Chemoembolization, Hepatic

Article Author:
Michael Young
Article Editor:
Savio John
Updated:
9/12/2018 1:45:58 PM
PubMed Link:
Chemoembolization, Hepatic

Introduction

Chemoembolization is the technique of injecting chemotherapy medication into the feeding arteries of a tumor along with particles designed to slow or stop the further arterial supply of oxygen and nutrients to that tumor. It has been performed since the late 1970s.[1],[2] It is one of several techniques used with the goal of treating either primary liver cancer or cancer metastatic to the liver. The most common primary liver cancer is hepatocellular carcinoma (HCC). Common types of metastases to the liver include those from the colon, breast, carcinoid, soft tissue sarcomas, and melanoma. Arterial chemoembolization also can be termed transarterial chemoembolization (TACE).

Anatomy

The liver is divided into lobes and segments; there are several classification schemes for describing these segments, but the most widely used is the Couinaud classification. In this classification, the segments and lobes are defined in part by their third order (third branch) portal venous supply and in part, by their systemic venous drainage.

The arterial liver supply is variable. The most common configuration is that of a single proper hepatic artery derived from the common hepatic artery in turn derived from the celiac artery, with the proper hepatic artery dividing into right and left branches to feed the right and left lobes of the liver, respectively. However, this configuration is probably present in less than 50% of humans; various sources give various percentages. Authors disagree regarding the terminology of the artery that supplies segment 4, which is termed a middle hepatic artery by some and a segment four branch by others.[3] The caudate lobe has particularly variable supply, often with multiple branches from both the right hepatic artery and the left hepatic artery.

The following are the 3 common potential accessory arterial supplies to liver tumors:

  • The right phrenic artery (sometimes called the inferior phrenic artery)
  • A replaced or accessory left hepatic artery
  • The right internal mammary artery (also called the internal thoracic artery)

The following 4 arteries should be kept in mind as common avenues for inadvertent chemoembolization (i.e., embolizing non-target healthy tissues):

  • The cystic artery
  • The right gastric artery
  • The falciform artery
  • The duodenal (or supraduodenal) artery

Indications

Perhaps the most widely used guidelines for management of cancer in the United States are those created by the National Comprehensive Network (NCCN). The NCCN is a non-profit organization composed of selected hospitals, mostly university hospitals, that choose member physicians from multiple specialties to sit on panels that make national guidelines for cancer treatment.

According to the NCCN, determining whether or not TACE is indicated involves a process of elimination. On the one hand, TACE is not as effective as surgery (either transplant or partial hepatic resection) for curing HCC or metastatic disease and is not in and of itself considered to be a curative treatment. On the other hand, TACE is a more effective treatment than others on the spectrum of treatments that may be considered to be purely palliative. In a minority of situations, TACE either can change a patient's status from "incurable" to "curable" (by downsizing one or more tumors to qualify the patient for surgery) or provide complete permanent tumor necrosis. Thus, on the one hand, a candidate for TACE is someone who has such advanced tumor status and/or overall poor health so as not to be able to withstand surgery or to gain a survival benefit from it as a first line option. This same person, on the other hand, must be healthy enough to withstand the potential side effects and toxicity of TACE and to have good enough odds of gaining at least several months of additional survival at a reasonable quality of life. This process of elimination for discerning which treatment is the best first-line treatment for an individual patient is variable and often subjective, but guidelines do exist to allow for some objectivity.

When considering treatment options for HCC and metastatic disease to the liver, the NCCN relies on several sets of criteria or "scores." These include scores, such as the Child-Pugh-Turcotte score, which is often referred to only as Child-Pugh score, and the United Network for Organ Sharing (UNOS) score, which is commonly referred to instead as the Model for End-stage Liver Disease (MELD) score. The Child-Pugh score is a measure of liver function that depends on a patient's levels of creatinine, INR, total bilirubin, encephalopathy, and ascites. The UNOS score is a measure of liver and renal function. It depends on the creatinine, INR, total bilirubin, sodium, and recent use of hemodialysis.

Additionally, the decision for or against transplant relies on tumor burden. The predominantly used set of criteria to define this are called the Milan criteria, which were established based on a study of 48 patients at the University of Milan.[4]. These criteria state that a patient is a candidate for liver transplant as a preferred first-line treatment for HCC if the liver contains no more than one tumor up to 5 cm in maximum span, or if there are multiple tumors, then there are no more than3e tumors with each tumor measuring no more than 3 cm in maximum span. Although these are the criteria used by the NCCN, there are alternative tumor burden criteria available, such as from the University of California, San Francisco.

The NCCN usually relies on the American Joint Committee on Cancer staging system to create algorithms for the treatment of various cancers based on cancer staging. However, the AJCC staging system does not take into account liver function, which is a critical component in determining prognosis and potential survival benefit. Multiple other HCC staging systems based on patient cohorts with accumulated survival data have been proposed that estimate the survival of newly diagnosed patients with HCC based on the severity of their tumor burden, liver function, and/or other health factors. HCC has a variable, poorly understood natural history based on its underlying etiology, for example, secondary to hepatitis C versus hepatitis B versus alcohol-induced versus other, and based on its molecular markers. The tumor size and number affect prognosis but may not be as meaningful a predictor of prognosis as the previously mentioned factors. For example, persons in China are relatively more susceptible to developing HCC from hepatitis B, persons in Japan are relatively more susceptible to developing HCC from hepatitis C, and Caucasians are relatively more susceptible to developing HCC from alcohol-induced cirrhosis or steatohepatitis. Consistent with the previous statements, research studies of these different populations that have compared survival in patients with untreated HCC against survival in patients having undergone various treatments for HCC have found moderately different survival estimates. Thus, the prognosis for a person with HCC is best determined by using a study that has evaluated persons with the same set of circumstances. Since staging is designed to correlate with prognosis in order to help decide how aggressive to be with treatment recommendations for a given person, the tumor staging system that is used should ideally be based on patients who correspond most similarly to the patient at hand or at least most closely to the population at that particular hospital.

Available staging systems include but are not limited to the following:

  • Okuda, 1985, Japan[5]
  • Cancer of the Liver Italian Program, 1998, Italy[6]
  • Barcelona Clinic Liver Cancer, 1999, Spain[7]
  • Chinese University Prognostic Index, 2002, China[8]
  • Japan Integrated Staging, 2003, Japan[9]
  • American Joint Committee on Cancer, 2010 United States[10]

A review of the differences, strengths, and weaknesses of these and other staging systems is provided by Kinoshita[11] and in the 2018 NCCN guidelines. There is much overlap between these systems, and the NCCN does not favor the use of one over another. The Barcelona Clinic Liver Cancer staging system (BCLC) is endorsed by the American Association for the Study of Liver Disease and is likely the most widely used staging system in the United States. It is the focus here and will be discussed in detail. The BCLC itself is a conglomeration of other staging systems, including the Child-Pugh score and the Eastern Cooperative Oncology Group (ECOG) Performance Status (PS).

The Child-Pugh and PST scoring systems and the BCLC treatment algorithm are presented in the graphics below.

In the BCLC, patients are divided into stages 0, A, B, C, and D from least to most severe condition. BCLC stage-B patients are an extremely heterogeneous group, ranging from having four subcentimeter tumors to having one tumor over 5 cm to having a liver to replaced with a tumor. 

The BCLC and NCCN recommend TACE as first-line treatment if:

  • The patient's HCC tumor burden is non-resectable
  • The patient's liver function is no worse than Child-Pugh B, and
  • The patient's overall function is no worse than PS 2.

The following is a breakdown of patient factors that determine how TACE may be used based on the NCCN guidelines. All patients who are candidates for TACE below are either not a candidate for (ECOG PS greater than 0) or choose against hepatectomy/transplant, or Child-Pugh class A or B.

Patient with HCC

TACE intends to keep the patient a candidate for transplant ("bridging" therapy).

  •  No evidence of vascular invasion on imaging and
  •  No evidence of extrahepatic spread on imaging and
  •  ECOG PS remains 2 or less and
  •  Patient meets Milan criteria

TACE intends to downstage the tumor(s) so that the patient qualifies for a transplant.

  • As above, but tumor burden is just outside of the Milan criteria

The intent of TACE is to palliate.

  • Any vascular invasion or
  • Any extrahepatic spread or
  • ECOG PS 3-4 or
  • Tumor burden is not just outside of the Milan criteria 

Patient with Metastasis to the Liver

TACE intends to cure.

  • All liver and primary lesions are considered potentially curable by thermal/chemical ablation or by resection and
  • The patient is willing to be treated as part of a clinical trial

The intent of TACE is to downstage to enable resection.

  • All metastatic lesions still qualify for eventual resection and
  • Initial chemotherapy has failed and
  • The patient is willing to be treated as part of a clinical trial.

The intent of TACE is to palliate.

  • At least one lesion does not affect quality for resection regardless of the outcome of TACE and
  • Initial chemotherapy has failed and
  • The hepatic tumor burden is predominant/is the main cause of symptoms and
  • The patient understands that TACE may be of little to no benefit in terms of extending quality of life.

Contraindications

Relative contraindications to TACE include but are not limited to the following:

  • Poor expected survival. This can be predicted if the patient has a PST greater than 3, in other words, patient completely disabled, cannot self-care, or confined to a bed or chair. 
  • Contraindication to chemotherapy, such as heart or kidney failure and leukopenia
  • Unwilling or unable to comply with follow-up guidelines
  • Extra-hepatic metastases
  • Malignant ascites
  • Tumor greater than 5 cm
  • Poor baseline liver function (as defined by reference)
  • Patients with end-stage cirrhosis (Child-Pugh)
  • Encephalopathy
  • Jaundice
  • Active alcohol consumer
  • Hypovascular tumor based on appearance on MRI or CT
  • Main portal vein thrombosis associated with a high risk of post-treatment liver failure
  • Biliary obstruction or bilirubin greater than 3 mg/dL, unless segmental injections can be performed
  • Patient eligible for a potentially more effective therapy

In general, no more than 50% of liver volume should be chemo-embolized at a time. Therefore, if a patient has a tumor occupying more than 50% of the liver volume, then that patient is best treated with 2 TACE procedures.

Portal vein thrombosis is not a contraindication to palliative TACE if there is adequate collateral hepatopetal flow to supply the liver parenchyma to be embolized. However, in patients with portal vein thrombosis, it is wise to avoid embolizing normal liver parenchyma as much as possible.

Many physicians treat bile duct obstruction before offering TACE, which could exacerbate bile duct obstruction.

The NCCN does not include TACE in its treatment algorithm for primary cholangiocarcinoma.

Equipment

TACE can be divided into 2 major categories of chemotherapy delivery:

  1. TACE with drug-eluting embolization particles, and
  2. TACE in which the active chemotherapy drug and the embolization particles are separate agents (i.e., conventional).

Conventional TACE (cTACE) is a mixture of three agents: lipiodol contrast agent, a chemotherapy drug, and an embolization agent. TACE using drug-eluting beads (TACE-DEB or DEB-TACE) uses resin beads that slowly release chemotherapy. Currently, only two chemotherapy drugs are FDA-approved for use in this manner. Doxorubicin is used to treat hypervascular primary hepatic tumors and metastases. Irinotecan is used to treat metastases from colorectal cancer.

Preparation

Imaging

Cross-sectional imaging with contrast-enhanced CT or MRI should be done for diagnostic and treatment planning purposes. Such imaging can determine whether there is anatomy or pathology that may prevent TACE from being safe or effective, such as whether the main portal vein is thrombosed. 

Biopsy

No biopsy is necessary if:

  • A tumor meets the criteria for HCC based on its enhancement pattern on multi-phase CT or MRI in a patient with risk factors for developing HCC or
  • There is clear evidence of an extra-hepatic primary tumor on imaging along with tumors in the liver that have behaved on contrast-enhanced imaging as expected for metastases. 

The NCCN suggests biopsy consideration before treatment in the following presentations:

  • A liver lesion is suspicious for malignancy but does not meet imaging criteria for HCC (such as defined by the American College of Radiology Liver Reporting and Data System).
  • A liver lesion meets imaging criteria for HCC but the patient:
  1. Is not considered to have any risk factors for HCC, such as cirrhosis or chronic hepatitis,
  2. Has risk factors for cholangiocarcinoma instead of HCC, such as elevated serum CA 19-9 or CEA level, or
  3. Is part of a research trial in which histologic grading or molecular characterization is needed

Prevention of Nontarget Embolization

To avoid inadvertently performing non-target chemoembolization, radiologists often will use platinum coils to embolize arteries near the artery planned for delivering chemotherapy (as discussed in the anatomy section above). Although it is not mandatory, some radiologists have patients undergo a "planning" arteriogram before the arteriogram for delivery of chemotherapy, at which time such coils would be placed.

Anesthesia

TACE typically is performed using conscious sedation. Determination of periprocedural anesthesia risk is site dependent. Many hospitals require physicians to assess the patient using the American Society of Anesthesiology (ASA) physical classification system and a Mallampati score. If the patient is ASA class 4 or higher and/or has any other anesthetic risk factors, such as a high-risk airway, then some institutions and authors recommend that the patient should undergo consultation with an anesthesiologist and/or medical specialist, such as a cardiologist, to address the pertinent risk factors.

Hydration

Many radiologists administer normal intravenous saline intravenously for hydration.

Infection Prevention

Because chemoembolization creates a bed of necrotic tissue, and such tissue may form an abscess, nearly all radiologists prescribe prophylactic antibiotics at the time of the procedure. Regimens should cover gram-positive cocci, gram-negative rods, and in the case of patients without an intact sphincter of Oddi from previous surgery, sphincterotomy or biliary drainage, anaerobes. This is discussed in more detail by the Society of Interventional Radiology (SIR) guidelines[12] with regard to incidences of abscess infection[13],[14],[15] and suggested antibiotic regimens.[16],[17],[18]. If a bilioenteric anastomosis or biliary stent is present, then some radiologists also prescribe a bowel cleansing preparation, such as oral neomycin-erythromycin.

Bleeding Prevention

Parameters for prevention of bleeding complications (lab tests and medication withdrawal) are specified by the Society of Interventional Radiology 2013 guidelines.[19]

Other Symptom Control

In patients being treated for carcinoid tumors, pre-procedure or intra-procedure administration of octreotide may prevent or diminish the side effects of serotonin release ("carcinoid crisis").

Other pre-procedure medications may include antiemetics and steroids. However, some radiologists only administer this post-procedure as routine or on an as-needed basis.

Technique

Arterial catheter access is obtained, and arteriography is performed to document the arterial supply to the single or multiple tumors.

  • Arteries that pose a high risk for enabling non-target embolization are occluded, usually with coils.
  • A catheter with an outer diameter of about 1 mm called a microcatheter is usually needed to reach inside the liver to the artery or arteries feeding the tumor.
  • When the catheter or microcatheter is placed as close to the location that is thought to result in successful embolization of the artery or arteries feeding the tumor, then the embolization particles, contrast, and chemotherapy are administered until stasis of arterial flow is seen during fluoroscopy.
  • Follow-up arteriography is performed to document persistence or absence of flow to the region of interest.
  • The maximum of chemotherapy administered (for example, 75 mg doxorubicin) is precalculated based on whether there is the tumor in 1 lobe or 2 lobes of the liver.

Complications

Major complications occur in approximately 5 to 10 out of 100 people who undergo TACE.[20] The most common major complications are:

  • Liver failure
  • Death from any cause
  • Abscess

Besides these complications, other major complications have included[21],[22],[23]:

  • Tumor rupture
  • Cholecystitis
  • Biloma
  • Permanent biliary stricture
  • Arterial dissection
  • Pulmonary emboli
  • Tissue injury from non-target embolization, with sequelae such as gastrointestinal hemorrhage

Clinical Significance

The number of persons that need to be treated in order to prevent 1 death over a given time period (such as 1 year) has not been published, since no studies have evaluated an absolute risk reduction for TACE, and the number may be very high.

The Society of Interventional Radiology defined technical success as expected catheter placement and administration of the selected particles and drug, which should occur at a rate of at least 98%.[20]

Clinical success is defined as successful tumor necrosis resulting in either down-staging or lengthened survival. No national organization is known to have set a recommended threshold for this parameter. Survival rates significantly improve in patients just missing meeting criteria for surgery who have:

  • Good performance status
  • Good underlying liver function
  • Low tumor burden

HCC Downstaging

Down-staging by the “best minimally invasive method” (for example, RFA, TACE, PEI, or some combination) was successful in 21 of 30 patients that met the following criteria as reported by Yao[24]:

  • One lesion 5 cm - 8 cm
  • Two or 3 lesions, at least 1 of which was between 3 to 5 cm, with total tumor diameter less than 8 cm, or
  • Four to 5 lesions all less than 3 cm with total tumor diameter less than 8 cm

In a study that included patients under 65 years old who had no contraindications for liver transplant other than not meeting the Milan criteria, 34 of 62 were down-staged.[25]

However, a given patient's chance of success for downstaging may be much lower if the patient does not share similar baseline characteristics.

HCC Lengthened Survival

Three randomized trials[26],[27],[28] have demonstrated improved patient survival after TACE versus no HCC treatment at all. In each study, however, selected patients underwent repeat TACE sessions, meaning that it could not be concluded that an indivual session of TACE improves survival.

Patients at an intermediate stage (BCLC stage-B) were found to have a median survival of about 16 months. With 1 or more TACE sessions in the setting of HCC, patient survival extended to a median of up to 19 to 20 months.[26]

Metastatic Disease

The expected survival benefit for patients with tumors metastatic to the liver is even more variable than it is for patients with HCC, and results generally are not as encouraging as for patients with HCC. TACE is typically used for palliation only following systemic chemotherapy. 

Alternatives to TACE depend on the patient's liver tumor and overall functional status as mentioned above. Other than opting for no treatment, other potential mainstream therapies accepted by the NCCN depending on the patient include:

  • Intravenous (IV) chemotherapy
  • External beam radiation
  • Tumor ablation with heat (microwaves or radio waves) or cold (cryoablation) via percutaneous or open surgical approaches
  • Embolization of the tumor's feeding arteries with inert particles only (bland embolization) or with radioactive particles (radioembolization).

No randomized controlled trial has found a survival benefit for TACE over bland embolization. One randomized controlled trial[29] compared TACE to radioembolization for patients with HCC and found that patients in the Y90 radioembolization group experienced a significantly longer median time to local progression of tumor (greater than 26 months) than patients in the TACE group (6.8 months). Despite this, these Y90 patients did not end up having a greater chance of undergoing a liver transplant and were not shown to benefit by having an overall increased rate of survival. A significantly greater proportion of patients in the TACE group developed side effects from treatment of diarrhea or hypoalbuminemia.