Department of Oncology, Institut Curie-St Cloud, 92210, Saint Cloud, France.
Department of Genetics, Institut Curie-Paris , 75005, Paris, France.
Neuro Oncol. 2023 Feb 14;25(2):365-374. doi: 10.1093/neuonc/noac180.
Patients with HER2-positive breast cancer (HER2 + BC) develop central nervous system metastases twice as often as patients with luminal HER2-negative breast cancer. Leptomeningeal progression results in a drastically altered prognosis with limited therapeutic options. This phase II study was conducted to assess the efficacy of intrathecal (IT) trastuzumab in HER2 + BC patients with leptomeningeal metastasis (LM), based on a phase I dose-escalation study that had determined the recommended weekly dose of 150 mg for phase II.
Eligible patients received weekly administrations of 150 mg of IT trastuzumab. The primary endpoint was clinical neurologic progression-free survival (LM-related-PFS) after 8 weeks. Overall survival (OS), toxicities, and quality of life (QoL) were secondary endpoints.
Among the 19 enrolled patients, 16 (84%) had concomitant brain metastases, 15 of them had received prior radiotherapy to the brain. All patients had received at least one line of systemic anti-HER2 therapy. After 8 weeks, 14 patients (74%) were free of neurological progression. The median LM-related-PFS was 5.9 months and the median OS was 7.9 months. According to the QLQ-C30 and BN20 scales, the global health-related QoL status seemed preserved and no toxicity above grade 3 was observed.
Conducting studies on patients with LM poses significant challenges and ethical dilemmas inherent to this population. Despite some limits, this phase II study's findings in terms of clinical neurologic response and QoL's control confirms weekly administration of 150 mg of IT trastuzumab as a valuable option for HER + BC patients with LM and support the interest for further investigations.
HER2 阳性乳腺癌(HER2+BC)患者发生中枢神经系统转移的频率是 luminal HER2 阴性乳腺癌患者的两倍。软脑膜进展导致预后明显恶化,治疗选择有限。本 II 期研究旨在评估鞘内(IT)曲妥珠单抗治疗 HER2+BC 伴软脑膜转移(LM)患者的疗效,该研究基于 I 期剂量递增研究,确定了 II 期每周 150mg 的推荐剂量。
符合条件的患者每周接受 150mg IT 曲妥珠单抗治疗。主要终点是 8 周后临床神经进展无进展生存期(LM 相关-PFS)。总生存期(OS)、毒性和生活质量(QoL)为次要终点。
在 19 名入组患者中,16 名(84%)伴有脑转移,其中 15 名患者曾接受过脑部放疗。所有患者均接受过至少一线抗 HER2 系统治疗。8 周后,14 名患者(74%)无神经进展。LM 相关-PFS 的中位数为 5.9 个月,OS 的中位数为 7.9 个月。根据 QLQ-C30 和 BN20 量表,全球健康相关 QoL 状况似乎得到维持,未观察到 3 级以上的毒性。
针对 LM 患者开展研究具有挑战性,且存在该人群特有的伦理难题。尽管存在一些局限性,但本 II 期研究在临床神经反应和 QoL 控制方面的结果证实了每周给予 150mg IT 曲妥珠单抗对 HER2+BC 伴 LM 患者是一种有价值的选择,并支持进一步研究的兴趣。