Schipper Paul H, Nichols Francis C, Thomse Kristine M, Deschamps Claude, Cassivi Stephen D, Allen Mark S, Pairolero Peter C
Division of General Thoracic Surgery, Mayo Clinic, Rochester, Minnesota 55905, USA.
Ann Thorac Surg. 2008 Jan;85(1):257-64; discussion 264. doi: 10.1016/j.athoracsur.2007.06.066.
Malignant pleural mesothelioma is a rare, aggressive, and deadly malignancy. Despite increasing incidence, no treatment modality is accepted standard of care. This report analyzes our experience with surgical management of mesothelioma.
All patients with surgery for mesothelioma from January 1985 through December 2003 were retrospectively reviewed.
There were 285 patients with a median age of 66 years (range, 26 to 91 years). One hundred forty-six patients (51%) had biopsy only, 73 (26%) had extrapleural pneumonectomy, 34 (12%) had subtotal parietal pleurectomy, 22 (8%) underwent exploration without resection, and 10 (3%) had total pleurectomy. Histopathology was epithelial, nonepithelial, and unclassified in 134, 108, and 43 patients, respectively. Twenty patients were stage IA, 82 patients were stage IB, 24 patients were stage II, 75 patients were stage III, 60 patients were stage IV, and 24 patients were of unknown stage. Fifty-three patients (19%) had chemotherapy alone, 16 (5.6%) had radiation alone, and 42 (14.7%) had both. Thirty-day operative mortality was 6.3% and was not significantly associated with the operative procedure (p = 0.79). Fifty-one percent of extrapleural pneumonectomy patients had major complications, significantly greater than patients having any other procedure (p < 0.001). Median follow-up was 11 months (range, 0 to 7 years). Overall median survival was 10.7 months; however, for patients having extrapleural pneumonectomy, median survival was 16 months. One-, 2-, and 3-year survival after extrapleural pneumonectomy was 61%, 25%, and 14%, respectively.
Extrapleural pneumonectomy can be performed with similar 30-day mortality as other procedures for malignant pleural mesothelioma with a median survival better than subtotal pleurectomy, exploration without resection, and biopsy alone. However, extrapleural pneumonectomy has significant morbidity and a 3-year survival of only 14%.
恶性胸膜间皮瘤是一种罕见、侵袭性强且致命的恶性肿瘤。尽管发病率不断上升,但尚无被认可的标准治疗方式。本报告分析了我们在间皮瘤手术治疗方面的经验。
对1985年1月至2003年12月间接受间皮瘤手术的所有患者进行回顾性分析。
共285例患者,中位年龄66岁(范围26至91岁)。146例患者(51%)仅接受活检,73例(26%)接受胸膜外全肺切除术,34例(12%)接受壁层胸膜大部分切除术,22例(8%)接受探查但未行切除术,10例(3%)接受全胸膜切除术。组织病理学检查结果显示,134例为上皮型,108例为非上皮型,43例为未分类型。20例为ⅠA期,82例为ⅠB期,24例为Ⅱ期,75例为Ⅲ期,60例为Ⅳ期,24例分期不明。53例患者(19%)仅接受化疗,16例(5.6%)仅接受放疗,42例(14.7%)同时接受放化疗。30天手术死亡率为6.3%,与手术方式无显著相关性(p = 0.79)。胸膜外全肺切除术患者中有51%发生严重并发症,显著高于接受其他手术的患者(p < 0.001)。中位随访时间为11个月(范围0至7年)。总体中位生存期为10.7个月;然而,接受胸膜外全肺切除术的患者中位生存期为16个月。胸膜外全肺切除术后1年、2年和3年生存率分别为61%、25%和14%。
胸膜外全肺切除术的30天死亡率与恶性胸膜间皮瘤的其他手术方式相似,中位生存期优于壁层胸膜大部分切除术、探查未切除术和单纯活检。然而,胸膜外全肺切除术有显著的并发症,3年生存率仅为14%。