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恶性胸膜间皮瘤的外科评估:我们是否已经到达关键阶段?

Surgical assessment of malignant pleural mesothelioma: have we reached a critical stage?

机构信息

Department of Thoracic Surgery, Glenfield Hospital, Groby Road, Leicester LE3 9QP, UK.

出版信息

Eur J Cardiothorac Surg. 2010 Jun;37(6):1457-63. doi: 10.1016/j.ejcts.2009.12.039. Epub 2010 Feb 6.

Abstract

OBJECTIVE

The International Mesothelioma Interest Group (IMIG) classification is the most widely used staging system but is based on post-resectional parameters. We aimed to test the association between clinical and pathological staging and to identify possible discrepancies.

METHODS

We identified 164 consecutive patients (144 males and 20 females, with mean age 58 years) who underwent radical surgery (114 extrapleural pneumonectomy; 50 radical pleurectomy/decortication) for malignant pleural mesothelioma (MPM). The patients were clinically staged with CT + or - MRI (CT, computed tomography; MRI, magnetic resonance imaging).

RESULTS

Clinical T (cT) stage proved to be the same as pathological T (pT) stage in 44%; understaged in 46% and overstaged in 10%. Clinical N (cN) stage proved to be the same as pathological N (pN) stage in 56%; understaged in 31% and overstaged in 13%. Disease-free interval (DFI) was associated with cT stage (median DFI 29 months, SE 13, 95% CI 3-54 months for cT1; median 5, SE 3, 95% CI 3-6 months for cT4, p=0.02) but not clinical N stage (median DFI 12 months, SE 1, 95% CI 9-15 months for cN0; median DFI 11 months, SE 0.3, 95% CI 10-12 months for cN2, p=0.5) and was associated with both pT (median DFI 31 months, SE 17, 95% CI 0-64 months for pT1; median DFI 8 months, SE1, 95% CI 6-11 months for pT4, p=0.03) and pN stage (median DFI 14 months, SE 3, 95% CI 9-20 months for pN0; median DFI 10 months, SE 1, 95% CI 8-13 months for pN2, p=0.02). Overall survival was associated with cT stage (median survival 25 months, SE 3, 95% CI 20-30 months for cT1; median survival 11 months, SE 3, 95% CI 10-11 months for cT4, p=0.01) but not cN stage (median survival 15 months, SE 2, 95% CI 11-19 months for cN0; median survival 15 months, SE 2, 95% CI 12-19 months for cN2, p=0.49) and pN stage (median survival 22 months, SE 3, 95% CI 19-27 months for pN0; median survival 14 months, SE 1, 95% CI 12-17 months for pN2, p=0.01) but not pT stage (median survival 27 months, SE 4, 95% CI 19-35 months for pT1; median survival 12 months, SE 2, 95% CI 9-15 months for pT4, p=0.06). Pathological IMIG stage was associated with DFI and overall survival; however, preoperative IMIG stage was less useful.

CONCLUSIONS

There are deficiencies in the current staging system for MPM and discrepancies between clinical and pathological systems. Future improvements are needed in clinical descriptors of nodal status and pathological descriptors of T stage. Subsequent IMIG stage grouping also needs revision.

摘要

目的

国际间皮瘤兴趣小组(IMIG)分类是最广泛使用的分期系统,但基于术后参数。我们旨在检验临床和病理分期之间的相关性,并确定可能存在的差异。

方法

我们确定了 164 名连续患者(144 名男性和 20 名女性,平均年龄 58 岁),他们接受了根治性手术(114 例胸膜外全肺切除术;50 例根治性胸膜切除术/剥脱术)治疗恶性胸膜间皮瘤(MPM)。患者接受 CT+/-MRI(CT,计算机断层扫描;MRI,磁共振成像)进行临床分期。

结果

临床 T(cT)分期与病理 T(pT)分期一致的占 44%;分期不足的占 46%,分期过度的占 10%。临床 N(cN)分期与病理 N(pN)分期一致的占 56%;分期不足的占 31%,分期过度的占 13%。无病间隔(DFI)与 cT 分期相关(cT1 的中位 DFI 为 29 个月,SE 为 13,95%CI 为 3-54 个月;cT4 的中位 DFI 为 5 个月,SE 为 3,95%CI 为 3-6 个月,p=0.02),但与临床 N 分期无关(cN0 的中位 DFI 为 12 个月,SE 为 1,95%CI 为 9-15 个月;cN2 的中位 DFI 为 11 个月,SE 为 0.3,95%CI 为 10-12 个月,p=0.5),并与 pT(pT1 的中位 DFI 为 31 个月,SE 为 17,95%CI 为 0-64 个月;pT4 的中位 DFI 为 8 个月,SE1,95%CI 为 6-11 个月,p=0.03)和 pN 分期(pN0 的中位 DFI 为 14 个月,SE 为 3,95%CI 为 9-20 个月;pN2 的中位 DFI 为 10 个月,SE 为 1,95%CI 为 8-13 个月,p=0.02)相关。总生存与 cT 分期相关(cT1 的中位生存时间为 25 个月,SE 为 3,95%CI 为 20-30 个月;cT4 的中位生存时间为 11 个月,SE 为 3,95%CI 为 10-11 个月,p=0.01),但与 cN 分期无关(cN0 的中位生存时间为 15 个月,SE 为 2,95%CI 为 11-19 个月;cN2 的中位生存时间为 15 个月,SE 为 2,95%CI 为 12-19 个月,p=0.49)和 pN 分期(pN0 的中位生存时间为 22 个月,SE 为 3,95%CI 为 19-27 个月;pN2 的中位生存时间为 14 个月,SE 为 1,95%CI 为 12-17 个月,p=0.01),但与 pT 分期无关(pT1 的中位生存时间为 27 个月,SE 为 4,95%CI 为 19-35 个月;pT4 的中位生存时间为 12 个月,SE 为 2,95%CI 为 9-15 个月,p=0.06)。病理 IMIG 分期与 DFI 和总生存相关;然而,术前 IMIG 分期的作用较小。

结论

目前的 MPM 分期系统存在缺陷,临床和病理系统之间存在差异。需要改进临床描述淋巴结状态和病理描述 T 分期的方法。随后的 IMIG 分期分组也需要修订。

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