Lauk Olivia, Bruestle Karina, Neuer Thomas, Battilana Bianca, Nguyen Thi Dan Linh, Frauenfelder Thomas, Stahel Rolf, Weder Walter, Curioni-Fontecedro Alessandra, Opitz Isabelle
Department of Thoracic Surgery, University Hospital Zurich, Zurich, Switzerland.
Institute of Diagnostic and Interventional Radiology, University Hospital Zurich, Zurich, Switzerland.
Front Oncol. 2020 Nov 13;10:588563. doi: 10.3389/fonc.2020.588563. eCollection 2020.
Adding bevacizumab, an anti-Vascular Endothelial Growth Factor (VEGF), to platinum-based chemotherapy/pemetrexed in 1 line treatment of advanced malignant pleural mesothelioma (MPM), significantly improved overall survival. However, increased high grade bleeding after operation was reported in patients with colorectal cancer who previously received bevacizumab. In the present analysis, we assessed for the first time the impact of adding bevacizumab to induction chemotherapy prior to surgery for mesothelioma patients.
Two hundred twenty-seven MPM patients, intended to be treated with induction chemotherapy followed by surgery at the University Hospital of Zurich between 2002 and December 2018, were included in the present analysis. After propensity score matching for gender, histology and age (1:3 ratio), data from 88 patients were analyzed. Sixty-six patients underwent induction chemotherapy (with cis-/carboplatin and pemetrexed: control group) alone and 22 patients underwent induction chemotherapy with the addition of bevacizumab (bevacizumab group) prior macroscopic complete resection (MCR). Perioperative and long-term outcome variables were analyzed.
Patients undergoing combination treatment with bevacizumab had a significantly better response than with chemotherapy alone as assessed by modified RECIST (p=0.046). Intraoperative complications in the bevacizumab group (one patient), or in the control group (three patients) were not related to intraoperative bleeding. Postoperative transfusion of blood products occurred in a larger amount in the control group than in the bevacizumab group (p=0.047). Overall survival was not statistically different between both groups.
These initial data demonstrate that MCR can be performed safely after triple induction chemotherapy with bevacizumab without increased intra- and postoperative bleeding complications. Response rates were significantly improved by the addition of bevacizumab.
在晚期恶性胸膜间皮瘤(MPM)的一线治疗中,将抗血管内皮生长因子(VEGF)的贝伐单抗添加到铂类化疗/培美曲塞中,可显著提高总生存期。然而,先前接受过贝伐单抗治疗的结直肠癌患者术后高级别出血增加。在本分析中,我们首次评估了在间皮瘤患者手术前将贝伐单抗添加到诱导化疗中的影响。
纳入2002年至2018年12月在苏黎世大学医院接受诱导化疗后手术治疗的227例MPM患者进行本分析。在按性别、组织学和年龄进行倾向评分匹配(1:3比例)后,分析了88例患者的数据。66例患者仅接受诱导化疗(使用顺铂/卡铂和培美曲塞:对照组),22例患者在宏观完全切除(MCR)前接受添加贝伐单抗的诱导化疗(贝伐单抗组)。分析围手术期和长期结局变量。
根据改良RECIST评估,接受贝伐单抗联合治疗的患者比单纯化疗患者的反应明显更好(p=0.046)。贝伐单抗组(1例患者)或对照组(3例患者)的术中并发症与术中出血无关。对照组术后输血的血液制品量比贝伐单抗组多(p=0.047)。两组的总生存期无统计学差异。
这些初步数据表明,在使用贝伐单抗进行三联诱导化疗后可以安全地进行MCR,且术中和术后出血并发症不会增加。添加贝伐单抗可显著提高缓解率。