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在转移性去势抵抗性前列腺癌中,阿帕他胺联合阿比特龙与安慰剂联合阿比特龙的安全性概况

Safety Profile of Ipatasertib Plus Abiraterone vs Placebo Plus Abiraterone in Metastatic Castration-resistant Prostate Cancer.

作者信息

Matsubara Nobuaki, de Bono Johann, Sweeney Christopher, Chi Kim N, Olmos David, Sandhu Shahneen, Massard Christophe, Garcia Josep, Chen Geng, Harris Adam, Schenkel Fanny, Sane Rucha, Hinton Healther, Bracarda Sergio, Sternberg Cora N

机构信息

Division of Breast and Medical Oncology, National Cancer Center Hospital East, Chiba, Japan.

The Institute of Cancer Research and the Royal Marsden Hospital, London, UK.

出版信息

Clin Genitourin Cancer. 2023 Apr;21(2):230-237.e1. doi: 10.1016/j.clgc.2023.01.001. Epub 2023 Jan 7.

Abstract

PURPOSE

Adding ipatasertib to abiraterone and prednisone/prednisolone significantly improved radiographic progression-free survival for patients with metastatic castration-resistant prostate cancer (mCRPC) with PTEN-loss tumours by immunohistochemistry in the IPATential150 trial (NCT03072238). Here we characterise the safety of these agents in subpopulations and assess manageability of key adverse events (AEs).

MATERIALS AND METHODS

In this randomised, double-blind, phase 3 trial, patients with previously untreated asymptomatic or mildly symptomatic mCRPC were randomised 1:1 to receive ipatasertib-abiraterone or placebo-abiraterone (all with prednisone/prednisolone). AEs were analysed, focusing on key AEs of diarrhoea, hyperglycaemia, rash and transaminase increased.

RESULTS

1097 patients received study medication and were assessed for safety (47% with PTEN-loss tumours by immunohistochemistry and 20% were Asian). Ipatasertib was associated with increased Grade 3/4 AEs and AEs leading to treatment discontinuation vs placebo. The rate of discontinuation of ipatasertib was 18% in patients with PTEN-loss and 21% overall. The frequencies of all-grade, Grade 3/4 and serious AEs were similar between the PTEN-loss and overall populations. Diarrhoea, hyperglycaemia, rash and transaminase elevation were more frequent in ipatasertib-treated patients, appearing rapidly after treatment initiation (median onset: 8-43 days for ipatasertib arm and 56-104 days for placebo). The ipatasertib discontinuation rate was 32% and 18% in Asian and non-Asian patients, respectively, despite similar baseline characteristics and Grade 3/4 AE frequencies between groups.

CONCLUSIONS

Ipatasertib plus abiraterone had an overall tolerable safety profile consistent with known toxicities. More AEs leading to drug discontinuation were observed with ipatasertib than placebo, but incidence would likely be lessened with prophylactic measures.

摘要

目的

在IPATential150试验(NCT03072238)中,通过免疫组化法检测,对于携带PTEN缺失肿瘤的转移性去势抵抗性前列腺癌(mCRPC)患者,在阿比特龙和泼尼松/泼尼松龙基础上加用ipatasertib可显著改善影像学无进展生存期。在此,我们对这些药物在亚组人群中的安全性进行了特征分析,并评估了关键不良事件(AE)的可管理性。

材料与方法

在这项随机、双盲、3期试验中,将既往未接受治疗的无症状或轻度症状性mCRPC患者按1:1随机分组,分别接受ipatasertib-阿比特龙或安慰剂-阿比特龙(均联合泼尼松/泼尼松龙)治疗。对不良事件进行分析,重点关注腹泻、高血糖、皮疹和转氨酶升高这些关键不良事件。

结果

1097例患者接受了研究药物治疗并进行了安全性评估(免疫组化法检测显示47%为PTEN缺失肿瘤患者,20%为亚洲患者)。与安慰剂相比,ipatasertib与3/4级不良事件及导致治疗中断的不良事件增加相关。在PTEN缺失患者中,ipatasertib的停药率为18%,总体停药率为21%。PTEN缺失人群和总体人群中,所有级别、3/4级及严重不良事件的发生率相似。腹泻、高血糖、皮疹和转氨酶升高在接受ipatasertib治疗的患者中更为常见,在治疗开始后迅速出现(中位发病时间:ipatasertib组为8 - 43天,安慰剂组为56 - 104天)。尽管两组患者的基线特征和3/4级不良事件发生率相似,但亚洲和非亚洲患者中ipatasertib的停药率分别为32%和18%。

结论

Ipatasertib联合阿比特龙的总体安全性可耐受,与已知毒性相符。与安慰剂相比,观察到更多因ipatasertib导致停药的不良事件,但采取预防措施可能会降低其发生率。

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