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TACE Treatment - Transarterial Chemoembolization
Interventional Radiology

TACE Treatment - Transarterial Chemoembolization

About This Department

 
Interventional Oncology

A liver tumor feeds from the artery. The rest of the liver mostly does not. TACE uses that difference to starve and poison the tumor from inside its own blood supply.

No treatment before it had lengthened the lives of people with liver cancer that could not be removed. Transarterial chemoembolization did, in randomized trials. In a Barcelona trial, two-year survival rose from 27 percent to 63 percent, and a Hong Kong trial run in the same year found the same direction. Twenty years on it remains the standard treatment for the middle stage of the disease, and the trials since have refined who gains from it, which beads to use and which drugs to add. Send us your scans, your liver blood tests and your tumor board notes, and a hepatologist and an interventional radiologist will tell you whether TACE is your stage.

63% vs 27%
Two-year survival, TACE against supportive care
25 vs 13.5
Months without progression, TACE plus sorafenib against TACE
1 night
Usual hospital stay per session
Free
Review of your scans and liver tests
Free consultation
TACE in one paragraph
Transarterial chemoembolization, TACE, treats liver cancer from inside its blood vessels. A catheter is threaded from an artery in the wrist or groin into the branch of the hepatic artery that feeds the tumor, and a chemotherapy drug is injected there together with particles that block the vessel. The tumor receives a dose of drug many times higher than a vein could deliver, and at the same time loses the blood it lives on. The healthy liver, which draws most of its blood from the portal vein, is largely spared. The procedure is repeated when the tumor regrows, and it is the standard treatment for liver cancer that is too large or too numerous for surgery or ablation and has not spread beyond the liver.

How does it work, and what did the trials find?

Reaching the artery
Under local anesthetic and sedation, a needle enters the radial artery at the wrist or the femoral artery in the groin, and a thin catheter is advanced under X-ray guidance to the artery of the liver. Contrast injected there maps every branch and shows which ones feed the tumor.
Going in close
A microcatheter goes next. Thinner than a millimeter, it is steered into the branch that supplies the tumor and as far into it as it will go, so that the treatment reaches the tumor and as little of the surrounding liver as possible. When several tumors sit in different segments, each branch is treated in turn.
Drug and blockade
Either an emulsion of chemotherapy in an oily contrast agent followed by particles, or beads a fraction of a millimeter across that have been loaded with the drug, is injected slowly until flow in the branch stops. The catheter is withdrawn, the artery at the wrist or groin is sealed, and the whole session has taken one to two hours.
  • A normal liver receives about three quarters of its blood from the portal vein and one quarter from the hepatic artery. Hepatocellular carcinoma reverses that, drawing nearly all of its supply from the artery. Blocking the artery therefore hurts the tumor far more than the liver around it.
  • Drug delivered straight into that artery reaches the tumor at concentrations that intravenous chemotherapy cannot approach, and the blockade keeps it there.
  • The blockade also causes the deep, sudden death of tumor tissue that scans show as a loss of enhancement, which is the sign of a successful session.
  • The same anatomy sets the limit. When the portal vein is itself blocked by tumor, the liver depends on the artery, and embolizing it can cause liver failure. Portal vein invasion is the classic reason TACE is refused.
Conventional TACE or drug-eluting beads
The original method mixes doxorubicin or cisplatin with an oily contrast agent that tumors retain, and follows it with gelatin sponge particles. Drug-eluting beads carry the same drug on their surface and release it over days while blocking the vessel. In the PRECISION V trial, 212 patients with cirrhosis and unresectable tumors were randomized between the two. Tumor response at six months was higher with beads, 52 against 44 percent, without reaching statistical significance, while serious liver toxicity and the drug's own side effects, hair loss, marrow suppression and heart strain among them, were significantly lower. Patients with poorer liver function, worse fitness, disease in both lobes or recurrent tumors gained the most from beads. Both methods remain in use, and the choice is made per patient.

The trials that made TACE the standard

Two randomized trials published in 2002 settled a question that had been argued for a decade. In Barcelona, 903 patients with liver cancer were screened and 112 met the strict criteria, a tumor that could not be cured by surgery or ablation, preserved liver function and no spread beyond the liver, and they were randomized to embolization, to chemoembolization with doxorubicin, or to supportive care.

Early stopping followed once the chemoembolization arm pulled ahead. Survival at one and two years was 82 and 63 percent with chemoembolization against 63 and 27 percent with supportive care, and the risk of death was halved. Hong Kong followed the same year. There, 80 of 279 patients met similar criteria and were randomized to chemoembolization with cisplatin or to supportive care, and survival at three years was 26 percent against 3 percent.

Twelve percent of those screened were suitable.

Hold on to it. The Barcelona investigators used the phrase stringently selected patients in their conclusion, and the Barcelona investigators used the phrase stringently selected patients in their conclusion. TACE lengthens life in the right patient, and the right patient is defined by the liver's reserve as much as by the tumor.

Chemoembolisation improved survival of stringently selected patients with unresectable hepatocellular carcinoma.
Conclusion of the Barcelona randomized trial, The Lancet, 2002

Adding drugs to the procedure

Drugs can extend the gain.

The Japanese TACTICS trial asked whether a targeted drug, sorafenib, taken before and between sessions, could hold the tumor longer. Among 156 patients, the median time before the disease progressed beyond what TACE could treat was 25.2 months with the combination and 13.5 months with TACE alone, and two-year survival was 82.7 against 64.6 percent. Immunotherapy combinations now face the same test. Ask whether drug treatment alongside TACE is planned for you, and on what evidence.

Median progression-free survival was 25.2 months with TACE plus sorafenib and 13.5 months with TACE alone.
TACTICS trial, Gut, 2020
Radioembolization, the sibling treatment
Transarterial radioembolization, TARE, uses the same catheter route to deliver microscopic glass or resin spheres loaded with the radioactive isotope yttrium-90, which irradiates the tumor from inside over days. It causes less pain and fever than TACE and is used for larger tumors and for tumors that have invaded a branch of the portal vein, where TACE is unsafe. It needs a preparatory session to map the vessels and measure any shunting to the lungs, so it takes two visits. The 2022 update of the Barcelona staging strategy lists it as an option in selected patients, and the reply to your file will say which of the two fits.

Who is TACE for?

The Barcelona Clinic Liver Cancer system stages liver cancer by weighing the tumor, the liver's reserve and the patient's fitness together and assigns a treatment to each stage. Its 2022 update, published in the Journal of Hepatology, places TACE at the intermediate stage and describes when a patient can move between stages.

This table scrolls sideways on a narrow screen. Swipe or drag to see every column.

Where TACE sits in the Barcelona staging strategy
Stage What it means First-line treatment TACE
Very early and early One tumor, or up to three of three centimeters or less, with preserved liver function Surgery, ablation or transplant Used as a bridge while waiting for a transplant, or when ablation is not possible
Intermediate Several tumors or a large one, confined to the liver, with preserved liver function and good fitness TACE The standard. Repeated on demand while the tumor responds and the liver tolerates it
Advanced Tumor in the portal vein or spread beyond the liver, or a patient with symptoms Drug treatment, now immunotherapy combinations Not advised. Blocking the artery when the portal vein is invaded risks liver failure
Terminal Liver failure or a patient confined to bed Supportive care Not advised

How do I prepare, and what does the day involve?

Preparation is short.

The liver tests decide more than anything you do, and they are read twice, once before the procedure is agreed and once on the morning it is done.

This table scrolls sideways on a narrow screen. Swipe or drag to see every column.

Preparing for TACE
When What happens
With your first message Send the contrast CT or MRI of the liver with images, the blood tests that grade the liver, any biopsy or AFP result, the medication list, and the notes of any tumor board that has seen you.
One to two weeks before Blood thinners are planned with the prescribing doctor. Kidney function is checked because contrast is used. A hepatitis B carrier starts or continues antiviral tablets, since chemotherapy can reactivate the virus.
The day before Eat normally. Fast from midnight. Bring someone with you.
The morning of A cannula, intravenous fluid, anti-sickness and pain medication before the procedure begins, and antibiotics where the bile ducts have been operated on.
  • Bilirubin, albumin, clotting and platelet count, which together grade the liver's reserve and decide whether TACE is safe.
  • Creatinine, for the contrast dose.
  • Hepatitis B and C status, and whether antiviral treatment is under way.
  • AFP, the tumor marker, as a baseline for follow-up.
  • Any previous TACE, ablation or surgery, with the dates and the images afterward.
Sedation, pain and the night in hospital
TACE is done under local anesthetic at the puncture site with intravenous sedation, and general anesthetic is used for patients who cannot lie still or whose procedure will be long. Pain during the injection is expected and is treated as it happens. Most patients stay one night, because the hours after embolization bring the pain, fever and nausea described below, and because the puncture site needs a few hours of lying flat if the groin was used. Wrist access shortens that to an hour of sitting.
Tell the team before the procedure
Blood thinners and when you last took them. Contrast allergy. Kidney disease. Diabetes and its treatment. Hepatitis B or C. Previous surgery on the bile ducts or a stent in them. A pacemaker. Pregnancy. Any earlier reaction to sedation.
  1. Arrival. Checks, a cannula, fluids and pre-medication. Consent through your interpreter.
  2. The procedure. One to two hours in the angiography suite, lying flat, with the radiologist talking you through the steps.
  3. Recovery. Lying flat for a few hours after groin access, with pain relief and fluids, and a check of the puncture site.
  4. The night. Fever, right upper abdominal pain and nausea for one to three days are expected and are treated with fluids, painkillers and anti-sickness drugs.
  5. Discharge. Blood tests in the morning, a check that the liver enzymes have not risen too far, and home with painkillers and instructions.

Post-embolization syndrome

A dying tumor releases the contents of its cells. The body responds with fever, pain and nausea that begin within hours and last one to three days. Doctors call it post-embolization syndrome, and it follows most sessions to some degree. It signals that the embolization has worked, and fluids and medication manage it, so that a patient who feels wretched on the second night can be told, truthfully, that the treatment is doing what it was meant to do. Fever that persists beyond three days, or pain that worsens after improving, needs a scan to look for infection or bile leak.

Chemoembolization was repeated every two to three months unless there was evidence of contraindication or progressive disease, with a median of 4.5 courses per patient.
Hong Kong randomized trial, Hepatology, 2002
Four to six weeks later
A contrast CT or MRI shows how much of the tumor has lost its blood supply. Complete loss of enhancement means the session succeeded. Residual enhancement means a second session aimed at the surviving part.
Repeat on demand
Sessions are repeated when imaging shows regrowth or new tumors, at intervals of two to four months in the trials, and each session is preceded by liver blood tests. Some patients need two sessions and some need eight.
Knowing when to stop
TACE stops helping when the tumor no longer responds after two sessions, when it spreads into the portal vein or outside the liver, or when the liver's reserve falls. The Barcelona strategy calls this stage migration. Drug treatment then takes over, because continuing TACE past that point damages the liver without controlling the tumor.

What are the risks, how many days do I need, and what decides the cost?

TACE threatens the liver before anything else. Blocking arterial blood in a cirrhotic liver can tip it toward failure. Bilirubin rises. Fluid collects. Confusion follows. In the Hong Kong trial, deaths from liver failure were more frequent after chemoembolization while survival overall was longer, and for that reason the liver tests are read before every session and patients with poor reserve are refused.

Other complications are rarer. Infection in the dead tumor tissue, an abscess, occurs in a small minority, above all in patients whose bile ducts have been operated on, and they receive antibiotics for that reason. Bleeding or a false aneurysm at the puncture site, damage to the bile ducts, an ulcer in the stomach or duodenum from particles that strayed into their arteries, and a reaction to the contrast are each rare. The chemotherapy itself causes little of the hair loss and marrow suppression seen with intravenous treatment, because so little of it reaches the rest of the body. Beads lower those effects further.

Watch for warning signs after discharge. Fever above 38 degrees that returns or persists beyond three days. Abdominal pain that worsens after it had settled. Yellowing of the eyes, swelling of the abdomen or legs, confusion or unusual sleepiness, black stools or vomiting blood, and a swelling or bleeding at the puncture site. Each needs a hospital the same day.

One session needs five days in the city.

Two days cover the consultation, the liver tests and any imaging that needs repeating, the procedure and its night in hospital come next, and a day or two of rest follows while the fever and pain settle, which for the majority means a hotel room, a light diet and painkillers taken by the clock. Fly three to four days after the procedure. Pain must be controlled first. Blood tests must be stable. The follow-up scan at four to six weeks can be done at home and sent for review, and a second session, when needed, means a second trip or a stay of six to eight weeks that covers both.

Price follows two things.

Method and liver set the price of a session. Drug-eluting beads cost more than the conventional oil and drug mixture, and that difference, which published packages in Istanbul put at a fifth to a third of the session, is the largest single variable in the quote. The chemotherapy dose, the contrast, the microcatheters and the closure device for the artery are consumables charged to the session. General anesthetic adds an anesthesiologist. Most quotes include one night, and charge for a second when recovery is slow. Pre-procedure imaging and the follow-up scan sit on separate lines, as are any drug treatment taken alongside and any treatment of a complication. The patient's own liver moves the figure, since poor reserve means more monitoring and a longer stay, and a hepatitis B carrier needs antiviral tablets. Packages published by hospitals in Istanbul for TACE cover the procedure, the interventional radiologist's fee and one night in hospital, and leave the scans, the drugs and the hotel outside. Compare quotes per session and ask what a repeat session costs, because few patients need only one. Your own figure follows the free review of your scans and liver tests.

One coordinator from the international patients team is assigned from your first message and stays with you until you fly. The team works in English, Arabic, French, Russian, Serbian, Romanian and Spanish and arranges interpreting in other languages on request, and an interpreter attends the consultation and consent. An invitation letter naming the hospital and the treating physician is sent about ten days before travel. The international patients office arranges the airport transfer, the hotel for you and a companion, and the rides to the hospital, and a companion is needed on the day of the procedure. Your room that night has a companion bed. Halal, vegetarian and diabetic meals come from the hospital kitchen, and a low-salt diet is prepared for patients with ascites. A prayer room is on site. Ask early for a female doctor if you would prefer one. The request is passed to the department and met wherever the rota allows.

Nobody changes hospital for the next step.

Hepatology, interventional radiology, surgery and medical oncology share one site, so the tumor board that recommends TACE can also arrange ablation, surgery or drug treatment without a change of hospital. Back home, the coordinator stays reachable on the same WhatsApp number. Send the follow-up scan and blood tests there, and the treating team decides on the next session from them, so that you travel only when there is something to treat.

TACE FAQ

Is TACE a cure for liver cancer?
No. It controls the tumor and lengthens life, and in the Barcelona trial two-year survival rose from 27 to 63 percent. It can shrink a tumor enough to make surgery, ablation or transplant possible, and it holds patients on a transplant waiting list.
How many TACE sessions will I need?
It depends on the response. In the Hong Kong trial the median was 4.5 sessions, repeated every two to three months. Some patients need two and some eight, and the scan at four to six weeks after each session decides the next.
Is TACE painful?
Pain during the injection and for one to three days afterward is expected, together with fever and nausea, as the tumor dies. It is treated with fluids, painkillers and anti-sickness drugs, and most patients stay one night.
What is the difference between TACE and TARE?
TACE delivers chemotherapy and blocks the artery. TARE delivers radioactive microspheres through the same route without blocking it. TARE causes less pain and fever and can be used when a branch of the portal vein is invaded, but it needs a mapping session first, so it takes two visits.
How long do I need to stay in Istanbul?
Five days for one session, covering the tests, the procedure, one night in hospital and two days of rest. You can fly three to four days after the procedure.
Can my family come with me?
Yes. The international patients office arranges a hotel for you and a companion, and your room on the night of the procedure has a companion bed.

References

  1. Llovet JM, Real MI, Montana X, et al. Arterial embolisation or chemoembolisation versus symptomatic treatment in patients with unresectable hepatocellular carcinoma: a randomised controlled trial. Lancet. 2002;359(9319):1734-1739.
  2. Lo CM, Ngan H, Tso WK, et al. Randomized controlled trial of transarterial lipiodol chemoembolization for unresectable hepatocellular carcinoma. Hepatology. 2002;35(5):1164-1171.
  3. Lammer J, Malagari K, Vogl T, et al. Prospective randomized study of doxorubicin-eluting-bead embolization in the treatment of hepatocellular carcinoma: results of the PRECISION V study. Cardiovascular and Interventional Radiology. 2010;33(1):41-52.
  4. Kudo M, Ueshima K, Ikeda M, et al. Randomised, multicentre prospective trial of transarterial chemoembolisation (TACE) plus sorafenib as compared with TACE alone in patients with hepatocellular carcinoma: TACTICS trial. Gut. 2020;69(8):1492-1501.
  5. Reig M, Forner A, Rimola J, et al. BCLC strategy for prognosis prediction and treatment recommendation: The 2022 update. Journal of Hepatology. 2022;76(3):681-693.

Editor's note

Written by the Biruni Hospital medical editorial team. Reviewed by Prof. Dr. Birnur YILMAZ, Radiology.

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