Dose-volume metrics

D0.03cc / Near-Max Dose

The minimum dose received by the hottest small volume of a structure — a more robust stand-in for a single-point maximum.

What is it?

A near-maximum dose is the dose to a small, fixed amount of the hottest part of a structure. In AAPM TG-263 terms it is a Dx metric: the minimum dose received by the hottest sub-volume of size x. D0.03cc[Gy], for example, is the dose that the hottest 0.03 cc receives or exceeds.

The small volume is set in two ways:

  • An absolute volume for organs at risk. NRG protocol templates define the maximum dose as D0.03cc. The UT Southwestern SBRT tables (Timmerman 2022) treat 0.035 cc or less as a "point", and the UK 2022 SABR consensus quotes several limits at 0.035 cc.
  • A percentage for targets. The ICRU Report 83 homogeneity index uses D2%, the dose to the hottest 2% of the target, to stand for its maximum.

Why does it matter?

A single hottest voxel depends on the calculation grid size and placement. A small volume is more stable, so it is a more reproducible way to report and compare the "maximum". NRG templates, for example, define their maximum on 0.03 cc rather than on a point.

The small volumes are similar but not interchangeable. A limit set at 0.03 cc is not automatically the same as one at 0.035 cc, 0.1 cc or 0.5 cc, so read the metric at the volume your source uses.

How is it evaluated?

  1. Check the volume in the limit — 0.03 cc, 0.035 cc, 2% or another.
  2. In the structure's DVH, read the dose at that volume (on a cumulative DVH, the dose where the curve crosses that volume).
  3. Look at where the hottest region sits in the plan, not just its value.

For small structures, the difference between a cc limit and a % limit matters: 2% of a very small organ (under 1.5 cc) is less than 0.03 cc, and 2% of a large one is much more.

Example

D0.03cc = minimum dose received by the hottest 0.03 cc
D2% = minimum dose received by the hottest 2% of the structure
Volume (cc)Dose →0.03D0.03ccDmaxsingle hottest voxelhigh-dose tail only
Schematic only. D0.03cc is read where the curve crosses 0.03 cc; the point maximum sits at the very end of the tail.

Illustrative numbers only. For an organ contour of 60 cc, 2% of it is 1.2 cc — forty times the 0.03 cc volume — so D2% and D0.03cc would describe very different parts of the DVH.

Authoritative resources

Clinical resourceSource Verified
NRG Oncology Protocol Development Template for Radiation Therapy — Lung: SBRT
Matuszak M, Chetty I, Robinson C, Weldon M, Timmerman R · NRG Oncology Medical Physics Subcommittee / Radiation Oncology Committee · 2016

The template NRG Oncology gives investigators for writing the radiation section of a lung SBRT trial. Its imaging section allows PET/CT or MRI for structure definition, asks that the images be registered accurately to the planning scan (following AAPM TG-132 for deformable registration), notes that PET may be needed to separate tumor from atelectasis or fibrosis, and suggests an extra margin when a fused image is the primary image for the GTV. Its target and planning sections (5.2.4 and 5.2.6–5.2.8) define the plan-quality measures for lung SBRT trials: the prescription as the dose covering 95% of the PTV, a D99% requirement, R100% (prescription isodose volume ÷ PTV), R50% (50% prescription isodose volume ÷ PTV) and D2cm (maximum dose at 2 cm from the PTV in any direction, as a percentage of the prescription), with a table of allowable dose spillage by PTV volume. It describes a 20 mm PTV expansion structure used to control intermediate dose spillage, asks that dose above 105% of prescription be avoided outside the PTV, describes a deliberately heterogeneous dose with the hotspot in the central GTV, defines the maximum dose on a 0.03 cc volume, and ranks planning priorities when target coverage and organ limits conflict.

Clinical resourceSource Verified
NRG Oncology Protocol Development Template for Radiation Therapy — Brain: SRS
Cui Y, Ogunleye T, Kirkpatrick J, Xiao Y, Sperduto P, et al. · NRG Oncology Medical Physics Subcommittee / Radiation Oncology Committee · 2016

The NRG Oncology template for the radiation section of a brain radiosurgery trial. Its example text asks for CT slices of 1.25 mm or less, strongly encourages MRI (contrast T1 and a 3D gradient-echo sequence) for target delineation, recommends fusing FDG-PET/CT when available, and asks that the fusion be done by a medical physicist and reviewed by the attending physician. Its plan-evaluation section defines the conformity index (CI, or R100%) as the prescription isodose volume ÷ PTV volume, R50% as the 50% prescription isodose volume ÷ target volume ("R50% defines dose falloff outside the target"), a heterogeneity index D5% ÷ D95%, and coverage as the PTV volume receiving the prescription dose ÷ PTV volume, and notes that criteria such as the CI should account for target size and treatment technology.

Review articleSource Verified
A Story of Hypofractionation and the Table on the Wall
Timmerman R · UT Southwestern Medical Center · 2022

An editorial history of the UT Southwestern SABR constraint tables — often called the “Timmerman tables” — covering how they were developed and revised, and their relationship to AAPM TG-101 and NRG/RTOG protocols. Tables 2–11 separate serial tissues (listed with a volume, a volume max and a max point dose) from parallel tissues (listed with a critical volume and a critical-volume dose max). In Tables 2–7 a footnote defines “point” as ≤0.035 cm³; Tables 8–11 add a contouring-instructions column for each structure.

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.

AAPM reportSource Verified
AAPM TG-263: Standardizing Nomenclatures in Radiation Oncology
Mayo CS, Moran JM, Bosch W, et al. · AAPM · 2018

Recommendations for standardized naming of targets, organs at risk and dose-volume metrics. Section 9 sets out the DVH-metric nomenclature DoseLab follows: Vx (volume receiving at least dose x), Dx (minimum dose to the hottest sub-volume x), CVx and DCx (the "cold" complements), output units in square brackets (Gy or % of prescription; cc or % of the structure), and an EQD2Gy unit with the α/β written in parentheses — for example D90%(10)[EQD2Gy]. Section 10 asks that DVH metrics say whether a lower-dose PTV is segmented (excludes the higher-dose PTV) or not. Read in the AAPM report PDF.

Professional guidelineUnder Review
ICRU Report 83: Prescribing, Recording, and Reporting Photon-Beam Intensity-Modulated Radiation Therapy (IMRT)
DeLuca P, Jones D, Gahbauer R, et al. · International Commission on Radiation Units and Measurements (ICRU) · 2010

ICRU report on prescribing, recording and reporting intensity-modulated photon therapy. DoseLab has not read the report itself (it is sold by the ICRU). Its homogeneity index, (D2% − D98%) / D50%, is checked as quoted in the open-access Yan 2019 paper.

Planning studySource Verified

Proposes a new homogeneity index. Its introduction lists the indices in use — Dmax/Dp, D5/D95, (D2 − D98)/Dp and the ICRU Report 83 version (D2 − D98)/D50 — notes that lower values of the last two mean a more homogeneous dose, and that each is based on only two or three points of the DVH. Full text read in Europe PMC (PMC6839365).

TPS guidance

Eclipse

Step-by-step guidance planned. Added only once verified.

Coming soon
RayStation

Step-by-step guidance planned. Added only once verified.

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