在局部晚期或转移性尿路上皮癌患者接受atezolizumab治疗时,同时给予抗组胺与改善生存结果相关。IMvigor210和IMvigor211的个体参与者数据分析。

IF 2.4 3区 医学 Q3 ONCOLOGY
Giuseppe Fallara, Federico Belladelli, Daniele Robesti, Bernard Malavaud, Côme Tholomier, Sharada Mokkapati, Francesco Montorsi, Colin P Dinney, Pavlos Msaouel, Alberto Martini
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引用次数: 0

摘要

目的:转移性尿路上皮癌(mUC)患者的生存结果仍然不理想,增强免疫肿瘤学(IO)化合物反应的策略正在审查中。在临床前研究中,已经证明抗组胺药可以逆转巨噬细胞免疫抑制,重新激活T细胞毒性,增强免疫治疗反应。我们的目的是评估同时使用抗组胺药对mUC患者肿瘤预后的影响。材料和方法:我们依赖IMvigor210(二线atezolizumab治疗mUC的II期单组试验)和IMvigor211试验(二线atezolizumab与化疗治疗mUC的III期随机试验)的个体患者数据。在接受IO治疗的个体中,我们确定了接受和未接受抗组胺药治疗的患者。多变量Cox或竞争风险回归模型用于预测无进展生存期(PFS)、总生存期(OS)和癌症特异性生存期(CSS)。在调整潜在混杂因素后,评估抗组胺药对结果的影响。结果:896例局部晚期或转移性尿路上皮癌患者在一线化疗后进展,155例(17 %)在IO分娩期间接受抗组胺药治疗。接受抗组胺药物治疗的患者生存期更长(风险比[HR]:0.59;95 %置信区间[CI]: 0.47-0.74;P 结论:在接受atezolizumab作为mUC二线治疗的患者中,同时服用抗组胺药与改善OS、CSS和PFS相关。需要进一步的机制和临床研究来阐明抗组胺药在IO中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concomitant antihistamine administration is associated with improved survival outcomes in patients with locally advanced or metastatic urothelial carcinoma treated with atezolizumab. Analysis of individual participant data from IMvigor210 and IMvigor211.

Objectives: Survival outcomes of patients with metastatic urothelial carcinoma (mUC) are still suboptimal and strategies to enhance response to immune-oncology (IO) compounds are under scrutiny. In preclinical studies, it has been demonstrated that antihistamines may reverse macrophage immunosuppression, reactivate T cell cytotoxicity, and enhance the immunotherapy response. We aimed to evaluate the role of concomitant antihistamines administration on oncological outcomes among patients with mUC.

Materials and methods: We relied on individual patient data from IMvigor210 (phase II single-arm trial on second line atezolizumab for mUC) and IMvigor211 trials (phase III randomized trial on second line atezolizumab vs chemotherapy for mUC). Among individuals treated with IO we identified patients who did and did not receive antihistamines. Multivariable Cox or competing-risks regression models were used to predict progression-free survival (PFS), overall survival (OS), and cancer-specific survival (CSS). The impact of antihistamines on the outcomes was assessed after adjusting for potential confounders.

Results: Among 896 patients with locally advanced or metastatic urothelial cancer who had progressed after first-line chemotherapy, 155 (17 %) received antihistamines during the delivery of IO. Patients receiving antihistamines had longer OS (Hazard Ratio [HR]:0.59; 95 % Confidence interval [CI]: 0.47-0.74; P < 0.001), PFS (HR:0.70; 95 %CI: 0.57-0.87; P = 0.001) and CSS [sHR:0.58; 95 %CI:0.45-0.75; P < 0.001)] relative to those who had not used antihistamine drugs. A sensitivity analysis, after the exclusion of patients who experienced adverse events and received antihistamines, yielded similar findings of prolonged CSS (sHR 0.78; 95 %CI: 0.59-0.98, P = 0.031) and OS (HR 0.71; 95 %CI: 0.52-0.94, P = 0.021).

Conclusions: Concomitant antihistamines administration was associated with improved OS, CSS, and PFS in patients receiving atezolizumab as second line treatment for mUC. Further mechanistic and clinical investigation is warranted to elucidate the role of antihistamines in IO.

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来源期刊
CiteScore
4.80
自引率
3.70%
发文量
297
审稿时长
7.6 weeks
期刊介绍: Urologic Oncology: Seminars and Original Investigations is the official journal of the Society of Urologic Oncology. The journal publishes practical, timely, and relevant clinical and basic science research articles which address any aspect of urologic oncology. Each issue comprises original research, news and topics, survey articles providing short commentaries on other important articles in the urologic oncology literature, and reviews including an in-depth Seminar examining a specific clinical dilemma. The journal periodically publishes supplement issues devoted to areas of current interest to the urologic oncology community. Articles published are of interest to researchers and the clinicians involved in the practice of urologic oncology including urologists, oncologists, and radiologists.
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