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恶性间皮瘤的临床特征、治疗及生存结果:土耳其18年经验

Clinical characteristics, treatment and survival outcomes in malignant mesothelioma: eighteen years' experience in Turkey.

作者信息

Berk Serdar, Dogan Omer Tamer, Kilickap Saadettin, Epozturk Kursat, Akkurt Ibrahim, Seyfikli Zehra

机构信息

Department of Chest Diseases, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey.

出版信息

Asian Pac J Cancer Prev. 2012;13(11):5735-9. doi: 10.7314/apjcp.2012.13.11.5735.

Abstract

BACKGROUND

Malignant mesothelioma (MM) is an insidious tumor with poor prognosis, arising from mesothelial surfaces such as pleura, peritoneum and pericardium. We here aimed to evaluate the demographic, clinical, and radiological features of patients with MM followed in our center as well as their survival.

METHODS

The study included 228 patients (131 male, 97 female) who were followed up in our institution between 1993 and 2010 with the diagnosis of MM.

RESULTS

The mean age was 59.1 years in men and 58.7 years in women and the sex ratio was 1.4:1 in favor of males. Environmental asbestos exposure was present in 86% of the patients for a mean duration of 40±20 years (range: 3-70). Pleural effusion and thoracic/abdominal pain were the most common presenting signs and symptoms (70.2% and 57.8%, respectively). One hundred-thirteen (66%) patients were treated with platinum-based combination chemotherapy (PBCT) plus supportive care (SC) and 67 (34%) patients received SC alone. The median follow-up time was 10.0 months. The median overall survival was significantly improved with PBCT plus SC compared to SC alone (11.4 vs. 5.1 months; p=0.005). The 6, 12, 18, and 24-month survival rates were significantly improved with PBCT plus SC compared to SC alone (72%, 43%, 19%, and 2% vs. 49%, 31%, 11%, and 1%).

CONCLUSION

The survival of patients with MM improved in patients treated with PBCT. The survival advantage continued 12- and 24-month after the initial time of combination chemotherapy.

摘要

背景

恶性间皮瘤(MM)是一种预后较差的隐匿性肿瘤,起源于胸膜、腹膜和心包等间皮表面。我们旨在评估在本中心接受随访的MM患者的人口统计学、临床和放射学特征及其生存率。

方法

该研究纳入了1993年至2010年间在我们机构接受随访且诊断为MM的228例患者(男性131例,女性97例)。

结果

男性的平均年龄为59.1岁,女性为58.7岁,性别比为1.4:1,男性居多。86%的患者有环境石棉暴露史,平均暴露时间为40±20年(范围:3 - 70年)。胸腔积液和胸/腹痛是最常见的首发症状和体征(分别为70.2%和57.8%)。113例(66%)患者接受了铂类联合化疗(PBCT)加支持治疗(SC),67例(34%)患者仅接受了SC。中位随访时间为10.0个月。与单纯SC相比,PBCT加SC显著提高了中位总生存期(11.4个月对5.1个月;p = 0.005)。与单纯SC相比,PBCT加SC显著提高了6个月、12个月、18个月和24个月的生存率(分别为72%、43%、19%和2%对49%、31%、11%和1%)。

结论

接受PBCT治疗的MM患者生存率有所提高。联合化疗初始时间后的12个月和24个月,生存优势依然存在。

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