# RapidPlan Knowledge-Based Radiotherapy Planning Compared to Manual Planning in Locally Advanced Non-Small-Cell Lung Cancer

**Authors:** Tal Falick Michaeli, Tamar Abu Said, Stanislav Raskin, Antoni Skripai, Yakir Rottenberg, Johnathan Arnon, Philip Blumenfeld

PMC · DOI: 10.3390/cancers17223654 · Cancers · 2025-11-14

## TL;DR

This study compares automated and manual radiotherapy planning for lung cancer, finding that automated planning reduces risks to some organs but increases lung dose.

## Contribution

The study demonstrates the dosimetric and clinical benefits of knowledge-based planning in lung cancer radiotherapy.

## Key findings

- RapidPlan reduced heart, esophagus, and spinal cord doses compared to manual planning.
- Lung toxicity was strongly linked to worse survival outcomes.
- VMAT-RP plans showed better cardiac and esophageal sparing than manual VMAT plans.

## Abstract

We retrospectively analyzed 50 patients with stage III NSCLC treated with concurrent chemoradiation between 2015 and 2021 to compare knowledge-based planning (RP) with manually optimized IMRT/VMAT plans. RP achieved comparable target coverage while significantly reducing mean doses to the heart (−2.5 Gy), esophagus (−3.9 Gy), and spinal cord (−4.1 Gy), though with a modest increase in lung V20 (+2.1%). Normal tissue complication probability estimates predicted lower cardiac and esophageal toxicity with RP but no clear improvement for lung or spinal cord. Clinically, lung toxicity ≥ grade 2 strongly correlated with inferior overall survival (16.2 vs. 51.8 months, p < 0.001). RP thus enhanced organ-at-risk sparing, particularly for cardiac and esophageal structures, but required attention to pulmonary dose trade-offs. These findings underscore both the potential and the limitations of knowledge-based planning and highlight the need for individualized optimization strategies in stage III NSCLC radiotherapy.

Background/Objectives: Treatment planning for stage III non–small cell lung cancer (NSCLC) presents dosimetric challenges due to the proximity of critical structures. RapidPlan (RP), a knowledge-based planning (KBP) system, offers the potential for improved plan consistency and organ-at-risk (OAR) sparing. The objective of this study was to compare dosimetric and clinical outcomes of RP-generated plans versus manually optimized plans in patients with stage III NSCLC undergoing IMRT or VMAT. Methods: In this retrospective analysis, 50 patients treated with concurrent chemoradiation for stage III NSCLC at Hadassah Medical Center (2015–2021) were analyzed. RP plans were generated using a lung-specific model in the Eclipse treatment planning system and compared with the original clinical manual plans. Dosimetric parameters for target volumes and OARs were evaluated, and subgroup analyses were performed by technique (IMRT vs. VMAT). Toxicity and survival outcomes were analyzed, and Normal Tissue Complication Probability (NTCP) modeling was conducted. Results: RP significantly reduced mean heart dose (Δ = −2.54 Gy, p < 0.001), spinal cord maximum dose (Δ = −4.08 Gy, p < 0.001), and esophageal mean dose (Δ = −3.89 Gy, p < 0.001) compared with manual plans. Lung doses were slightly higher in RP plans (V20 Δ = +2.12%, p < 0.001). VMAT-RP plans demonstrated greater cardiac and esophageal sparing than VMAT-manual plans. RP yielded significant NTCP reductions for the heart (0.34% → 0.20%) and esophagus (16.6% → 11.5%), but no improvement for lung or spinal cord. Lung toxicity ≥ grade 2 was associated with reduced overall survival (16.2 vs. 51.8 months, p < 0.001). Conclusions: RapidPlan-based knowledge-based planning enhances OAR sparing while maintaining target coverage in locally advanced NSCLC. Slight increases in lung dose highlight the need for ongoing model refinement. An association between lung toxicity and reduced survival was observed, underscoring the impact of treatment-related morbidity on outcomes.

## Linked entities

- **Diseases:** non-small-cell lung cancer (MONDO:0005233)

## Full-text entities

- **Diseases:** NSCLC (MESH:D002289), Toxicity (MESH:D064420), Lung toxicity (MESH:D008171)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12651467/full.md

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Source: https://tomesphere.com/paper/PMC12651467