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arXiv 2104.15032physics.med-ph
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作为逆向规划方法的基于深度学习的注量图预测的可推广性

Generalizability of deep learning based fluence map prediction as an inverse planning approach

Lin Ma, Mingli Chen, Xuejun Gu, Weiguo Lu

摘要:

文献中已经报道了基于深度学习的注量图预测(DL-FMP)方法,该方法通过基于深度神经网络(DNN)的逆映射生成期望剂量的注量图。我们假设DL-FMP与一般注量图优化(FMO)相似,因为它在理论上基于一般逆映射。我们设计了四个实验来验证DL-FMP对除了训练数据之外的其他类型的计划的通用性,其中仅包含临床头颈部(HN)全弧VMAT计划。前三个实验分别量化了DL-FMP对多个解剖部位、不同递送方式和各种调制度(DOM)的普遍性。实验四探讨了对不可行剂量输入的泛化性和稳定性。第一次实验的结果表明,DL-FMP可以推广到肺、肝、食管和前列腺,其γ通过率(GPR)高于95%(2%/2 mm)。第二个实验表明,DL-FMP可以推广到部分弧计划和预测部分弧通量。GPR(3 mm/3%)范围为96%-99%。DL-FMP无法生成IMRT输入的离散射束角度的注量图。但在93%GPR(5%/5 mm)下,预测剂量仍与真实剂量一致。第三次实验表明,DL-FMP可以推广到各种DOM,GPR(3%/3 mm)范围为94%-98%。此外,预测的注量图的DOM相应地与输入剂量的最优性相关。第四个实验表明,DL-FMP可以对不可行的剂量输入进行稳定的预测。总之,我们验证了DL-FMP可以推广到多个解剖部位的计划、不同输送方式的计划和具有各种DOM的计划。对不可行输入也能做出稳定的预测。

英文摘要:

Deep learning-based fluence map prediction(DL-FMP) method has been reported in the literature, which generated fluence maps for desired dose by deep neural network(DNN)-based inverse mapping. We hypothesized that DL-FMP is similar to general fluence map optimization(FMO) because it's theoretically based on a general inverse mapping. We designed four experiments to validate the generalizability of DL-FMP to other types of plans apart from the training data, which contained only clinical head and neck(HN) full-arc VMAT plans. The first three experiments quantified the generalizability of DL-FMP to multiple anatomical sites, different delivery modalities, and various degree of modulation(DOM), respectively. The fourth experiment explored the generalizability and stability to infeasible dose inputs. Results of the first experiment manifested that DL-FMP can generalize to lung, liver, esophagus and prostate, with gamma passing rates (GPR) higher than 95%(2%/2mm). The second experiment showed that DL-FMP can generalize to partial-arc plans and predict partial-arc fluences. GPR(3mm/3%) ranged from 96% to 99%. DL-FMP cannot generate fluence maps in discrete beam angles for IMRT input. But the predicted dose still agreed with ground truth dose with 93% GPR(5%/5mm). The third experiment demonstrated that DL-FMP can generalize to various DOMs, with GPRs(3%/3mm) ranged in 94%-98%. Moreover, the DOM of predicted fluence maps correlated to the optimality of the input dose accordingly. The fourth experiment exemplified that DL-FMP can make stable predictions for infeasible dose input. In conclusion, we validated that DL-FMP can generalize to plans for multiple anatomical sites, plans of different delivery modalities and plans with various DOM. It can also make stable prediction for infeasible input.

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