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含依维莫司的治疗与常规治疗在治疗有 PI3K/AKT/mTOR 突变的难治性乳腺癌患者中的比较:一项回顾性研究。

Everolimus-containing therapy vs conventional therapy in the treatment of refractory breast cancer patients with PI3K/AKT/mTOR mutations: A retrospective study.

机构信息

Department of Breast Medical Oncology, Zhejiang Cancer Hospital, Hangzhou, China.

The Medical Department, 3D Medicines Inc, Shanghai, China.

出版信息

Cancer Med. 2019 Sep;8(12):5544-5553. doi: 10.1002/cam4.2460. Epub 2019 Aug 6.

Abstract

BACKGROUND

Previous case reports have shown the promising antitumor activity of everolimus in solid tumors containing molecular aberrations in PI3K/ATK/mTOR pathway, however, whether it is effective in patients with breast cancer remains unknown. Therefore, we conducted this retrospective cohort study to compare the efficacy of molecularly matched targeted therapy with everolimus to conventional therapy in refractory breast cancer patients harboring PI3K/ATK/mTOR pathway activating mutations.

METHODS

Refractory metastatic breast cancer patients who have received molecular screening using next-generation sequencing (NGS) between September 8, 2015 and October 30, 2017 in two sites were screened for this study. The primary outcome was progression-free survival (PFS). The secondary outcomes were overall response rate (ORR), disease control rate (DCR), and safety profile.

RESULTS

A total of 78 patients were screened for analysis, amongst all, 52 (66.7%) had at least one gene mutation in PI3K/AKT/mTOR pathway. The most common mutation fell in PIK3CA (76.9%, 40/52) with a mutational prevalence of 51.3%. Of the 32 patients who were eligible for efficacy analysis, patients in the everolimus group (n = 19) exhibited shorter PFS than those in the conventional group (n = 13) (median, 1.9 vs 6.1 months; HR, 3.6; 95% CI, 1.48-8.81; P = .0005). ORR was 15.4% (2/13) in the everolimus group and 23.1% (3/13) in the conventional group (P = 1.000), and DCR was 30.8% (4/13) and 100% (13/13) for each group, respectively (P = .000). The incidence of grade 3-5 adverse events was relatively higher in the conventional group (38.5%, 5/13) than that in the everolimus group (26.3%, 5/19).

CONCLUSIONS

Our findings suggested that everolimus might not be effective for cancer patients harboring mutations in PI3K/ATK/mTOR pathway and physicians should be cautious about its off-label use in clinical practice.

摘要

背景

先前的病例报告显示,依维莫司在含有 PI3K/AKT/mTOR 通路分子异常的实体肿瘤中具有有前景的抗肿瘤活性,然而,其在乳腺癌患者中的疗效尚不清楚。因此,我们进行了这项回顾性队列研究,以比较分子匹配靶向治疗与依维莫司与常规治疗在携带 PI3K/AKT/mTOR 通路激活突变的难治性乳腺癌患者中的疗效。

方法

2015 年 9 月 8 日至 2017 年 10 月 30 日期间,在两个地点使用下一代测序(NGS)对难治性转移性乳腺癌患者进行了分子筛选,筛选出符合条件的患者参加本研究。主要结局是无进展生存期(PFS)。次要结局是总缓解率(ORR)、疾病控制率(DCR)和安全性。

结果

共有 78 名患者接受了分析,其中 52 名(66.7%)患者至少有一种 PI3K/AKT/mTOR 通路的基因突变。最常见的突变发生在 PIK3CA(76.9%,40/52),突变率为 51.3%。在 32 名符合疗效分析条件的患者中,依维莫司组(n=19)的患者 PFS 短于常规组(n=13)(中位数,1.9 与 6.1 个月;HR,3.6;95%CI,1.48-8.81;P=0.0005)。依维莫司组的 ORR 为 15.4%(2/13),常规组为 23.1%(3/13)(P=1.000),DCR 分别为 30.8%(4/13)和 100%(13/13)(P=0.000)。常规组不良事件发生率(38.5%,5/13)明显高于依维莫司组(26.3%,5/19)。

结论

我们的研究结果表明,依维莫司可能对携带 PI3K/AKT/mTOR 通路突变的癌症患者无效,医生在临床实践中应谨慎使用其作为标签外用药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365d/6745827/67895966e995/CAM4-8-5544-g001.jpg

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