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基线皮质类固醇对晚期黑色素瘤患者免疫治疗疗效的影响。

Impact of Baseline Corticosteroids on Immunotherapy Efficacy in Patients With Advanced Melanoma.

机构信息

Cancer Centre of Southeastern Ontario.

Departments of Oncology.

出版信息

J Immunother. 2021 May 1;44(4):167-174. doi: 10.1097/CJI.0000000000000360.

Abstract

This is a 2-center, retrospective study which aimed to evaluate the effect of baseline corticosteroid use on immunotherapy efficacy in patients with advanced melanoma. We included all patients with advanced unresectable and metastatic melanoma on single-agent programmed cell death protein 1 (PD-1) inhibitors at the Cancer Centre of Southeastern Ontario and London Regional Cancer Program. We defined baseline corticosteroid use as prednisone-equivalent of ≥10 mg within 30 days of immunotherapy initiation. Our study had 166 patients in total, and 25 were taking corticosteroids at the initiation of the PD-1 inhibitor. Baseline prednisone-equivalent ≥10 mg did not have effect on median overall survival (hazard ratio=1.590, 95% confidence interval: 0.773-3.270, P=0.208). However, a higher dose of baseline prednisone-equivalent ≥50 mg was independently associated with poor median overall survival (hazard ratio=2.313, 95% confidence interval: 1.103-4.830, P=0.026) when compared with baseline prednisone-equivalent 0-49 mg, even when controlled for confounders including baseline Eastern Cooperative Oncology Group ≥2 and baseline brain metastasis. Consideration should be made to decrease the use of unnecessary steroids as much as possible before initiation of PD-1 inhibitor treatment.

摘要

这是一项 2 中心、回顾性研究,旨在评估基线皮质类固醇使用对晚期黑色素瘤患者免疫治疗疗效的影响。我们纳入了在安大略省东南部癌症中心和伦敦地区癌症项目接受单药程序性死亡蛋白 1(PD-1)抑制剂治疗的所有晚期不可切除和转移性黑色素瘤患者。我们将基线皮质类固醇使用定义为在免疫治疗开始前 30 天内泼尼松等效剂量≥10mg。我们的研究共有 166 例患者,其中 25 例在 PD-1 抑制剂起始时使用皮质类固醇。基线泼尼松等效剂量≥10mg 对中位总生存期无影响(危险比=1.590,95%置信区间:0.773-3.270,P=0.208)。然而,与基线泼尼松等效剂量 0-49mg 相比,基线泼尼松等效剂量≥50mg 与中位总生存期较差独立相关(危险比=2.313,95%置信区间:1.103-4.830,P=0.026),即使在控制包括基线东部合作肿瘤学组≥2 和基线脑转移等混杂因素后也是如此。在开始 PD-1 抑制剂治疗之前,应考虑尽可能减少不必要的类固醇使用。

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