Fuchs Talia L, Chou Angela, Aksoy Yagiz, Mahjoub Mahiar, Sheen Amy, Sioson Loretta, Ahadi Mahsa, Gill Anthony J
Cancer Diagnosis and Pathology Group, Kolling Institute of Medical Research, Royal North Shore Hospital, St Leonards.
Department of Anatomical Pathology, NSW Health Pathology, Royal North Shore Hospital.
Am J Surg Pathol. 2022 Jun 1;46(6):774-785. doi: 10.1097/PAS.0000000000001854. Epub 2021 Dec 15.
Although there is early support for schemes based on nuclear grade, necrosis and mitotic rate, there is currently no widely implemented grading system for diffuse pleural mesothelioma (DPM). We investigated current systems and propose a novel Mesothelioma Weighted Grading Scheme (MWGS). The MWGS assigns weighted scores from 0 to 10 based on age (≤74, >74 yrs: 0,1); histologic type (epithelioid, biphasic, sarcomatoid: 0,1,2); necrosis (absent, present: 0,2); mitotic count per 2 mm2 (≤1, 2 to 4, ≥5: 0,1,2); nuclear atypia (mild, moderate, severe: 0,1,2); and BRCA1-associated protein 1 (BAP1) expression (lost, retained: 0,1). A score of 0 to 3 is low grade, 4 to 6 intermediate grade, and 7 to 10 high grade. In 369 consecutive DPMs, median survival was 17.1, 10.1, and 4.1 months for low, intermediate, and high grades (P<0.0001). A progressive increase in score correlated with worsening overall survival (P<0.0001). Interobserver concordance was substantial (κ=0.588), with assessment of nuclear grade being the most subjective parameter (κ=0.195). We compared the MWGS to the 2-tiered system discussed in the World Health Organization (WHO) fifth edition. The WHO system predicted median survival in epithelioid (median 18.0 vs. 11.3 mo, P=0.003) and biphasic (16.2 vs. 4.2 mo, P=0.002), but not sarcomatoid DPM (5.4 vs. 4.7 mo, P=0.407). Interestingly, the WHO grading system was prognostic in cases with BAP1 loss (median survival 18.7 vs. 10.4 mo, P<0.0001), but not retained BAP1 expression (8.9 vs. 6.2 mo, P=0.061). In conclusion, the WHO scheme has merit in epithelioid/biphasic and BAP1-deficient DPM, however, the MWGS can be used for risk stratification of all DPMs, regardless of histologic subtype and BAP1 status.
尽管基于核分级、坏死和有丝分裂率的方案早期得到了支持,但目前弥漫性胸膜间皮瘤(DPM)尚无广泛实施的分级系统。我们研究了现有系统并提出了一种新的间皮瘤加权分级方案(MWGS)。MWGS根据年龄(≤74岁、>74岁:0、1);组织学类型(上皮样、双向性、肉瘤样:0、1、2);坏死(无、有:0、2);每2平方毫米的有丝分裂计数(≤1、2至4、≥5:0、1、2);核异型性(轻度、中度、重度:0、1、2);以及乳腺癌1号相关蛋白1(BAP1)表达(缺失、保留:0、1)赋予0至10的加权分数。0至3分为低级别,4至6分为中级别,7至10分为高级别。在369例连续的DPM中,低、中、高级别的中位生存期分别为17.1个月、10.1个月和4.1个月(P<0.0001)。分数的逐步增加与总体生存期的恶化相关(P<0.0001)。观察者间的一致性较高(κ=0.588),其中核分级评估是最主观的参数(κ=0.195)。我们将MWGS与世界卫生组织(WHO)第五版中讨论的两级系统进行了比较。WHO系统预测了上皮样(中位生存期18.0个月对11.3个月,P=0.003)和双向性(16.2个月对4.2个月,P=0.002)DPM的中位生存期,但对肉瘤样DPM无效(5.4个月对4.7个月,P=0.407)。有趣的是,WHO分级系统在BAP1缺失的病例中具有预后价值(中位生存期18.7个月对10.4个月,P<0.0001),但在BAP1表达保留的病例中无此价值(分别为8.9个月和6.2个月,P=0.061)。总之,WHO方案在上皮样/双向性和BAP1缺陷型DPM中具有优点,然而,MWGS可用于所有DPM的风险分层,无论其组织学亚型和BAP1状态如何。