Institute of Biomedical and Health Engineering, Chinese Academy of Sciences Shenzhen Institutes of Advanced Technology, Shenzhen, China.
Department of Clinical Oncology, University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Front Immunol. 2022 Jun 21;13:768811. doi: 10.3389/fimmu.2022.768811. eCollection 2022.
Radiation-induced lymphopenia is known for its survival significance in patients with breast cancer treated with radiation therapy. This study aimed to evaluate the impact of radiotherapy on lymphocytes by applying machine learning strategies. We used Extreme Gradient Boosting (XGboost) to predict the event of lymphopenia (grade≥1) and conduced an independent validation. Then, we induced feature attribution analysis (Shapley additive explanation, SHAP) in explaining the XGboost models to explore the directional contribution of each feature to lymphopenia. Finally, we implemented the proof-of-concept clinical validation. The results showed that the XGboost models had rigorous generalization performances (accuracies 0.764 and ROC-AUC 0.841, respectively) in the independent cohort. The baseline lymphocyte counts are the most protective feature (SHAP = 5.226, direction of SHAP = -0.964). Baseline platelets and monocytes also played important protective roles. The usage of taxane only chemotherapy was less risk on lymphopenia than the combination of anthracycline and taxane. By the contribution analysis of dose, we identified that firstly lymphocytes were sensitive to a radiation dose less than 4Gy; secondly the irradiation volume was more important in promoting lymphopenia than the irradiation dose; thirdly the irradiation dose promoted the event of lymphopenia when the irradiation volume was fixed. Overall, our findings paved the way to clarifying the radiation dose volume effect. To avoid radiation-induced lymphopenia, irradiation volume should be kept to a minimum during the planning process, as long as the target coverage is not compromised.
辐射诱导性淋巴细胞减少症在接受放射治疗的乳腺癌患者中具有生存意义,这是已知的。本研究旨在通过应用机器学习策略来评估放射治疗对淋巴细胞的影响。我们使用极端梯度提升(XGboost)来预测淋巴细胞减少症(等级≥1)的发生,并进行了独立验证。然后,我们在解释 XGboost 模型时进行了特征归因分析(Shapley 加性解释,SHAP),以探索每个特征对淋巴细胞减少症的定向贡献。最后,我们实施了概念验证的临床验证。结果表明,XGboost 模型在独立队列中具有严格的泛化性能(准确性分别为 0.764 和 ROC-AUC 为 0.841)。基线淋巴细胞计数是最具保护作用的特征(SHAP = 5.226,SHAP 方向=-0.964)。基线血小板和单核细胞也起着重要的保护作用。与蒽环类药物和紫杉烷联合化疗相比,仅使用紫杉烷的化疗发生淋巴细胞减少症的风险较低。通过剂量的贡献分析,我们确定了首先淋巴细胞对小于 4Gy 的辐射剂量敏感;其次,与辐射剂量相比,照射体积对促进淋巴细胞减少症更为重要;第三,当照射体积固定时,照射剂量会促进淋巴细胞减少症的发生。总体而言,我们的研究结果为阐明辐射剂量-体积效应铺平了道路。为了避免辐射诱导的淋巴细胞减少症,在规划过程中应尽量将照射体积保持在最低水平,只要目标覆盖范围不受影响。