Kahraman Deniz, Theurich Sebastian, Rothe Achim, Kuhnert Georg, Sasse Stephanie, Scheid Christoph, Dietlein Markus, Drzezga Alexander, von Bergwelt-Baildon Michael, Kobe Carsten
Department of Nuclear Medicine.
Leuk Lymphoma. 2014 Apr;55(4):811-6. doi: 10.3109/10428194.2013.819575. Epub 2013 Jul 29.
Brentuximab vedotin has emerged as a possible treatment option in patients suffering from relapsed and refractory Hodgkin lymphoma (HL). We investigated the role of 18-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) for monitoring treatment response to brentuximab vedotin in patients with relapsed and refractory HL. Twelve consecutive, heavily pretreated patients with relapsed and refractory HL treated with brentuximab vedotin were available for analysis. FDG-PET/CT studies were performed early during treatment after a median of 3 cycles (range, 2-5 cycles), and were analyzed visually using a 5-point scale (5PS) and quantitatively using the maximum standardized uptake value (SUV(max)) and the three-dimensional (3D) isocontour at 50% of the maximum pixel value (SUV(50)) in the hottest single lesion. The median follow-up in our study cohort was 16 months (range, 5-30 months). The median progression-free survival (PFS) was 12.5 months and PFS at 12 months was 58%. Patients treated with brentuximab vedotin and negative interim FDG-PET/CT assessed by visual or quantitative analysis demonstrated a significantly prolonged PFS compared to patients with positive interim FDG-PET/CT. The 1-year PFS was 100% in patients with negative interim FDG-PET/CT assessed by visual analysis, whereas patients with positive interim FDG-PET/CT had a worse outcome with a 1-year PFS of 38% (p = 0.033). The 1-year PFS was 75% in patients with negative interim FDG-PET/CT assessed by quantitative analysis using the SUV(50), whereas patients with positive interim FDG-PET/CT had a worse outcome with a 1-year PFS of 25% (p = 0.017) Interim FDG-PET/CT might be a suitable diagnostic approach to predict response to brentuximab vedotin in relapsed and refractory HL.
本妥昔单抗已成为复发难治性霍奇金淋巴瘤(HL)患者可能的治疗选择。我们研究了18-氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET/CT)在监测复发难治性HL患者对本妥昔单抗治疗反应中的作用。连续12例接受本妥昔单抗治疗的复发难治性HL患者,均经过大量预处理,可供分析。FDG-PET/CT检查在治疗早期进行,中位周期数为3个周期(范围2-5个周期),采用5分制(5PS)进行视觉分析,并使用最大标准化摄取值(SUV(max))和最热点单个病灶中最大像素值50%处的三维(3D)等轮廓线(SUV(50))进行定量分析。我们研究队列的中位随访时间为16个月(范围5-30个月)。中位无进展生存期(PFS)为12.5个月,12个月时的PFS为58%。与中期FDG-PET/CT阳性的患者相比,经视觉或定量分析评估为中期FDG-PET/CT阴性且接受本妥昔单抗治疗的患者PFS显著延长。经视觉分析评估为中期FDG-PET/CT阴性的患者1年PFS为100%,而中期FDG-PET/CT阳性的患者预后较差,1年PFS为38%(p = 0.033)。使用SUV(50)进行定量分析评估为中期FDG-PET/CT阴性的患者1年PFS为75%,而中期FDG-PET/CT阳性的患者预后较差,1年PFS为25%(p = 0.017)。中期FDG-PET/CT可能是预测复发难治性HL患者对本妥昔单抗治疗反应的合适诊断方法。