ArticleCurrent problems in diagnostic radiology
Volume Doubling Times of Benign and Malignant Nodules in Lung Cancer Screening.
Article in Current problems in diagnostic radiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 10 citations in OpenAlex.
- Towards optimized CT lung cancer screening scan protocols.The British journal of radiology · 2026Article
- The role of growth heterogeneity in solid nodular non-small cell lung cancer in clinical practice: a narrative review.Journal of thoracic disease · 2026Review
- Biopsy-Proven Pulmonary Tumors Detected by LDCT: A 10-Year Single-Center Study of Growth Patterns and Diagnostic Pitfalls.International journal of medical sciences · 2026Article
- Influencing factors and prediction of growth heterogeneity in solid nodule non-small cell lung cancer based on artificial intelligence: a prospective study.Translational lung cancer research · 2025Article
- Exploration of optimal thresholds for predicting the invasive nature of stage T1 lung adenocarcinoma using artificial intelligence-based 3D solid component volume segmentation.Quantitative imaging in medicine and surgery · 2025Article
- Growth dynamics of lung nodules: implications for classification in lung cancer screening.Cancer imaging : the official publication of the International Cancer Imaging Society · 2024Article
- Prediction of subsolid pulmonary nodule growth rate using radiomics.BMC medical imaging · 2023Article
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
The purpose of this study was to measure the fractions of benign and malignant nodules in lung cancer screening that grow on follow-up, and to measure the volume doubling time (VDT) of those that grow. In this retrospective study, we included nodules from CT lung cancer screening in our healthcare network, for which a follow-up CT performed at least 2 months later showed the nodule to be persistent. The nodules were measured using semiautomated volumetric segmentation software at both timepoints. Growth was defined as an increase in volume by 25%. VDTs were calculated, and the fraction <400 days was recorded. Categorical variables were compared with Fisher's exact test, and continuous variables by the Wilcoxon test. The study included 153 nodules, of which 44 were malignant and 109 benign. Thirty (68%) of malignant nodules and 36 (33%) of benign nodules grew (P < 0.001). For growing nodules, VDT was 318 days for malignant nodules and 389 for benign nodules (P = 0.21). For growing solid nodules, VDT was 204 days for malignant nodules and 386 days for benign nodules (P = 0.01); of these, VDT was <400 days for 12/13 (92%) of malignant nodules and 15/26 (58%) of benign nodules. In conclusion, malignant nodules were more likely to grow, and solid malignant nodules grew faster, than benign nodules. However, there was substantial overlap between benign and malignant nodules. This limits the utility of volume doubling time in determining malignant nodules.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.