Bobeff Katarzyna, Krajewska Karolina, Baranska Dobromila, Kotulska Katarzyna, Jozwiak Sergiusz, Mlynarski Wojciech, Trelinska Joanna
Department of Pediatrics, Oncology and Hematology, Medical University of Lodz, Lodz, Poland.
Department of Pediatric Radiology, Medical University Hospital, Lodz, Poland.
Front Neurol. 2021 Apr 9;12:581102. doi: 10.3389/fneur.2021.581102. eCollection 2021.
The aim of this EMINENTS prospective, single-center, open-label, single-arm study was to evaluate the cumulative efficacy and safety of reduced doses of everolimus (maintenance therapy) in patients with tuberous sclerosis and subependymal giant cell astrocytoma (SEGA). The trial included 15 patients who had undergone at least 12 months of treatment with a standard everolimus dose. The dose of everolimus was reduced to three times a week, with a daily dose as in standard regimen. Data of 14 patients were analyzed. SEGA volume (SV) was evaluated at study entry and subsequent time points by an experienced radiologist. Adverse events (AEs) noted during maintenance therapy were compared to the AEs of standard dose period. Patients were followed over a mean duration 58.37 months (95%CI: 45.95-70.78). The differences in SEGA volume between subsequent time points (0, 3, 6,12, 18, 24, 36, 48, and 60 months) were not statistically significant ( = 0.16). At the end of the study, 7 out of 10 patients had stable SEGA volume. No clinical symptoms of progression were observed in any patients. No patient or tumor-related risk factors of progression were identified. Regarding AEs, infections (stomatitis, bronchitis, diarrhea) and laboratory abnormalities (neutropenia, anemia, hyperglycemia) occurred less frequently during maintenance therapy compared to the standard dose regimen. Final results from EMINENTS study confirm that maintenance therapy with everolimus might represent a rational therapeutic option for patients TSC and SEGA after effective full dose treatment. It could be an option for patients who experienced everolimus-related AEs, instead of discontinuation of therapy. Careful evaluation of possible progression, especially concerning first six months of maintenance therapy should be advised. www.drks.de, identifier DRKS00005584.
这项EMINENTS前瞻性、单中心、开放标签、单臂研究的目的是评估低剂量依维莫司(维持治疗)对结节性硬化症和室管膜下巨细胞星形细胞瘤(SEGA)患者的累积疗效和安全性。该试验纳入了15名接受标准依维莫司剂量治疗至少12个月的患者。依维莫司剂量减至每周三次,每日剂量与标准方案相同。分析了14名患者的数据。由经验丰富的放射科医生在研究入组时及后续时间点评估SEGA体积(SV)。将维持治疗期间记录的不良事件(AE)与标准剂量期的AE进行比较。对患者进行了平均58.37个月(95%CI:45.95 - 70.78)的随访。后续时间点(0、3、6、12、18、24、36、48和60个月)之间SEGA体积差异无统计学意义( = 0.16)。研究结束时,10名患者中有7名SEGA体积稳定。未观察到任何患者出现进展的临床症状。未发现患者或肿瘤相关的进展危险因素。关于AE,与标准剂量方案相比,维持治疗期间感染(口腔炎、支气管炎、腹泻)和实验室异常(中性粒细胞减少、贫血、高血糖)的发生频率较低。EMINENTS研究的最终结果证实,依维莫司维持治疗可能是结节性硬化症和SEGA患者在有效全剂量治疗后的合理治疗选择。对于经历过依维莫司相关AE的患者,这可能是一种选择,而不是停止治疗。建议仔细评估可能的进展,尤其是在维持治疗的前六个月。www.drks.de,标识符DRKS00005584