently underway to clarify the survival benefit of HAIC. Moreover, various novel systemic chemotherapeutic agents are currently under development in Japan, and further improvements in the treatment outcomes are expected (17). High efficacy and safety of a new combination therapy comprising of cisplatin-lipiodol suspension and 5-FU for HCC with PVTT, referred to as NewFP, has been reported; a high response rate at 86.3% and a MST of 33 months has been reported with this therapy regimen (18). In patients with advanced HCC and major PVTT, survival was significantly longer in those treated with HAIC combined with RT than it was with sorafenib (19).

This study aimed to investigate the efficacy and safety of NewFP plus 3D-CRT for MVI as the initial treatment and additionally that of sorafenib as the secondary treatment in patients with advanced HCC showing MVI.

Patients and methods

Patients

This retrospective study enrolled patients from our institute with unresectable advanced HCC who were treated with NewFP plus 3D-CRT for MVI between January 2009 and December 2017. In total, 32 HCC patients with MVI were registered retrospectively. Of these patients, 18 were treated with NewFP plus 3D-CRT for MVI and 14 were treated with sorafenib after NewFP plus 3D-CRT for MVI.

The diagnosis of HCC was made on the basis of the American Association for the Study of Liver Disease (AASLD) guidelines (6). Inclusion criteria were as follows: (i) HCC with PVTT in the first portal branch (Vp3) or in the main portal trunk or contralateral portal branch (Vp4); (ii) HCC with invasion to right or middle or left hepatic vein (Vv2) or IVCTT (Vv3); (iii) removal of all detected tumors is impossible with a sufficient hepatic functional reserve even if thrombectomy using the peel-off technique is considered (20); (iv) Child-Pugh score of 5–8; (v) an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0–2 (21); and (vi) no history of radiotherapy to the liver or of sorafenib treatment.

After estimating the response to the initial treatment with NewFP plus 3D-CRT for MVI, sorafenib was given to patients who were not able to undergo curative therapies such as hepatectomy and radiofrequency ablation (RFA) as a secondary treatment.

This study was conducted in accordance with the 1975 Declaration of Helsinki after receiving approval from the institutional review board of the Kagawa University, Kagawa, Japan (approval no. Heisei29-192). The requirement for informed consent from the participants was waived because of the retrospective nature of the study.

Implantation of arterial catheter

An indwelling catheter (5-Fr W and G spiral Catheter; Piolax, Tokyo, Japan) was inserted through the femoral artery, with the distal end extended into the hepatic or gastroduodenal artery with the proximal end connected to the port system (P-U CELSITE PORT; TORAY, Tokyo, Japan), which was implanted subcutaneously. The right gastric, gastroduodenal, and posterior superior pancreaticoduodenal arteries were occluded with microcoils to prevent gastroduodenal ulcers caused by anticancer agents.

Chemotherapy

HAIC involved cisplatin (50 mg fine powder in 5–10 ml lipiodol) and a continuous infusion of 5-FU (1,500 mg/5 days), referred to as NewFP. On day 1 of treatment, cisplatin with lipiodol was injected through the reservoir catheter, followed by 5-FU (250 mg). Following this, 5-FU (1,250 mg) was continuously infused for 5 days using a balloon pump (SUREFUSER PUMP, Nipro Pharma Corporation, Osaka, Japan). This regimen was administered once per week during the first 2 weeks of admission. Subsequently, a combination of 20–30 mg cisplatin with 2–6 ml lipiodol and 500–1,000 mg 5-FU was infused every 2 weeks at the out-patient department for as long as possible (18). Treatment was discontinued in cases of occurrence of grade 3 or higher adverse effects according to the ECOG classification, with the exception of total bilirubin >3.0 mg/dl, platelet count <5×104/µl, and leukocyte count <1,500/µl.

Radiotherapy

Planning computed tomography (CT) scans were obtained under free-breathing conditions using scans with a scan time of 3 sec per section. All patients underwent 3D-CRT, planned using a radiation treatment planning system. The gross tumor volume (GTV) consisted of the PVTT or IVCTT. A clinical target volume (CTV) was defined as the GTV with or without the main tumor. If the main tumor existed close to the GTV, the main tumor was included in the CTV when possible. The planning target volume (PTV) consisted of the CTV plus 8–10 mm margins. In principle, a prescribed dose at an isocenter was 50 Gy in 25 fractions with 2 Gy per fraction once daily using 6–10 MV photon beams delivered by a linear accelerator. 3D-CRT was started with the first cycle of HAIC.

Sorafenib treatment

Eligibility criteria for treatment with sorafenib were as follows: (i) unresectable advanced HCC; (ii) no effect of TACE; (iii) no previous sorafenib treatment for the liver tumor; (iv) Child-Pugh class A or B (up to a score of 7 points) hepatic function; (v) an ECOG performance status of 0–2 (21); and (vi) the following laboratory findings: Leukocyte count >1,500/µl, platelet count >7.5×104/µl, and serum hemoglobin level >8.5 g/dl. Sorafenib was administered orally as a 400–800 mg dose daily per the discretion of the chief physician. Dose reductions and treatment interruptions were allowed according to drug-related toxicity grades, as recommended.

Assessment of tumor response

To determine the therapeutic effect, baseline tumor measurements were obtained within 1 month before treatment by combining the largest diameters of selected target lesions in each patient, as measured using CT or MRI. CT or MRI was performed 4–6 weeks after the initial treatment cycle and every 2–3 months thereafter. The therapeutic effect was determined according to the best overall response, which was defined by the Modified RECIST (mRECIST) criteria (22). This was as follows: Complete response (CR), the disappearance of any intratumoral arterial enhancement in all target lesions; partial response (PR), at least a 30% decrease in the sum of diameters of viable (contrast enhancement in the arterial phase) target lesions, taking as reference the baseline sum of the diameters of target lesions; progressive disease (PD), an increase of at least 20% in the sum of the diameters of viable (enhancing) target lesions, taking as reference the smallest sum of the diameters of viable (enhancing) target lesions recorded since treatment initiation; and stable disease (SD), any case that does not qualify for either PR or PD. Patients who died before their first radiographic assessment were classified as having PD. Data from patients who died without tumor progression were censored. The response rate was defined on the basis of the independent radiologic review as the percentage of patients whose best-response mRECIST rating of CR or PR was maintained for at least 1 month after the first demonstration of such a rating. The disease-control rate was defined on the basis of independent radiologic review as the percentage of patients whose best-response mRECIST rating of CR, PR, or SD was maintained for at least 1 month after the first demonstration of such a rating.

Statistical analysis

All statistical analyses were performed using JMP software (SAS Institute, Inc., Cary, NC, USA), version 13. Baseline patient characteristics were analyzed using the Chi-square test, the Welch's t test, or Fisher's exact probability test. Overall survival rates and progression-free survival (PFS) were calculated using the Kaplan-Meier method and compared using the log-rank test. Changes in hepatic function using Child-Pugh scores before and after 3D-CRT were analyzed using the Wilcoxon signed-rank test. The Cox proportional-hazards model was used to evaluate the interaction between baseline characteristics and overall survival or therapeutic effect. All P values were two-tailed, and values less than 0.05 were considered statistically significant.

Results

Patient characteristics

Of the 32 HCC patients, 18 were treated with NewFP plus 3D-CRT for MVI (NewFP+3D-CRT group) and 14 were treated with sorafenib after NewFP plus 3D-CRT for MVI (sorafenib after NewFP+3D-CRT group). Comparisons of the clinical features between the two groups are shown in Table I. There were no significant differences in the baseline characteristics between groups.

Table I.

Patient characteristics (n=32). Baseline patient characteristics were analyzed using the chi-square test, Welch's t test, or Fisher's exact probability test.

Variables	NewFP+3D-CRT (n=18)	Sorafenib after NewFP+3D-CRT (n=14)	P-value
Age, median (range)	68 (37–83)	68.5 (53–80)	0.9130
Sex, n (%)			0.2379
Male	15 (83.3)	14 (100)
Female	3 (16.7)	0 (0)
HBs antigen, n (%)			0.2302
Present	6 (33.3)	2 (14.3)
Absent	12 (66.7)	12 (85.7)
HCV antibody, n (%)			0.1641
Present	7 (38.9)	9 (64.3)
Absent	11 (61.1)	5 (35.7)
Child-Pugh score, n (%)			0.0590
5	1 (5.6)	1 (7.1)
6	6 (33.3)	8 (57.1)
7	7 (38.9)	5 (35.7)
8	4 (22.2)	0 (0)
Tumor size, maximum, median (mm)	190, 66	137, 50	0.1587
Number of tumors, n (%)			0.7120
<4	7 (38.9)	4 (28.6)
≥4	11 (61.1)	10 (71.4)
Tumor extent, n (%)			0.7178
Unilobar involvement	12 (66.7)	8 (57.1)
Bilobar involvement	6 (33.3)	6 (42.9)
AFP (ng/ml), n (%)			0.0993
<1,000	5 (27.8)	8 (57.1)
≥1,000	13 (72.2)	6 (42.9)
DCP median (mAU/ml), n (%)			0.3893
<1,000	5 (27.8)	6 (42.9)
≥1,000	13 (72.2)	8 (57.1)
Grade of portal vein invasion, n (%)			0.6744
Vp4	4 (22.2)	3 (21.4)
Vp3	14 (77.8)	7 (50)
Hepatic vein invasion, n (%)			0.1103
Present	2 (11.1)	4 (28.6)
Absent	16 (88.9)	10 (71.4)
Extra-hepatic spread			0.5828
Present	4 (22.2)	2 (14.3)
Absent	14 (77.8)	12 (85.7)

NewFP, new 5-fluorouracil and cisplatin therapy; HBs, hepatitis B surface; HCV, hepatitis C virus; AFP, a-fetoprotein; DCP, des-g-carboxy prothrombin; 3D-CRT, three-dimensional conformal radiotherapy.

The NewFP+3D-CRT group (n=18) included 15 men (83.3%) and 3 women (16.7%), with a mean age of 68 years (Table I). Chronic hepatitis C virus infection was the predominant cause of HCC (n=7; 38.9%), followed by chronic hepatitis B virus infection (n=6; 33.3%). Of the 18 patients, 7 patients (38.8%) had Child-Pugh class A hepatic function and 11 patients (61.1%) had Child-Pugh class B hepatic function. The median maximum tumor diameter was 190 mm. HCC showed portal vein invasion, with 4 patients (22.2%) presenting with Vp4 and 14 patients (77.8%) with Vp3 type of invasion. Four patients (22.2%) had extrahepatic spread (EHS).

The sorafenib after NewFP+3D-CRT group (n=14) included 14 men (100%), with a mean age of 68.5 years (Table I). Chronic hepatitis C virus infection was the predominant cause of HCC (n=9; 64.3%), followed by chronic hepatitis B virus infection (n=2; 14.3%). Of the 14 patients, 9 patients (64.2%) had Child-Pugh class A hepatic function and 5 patients (35.7%) had Child-Pugh class B hepatic function. The median maximum tumor diameter was 137 mm. HCC showed portal vein invasion, with 3 patients (21.4%) having Vp4 and 7 patients (50%) having Vp3. Two patients (14.3%) had EHS.

Overall response and efficacy

Table II shows the results at the first radiologic assessment according to the mRECIST. Of the 32 patients treated with NewFP plus 3D-CRT for MVI, 3 (9.4%), 16 (50%), and 7 (21.9%) patients had CR, PR, and SD, respectively. The overall response rate was 59.4%, and the disease control rate was 81.3%.

Table II.

Therapeutic effects in all patients (n=32).

Therapeutic effects	NewFP+3D-CRT (n=32)
CR	3
PR	16
SD	7
PD	6
ORR (CR+PR), n (%)	19 (59.4)
DCR (CR+PR+SD), n (%)	26 (81.3)

NewFP, new 5-fluorouracil and cisplatin therapy; 3D-CRT, three-dimensional conformal radiotherapy; CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; ORR, overall response rate; DCR, disease control rate.

Cumulative overall survival curves of patients treated with NewFP plus 3D-CRT for MVI or sorafenib after NewFP plus 3D-CRT for MVI are shown in Fig. 1. The MST was 6.7 months for patients treated with NewFP plus 3D-CRT for MVI and 49.2 months for those treated with sorafenib after NewFP plus 3D-CRT for MVI (P=0.0003). The PFS in patients showing MVI who were treated either with NewFP plus 3D-CRT or with sorafenib after NewFP plus 3D-CRT are shown in Fig. 2. The median PFS was 4.3 and 6.8 months for patients treated either with NewFP plus 3D-CRT for MVI or those treated with sorafenib after NewFP plus 3D-CRT, respectively (P=0.0219). Sorafenib, administered as the secondary treatment after NewFP plus 3D-CRT for MVI was associated with a significantly higher overall response rate, disease control rate, and longer overall survival in HCC patients showing MVI.

Figure 1.

Kaplan-Meier analysis of overall survival in patients treated with NewFP plus 3D-CRT for MVI (solid line; n=18) and those treated with sorafenib after NewFP plus 3D-CRT for MVI (dotted line; n=14). The median survival times were 6.7 and 49.2 months, respectively. The overall survival rates were compared using the log-rank test. NewFP, new 5-fluorouracil and cisplatin therapy; 3D-CRT, three-dimensional conformal radiotherapy; MVI, macroscopic vascular invasion.

Figure 2.

Kaplan-Meier analysis of PFS in patients treated with NewFP plus 3D-CRT for MVI (solid line; n=18) and those treated with sorafenib after NewFP plus 3D-CRT for MVI (dotted line; n=14). The median PFS were 4.3 and 6.8 months, respectively. The PFS rates were compared using the log-rank test. PFS, progression-free survival; NewFP, new 5-fluorouracil and cisplatin therapy; 3D-CRT, three-dimensional conformal radiotherapy; MVI, macroscopic vascular invasion.

Factors associated with survival outcomes

The significant prognostic factors for overall survival, according to univariate analysis, were response to initial treatment with NewFP plus 3D-CRT (PR or CR, P=0.0479) and the number of tumors (<4, P=0.0260). Multivariate analysis confirmed that initial treatment with NewFP plus 3D-CRT (PR or CR, hazard ratio, 0.2264; 95% confidence interval, 0.0737–0.6320; P=0.0060) was an independent factor for overall survival (Table III).

Table III.

Factors associated with overall survival. The Cox proportional hazards model was used to evaluate the interaction between baseline characteristics and overall survival or therapeutic effect. Two-tailed values of P<0.05 were considered to indicate a statistically significant result.

	Univariate analysis	Multivariate analysis
Variables	P-value	HR (95% CI)	P-value
Age (<75/75≤ years)	0.3617
Child-Pugh (A/B)	0.1069
AFP (<1,000/1,000≤ ng/ml)	0.3891
DCP (<1,000/1,000≤ mAU/ml)	0.6205
Tumor number (<4/4≤)	0.0260[a]	0.9731 (0.2995–3.0632)	0.9628
Tumor localization (unilobar/bilobar)	0.3699
Vv2-3 (absent/present)	0.1536
Vp3-4 (absent/present)	0.1536
TACE-refractory (abscent/present)	0.5228
Treatment response to NewFP+3D-CRT (PR+CR/SD+PD)	0.0479[a]	0.2264 (0.0737–0.6320)	0.0060[b]

Analyzed using univariate analysis

analyzed using multivariate analysis. AFP, alpha-fetoprotein; DCP, des-gamma-carboxy prothrombin; NewFP, new 5-fluorouracil and cisplatin therapy; 3D-CRT, three-dimensional conformal radiotherapy; CR, complete response; PR, partial response; SD, stable disease; PD, progressive disease; HR, hazard ratio; CI, confidence interval.

Safety and adverse events

Changes in hepatic function using Child-Pugh scores before and after 3D-CRT are shown in Fig. 3. In surviving cases, no significant hepatic function decline was seen after 3D-CRT. On the other hand, Child-Pugh scores decreased after 3D-CRT; hepatic function improved in several patients.

Figure 3.

Changes in hepatic function using Child-Pugh scores before and after 3D-CRT. In surviving cases, no significant hepatic functional decline was observed after 3D-CRT. 3D-CRT, three-dimensional conformal radiotherapy. N.S., not statistically significant.

Serious adverse events such as gastrointestinal bleeding due to radiation gastritis were observed in 3 patients, 1 in the NewFP+3D-CRT group and 2 in the sorafenib after NewFP+3D-CRT group. In all 3 cases, healing occurred using argon plasma coagulation delivered via endoscopy. Treatment-related mortality was not observed in the two groups.

Discussion

In the present study, for patients with advanced HCC showing MVI, sorafenib after NewFP plus 3D-CRT for MVI was associated with a significantly higher overall response and disease control rate relative to sorafenib monotherapy. Furthermore, patients administered sorafenib after NewFP plus 3D-CRT for MVI had a good prognosis, with an MST of 49.2 months.

MVI is a prognostic factor for lower overall survival among HCC patients. PVTT causes portal hypertension-related complications such as varix or ascites, and is associated with exacerbating factors such as a larger tumor size, higher tumor grade, and alpha-fetoprotein elevation (23). Because blood from the inferior vena cava flows into the pulmonary vessels, lung metastasis and pulmonary embolism would be expected to be frequent in patients with IVCTT. If the MVI cannot be reduced, it may lead to a decrease in the portal vein blood flow; this may result in a further decline in hepatic function, increasing the risk of sudden death. Therefore, quick reduction of MVI is important to facilitate subsequent treatment.

Sorafenib is recommended by BCLC guidelines as the first-line therapy for advanced HCC, but its efficacy is limited (24). In the SHARP trial, the MST of patients with HCC showing MVI who were treated with sorafenib was 8.1 months; the incidence of objective responses was low (7). Several studies have reported various combination strategies for HCC showing MVI (25). In a randomized clinical trial for advanced HCC showing MVI, initial treatment with TACE plus RT was well tolerated and conferred an improved progression-free survival, objective response rate, time to progression, and overall survival, compared with sorafenib treatment (26). On the other hand, HAIC combined with RT was associated with a longer MST for HCC with PVTT compared with sorafenib (19). In the present study, immediate therapeutic response was obtained by using NewFP (associated with a high response rate) plus 3D-CRT (associated with a high local control rate) for MVI.

Although regorafenib and lenvatinib can currently be administered as alternatives to sorafenib as molecular target drugs for HCC patients showing MVI, they are limited to Child-Pugh class A hepatic function (27–29). When sorafenib was withdrawn, the introduction of secondary treatments was difficult, due to a decline in hepatic functional reserve, fatigue, and a decline in PS; as recorded in previous reports (30). In the present study, HCC patients showing MVI of Child-Pugh class B hepatic function were safely able to undergo NewFP plus 3D-CRT for MVI as the initial treatment. In addition, several patients in whom hepatic function improved after the initial treatment from Child-Pugh class B to A, were able to receive sorafenib. Furthermore, in the multivariate analysis, initial treatment was extracted as a significant factor associated with overall survival. As the initial treatment, NewFP plus 3D-CRT for MVI was well tolerated and provided a chance for secondary treatment. On the other hand, we compared our study to a previous open label, non-comparative, phase II trial in patients with advanced HCC. Patients who received HAIC and were responders were continued on HAIC and were expected to have good prognoses, while the HAIC non-responders were switched to sorafenib (31). The MST of HCC patients showing MVI was 25.4 months in this previous trial. Although there were few differences between our study and the previous trial, the results of sorafenib after NewFP plus 3D-CRT for MVI in our study was superior to that of the previous trial. The reason for our favorable results could be that immediate therapeutic response was obtained by using NewFP (associated with a high response rate) plus 3D-CRT (associated with a high local control rate) for MVI. In addition, avoiding the unnecessary stenosis of hepatic artery by catheter therapy, the reduction of sensitivity to the drug, deterioration of liver function, and appearance of collateral arteries could also explain the favorable results (32,33). We postulated that shifting to the secondary treatment promptly, while maintaining hepatic function, would lead to improvement in prognosis for advanced HCC showing MVI.

Sorafenib, an oral multikinase inhibitor that blocks tumor cell proliferation and angiogenesis, significantly improved overall survival compared with placebo in patients with advanced HCC (7,9). In preclinical studies, sorafenib was shown to exert a synergistic anticancer effect on cisplatin (34). A recent study investigating sorafenib combined with HAIC suggested that combining systemic therapy and regional cytotoxic chemotherapy could enhance antitumor activity (35). Therefore, we speculate that the combination of NewFP and sorafenib synergistically produced an antitumor effect, leading to the higher overall response. Because a considerable proportion of HCC patients showing MVI are unable to receive curative treatment, it is important to explore multimodal strategies for such patients. To the best of our knowledge, NewFP was associated with the longest survival of HCC patients showing MVI in all studies reported so far. No combined modality therapy of NewFP plus 3D-CRT and sorafenib has yet to show a clear survival benefit. The present study is the first reported to show that the combined modality therapy of NewFP plus 3D-CRT and sorafenib is a feasible and promising treatment option for HCC patients showing MVI.

There are several possible limitations to this study. Since this investigation was a retrospective single-center study, the possibility of unintentional selection bias during patient selection cannot be fully excluded. Additionally, the number of cases was small. Therefore, it is necessary to investigate this treatment strategy at multiple centers via a prospective study to confirm our findings.

In conclusion, for patients with advanced HCC showing MVI, the initial treatment with NewFP plus 3D-CRT for MVI was well tolerated, and administration of sorafenib as the secondary treatment after NewFP plus 3D-CRT for MVI was associated with a significantly higher overall response rate, disease control rate, and longer overall survival. Our results suggest that a good prognosis could be obtained by performing sorafenib treatment after chemoradiotherapy for advanced HCC showing MVI.