Batirel Hasan Fevzi, Metintas Muzaffer, Caglar Hale Basak, Yildizeli Bedrettin, Lacin Tunc, Bostanci Korkut, Akgul Asli Gul, Evman Serdar, Yuksel Mustafa
Marmara University Hospital, Department of Thoracic Surgery, Istanbul, Turkey.
J Thorac Oncol. 2008 May;3(5):499-504. doi: 10.1097/JTO.0b013e31816fca1b.
Multimodality treatment has achieved significant success in local control and treatment of early-stage malignant pleural mesothelioma patients. However, its favorable effect on survival is questionable.
We have instituted a trimodality treatment protocol consisting of extrapleural pneumonectomy, adjuvant high-dose (54 Gy) hemithoracic irradiation, and platin-based chemotherapy in a multi-institutional setting. Preoperative pulmonary function tests, echocardiogram, chest computed tomography, and magnetic resonance imaging scans were performed in all patients. Twenty patients have been treated with this protocol during 2003-2007. Seventeen had a history of environmental asbestos/erionite exposure. Clinical stages were T1-3N0-2.
Median age was 56 (41-70, 8 female). There was one postoperative mortality (% 5) due to ARDS. Morbidity occurred in 11 patients (% 55). Histology was epithelial in 17, mixed in 2, and sarcomatoid in 1. Sixteen patients underwent extrapleural pneumonectomy. Microscopic margin positivity was present in 14 patients with macroscopic complete resection. Twelve patients completed all three treatments. Median follow-up was 16 months (1-43). Overall median survival was 17 months (24% at 2 years). Eight patients had extrapleural lymph node involvement (internal mammary [n = 3], subcarinal [n = 2], pulmonary ligament [n = 1], diaphragmatic [n = 1], subaortic [n = 1]). There was better survival in patients without lymph node metastasis (24 versus 13 months median survival, p = 0.052). Currently, 7 patients are alive, 6 without recurrence, and 2 patients at 40 and 45 months.
Trimodality treatment in malignant pleural mesothelioma seems to prolong survival in patients without lymph node metastasis. Novel techniques are needed for preoperative assessment of extrapleural lymph nodes.
多模式治疗在早期恶性胸膜间皮瘤患者的局部控制和治疗方面取得了显著成功。然而,其对生存的有利影响尚存在疑问。
我们制定了一项三模式治疗方案,包括在多机构环境下进行胸膜外全肺切除术、辅助高剂量(54 Gy)半胸照射以及铂类化疗。所有患者均进行了术前肺功能测试、超声心动图、胸部计算机断层扫描和磁共振成像扫描。2003年至2007年期间,有20例患者接受了该方案治疗。其中17例有环境石棉/毛沸石接触史。临床分期为T1 - 3N0 - 2。
中位年龄为56岁(41 - 70岁,8名女性)。有1例患者因急性呼吸窘迫综合征术后死亡(5%)。11例患者发生并发症(55%)。组织学类型为上皮型17例、混合型2例、肉瘤样型1例。16例患者接受了胸膜外全肺切除术。14例肉眼完全切除的患者镜下切缘阳性。12例患者完成了所有三种治疗。中位随访时间为16个月(1 - 43个月)。总体中位生存期为17个月(2年生存率为24%)。8例患者有胸膜外淋巴结受累(乳内淋巴结[n = 3]、隆突下淋巴结[n = 2]、肺韧带淋巴结[n = 1]、膈淋巴结[n = 1]、主动脉下淋巴结[n = 1])。无淋巴结转移患者的生存期更长(中位生存期分别为24个月和13个月,p = 0.052)。目前,7例患者存活,6例无复发,2例分别在40个月和45个月。
恶性胸膜间皮瘤的三模式治疗似乎可延长无淋巴结转移患者的生存期。术前评估胸膜外淋巴结需要新技术。