Kirzinger Lukas, Boy Sandra, Marienhagen Jörg, Schuierer Gerhard, Neu Reiner, Ried Michael, Hofmann Hans-Stefan, Wiebe Karsten, Ströbel Philipp, May Christoph, Kleylein-Sohn Julia, Baierlein Claudia, Bogdahn Ulrich, Marx Alexander, Schalke Berthold
Department of Neurology, University of Regensburg, Regensburg, Germany.
Department of Nuclear Medicine, University of Regensburg, Regensburg, Germany.
PLoS One. 2016 Dec 16;11(12):e0168215. doi: 10.1371/journal.pone.0168215. eCollection 2016.
Therapeutic options to cure advanced, recurrent, and unresectable thymomas are limited. The most important factor for long-term survival of thymoma patients is complete resection (R0) of the tumor. We therefore evaluated the response to and the induction of resectability of primarily or locally recurrent unresectable thymomas and thymic carcinomas by octreotide Long-Acting Release (LAR) plus prednisone therapy in patients with positive octreotide scans. In this open label, single-arm phase II study, 17 patients with thymomas considered unresectable or locally recurrent thymoma (n = 15) and thymic carcinoma (n = 2) at Masaoka stage III were enrolled. Octreotide LAR (30 mg once every 2 weeks) was administered in combination with prednisone (0.6 mg/kg per day) for a maximum of 24 weeks (study design according to Fleming´s one sample multiple testing procedure for phase II clinical trials). Tumor size was evaluated by volumetric CT measurements, and a decrease in tumor volume of at least 20% at week 12 compared to baseline was considered as a response. We found that octreotide LAR plus prednisone elicited response in 15 of 17 patients (88%). Median reduction of tumor volume after 12 weeks of treatment was 51% (range 20%-86%). Subsequently, complete surgical resection was achieved in five (29%) and four patients (23%) after 12 and 24 weeks, respectively. Octreotide LAR plus prednisone treatment was discontinued in two patients before week 12 due to unsatisfactory therapeutic effects or adverse events. The most frequent adverse events were gastrointestinal (71%), infectious (65%), and hematological (41%) complications. In conclusion, octreotide LAR plus prednisone is efficacious in patients with primary or recurrent unresectable thymoma with respect to tumor regression. Octreotide LAR plus prednisone was well tolerated and adverse events were in line with the known safety profile of both agents.
治疗晚期、复发性和不可切除胸腺瘤的选择有限。胸腺瘤患者长期生存的最重要因素是肿瘤的完整切除(R0)。因此,我们评估了长效奥曲肽(LAR)联合泼尼松治疗对奥曲肽扫描阳性患者的原发性或局部复发性不可切除胸腺瘤和胸腺癌的反应以及可切除性的诱导情况。在这项开放标签的单臂II期研究中,纳入了17例Masaoka III期被认为不可切除或局部复发胸腺瘤(n = 15)和胸腺癌(n = 2)的患者。给予奥曲肽LAR(每2周30 mg)联合泼尼松(每天0.6 mg/kg),最长治疗24周(研究设计根据Fleming的II期临床试验单样本多重检验程序)。通过容积CT测量评估肿瘤大小,与基线相比,第12周时肿瘤体积至少减少20%被视为有反应。我们发现,17例患者中有15例(88%)对奥曲肽LAR联合泼尼松有反应。治疗12周后肿瘤体积的中位数减少了51%(范围为20%-86%)。随后,分别在12周和24周后,5例(29%)和4例(23%)患者实现了完整手术切除。由于治疗效果不佳或不良事件,2例患者在第12周前停止了奥曲肽LAR联合泼尼松治疗。最常见的不良事件是胃肠道并发症(71%)、感染并发症(65%)和血液学并发症(41%)。总之,对于原发性或复发性不可切除胸腺瘤患者,奥曲肽LAR联合泼尼松在肿瘤消退方面是有效的。奥曲肽LAR联合泼尼松耐受性良好,不良事件与两种药物已知的安全性特征相符。