单克隆抗体免疫治疗反应仪在3pm引导下的泛癌治疗中分层和成本效益个性化方法。

IF 5.9 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
The EPMA journal Pub Date : 2025-03-22 eCollection Date: 2025-06-01 DOI:10.1007/s13167-025-00403-w
Salem Baldi, Mohammed Alnaggar, Maged Al-Mogahed, Khalil A A Khalil, Xianquan Zhan
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引用次数: 0

摘要

背景:免疫检查点抑制剂(ICIs),如抗pd -1、抗pd - l1和抗ctla -4疗法,通过利用人体免疫系统消除癌细胞,已经彻底改变了癌症治疗。尽管ICIs具有相当大的前景,但其疗效因肿瘤类型和特定患者情况而显着差异,这突出了在预测性预防性个性化医学(PPPM)框架中采用个性化方法的必要性;下午3点)。主体:本综述提出了一种3PM框架下的分层工具,以提高ICIs对泛癌的治疗效果。需要利用预测方法来提高国际信息系统的有效性。例如,生物标志物,如特定的遗传改变和代谢途径,提供了患者治疗反应的关键信息。为了预测治疗结果,揭示耐药机制和定制药物,我们检查了包括PDL-1和CTLA4在内的生物标志物。重点关注黑色素瘤、膀胱癌和肾细胞癌等癌症,我们强调了联合治疗和细胞方法克服耐药性的进展。我们对临床试验和公共数据集(TCGA, GEO)进行了分析,以评估多种癌症类型的ICI反应。生存分析采用Kaplan-Meier曲线和Cox回归。泛癌症分析显示,当联合治疗时,膀胱癌的缓解率为19.8%,黑色素瘤的缓解率为50.39%,强调了3PM改善预后的潜力。通过探索耐药机制和新兴的治疗创新,我们提出了一种具有成本效益的模式,以更好地对患者进行分层和护理。该模型的验证需要标准化的生物标志物和前瞻性试验,有望向精确肿瘤学转变。结论:在3PM框架内,本综述解决了迫切需要具有成本效益的分层工具和适应性组合策略来优化结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Monoclonal antibody immune therapy response instrument for stratification and cost-effective personalized approaches in 3PM-guided pan cancer management.

Background: Immune checkpoint inhibitors (ICIs), such as anti-PD-1, anti-PD-L1, and anti-CTLA-4 therapies, have revolutionized cancer treatment by harnessing the body's immune system to eliminate cancer cells. Despite their considerable promise, the efficacy of ICIs significantly differs based on tumor types and specific patient conditions, highlighting the necessity for personalized approaches in the framework of predictive preventive personalized medicine (PPPM; 3PM).

Main body: This review proposes a stratification instrument within the 3PM framework to enhance the therapeutic efficacy of ICIs across Pan-cancer. Predictive approaches need to be utilized to enhance the effectiveness of ICIs. For example, biomarkers such as particular genetic alterations and metabolic pathways provide key information on patient treatment responses. To predict treatment outcomes, uncover resistance mechanisms, and tailor medications, we examine biomarkers including PDL-1 and CTLA4. Focusing on cancers like melanoma, bladder, and renal cell carcinoma, we highlight advances in combination therapies and cellular approaches to overcome resistance. We conducted an analysis of clinical trials and public datasets (TCGA, GEO) to evaluate ICI responses across number of cancer types. Survival analysis employed Kaplan-Meier curves and Cox regression. Pan-cancer analysis shows response rates ranging from 19.8% in bladder cancer to > 39% in melanoma when combination therapy is used, emphasizing the potential of 3PM to improve outcomes. By exploring resistance mechanisms and emerging therapeutic innovations, we propose a cost-effective model for better patient stratification and care. Validation of this model requires standardized biomarkers and prospective trials, promising a shift toward precision oncology.

Conclusion: Within the 3PM framework, this review addresses the urgent need for cost-effective stratification tools and adaptive combinatorial strategies to optimize outcomes.

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