Variogram Modeling of Spatially Variant Early Response to Therapy in Advanced Non-Small Cell Lung Cancer.

AMIA ... Annual Symposium proceedings. AMIA Symposium Pub Date : 2025-05-22 eCollection Date: 2024-01-01
Faisal Yaseen, Daniel S Hippe, Parth V Soni, Shouyi Wang, Chunyan Duan, John H Gennari, Stephen R Bowen
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Abstract

Predicting heterogeneity in treatment response for non-small cell lung cancer (NSCLC) at multiple scales, both between patients and spatially within each patient, can support clinical decisions that personalize oncologic management. In this study, we evaluated different variogram models of voxel-level spatial correlation in tumor response in locally advanced NSCLC and metastatic NSCLC from two different clinical trials. The Stable model achieved the lowest root mean squared error (RMSE) on average (mean: 5.2-5.5%), followed by the Matérn model (mean: 5.8-7.4%), both of which performed better than most other models. In contrast, the Exponential model had the highest RMSE (mean: 9.4-15.6%). These results remained consistent across two different cohorts of NSCLC. Given the robust performance of the Stable model, it may generalize for modeling spatial response in other clinical settings beyond NSCLC and should be further studied.

晚期非小细胞肺癌早期治疗反应空间变异的变异图建模。
在多个尺度上预测非小细胞肺癌(NSCLC)治疗反应的异质性,包括患者之间和每个患者内部的空间异质性,可以支持个性化肿瘤治疗的临床决策。在这项研究中,我们评估了两项不同临床试验中局部晚期NSCLC和转移性NSCLC肿瘤反应体素水平空间相关性的不同变异函数模型。Stable模型的平均均方根误差(RMSE)最低(均值:5.2-5.5%),其次是mat模型(均值:5.8-7.4%),两者的表现都优于大多数其他模型。相比之下,指数模型的RMSE最高(平均值:9.4-15.6%)。这些结果在两个不同的非小细胞肺癌队列中保持一致。鉴于Stable模型的强大性能,它可以推广到非小细胞肺癌以外的其他临床环境中空间反应的建模,应该进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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