- Open Access
Radiation treatment with volumetric modulated arc therapy of hepatocellular carcinoma patients. Early clinical outcome and toxicity profile from a retrospective analysis of 138 patients
Radiation Oncologyvolume 7, Article number: 207 (2012)
To report early outcome and toxicity for inoperable patients with hepatocellular carcinoma (HCC) treated with volumetric modulated arc therapy (VMAT).
One hundred and thirty eight patients were retrospectively analysed. Dose prescription ranged from 45 to 66Gy with conventional fractionation regime. Based on AJCC staging, 88.4% presented stage III or IV. Two-thirds (69.6%) were Child-Pugh stage A, the remaining were stage B. According to Barcelona Clinic Liver Cancer staging, 72.5% of patients were classified as stage C.
Median age was 66 years, median tumor volume was 516cm3 (28 to 3620cm3). The most patients (83%) were treated with 60Gy. Median follow-up time was 9 months. One-year overall survival rate was 45% (100% for AJCC stage I, 83% for stage II, 45% for stage III and 28% for stage IV), median survival was 10.3 months (95% C.I. 7.2-13.3). Local control was achieved in 94% (of 109 assessable patients), stable disease in 29%, partial response in 53%, complete response in 11%, and progression in 6%. Radiation-induced liver disease was observed in 34 patients (25%). Gastrointestinal grade 3 toxicity was modest with a total of 17 (12.3%) cases for all endpoints.
Clinical results could suggest to introduce VMAT as an appropriate technique for the patients with HCC.
Hepatocellular carcinoma (HCC) is the third cause of cancer death and one of the most challenging oncological problems . Surgery, although providing survival rates up to 70% at 5 years , is viable in a small fraction of patients (less than 1/3) because of advanced stage at diagnosis. Patients also can be treated with transcatheter arterial chemoembolization (TACE), radiofrequency ablation (RFA), percutaneous ethanol injection (PEI), chemotherapy and targeted agents [3–6] with complex decision trees and limited impact on outcome. Radiotherapy was offered to HCC patients but it was limited by severe radiation induced liver disease (RILD) when excessive fractions of the liver were involved in the radiation field  and the important relationship between the volume of irradiated normal liver and the toxicity profile [8–10]. After the introduction of intensity modulated radiotherapy (IMRT), a new hope emerged for radiotherapy in HCC patients [11, 12]. Recently, IMRT evolved into the so-called volumetric modulated arc therapy (VMAT). VMAT was pioneered in its RapidArc mode by Otto  and technical details can be found elsewhere . In liver, clinical application of RapidArc was primarily limited to metastatic indications . A planning study from Kuo et al. demonstrated that RapidArc also play a role in HCC . Stereotactic body radiation therapy (SBRT) approaches have been hypothesized for smaller target and in cases requiring modest irradiation of entire liver (less than 1/4 of the volume) .
Here, we report about the clinical application of RapidArc to HCC in a cohort of patients, demonstrating the feasibility and the early clinical outcome on a large patient population. Conventional fractionation and total dose were adopted because of the stage and the large median tumor size.
Between February 2009 and December 2010, 138 consecutive HCC patients presented Barcelona Clinic Liver Cancer (BCLC) stage A to C and were eligible for curative or palliative radiotherapy (in eventual association to other therapeutic modalities) at the home institute. Figure 1 represents the institutional guidelines for HCC treatment. In brief, BCLC stages A to C, Child-Pugh stages A-B with single lesions larger than 5cm or multi-nodular lesions larger than 3cm were eligible for radiotherapy. All patients were inoperable or not eligible for TACE treatments and received radiotherapy as primary treatment. Portal vein thrombosis was present in about 50% of the cases. Relative contraindication to inclusion were: total bilirubin levels greater than 3 to 5 mg/dL; white blood count (WBC) less than 2500–1500 U/?L; Glutamic pyruvic transaminase (GPT) in the range 100–300 U/L. Absolute exclusion criteria included total bilirubin >5 mg/dL, WBC<1500 U/?L and GPT>300 U/L.
Dose prescription was of 45, 60 or 66Gy in 1.8 or 2.0Gy/fraction depending upon stage, location of target and its size and general conditions of patient. Plans were designed for single course treatments of for sequential boosting on reduced volumes technique. In case of boost, three schemed were adopted: i) 60Gy total dose in two courses: 40Gy+20Gy; ii) 45Gy in two courses: 36Gy+9Gy; iii) 45Gy in three courses: 27Gy+9Gy+9Gy. Patients receiving a single course were treated at 66Gy. For those patients with tumor near gastrointestine tract, 45Gy in two or three courses were designed by the shrinkage of tumor and prevention for gastrointestine. The dosage and boost scheme were predetermined by the decisions of the physician. If the dose constraints couldn’t be satisfied, boost schemes were applied to decrease normal tissue complications. As an example, for existing duonenal ulcer, gastric ulcer, reflux esophagitis patients, 36+9Gy boost was applied to minimize radiation-induced ulcer. When OARs included stomach, duodenum and colon, the 40+20Gy scheme was applied. The gross tumor volume (GTV) was defined as the primary tumor plus abnormal portal areas revealed on CT images (IV contrast was used for all patients except for the patients with renal dysfunction. For those renal insufficient patients, MRI was added and fused to planning CT for more precise target delineation). The clinical target volume (CTV) was defined as the GTV plus a 1cm margin. The planning target volume (PTV) was defined as the CTV plus 0.5cm axial and 1–2.5cm cranial-caudal individualized margins. Boost volumes were definied with repeated CT scans if needed.
Plans were normalized to 95% of the planning target volume (PTV) (D95%=100%). For all patients, in addition to the target volume PTV, the entire liver, the normal liver (liver-PTV), the kidneys, the stomach, the spinal cord and the lungs were outlined and considered during optimization. The following explicit planning objectives were defined: for the total liver V30Gy<60%, for the normal liver (liver-PTV); V15Gy<30%, for the PTV a minimum dose greater than 90%; and a maximum dose lower than 115-140%.
All patients were treated with VMAT in the form of RapidArc [13, 14] with 10 MV photons. Individualized optimization was performed using single or multiple, coplanar or non-coplanar, mono-isocentric arcs.
All patients were treated in supine position with arms placed overhead and were immobilized with an individualized vacuum cushion on the patient tray. A real-time infrared tracking device (ExacTrac; BrainLab AG, Heimstetten, Germany) was used for patient immobilization and reposition during the CT scan and treatment.
Dosimetric and technical parameters of delivery were scored including some delivery parameters as well as standard analysis of dose volume histograms (DVH). Guidelines of International Commission on Radiation Units and Measurements (ICRU) 83 report were applied as far as possible . Clinical evaluation was performed, with reference to baseline conditions determined before start of treatment, during treatment and at 1, 2, 3,6 months after treatment completion: basic treatment outcome was measured in terms of in-field local control (visits included laboratory assessment and CT and MRI imaging (at 2 to 3 month intervals for at least 2 years and at 6 month intervals thereafter)) and patient overall survival and it was scored continuously with a total follow-up of maximum 28 months. Tumor response was assessed using Response Evaluation Criteria in Solid Tumors (RECISTs) criteria. Local in field recurrence was defined by new enhancement or progressive disease with CT or MR imaging during follow-up. Actuarial survival and local control rates were determined by standard Kaplan-Meier analysis and several factors were tested to ascertain significant differences between subgroups of patients. Univariate and multivariate analysis were similarly performed to identify variables relevant for survival prediction. RILD (in absence of progressive liver disease), was defined by Lawrence’s criterion . Conventional definition of classical RILD  manifested within 4 months after the completion of irradiation as either anicteric elevation of alkaline phosphatase level to at least two-fold of the upper normal level and nonmalignant ascites, is not common in Asia. Instead, non-classic RILD is dominant and GPT elevation indicates hepatocyte damage. Bujold  defined non-classical RILD as a 5-time elevation in liver transaminases. The significant liver dysfunction is often difficult to differentiate treatment-induced hepatic toxicity from progressive tumor or dysfunction exist prior to treatment such as cirrhosis or previous treatment. Thus, we defined RILD as elevated transaminase of at least two-fold the upper limit of normal or pretreatment levels based on the National Cancer Institute Common Toxicity Criteria for Adverse Events (CTCAE) version 4.03. Gastrointestinal (GI) toxicity was also scored according to CTCAE 4.03. Endpoints included esophagitis, gastritis, gastric hemorrhage or ulceration, duodenal hemorrhage or ulceration and ascites.
Of the 138 patients treated with RapidArc included in the analysis, Twenty-nine patients were not assessed in terms of treatment response because either dead (21) or lost to follow-up (8). Table 1 reports the characteristics of the cohort of patients included in the study. Concerning stage, the vast majority of the cases presented advanced local diseases: BCLC stage C in 72.5% of the population, AJCC stage III and IV in 88.4% of the cases. About half of the cases were with portal vein thrombosis; 86.2% had history of hepatitis. For all patients, median tumor volume was 516 cm3 (ranging up to 3621cm3) corresponding to 33% of the median total liver volume.
Almost (88.4%) patients received either 60 or 66Gy and about 61% were treated with one or more volume reductions (cone-down). About 88% of the patients were treated with 2Gy/fraction, 12% with 1.8Gy/fraction. Nearly 99% of the patients were treated with multiple partial arcs and 93% were optimized with a non-coplanar setting.
Table 2 shows results from the dose-volume histogram (DVH) analysis for target volumes and organs at risk. The planning objective on V30Gy for total liver and on V15Gy for normal liver (liver-PTV) were on average respected together with a substantially full coverage of the PTV (V95% and D95% showed a minimum value of 96% and 96.8%).
Figure 2 shows survival estimates after Kaplan-Meier analysis for the whole cohort of patients (n=138) and factorized according to some of the variables leading to significant differences. Mean survival time resulted 13.5 months (95% C.I.: 11.6–15.3 months), median resulted 10.3 months (95% C.I.: 7.2-13.3 months). Overall survival (OS) at 12 months resulted 45±5%, at 24 months 28±5%. One-year OS based on AJCC stage was: stage I: 100%; stage II: 83%; stage III: 45%; stage IV: 28%. The same OS classified by BCLC is: stage A 85.1% (4 patients alive), B 74.1% (19 patients alive), C 32.5% (24 patients alive). Table 3 summarizes the mean OS time factorized according to some of the main significant variables. Univariate analysis lead to the result that the following variables are significant with respect to survival (in parenthesis the significance): sex (p=0.05), age (p=0.006), total dose (p=0.01), tumor volume (p<0.001), localization (p=0.03), portal vein thrombosis (p<0.001), AJCC stage (p<0.001), BCLC stage (p<0.001), normal liver volume (p<0.001), T stage (p<0.001), baseline alpha fetoprotein (AFP) level at before therapy (p=0.03), volume of total liver receiving more than 30Gy (p=0.001). In a multivariate analysis, the following variables resulted statistically significant: total liver volume (p=0.001), tumor volume (p=0.002), total liver volume irradiated more than 30Gy (p=0.02), portal vein thrombosis (p=0.001), T stage (p=0.001), AJCC stage (p=001), BCLC stage (p<0.001) and baseline alpha fetoprotein level (p=0.02). Survival did not resulted significantly different (p=0.11) if factorized according to Okuda stage I and II.
Response and toxicity
The mean time to local response was 8.8 months (95% C.I.: 7.9–9.7 months). The responses were: progressive disease (PD): 6.4% (7 of 109 assessed patients) with a mean time to progression detection of 3.1±2.3 months (range 1.1 to 7.2 months); stable disease (SD): 29.4% (32 patients) with mean time to detection of 4.0±1.3 months (range: 1.4-6.8 months); partial response (PR): 53.2% (58 patients) mean time to response of 4.6±1.3 months (range: 1.2-8.9 months); complete response (CR): 11.0% (12 patients), mean time to complete response of 4.9±1.7 months (range: 3.0-9.8 months). Twenty-nine patients were not assessable as described above. Hundred and two patients responded with progression-free (SD+PR+CR), 93.5% of the assessed group or 73.9% of the entire cohort of 138 patients.
AFP level was monitored and its reduction from baseline (before treatment) to the end of radiotherapy resulted highly significant for the entire cohort of patients (20% reduction, p<0.01). Total reduction and significance remained high at 1, 3 and 6 months (reduction of 27%, 27% and 29%; p=0.01, p<0.01 and p=0.03). Different trends were observed for the two risk groups (baseline AFP between normal level to 400ng/L versus greater than 400ng/L). For the first risk group, AFP increased during treatment and follow-up: +22% at end of treatment, +173% at 1 month after end of treatment and +228% at 3 months with high significance of differences. The patients belonging to the highest risk group, showed, on the contrary, a remarkable reduction of AFP: 20% at the end of treatment, 29% at one and 3 months (p<0.01, p<0.01, p=0.03). The relative majority of PR or CR (29/70) were observed in the AFP highest risk group. No impact was observed on total bilirubin levels between baseline and end of therapy. A significant drop in WBC was observed between baseline and end of therapy (p=0.01), partially recovered but still significant at 3 and 6 months. For hemoglobin levels, the trend is similar with WBC.
Concerning treatment toxicity, non-conventional RILD was observed in 34 cases (25% of 138 patients), but the most cases (24/34) were grade 1 or 2 toxicities (Table 4). Four patients with severe RILD (grade 3 or 4) were observed in the AFP first risk group (AFP from 8.04 to 400ng/mL) and 3 in each of the normal level or high risk groups. GI toxicity is summarized in Table 4 and resulted mild. For each endpoint grade 3 was observed in 1-2% of cases while grade 1–2 ranged from 2% (esophagitis) to 23% (ascites).
The current study demonstrated the possibility to treat HCC patients with RapidArc safely and effectively within a conventional fractionation scheme and total dose ranging from 45 to 66Gy. Patients treated were mostly in advanced stages (>90% in BCLC stages B and C) with frequent presence of portal vein thrombosis. Early results in terms of overall survival and local control demonstrated a high level of local control (94% of the assessable patients) and the overall survival at 12 months resulted 45% (significantly higher for earlier stages). A significant clinical effect at biochemical level was observed in the decline of the AFP levels at the end of treatment and during follow-up with a 30% reduction of AFP for the whole cohort and of more than 50% for the patients with poor baseline.
The application of non-coplanar rotational technique with intensity modulation is a unique characteristic in this study. RapidArc allowed to spare normal liver tissue and led to be an acceptable treatment option for those patients ineligible for surgery or other ablative treatments. Because of the advanced stage, it was not possible to add also hypo-fractionated regimen for these HCC patients. Therefore, although this modality has better or similar effect in tumor response as the standard treatment, any comparison against other published studies has to account for the trade-off between the innovative technique and the limits of conventional fractionation. Given the short follow-up, results might be time-biased (local control might be overestimated or toxicity under-estimated) in present study. However, it is important to position the new treatment technique in the frame of consolidated experience of other groups. Hsu  reported about bi-fractionated treatments with conformal therapy: from a pool of 121 patients, 1 year survival was 60%. Krishnan  reviewed studies of radiotherapy in liver including typically TACE, 1 year survival ranged from 42% to 94% for doses ranging from 30 to 66Gy. Seong  demonstrated 158 patients treated with conventional fractionation scheme and in combination with TACE. One-year and 2-year OS was 40% and 20% with a median survival of 10 months, respectively. Seong also found that total dose was the only significant factor influencing survival and the mean prescribed dose was 48Gy. Data from this study demonstrated a similar effect with a huge difference between the three-dose levels administered (although masked by several other prognostic factors in the dose level assignment). Seong reported comparable results in terms of local control compared to this study. Skinner  reported a small cohort of 29 patients demonstrating once more the relevance of total dose to improve outcome. Patients treated with lower total doses (biological effective dose <75Gy) resulted in 1-year OS of only 18% against 69% for the complementary group. Given these perspective and the results of the present study, it is conceivable to escalate the dose prescribed with RapidArc also for advanced stage patients with HCC. Yoon  analyzed clinical outcome for 412 patients treated with TACE and 3D conformal radiotherapy for HCC with portal vein thrombosis. For these patients, median survival was 10.6 months with 42.5% survival rate at one year consistent to the data reported in the present study (35% survival for PVT positive patients).
This study also allowed to identify some correlation between outcome and AFP levels before treatment. Patients within the highest risk group of AFP had the most significant reduction of the same during follow-up. Although no definitive answer can be provided here, one possible interpretation, might be related to the fact that non-significant AFP elevation will occur when either hepatitis reactivation or change of cirrhosis status will occur after radiotherapy. Thus, for those patients with lower AFP levels (first risk group), the AFP might be increasing because of the effects of inflammation/cirrhosis are higher than therapeutic effect in the early follow-up period. On the contrary, for those patients with higher AFP levels (high risk group), even assuming a similar proportion of tumor cell killing as within the first group, the absolute AFP values will decrease more.
Finally, an advantage of RapidArc is its effective ‘rapid’ delivery time. This might overcome most of the problem of respiratory motion in abdominal tumours, especially in HCC patients. In particular, conventional respiratory gating may not be feasible for HCC patients (breath hold or deep inspiration are impractical for the patients with huge HCC and massive ascites). While for most advanced stages, respiratory motion could be automatically accounted for by the extension of margins, for earlier stages, the usage of time resolved CT scan (4DCT) for planning might help to understand the liver excursion and to better individualise the margins to PTV. This is particularly important in those cases where dose escalation might be envisaged.
The cohort of 138 patients suffering of HCC was treated with VMAT. Early results in terms of OS and local control were adequate and consistent with similar reports demonstrating the appropriateness of the RapidArc technique for advanced HCC patients. Toxicity profile was mild. Dose escalation might be considered to improve survival, either increasing the total dose or, for earlier stages, considering the SBRT solution. Longer follow-up will allow to consolidate these early observations.
Altekruse SF, McGlynn KA, Reichman ME: Hepatocellular carcinoma incidence, mortality, and survival trends in the united states from 1975 to 2005. J Clin Oncol 2009, 27: 1485-1491. 10.1200/JCO.2008.20.7753
El-Serag HB, Mason AC: Rising incidence of hepatocellular carcinoma in the united states. N Engl J Med 1999, 340: 745-750. 10.1056/NEJM199903113401001
Bujold A, Dawson LA: Stereotactic radiation therapy and selective internal radiation therapy for hepatocellular carcinoma. Cancer Radiother 2011, 15: 54-63. 10.1016/j.canrad.2010.11.003
Dawson LA: Overview: where does radiation therapy fit in the spectrum of liver cancer local-regional therapies? Semin Radiat Oncol 2011, 21: 241-246. 10.1016/j.semradonc.2011.05.009
Feng M, Ben-Josef E: Radiation therapy for hepatocellular carcinoma. Semin Radiat Oncol 2011, 21: 271-277. 10.1016/j.semradonc.2011.05.002
Guy J, Kelley RK, Roberts J, et al.: Multidisciplinary management of hepatocellular carcinoma. Clin Gastroenterol Hepatol 2012, 10: 354-362. 10.1016/j.cgh.2011.11.008
Lawrence TS, Robertson JM, Anscher MS, et al.: Hepatic toxicity resulting from cancer treatment. Int J Radiat Oncol Biol Phys 1995, 31: 1237-1248. 10.1016/0360-3016(94)00418-K
Dawson LA, Ten Haken RK: Partial volume tolerance of the liver to radiation. Semin Radiat Oncol 2005, 15: 279-283. 10.1016/j.semradonc.2005.04.005
Pan CC, Kavanagh BD, Dawson LA, et al.: Radiation-associated liver injury. Int J Radiat Oncol Biol Phys 2010, 76: S94-S100. 10.1016/j.ijrobp.2009.06.092
Park HC, Seong J, Han KH, et al.: Dose–response relationship in local radiotherapy for hepatocellular carcinoma. Int J Radiat Oncol Biol Phys 2002, 54: 150-155.
Cheng JC, Wu JK, Huang CM, et al.: Dosimetric analysis and comparison of three-dimensional conformal radiotherapy and intensity-modulated radiation therapy for patients with hepatocellular carcinoma and radiation-induced liver disease. Int J Radiat Oncol Biol Phys 2003, 56: 229-234. 10.1016/S0360-3016(03)00091-9
Eccles CL, Bissonnette JP, Craig T, et al.: Treatment planning study to determine potential benefit of intensity-modulated radiotherapy versus conformal radiotherapy for unresectable hepatic malignancies. Int J Radiat Oncol Biol Phys 2008, 72: 582-588. 10.1016/j.ijrobp.2008.06.1496
Otto K: Volumetric modulated arc therapy: IMRT in a single gantry arc. Med Phys 2008, 35: 310-317. 10.1118/1.2818738
Fogliata A, Clivio A, Nicolini G, et al.: Intensity modulation with photons for benign intracranial tumours: a planning comparison of volumetric single arc, helical arc and fixed gantry techniques. Radiother Oncol 2008, 89: 254-262. 10.1016/j.radonc.2008.07.021
Scorsetti M, Alongi F, Castiglioni S, et al.: Feasibility and early clinical assessment of flattening filter free (FFF) based stereotactic body radiotherapy (SBRT) treatments. Radiat Oncol 2011, 6: 113. 10.1186/1748-717X-6-113
Kuo YC, Chiu YM, Shih WP, et al.: Volumetric intensity-modulated Arc (RapidArc) therapy for primary hepatocellular carcinoma: comparison with intensity-modulated radiotherapy and 3-D conformal radiotherapy. Radiat Oncol 2011, 6: 76. 10.1186/1748-717X-6-76
Tse RV, Hawkins M, Lockwood G, et al.: Phase I study of individualized stereotactic body radiotherapy for hepatocellular carcinoma and intrahepatic cholangiocarcinoma. J Clin Oncol 2008, 26: 657-664. 10.1200/JCO.2007.14.3529
ICRU: Report 83: prescribing, recording and reporting intensity modulated photon beam therapy (IMRT) (ICRU report 83). International Commission on Radiation Units and Measurements, Washington, DC; 2010.
Hsu WC, Chan SC, Ting LL, et al.: Results of three-dimensional conformal radiotherapy and thalidomide for advanced hepatocellular carcinoma. Jpn J Clin Oncol 2006, 36: 93-99. 10.1093/jjco/hyi242
Krishnan S, Dawson LA, Seong J, et al.: Radiotherapy for hepatocellular carcinoma: an overview. Ann Surg Oncol 2008, 15: 1015-1024. 10.1245/s10434-007-9729-5
Seong J, Park HC, Han KH, et al.: Clinical results of 3-dimensional conformal radiotherapy combined with transarterial chemoembolization for hepatocellular carcinoma in the cirrhotic patients. Hepatol Res 2003, 27: 30-35. 10.1016/S1386-6346(03)00162-1
Skinner HD, Sharp HJ, Kaseb AO, et al.: Radiation treatment outcomes for unresectable hepatocellular carcinoma. Acta Oncol 2011, 50: 1191-1198. 10.3109/0284186X.2011.592147
Yoon SM, Lim YS, Won HJ, et al.: Radiotherapy plus transarterial chemoembolization for hepatocellular carcinoma invading the portal vein: long-term patient outcomes. Int J Radiat Oncol Biol Phys 2012, 82: 2004-2011. 10.1016/j.ijrobp.2011.03.019
Dr. L. Cozzi is Head of Research at Oncology Institute of Southern Switzerland and acts as Scientific Advisor to Varian Medical Systems.
PMW and LC coordinated the entire study. Data collection was conducted by PMW, WCH, NNC, FLC. Data were analyzed by PMW, WCH, NNC, FLC, AF, LC. All authors read and approved the final manuscript.