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Inavolisib用于激素受体阳性、人表皮生长因子受体2阴性的晚期乳腺癌:临床试验及对患者可及性的影响

Inavolisib for HR-Positive, HER2-Negative Advanced Breast Cancer: Clinical Trials and Patient Access Implication.

作者信息

Arabshomali Arman, Goswami Swarnali, Masurkar Prajakta P

机构信息

Department of Pharmacy Administration, University of Mississippi School of Pharmacy, MS.

Neurocrine Biosciences, Inc., San Diego, CA.

出版信息

Am J Clin Oncol. 2025 Jul 11. doi: 10.1097/COC.0000000000001209.

Abstract

OBJECTIVES

Breast cancer remains the most prevalent cancer among women in the United States, with hormone receptor-positive (HR+) and HER2-negative subtypes comprising a significant proportion of cases. Despite advancements in treatment, resistance to endocrine therapies remains a substantial clinical challenge, especially in patients with mutations in the PIK3CA gene.

METHODS

A literature review was conducted to evaluate the safety and efficacy of inavolisib in breast cancer. Studies published through November 2024 were identified using PubMed, Google Scholar, and ClinicalTrials.gov. Phases I to III clinical trials in English were included. The review focused on safety outcomes (eg, serious adverse events) and efficacy outcomes (eg, progression-free survival), which were summarized narratively.

RESULTS

Inavolisib, a selective PI3Kα inhibitor, presents a promising option for patients with PIK3CA-mutated HR+HER2-negative advanced or metastatic breast cancer. In the INAVO120 trial, inavolisib combined with palbociclib and fulvestrant significantly extended progression-free survival (PFS) in patients with PIK3CA mutations. The median PFS was 15.0 months for the treatment arm compared with 7.3 months in the placebo group (hazard ratio: 0.43, P<0.001). The objective response rate (ORR) was 58.4% in the treatment arm, underscoring the drug's antitumor efficacy. Safety profiles revealed manageable adverse events, primarily hyperglycemia, neutropenia, and stomatitis. The incidence of these side effects was notable but manageable with appropriate supportive care. Inavolisib offers a new treatment for HR+HER2-negative advanced breast cancer, showing promising efficacy and safety. However, implementation challenges include high costs, insurance coverage issues, and limited access to required genetic testing through FoundationOne Liquid CDx assay, potentially creating barriers to equitable patient access.

CONCLUSIONS

Inavolisib represents a significant advancement in the treatment of advanced HR+HER2-negative breast cancer, offering an effective option for patients with PIK3CA mutations. However, to fully realize its potential, health care systems must address challenges related to patient access, insurance coverage, and the availability of companion diagnostics. Further long-term studies will be essential to assess the enduring impact of this treatment on patient outcomes.

摘要

目的

乳腺癌仍是美国女性中最常见的癌症,激素受体阳性(HR+)和人表皮生长因子受体2阴性(HER2-)亚型占相当大比例的病例。尽管治疗取得了进展,但对内分泌治疗的耐药性仍然是一个重大的临床挑战,尤其是在携带PIK3CA基因突变的患者中。

方法

进行了一项文献综述,以评估inavolisib在乳腺癌中的安全性和疗效。使用PubMed、谷歌学术和ClinicalTrials.gov检索截至2024年11月发表的研究。纳入了英文的I期至III期临床试验。该综述重点关注安全性结果(如严重不良事件)和疗效结果(如无进展生存期),并进行了叙述性总结。

结果

Inavolisib是一种选择性PI3Kα抑制剂,为携带PIK3CA突变的HR+HER2-晚期或转移性乳腺癌患者提供了一个有前景的选择。在INAVO120试验中,inavolisib联合哌柏西利和氟维司群显著延长了携带PIK3CA突变患者的无进展生存期(PFS)。治疗组的中位PFS为15.0个月,而安慰剂组为7.3个月(风险比:0.43,P<0.001)。治疗组的客观缓解率(ORR)为58.4%,突出了该药物的抗肿瘤疗效。安全性概况显示不良事件可控,主要为高血糖、中性粒细胞减少和口腔炎。这些副作用的发生率虽显著,但通过适当的支持性护理可得到控制。Inavolisib为HR+HER2-晚期乳腺癌提供了一种新的治疗方法,显示出有前景的疗效和安全性。然而,实施方面的挑战包括成本高昂、保险覆盖问题以及通过FoundationOne Liquid CDx检测进行所需基因检测的机会有限,这可能会给患者公平获得治疗带来障碍。

结论

Inavolisib代表了晚期HR+HER2-乳腺癌治疗的重大进展,为携带PIK3CA突变的患者提供了一种有效的选择。然而,要充分发挥其潜力,医疗保健系统必须应对与患者获得治疗、保险覆盖以及伴随诊断可用性相关的挑战。进一步的长期研究对于评估这种治疗对患者预后的持久影响至关重要。

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