Radikulus

Lung Nodule Volume Doubling Time Calculator

GrowTime · Calculate lung nodule volume doubling time from serial CT measurements and scan dates.

Criteria: BTS 2015Callister et al., British Thoracic Society guidelines for the investigation and management of pulmonary nodules. Thorax 2015;70 Suppl 2:ii1–ii54. PMID 26082159. Last checked for newer criteria 30 Oct 2026.

For solid pulmonary nodules measured with comparable CT technique. This calculator estimates growth; it does not calculate an individual cancer probability or select a complete follow-up pathway.

Measurement typeBTS 2015 recommends diameter measurements where volumetry is not possible or there is clear evidence of marked growth (Grade D).
Scan dateMeasured volume (mm³)Use checked volumetry measurements obtained with the same software and comparable CT technique across scans.Series (optional)Image (optional)2 scans
Calculated VDT display intervals
  • G1G1 is a Radikulus display label, not an official guideline category. <400 daysA shorter calculated volume doubling time indicates faster volume increase under the exponential-growth model. It does not diagnose malignancy.
  • G2G2 is a Radikulus display label, not an official guideline category. 400–<600 daysThis is the middle Radikulus display interval. Management also depends on measurement reliability, nodule characteristics and the applicable guideline.
  • G3G3 is a Radikulus display label, not an official guideline category. ≥600 daysA longer calculated volume doubling time does not establish benignity. Some lung cancers grow slowly.

G1/G2/G3 is a Radikulus display label, not an official guideline category.

This tool is for educational purposes only. Clinical decisions should be made by qualified healthcare professionals considering all relevant clinical information.

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What is it about?

Do not include patient names or other identifiers.

How to read this calculator

Enter the measurements, or press Simulate to load a case from the reviewed validation catalog. The calculator then shows three things, top to bottom:

  • Results: First-to-last VDT (days) and First-to-last comparison as plain numbers, with no interpretation attached.
  • Calculated VDT display intervals: the three steps, listed once below the nodules; each nodule’s card shows the step that applies to it, in its status colour.
  • Adjacent scan intervals: each consecutive scan pair, in date order.

About doubling time

Volume doubling time (VDT) is the time it takes a nodule to double in volume, assuming exponential growth. It is calculated as VDT = (t × ln 2) / ln(V2 / V1), where t is the interval between scans and V1 and V2 are the earlier and later volumes.

When volume is estimated from diameter by treating the nodule as a sphere (V = π/6 × D³), the volume ratio is the cube of the diameter ratio, so VDT = (t × ln 2) / (3 × ln(D2 / D1)).

Diameter doubling time is 3× VDT.

Interpreting volume doubling time

VDT bands use unrounded values: <400 days, 400–<600 days, and ≥600 days.

Horeweg’s screening analysis advocated VDT assessment for intermediate-size nodules; its size thresholds and participant probabilities are not a complete contemporary management algorithm.

BTS 2015 notes that rapid growth of a new nodule may imply an inflammatory process; rapid growth does not exclude a neoplasm.

In Hong’s selected cohort of resected invasive adenocarcinomas, median VDT for lepidic-predominant tumours was 1140.6 days; 19 of 26 were part-solid on CT. This is not a solid-nodule population reference value.

Each nodule is calculated separately. These calculations do not provide a combined cancer-risk assessment or select an index nodule for management. BTS 2015 recommends basing risk assessment in people with multiple pulmonary nodules on the largest nodule (Grade C).

Decision steps

G1/G2/G3 is a Radikulus display label, not an official guideline category.

StepCriterionMeaningDetail
G1Calculated VDT <400 daysShorter VDTA shorter calculated volume doubling time indicates faster volume increase under the exponential-growth model. It does not diagnose malignancy.
G2Calculated VDT 400–<600 daysIntermediate VDTThis is the middle Radikulus display interval. Management also depends on measurement reliability, nodule characteristics and the applicable guideline.
G3Calculated VDT ≥600 daysLonger VDTA longer calculated volume doubling time does not establish benignity. Some lung cancers grow slowly.

Worked example

Published case — Lim 2024, Figs. 2–3, PMID 38405419: glandular papilloma (benign). 9 → 10 → 13 mm at about one and two years. Calculation assumes 365 + 365 days because the publication gives approximate intervals. Single-diameter spherical estimates; the paper reports volume-based VDTs of 844.28 days over the first year and 369.45 days overall, which are not the calculator's single-diameter estimates.

What the calculator returns for this case. Dates are illustrative.
ItemValue
Scan 1Scan date: 2020-01-01; Maximum transverse diameter (mm): 9
Scan 2Scan date: 2020-12-31; Maximum transverse diameter (mm): 10
Scan 3Scan date: 2021-12-31; Maximum transverse diameter (mm): 13
First-to-last VDT (days)458.7
First-to-last comparisonScan 1 (2020-01-01) to scan 3 (2021-12-31): 730 days; 9 → 13 mm
Calculated VDT display intervalsG2 · Calculated VDT 400–<600 days
Scan 1 (2020-01-01) to scan 2 (2020-12-31)365 days; 9 → 10 mm. 800.4 days — Calculated VDT ≥600 days. Diameter change <1.7 mm is within the measurement variability discussed by BTS 2015; the calculated VDT may be unreliable.
Scan 2 (2020-12-31) to scan 3 (2021-12-31)365 days; 10 → 13 mm. 321.4 days — Calculated VDT <400 days

The recorded increase gives a calculated VDT in the 400–<600 days display interval. The latest measurement is ≥10 mm. VDT alone does not determine the next step. Scan 2 to scan 3 had a shorter calculated VDT: 321.4 days.

  • VDT estimated from one diameter assumes spherical, uniform growth and is less reliable than measured volumetry.

Measurement and display limitations

VDT estimated from one diameter assumes spherical, uniform growth and is less reliable than measured volumetry.

BTS 2015 uses a ≥25% volume change to define significant growth (Grade C); its account of NELSON likewise reports a requirement for at least 25% volume change.

For the evaluated protocols, the criterion that the percentage volume change should be >25% before calculating the VDT was ignored.

BTS assessment pathway

These recommendations belong to BTS 2015’s assessment pathway. Initial risk, morphology, reliable measurements, prior imaging and cancer context must be considered; GrowTime does not determine those conditions.

BTS 2015 recommends composite prediction models, based on clinical and radiological factors, to estimate the probability that a nodule ≥8 mm or ≥300 mm³ is malignant (Grade C). GrowTime does not calculate that probability, and its intermediate-size display range (5–<10 mm or 100–<300 mm³ on the first measurement) is a separate convention adapted from Horeweg’s NELSON analysis.

BTS 2015 recommends further diagnostic investigation—biopsy, imaging or resection—for clear growth or VDT <400 days assessed after three months and one year (Grade C).

For nodules in the BTS surveillance pathway with VDT 400–600 days, BTS 2015 offers ongoing yearly surveillance or biopsy according to patient preference (Grade C).

For VDT >600 days, BTS 2015 offers discharge or ongoing CT surveillance, taking account of patient preference, fitness and age (Grade C).

Within its solid-nodule surveillance pathway, BTS 2015 recommends discharge after stability (<25% volume change) on CT after one year (Grade C); a single endpoint comparison does not establish the complete pathway or exclude intervening growth.

When 2D diameter measurements are used to assess growth, BTS 2015 recommends CT follow-up for a total of two years (Grade D).

BTS 2015 recommends no nodule follow-up below 5 mm maximum diameter or 80 mm³ volume (Grade C); this is a separate size-based recommendation, not an inference from a calculated VDT.

Other guideline contexts

In ESTI’s screening pathway, a decrease may indicate a benign process, with ongoing follow-up to ensure shrinkage continues.

Lung-RADS v2022 defines growth as >1.5 mm increase in mean diameter within twelve months; slow-growing solid or part-solid nodules across multiple screening examinations may still be suspicious. GrowTime does not assign Lung-RADS categories.

Fleischner 2017 discusses VDT and the greater reproducibility of volumetry, but its incidental-nodule recommendations are not GrowTime’s three VDT display bands; applicability, morphology, size and prior imaging remain essential.

The 2023 AJR expert-panel review describes volumetry as the primary size method for solid nodules in the European screening position statement and BTS recommendations.

Criteria review

Calculation and contextual guidance reviewed 30 October 2026. BTS 2015 remains the published basis used here; a BTS pulmonary nodules consultation draft is open for comments until 1 December 2026 and is not implemented.

Frequently asked questions

What is the formula for volume doubling time?

VDT = (t × ln 2) / ln(V2 / V1), where t is the time between scans and V1 and V2 are the nodule volumes. If volumes are estimated from diameters assuming a sphere, VDT = (t × ln 2) / (3 × ln(D2 / D1)).

Should I use volume or diameter?

BTS 2015 recommends diameter measurements where volumetry is not possible or there is clear evidence of marked growth (Grade D). BTS 2015 describes NELSON’s failed-volumetry fallback as manually measuring maximum diameter in three perpendicular planes. Horeweg’s thesis manuscript describes estimating unavailable volumes from a manually measured diameter assuming a sphere, while its main diameter measurements were software-derived. These source descriptions differ; GrowTime’s single-diameter spherical estimate does not reproduce BTS’s three-plane account or NELSON’s semiautomated measurements.

What volume doubling time suggests lung cancer?

No calculated VDT diagnoses or excludes cancer. In Horeweg’s NELSON screening analysis, reported 2-year lung cancer probabilities among participants whose largest nodule measured 50–500 mm³ were 9.9% (95% CI 6.9–14.1) for VDT <400 days, 4.0% (1.8–8.3) for VDT 400–<600 days and 0.8% (0.4–1.7) for VDT ≥600 days. These are screening-cohort observations, not this patient’s calculated probability. Growth does not establish malignancy: benign nodules, including hamartomas, can have VDTs comparable to slow-growing cancers. A longer calculated volume doubling time does not establish benignity. Some lung cancers grow slowly.

Can growth be assessed on a 3-month follow-up CT?

BTS 2015 reports better VDT accuracy after one year than after three months, particularly for nodules <6 mm. For screen-detected nodules suitable for volumetry, ESTI’s 2025 recommendation uses substantial-growth thresholds of VDT <250 days at three months, <400 days at six months and <500 days at twelve months or later, accounting for measurement variability. GrowTime does not implement that screening pathway. Diameter change <1.7 mm is within the measurement variability discussed by BTS 2015; the calculated VDT may be unreliable.

References

  1. Callister et al., BTS guidelines, Thorax 2015;70 Suppl 2:ii1–ii54. doi:10.1136/thoraxjnl-2015-207168. PMID 26082159.
  2. Callister et al., BTS 2015, Summary of recommendations, p.ii2: risk assessment in people with multiple pulmonary nodules (Grade C).
  3. Horeweg et al., Lancet Oncol 2014;15(12):1332–1341. doi:10.1016/S1470-2045(14)70389-4. PMID 25282285. Read as the manuscript reprinted in chapter 6 (pp.147–177) of Horeweg’s Erasmus University Rotterdam doctoral thesis; the journal version of record was not inspected.
  4. Revel et al., Radiology 2004;231:453–458. doi:10.1148/radiol.2312030167. PMID 15128990. Abstract-derived evidence.
  5. Hong et al., Korean J Radiol 2021;22:464–475. doi:10.3348/kjr.2020.0592. PMID 33169551.
  6. Snoeckx et al., Eur Radiol 2026;36:135–147 (online 2025). doi:10.1007/s00330-025-11648-4. PMID 40593170.
  7. Prokop et al., Eur Radiol 2026;36:122–134 (online 2025). doi:10.1007/s00330-025-11647-5. PMID 40593169.
  8. MacMahon et al., Fleischner Society 2017. Radiology 2017;284:228–243. doi:10.1148/radiol.2017161659. PMID 28240562.
  9. ACR Lung-RADS v2022: https://www.acr.org/Clinical-Resources/Clinical-Tools-and-Reference/Reporting-and-Data-Systems/Lung-RADS
  10. Nair et al., AJR expert-panel review 2023;220:314–329. doi:10.2214/AJR.22.27830. PMID 36129224. Abstract-derived evidence.
  11. BTS October 2026 consultation draft (not implemented): https://www.brit-thoracic.org.uk/clinical-resources/guidelines/pulmonary-nodules-guideline-consultation/

Last updated: 30 Oct 2026