Division of Pediatric Hematology/Oncology, Department of Pediatrics, Nationwide Children's Hospital, Columbus, OH, USA.
Division of Neuroradiology, Department of Radiology, NYU Langone Health, New York, NY, USA.
J Neurooncol. 2018 Sep;139(3):749-755. doi: 10.1007/s11060-018-2922-5. Epub 2018 Jun 8.
Epidermal growth factor receptors EGFR and ErbB2 are overexpressed in schwannomas and meningiomas. Preclinical and clinical data indicate that lapatinib, an EGFR/ErbB2 inhibitor, has antitumor activity against vestibular schwannomas in neurofibromatosis type 2 (NF2) patients. Its antitumor activity against meningiomas, however, is unknown.
We conducted a retrospective review of patients with NF2 and progressive vestibular schwannomas treated on a phase 2 clinical trial with lapatinib (NCT00973739). We included patients with at least one volumetrically measurable meningioma (> 0.5 cm) who received at least five 28-day courses of treatment. Patients received lapatinib 1500 mg daily. Meningioma response was assessed using 3-dimensional MRI volumetrics. Progressive meningioma growth and response were defined as + 20 and - 20% change in tumor volume from baseline, respectively. Off-treatment was defined as any period > 5 months without lapatinib.
Eight patients (ages: 20-58 years) who met criteria had 17 evaluable meningiomas with a combined volume of 61.35 cc at baseline, 61.17 cc during treatment, and 108.86 cc (+ 77.44% change) off-treatment, p = 0.0033. Median time on-treatment and off-treatment was 15.5 and 16.7 months, respectively. On-treatment mean and median annualized growth rates were 10.67 and 1.32%, respectively. Off-treatment mean and median annualized growth rates were 20.05 and 10.42%, respectively. The best volumetric response was - 26.1% after 23 months on lapatinib. Two tumors increased > 20% volumetrically on-treatment, compared to eight tumors off-treatment.
These data suggest that lapatinib may have growth-inhibitory effects on meningiomas in NF2 patients, and support prospective studies of lapatinib for NF2 patients with progressive meningiomas.
表皮生长因子受体 EGFR 和 ErbB2 在神经鞘瘤和脑膜瘤中过度表达。临床前和临床数据表明,拉帕替尼,一种 EGFR/ErbB2 抑制剂,对神经纤维瘤病 2 型(NF2)患者的前庭神经鞘瘤具有抗肿瘤活性。然而,其对脑膜瘤的抗肿瘤活性尚不清楚。
我们对接受拉帕替尼(NCT00973739)二期临床试验治疗的 NF2 伴进行性前庭神经鞘瘤患者进行了回顾性研究。我们纳入了至少有一个可测量脑膜瘤(>0.5cm)的患者,这些患者至少接受了 5 个 28 天疗程的治疗。患者每天接受拉帕替尼 1500mg。使用 3 维 MRI 体积测量法评估脑膜瘤的反应。脑膜瘤进展和反应分别定义为肿瘤体积相对于基线增加或减少 20%。停药定义为任何无拉帕替尼治疗的时间>5 个月。
符合条件的 8 名患者(年龄 20-58 岁)共 17 个可评估脑膜瘤,基线时脑膜瘤的总体积为 61.35cc,治疗期间为 61.17cc,停药时为 108.86cc(增加 77.44%),p=0.0033。治疗中位时间和停药中位时间分别为 15.5 个月和 16.7 个月。治疗期间的平均和中位年化生长率分别为 10.67%和 1.32%。停药期间的平均和中位年化生长率分别为 20.05%和 10.42%。在拉帕替尼治疗 23 个月后,最佳的体积反应为 -26.1%。2 个肿瘤在治疗期间的体积增加超过 20%,而 8 个肿瘤在停药期间体积增加超过 20%。
这些数据表明,拉帕替尼可能对 NF2 患者的脑膜瘤有生长抑制作用,并支持对 NF2 患者进行前瞻性研究,以评估拉帕替尼对进展性脑膜瘤的疗效。