Furtner Julia, Schöpf Veronika, Seystahl Katharina, Le Rhun Emilie, Rudà Roberta, Roelcke Ulrich, Koeppen Susanne, Berghoff Anna Sophie, Marosi Christine, Clement Paul, Faedi Marina, Watts Colin, Wick Wolfgang, Soffietti Riccardo, Weller Michael, Preusser Matthias
Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria (J.F., V.S.); Department of Psychology, University of Graz, Graz, Austria (V.S.); BioTechMed, Graz, Austria (V.S.); Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland (K.S., M.W.); Department of Neuro-oncology, University Hospital, Lille, France (E.L.R.); Breast Cancer Department, Oscar Lambret Center, Lille, France (E.L.R.); PRISM Inserm U1191, Villeneuve D'Ascq, France (E.L.R.); Department of Neuro-Oncology, University of Torino, Torino, Italy (R.R., R.S.); Department of Neurology and Brain Tumor Center, Cantonal Hospital Aarau, Aarau, Switzerland (U.R.); Department of Neurology, University of Essen, Essen, Germany (S.K.); Department of Medicine I, Medical University of Vienna, Vienna, Austria (A.S.B., C.M., M.P.); Department of Oncology, KU Leuven, Leuven, Belgium (P.C.); Department of Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, Italy (M.F.); Department of Clinical Neurosciences, Division of Neurosurgery, University of Cambridge, Cambridge, England (C.W.); Neurology Clinic and National Center for Tumor Disease, University of Heidelberg, Heidelberg, Germany (W.W.); Clinical Cooperation Unit Neurooncology, German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Heidelberg, Germany (W.W.).
Neuro Oncol. 2016 Mar;18(3):401-7. doi: 10.1093/neuonc/nov183. Epub 2015 Sep 9.
The efficacy of systemic antineoplastic therapy on recurrent World Health Organization (WHO) grades II and III meningiomas is unclear.
We performed a retrospective multicenter analysis of serial cranial MRI in patients with recurrent WHO II and III meningiomas treated with antineoplastic systemic therapies. Growth rates for tumor volume and diameter, as well as change rates for edema size, were calculated for all lesions.
We identified a total of 34 patients (23 atypical, 11 anaplastic meningiomas) with a total of 57 meningioma lesions who had been treated at 6 European institutions. Systemic therapies included bevacizumab, cytotoxic chemotherapy, somatostatin analogues, and tyrosine kinase inhibitors. Overall, tumor growth rates decreased during systemic therapy by 51% for tumor diameter and 14% for tumor volume growth rates compared with the period before initiation of systemic therapy. The most pronounced decrease in meningioma growth rates during systemic therapy was evident in patients treated with bevacizumab, with a reduction of 80% in diameter and 59% in volume growth. Furthermore, a decrease in size of peritumoral edema after initiation of systemic therapy was exclusively observed in patients treated with bevacizumab (-107%).
Our data indicate that systemic therapy may inhibit growth of recurrent WHO grades II and III meningiomas to some extent. In our small cohort, bevacizumab had the most pronounced inhibitory effect on tumor growth, as well as some anti-edematous activity. Prospective studies are needed to better define the role of medical therapies in this tumor type.
全身抗肿瘤治疗对复发性世界卫生组织(WHO)II级和III级脑膜瘤的疗效尚不清楚。
我们对接受抗肿瘤全身治疗的复发性WHO II级和III级脑膜瘤患者的系列头颅MRI进行了回顾性多中心分析。计算所有病变的肿瘤体积和直径增长率以及水肿大小变化率。
我们共纳入了6家欧洲机构治疗的34例患者(23例非典型、11例间变性脑膜瘤),共57个脑膜瘤病变。全身治疗包括贝伐单抗、细胞毒性化疗、生长抑素类似物和酪氨酸激酶抑制剂。总体而言,与全身治疗开始前相比,全身治疗期间肿瘤直径增长率下降了51%,肿瘤体积增长率下降了14%。全身治疗期间,接受贝伐单抗治疗的患者脑膜瘤生长率下降最为明显,直径下降80%,体积增长下降59%。此外,仅在接受贝伐单抗治疗的患者中观察到全身治疗开始后瘤周水肿大小减小(-107%)。
我们的数据表明,全身治疗可能在一定程度上抑制复发性WHO II级和III级脑膜瘤的生长。在我们的小队列中,贝伐单抗对肿瘤生长的抑制作用最为明显,同时还有一定的抗水肿活性。需要进行前瞻性研究以更好地明确药物治疗在这种肿瘤类型中的作用。