Teijeira Lucía, Martínez Mireia, Moreno Amaia, de Elejoste Ibone, Ibáñez-Beroiz Berta, Arrazubi Virginia, Díaz de Corcuera Isabela, Elejalde Iñaki, Campillo-Calatayud Ana, Les Iñigo
Servicio de Oncología Médica, Hospital Universitario de Navarra, 31008 Pamplona, Spain.
Servicio de Oncología Médica, Hospital Universitario Araba, Servicio Vasco de Salud Osakidetza, 01009 Vitoria-Gasteiz, Spain.
Cancers (Basel). 2023 Dec 28;16(1):151. doi: 10.3390/cancers16010151.
Several factors have been associated with the occurrence of immune-related adverse events (irAEs) induced by immune checkpoint inhibitor (ICI) therapy. Despite their availability, the predictive value of circulating blood cell parameters remains underexplored. Our aim was to investigate whether baseline values of and early changes in absolute neutrophil count (ANC), absolute lymphocyte count (ALC), other blood cell counts, and lymphocyte-related ratios can predict irAEs and whether sex may differentially influence this potential predictive ability. Of the 145 patients included, 52 patients (35.8%) experienced at least one irAE, with a 1-year cumulative incidence of 41.6%. Using Fine and Gray competing risk models, we identified female sex (hazard ratio (HR) = 2.17, 95% confidence interval (CI) = 1.20-3.85), high ALC before ICI initiation (HR = 1.63, 95% CI = 1.09-2.45), and low ANC after ICI initiation (HR = 0.81, 95% CI = 0.69-0.96) as predictors of irAEs. However, ALC and ANC may only have an impact on the risk of irAEs in women (stratified for female sex, ALC-related HR = 2.61, 95% CI = 1.40-4.86 and ANC-related HR = 0.57, 95% CI = 0.41-0.81). Priority should be given to developing models to predict ICI-related toxicity and their validation in various settings, and such models should assess the impact of patient sex on the risk of toxicity.
多种因素与免疫检查点抑制剂(ICI)治疗诱发的免疫相关不良事件(irAE)的发生有关。尽管已有相关研究,但循环血细胞参数的预测价值仍未得到充分探索。我们的目的是研究绝对中性粒细胞计数(ANC)、绝对淋巴细胞计数(ALC)、其他血细胞计数以及淋巴细胞相关比值的基线值和早期变化是否能够预测irAE,以及性别是否会对这种潜在的预测能力产生不同影响。在纳入的145例患者中,52例患者(35.8%)经历了至少一次irAE,1年累积发病率为41.6%。使用Fine和Gray竞争风险模型,我们确定女性(风险比(HR)=2.17,95%置信区间(CI)=1.20 - 3.85)、ICI开始前高ALC(HR = 1.63,95% CI = 1.09 - 2.45)以及ICI开始后低ANC(HR = 0.81,95% CI = 0.69 - 0.96)为irAE的预测因素。然而,ALC和ANC可能仅对女性发生irAE的风险有影响(按女性分层,与ALC相关的HR = 2.61,95% CI = 1.40 - 4.86,与ANC相关的HR = 0.57,95% CI = 0.41 - 0.81)。应优先开发预测ICI相关毒性的模型并在各种环境中进行验证,并且此类模型应评估患者性别对毒性风险的影响。