Brakemeier Susanne, Vogt Lars, Adams Lisa, Zukunft Bianca, Diederichs Gerd, Hamm Bernd, Budde Klemens, Makowski Marcus R
Department of Nephrology and Medical Intensive Care, Charité, Berlin, Germany.
Department of Radiology, Charité, Berlin, Germany.
PLoS One. 2017 Dec 12;12(12):e0189132. doi: 10.1371/journal.pone.0189132. eCollection 2017.
Tuberous sclerosis complex (TSC)-associated renal angiomyolipoma (AML) have a high lifetime risk of acute bleeding. MTOR-inhibitors are a promising novel treatment for TSC-AML, however adequate response to therapy can be difficult to assess. Early changes in MRI signal may serve as a novel early indicator for a satisfactory response to mTOR-inhibitor therapy of AML.
Thirty-eight patients with the definite diagnosis of tuberous sclerosis receiving everolimus therapy and n = 19 patients without specific therapy were included. 1.5 Tesla MRI was performed including sequences with a selective fat suppression. Patients were investigated prior to the initiation of therapy (baseline) and after <3 months (n = 21 patients), 3 to 6 months (n = 32) and 18 to 24 months (n = 28). Signal and size changes of renal AMLs were assessed at all different timepoints. Signal-to-noise-ratio (SNR), contrast-to-noise-ratio (CNR) and size of angiomyolipomas were evaluated.
Signal changes in 273 AMLs were evaluated. A significant and strong decrease of the CNR of AMLs following the initiation of therapy was measured in the fat-suppressed MR sequence at all time points, compared to the baseline: From 7.41±6.98 to 3.84±6.25 (p ≤ 0.05p = 0.002), 3.36±6.93 (p<0.0001), and 2.50±6.68 (p<0.0001) after less than 3 months, 3-6 months or 18-24 months of everolimus treatment, respectively. Also, a significant, however less pronounced, reduction of angiomyolipoma size in the different groups was measured (from baseline 2022.2±2657.7 mm2 to 1854.4±1670.9 mm2 (p = 0.009), 1875.5±3190.1 mm2 (p<0.001), and 1365.8 ± 1628.8 mm2 (p<0.0001) after less than 3 months, 3-6 months or 18-24 months of everolimus treatment, respectively). No significant changes in CNR (p>0.05) and size (p>0.05) were measured in the control group.
mTOR inhibitor therapy in TSC patients results in an early and pronounced fatty transformation of AMLs on MRI. Fatty transformation could represent a novel early indicator of response to therapy in this patient collective.
结节性硬化症(TSC)相关肾血管平滑肌脂肪瘤(AML)终生有急性出血的高风险。雷帕霉素靶蛋白(mTOR)抑制剂是治疗TSC-AML的一种有前景的新型疗法,然而,对治疗的充分反应可能难以评估。MRI信号的早期变化可能是AML对mTOR抑制剂治疗产生满意反应的一种新型早期指标。
纳入38例确诊为结节性硬化症且接受依维莫司治疗的患者以及19例未接受特殊治疗的患者。采用1.5特斯拉MRI进行检查,包括选择性脂肪抑制序列。在治疗开始前(基线)以及治疗后<3个月(21例患者)、3至6个月(32例)和18至24个月(28例)对患者进行检查。在所有不同时间点评估肾AML的信号和大小变化。评估血管平滑肌脂肪瘤的信噪比(SNR)、对比噪声比(CNR)和大小。
评估了273个AML的信号变化。与基线相比,在所有时间点的脂肪抑制MR序列中,治疗开始后AML的CNR均显著且大幅下降:依维莫司治疗少于3个月、3至6个月或18至24个月后,分别从7.41±6.98降至3.84±6.25(p≤0.05,p = 0.002)、3.36±6.93(p<0.0001)和2.50±6.68(p<0.0001)。此外,不同组中血管平滑肌脂肪瘤大小也有显著但不太明显的减小(从基线的2022.2±2657.7mm²分别降至依维莫司治疗少于3个月、3至6个月或18至24个月后的1854.4±1670.9mm²(p = 0.009)、1875.5±3190.1mm²(p<0.001)和1365.8±1628.8mm²(p<0.0001))。对照组的CNR(p>0.05)和大小(p>0.05)无显著变化。
TSC患者的mTOR抑制剂治疗导致MRI上AML早期且明显的脂肪变性。脂肪变性可能是该患者群体对治疗反应的一种新型早期指标。