Overview

Stereotactic treatment of liver tumors in three or five fractions. The work is in controlling or measuring breathing motion, seeing the tumor at all — which usually takes multiphase contrast CT and MRI fusion — and keeping enough healthy liver below its dose limit while sparing the bowel, stomach and bile ducts close by.

Start here: I’m planning my first GI case — a step-by-step learning roadmap.

Schedules

Liver SBRT is used for hepatocellular carcinoma (HCC) and for liver metastases, and the two are planned differently because the healthy liver is different.

  • HCC usually arises in a cirrhotic liver with less reserve. One protocol gives 27.5–50 Gy in 5 fractions, choosing the dose by liver function (Child-Pugh score), the expected remaining liver and nearby organs — and the LARK trial ties the mean liver dose limit to the prescription.
  • Metastases usually arise in a healthy liver. Common schedules are 42–54 Gy in 3 fractions (preferred when organ limits allow) or 40–60 Gy in 5 fractions, with lower doses when a bowel or other serial organ is close.

Fractions are usually given every other day or so. The constraint table has a column for three and for five fractions; your protocol sets the prescription, the covering isodose and the fraction spacing.

Simulation & Setup

The liver moves with every breath and is hard to see on CT without contrast. Everything downstream depends on how motion is handled and how well the tumor can be seen.

Immobilization
A reproducible full-body setup and consistent fasting support the small margins of SBRT.

What is it?

Supine with the arms above the head in a full-length vacuum body bag, with fasting for a few hours before simulation and each treatment.

Why does it matter?

SBRT uses small margins and a steep dose fall-off, so the patient must return to the same position, and fasting keeps the stomach and duodenum in a similar place each day.

Motion management
Liver motion is controlled or measured, with one chosen strategy used from simulation through every treatment.

What is it?

Breath hold (at inspiration or expiration), free breathing with a 4DCT and an ITV, abdominal compression, or gating or tracking. A session before simulation helps choose the strategy, and the same one is used for simulation, planning and every treatment.

Why does it matter?

The liver moves mostly up and down with the diaphragm, and studies have measured motion of up to several centimeters. Controlling or measuring that motion lets the plan use smaller volumes and spare more healthy liver.

Fiducials
Markers near the tumor give the daily match something visible when the tumor itself isn't.

What is it?

Implanted gold markers near the tumor, placed a few days before simulation. Lipiodol left by previous chemoembolization, or surgical clips, can serve the same purpose.

Why does it matter?

On cone-beam CT the tumor is usually invisible and the liver edges are blurred, so a marker near the tumor is what the daily match is made to. Some tracking systems require them.

Multiphase contrast CT
Timed contrast phases make the tumor, and any thrombus in the vessels, visible for contouring.

What is it?

Contrast scans at several phases after injection — arterial, portal venous and delayed — acquired in the treatment breathing state, alongside a non-contrast scan used for dose calculation.

Why does it matter?

HCC is typically bright in the arterial phase and washes out in later phases; the portal venous phase shows tumor thrombus in the vessels. One NRG template describes each phase's purpose. Organs are usually drawn on the non-contrast planning scan.

Image fusion — MRI, PET/CT and diagnostic CT
Contrast MRI, PET/CT or diagnostic contrast CT fused with the planning CT.

What is it?

Image fusion aligns an outside scan with the planning CT so the target can be drawn using information the CT doesn't show. For liver SBRT the outside scans are a contrast-enhanced liver MRI, PET/CT or diagnostic contrast CT. MRI is recommended particularly for breath-hold treatment, ideally taken in the treatment position.

Why does it matter?

Contrast MRI is also recommended when contrast CT can't be done. Because the liver moves and deforms, the registration is focused on the involved part of the liver and matched to vessels, surgical clips, lipiodol or fiducials rather than the spine. Imaging in the treatment breath state makes the match more reliable.

Daily imaging
The target's position is confirmed before every fraction, because small margins depend on it.

What is it?

Cone-beam CT before each fraction, matched to fiducials, lipiodol or the liver itself, with the breath-hold level or gating checked. Imaging during delivery is increasingly used.

Why does it matter?

Small margins only work when the target's position is confirmed at every fraction. Motion during delivery can differ from what was seen at simulation.

Target Delineation

What each volume represents. Margins come only from your protocol.

GTV — Gross tumor

Definition

The tumor seen on the contrast CT phases and MRI — for HCC, including any tumor thrombus in the vessels.

Why it matters

Reviewing the contours with a diagnostic radiologist is often recommended, because different lesions show best on different phases or sequences.

Contouring resources

Organ contouring guides →

ITV — Motion

Definition

The GTV across its range of motion — required with free breathing, optional with breath hold, depending on the protocol. Concept page →

Why it matters

Covers the tumor wherever it is during delivery when motion isn't frozen.

Contouring resources

Organ contouring guides →

CTV — Microscopic spread

Definition

Often the same as the GTV or ITV for HCC; some protocols add a margin for cholangiocarcinoma.

Why it matters

Whether microscopic spread is covered by a separate expansion or by the dose fall-off around the tumor differs by disease type and protocol.

Contouring resources

Organ contouring guides →

PTV — Planning target volume

Definition

The CTV or ITV expanded for setup and residual motion uncertainty; margins can differ between directions. Concept page →

Why it matters

In SBRT the PTV is also what coverage, conformity and dose fall-off are measured against, so its size shapes both the plan and how it is judged.

Contouring resources

Organ contouring guides →

Organs at Risk & Dose Constraints

Click an organ for its anatomy, why it matters and contouring resources. Superscripts link to the source of each value.

Organ42–54 Gy / 3 fxLiver metastases27.5–60 Gy / 5 fxHCC or metastases
LiverLiver minus GTV. For HCC, favor the optimal limits; limits assume Child-Pugh A.
  • Mean ≤13 Gy (optimal), ≤15 Gy (mandatory)1
  • ≥700 cc of liver <15 Gy2
  • Mean ≤13 Gy (optimal), ≤15.2 Gy (mandatory)1
  • ≥700 cc of liver <15 Gy2
  • HCC: mean ≤13 Gy (50 Gy) to ≤17 Gy (27.5 Gy)2
Central Hepatobiliary TractA 1.5 cm expansion of the portal vein.
  • D21 cc <33.8 Gy, D24 cc <32 Gy2
  • Mean <19 Gy2
  • D21 cc <40 Gy, D24 cc <37.7 Gy2
Common Bile Duct
  • D0.1 cc ≤50 Gy1
  • D0.1 cc ≤50 Gy1
Duodenum
  • D0.1 cc ≤22.2 Gy1
  • D10 cc ≤11.4 Gy1
  • D0.1 cc ≤33 Gy (optimal), ≤35 Gy (mandatory)1
  • D10 cc ≤25 Gy1
Stomach
  • D0.1 cc ≤22.2 Gy1
  • D10 cc ≤16.5 Gy1
  • D0.1 cc ≤33 Gy (optimal), ≤35 Gy (mandatory)1
  • D10 cc ≤25 Gy1
Small Bowel
  • D0.1 cc ≤25.2 Gy1
  • D5 cc ≤17.7 Gy1
  • D0.1 cc ≤30 Gy (optimal), ≤35 Gy (mandatory)1
  • D10 cc ≤25 Gy1
Large Bowel / Sigmoid
  • D0.1 cc ≤28.2 Gy1
  • D0.1 cc ≤38 Gy1
Esophagus
  • D0.1 cc ≤25.2 Gy1
  • D0.1 cc ≤35 Gy1
  • D0.5 cc ≤32 Gy2
Heart / Pericardium
  • D0.1 cc ≤26 Gy (optimal), ≤30 Gy (mandatory)1
  • D0.1 cc ≤38 Gy1
  • D5 cc ≤30 Gy2
KidneysBoth kidneys (cortex) combined.
  • Mean ≤8.5 Gy1
  • ≥200 cc ≤16 Gy1
  • Mean ≤10 Gy1
  • ≥200 cc ≤17.5 Gy1
Spinal CordCord PRV or spinal canal.
  • D0.035 cc ≤20.3 Gy1
  • D0.035 cc ≤25.3 Gy1
Chest Wall / RibsShould not compromise target coverage.
  • D0.5 cc ≤37 Gy2
  • V30 Gy <30 cc3
  • D0.5 cc ≤39 Gy2
  • V30 Gy <30 cc3
GallbladderWithin about 1 cm of the gallbladder, one protocol suggests 5 fractions.—
  • D0.5 cc ≤55 Gy2
Skin
  • D0.1 cc ≤33 Gy1
  • D10 cc ≤30 Gy1
  • D0.1 cc ≤39.5 Gy1
  • D10 cc ≤36.5 Gy1
  • Kidneys: at least 200 cc of combined kidney must receive no more than the stated dose (a “cold” limit). The compiling protocol writes this as V16 Gy ≤200 cc and V17.5 Gy ≤200 cc, which is a different limit.
  • HCC liver mean (5 fx): the limit depends on the prescription — ≤13 Gy at 50 Gy, ≤15 Gy at 40–45 Gy, ≤15.5 Gy at 35 Gy, ≤16 Gy at 30 Gy and ≤17 Gy at 27.5 Gy (Child-Pugh A). For HCC the same trial asks for ≥800 cc of liver below 15 Gy.
  • Contour organs on the non-contrast planning scan; PRVs can be considered for the esophagus, stomach, duodenum, bowel, kidneys and cord.
References (3)
  1. UK SABR consensus 2022 — UK 2022 Consensus on Normal Tissue Dose-Volume Constraints for Oligometastatic, Primary Lung and Hepatocellular Carcinoma Stereotactic Ablative Radiotherapy. Clin Oncol (R Coll Radiol). 2022;34(5):288–300 Source
  2. LARK (TROG 17.03) — Study protocol of the LARK (TROG 17.03) clinical trial: a phase II trial investigating the dosimetric impact of Liver Ablative Radiotherapy using Kilovoltage intrafraction monitoring. BMC Cancer. 2021;21:494 (with Additional file 1) Source
  3. Dunlap 2010 — Chest wall volume receiving >30 Gy predicts risk of severe pain and/or rib fracture after lung stereotactic body radiotherapy. Int J Radiat Oncol Biol Phys. 2010;76(3):796–801 Source

Values quoted from eviQ 4026 (last reviewed 28 October 2025; review due 30 June 2028) and eviQ 4024 (last reviewed 28 October 2025; review due 30 June 2028), checked by DoseLab on 2026-09-29. Verify against your protocol, institutional policy and physician directive before clinical use.

Search all GI constraints in the Constraint Finder →

Protocols & Literature

Clinical protocolSource Verified

Protocol paper for an Australian and Danish phase 2 trial of liver SBRT with kilovoltage intrafraction monitoring. Its supplementary tables (Additional file 1) give organ constraints for HCC (5 fractions) and for liver metastases (3 and 5 fractions), and liver limits — including an HCC liver-mean limit for each prescription and a minimum volume of liver kept below 15 Gy. The constraints were adapted from existing recommendations and trials including UK CORE, RTOG 1112 and NRG BR001. DoseLab read the supplementary tables.

Consensus guidelineSource Verified

UK consensus on dose–volume constraints for SABR of oligometastases, primary lung cancer and hepatocellular carcinoma. Citation checked against Crossref. DoseLab read the tables in the authors' accepted manuscript (UCL Discovery and White Rose Research Online): Table 6 (intracranial, 1, 3 and 5 fractions) for the brain pages, and Tables 2, 3 and 5 (thoracic, abdominal and spinal) for the liver SBRT page. Each table gives optimal and mandatory limits by fraction count; the liver limits apply to patients with, at worst, Child-Pugh A6 liver disease. The kidney limit is written as a "cold" constraint — at least 200 cc must receive no more than the stated dose.

Clinical resourceSource Verified
NRG Oncology Protocol Development Template for Radiation Therapy — Liver: SBRT
Parker WA, Sohn JW, Wolfgang J · NRG Oncology Medical Physics Subcommittee · 2018

The template NRG Oncology gives investigators for the radiation therapy section of a liver SBRT trial, based on NRG GI-003. It strongly recommends implanted fiducials, allows several motion-management techniques, and describes the multiphase contrast CT used for hepatocellular carcinoma: non-contrast, arterial phase (hypervascular tumor), portal venous phase (vascular thrombus) and delayed phase (washout). Contrast-enhanced MRI is recommended when contrast CT can't be done.

Consensus guidelineSource Verified
Use of normal tissue complication probability models in the clinic
Marks LB, Yorke ED, Jackson A, et al. · QUANTEC · 2010

The QUANTEC overview paper, whose summary table gathers the approximate dose/volume/outcome data from each organ chapter. Its footnotes stress that the data are estimates from the literature, should be applied with caution, and largely do not reflect modern IMRT. DoseLab read the esophagus row (mean dose <34 Gy for grade ≥3 acute esophagitis, 5–20%, 3D-CRT) from the open-access manuscript, and the lung, heart, liver, kidney, stomach and small bowel rows used on the GI pages from the journal's full-text table.

Observational studySource Verified

Sixty patients treated with 3–5 fraction SBRT for peripheral lung lesions. The chest wall volume receiving 30 Gy best predicted severe pain or rib fracture; the authors advise limiting it to under 30 cm³ where possible without compromising coverage. DoseLab read the abstract.

AAPM reportSource Verified

AAPM task group report on respiratory motion in thoracic, abdominal and pelvic treatment. It groups management approaches into motion-encompassing methods, respiratory gating, breath-hold techniques, forced shallow breathing (such as abdominal compression) and respiration-synchronized (tracking) techniques. Read in the AAPM report PDF (Report No. 91, July 2006): using ICRU Report 62 nomenclature, the PTV adds margins to the CTV for respiratory (intrafraction) motion, interfraction motion and set-up error; without a respiratory management device the entire range of motion should be considered in the internal margin; and for lung tumors a maximum intensity projection (MIP) can give the motion-encompassing volume, provided there is no mediastinal involvement.

AAPM reportUnder Review

AAPM Task Group 132 report on image registration and fusion in radiotherapy. It reviews rigid and deformable registration, points out that every registration carries an uncertainty that should be understood and communicated, and gives recommendations for commissioning and quality assurance of registration software and for checking individual registrations. Citation checked against Europe PMC.

Clinical resourceSource Verified
Hepatic primary stereotactic EBRT (eviQ ID 4024)
eviQ, Cancer Institute NSW · 2025

Endorsed eviQ protocol for stereotactic treatment of primary liver cancer (hepatocellular carcinoma or intrahepatic cholangiocarcinoma) in five fractions. It covers motion management (breath hold, free breathing with 4DCT, compression or gating), triple-phase contrast CT, fiducials (including lipiodol and surgical clips), contrast-enhanced MRI and rigid co-registration of MRI, PET and CT in the region of the liver. Its organ table draws on the LARK (TROG 17.03) trial protocol and the UK 2022 SABR consensus.

Clinical resourceSource Verified
Hepatic metastases stereotactic EBRT (eviQ ID 4026)
eviQ, Cancer Institute NSW · 2025

Endorsed eviQ protocol for stereotactic treatment of liver metastases in three or five fractions (three preferred when organ limits allow). Its organ table gives a separate column for each fraction count. Patients with cirrhosis are treated as for hepatocellular carcinoma under the companion primary-liver protocol.

All GI literature →