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CAPItello-291 研究的通俗易懂总结:卡培他滨联合卡培他滨在激素受体阳性晚期乳腺癌中的应用。

A plain language summary of the CAPItello-291 study: Capivasertib in hormone receptor-positive advanced breast cancer.

机构信息

Royal Marsden Hospital, Institute of Cancer Research, London, UK.

Medical Oncology Department, Vall d'Hebron University Hospital, Barcelona, Spain.

出版信息

Future Oncol. 2024;20(37):2901-2913. doi: 10.1080/14796694.2024.2390791. Epub 2024 Sep 16.

Abstract

WHAT IS THIS SUMMARY ABOUT?: This is a summary of the article discussing the results of the CAPItello-291 study. In the study, participants had advanced breast cancer that could not be completely removed with surgery, and that was diagnosed as a type of breast cancer where tumor cells had hormone receptors (HR-positive) but did not have HER2 receptors (HER2-negative). All participants were also required to have previously received treatment with a type of therapy called an aromatase inhibitor (with or without a CDK4/6 inhibitor), but over time their cancer cells had still grown or spread. The CAPItello-291 study researchers wanted to find out if a treatment combination of the medications capivasertib plus fulvestrant worked better than placebo plus fulvestrant. Capivasertib is a drug that blocks the activity of a protein called AKT, which is found inside breast cancer cells.

WHAT ARE THE KEY TAKEAWAYS?: The main finding was that participants who took capivasertib plus fulvestrant lived longer without their disease getting worse (progressing) compared with those treated with placebo plus fulvestrant. This is called progression-free survival. This result was seen across all participants (median progression-free survival of 7.2 months with capivasertib plus fulvestrant vs 3.6 months with placebo plus fulvestrant). It was also seen in participants whose tumors had detectable genetic alterations in genes called PIK3CA, AKT1, and/ or PTEN (median progression-free survival of 7.3 months with capivasertib plus fulvestrant vs 3.1 months with placebo plus fulvestrant). The most common side effects experienced by participants included diarrhea and different types of rash. These were as expected (given how capivasertib works). The CAPItello-291 study is still ongoing, and more results are expected to be released in the future.

WHAT WERE THE MAIN CONCLUSIONS REPORTED BY THE RESEARCHERS?: Results from the CAPItello-291 study showed that capivasertib plus fulvestrant compared with placebo plus fulvestrant improved progression-free survival in participants with HR-positive/ HER2-negative advanced breast cancer whose cancer had grown or spread despite hormone therapy (with/without a CDK4/6 inhibitor). NCT04305496 (CAPItello-291) (ClinicalTrials.gov).

摘要

这是一篇关于 CAPItello-291 研究结果的摘要。在这项研究中,参与者患有无法通过手术完全切除的晚期乳腺癌,且被诊断为一种激素受体阳性(HR 阳性)但无 HER2 受体(HER2 阴性)的乳腺癌。所有参与者还必须接受过一种称为芳香酶抑制剂的治疗(有或没有 CDK4/6 抑制剂),但随着时间的推移,他们的癌细胞仍在生长或扩散。CAPItello-291 研究人员想了解药物 capivasertib 加 fulvestrant 的治疗组合是否比安慰剂加 fulvestrant 效果更好。Capivasertib 是一种抑制一种名为 AKT 的蛋白质活性的药物,该蛋白质存在于乳腺癌细胞内。

主要发现是,与安慰剂加 fulvestrant 相比,接受 capivasertib 加 fulvestrant 治疗的参与者疾病恶化(进展)的时间更长,无进展生存期更长。这称为无进展生存期。这一结果在所有参与者中均可见(capivasertib 加 fulvestrant 的中位无进展生存期为 7.2 个月,安慰剂加 fulvestrant 为 3.6 个月)。在肿瘤存在称为 PIK3CA、AKT1 和/或 PTEN 的基因可检测遗传改变的参与者中也可见到这一结果(capivasertib 加 fulvestrant 的中位无进展生存期为 7.3 个月,安慰剂加 fulvestrant 为 3.1 个月)。参与者经历的最常见副作用包括腹泻和不同类型的皮疹。这些副作用是可以预期的(鉴于 capivasertib 的作用方式)。CAPItello-291 研究仍在进行中,预计未来会有更多结果公布。

CAPItello-291 研究的结果表明,与安慰剂加 fulvestrant 相比,capivasertib 加 fulvestrant 改善了 HR 阳性/HER2 阴性晚期乳腺癌患者的无进展生存期,这些患者的癌症在激素治疗(有/无 CDK4/6 抑制剂)后仍在生长或扩散。NCT04305496(CAPItello-291)(ClinicalTrials.gov)。

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