Department of Pathology, Gustave Roussy, Villejuif, France.
INSERM 981, Gustave Roussy Cancer Campus, Villejuif, France.
Virchows Arch. 2021 May;478(5):885-891. doi: 10.1007/s00428-020-02939-w. Epub 2020 Oct 3.
The morphological distinction between the various types of mucinous ovarian tumors has major prognostic implications but may be challenging. The aims of our study were to describe inter-observer reproducibility in the morphological diagnosis of mucinous ovarian tumors, to evaluate the clinical relevance of possible diagnostic discrepancies, and to identify molecular abnormalities correlated with the histological type. Seventy-nine ovarian mucinous borderline tumors (MOB) and either expansile or infiltrative carcinomas (MOC) were independently reviewed by two gynecological pathologists. Molecular analysis was performed in 32 cases. Concordance between the two pathologists was reached in 67 cases (k: 0.78). The main discrepancies (8/12) were the evaluation of nuclear grade 3 or that of microfoci (< 5 mm) of infiltrative-type carcinoma in an otherwise typical expansile MOC. Our follow-up analysis showed that infiltrative MOC had a lower overall survival (OS) (p < 0.0024) and progression-free survival (PFS) (p = 0.0060) as compared with MOB and expansile MOC. The presence of nuclear grade 3 or microfoci (< 5 mm) of infiltrative-type pattern of invasion in an otherwise typical expansile MOC did not alter the prognosis as compared with expansile MOC without these features, in terms of OS (p < 0.0028) and PFS (p = 0.0074). KRAS mutations were more frequent in MOB (71%), than in expansile (50%) and infiltrative MOC (14%). In contrast, the prevalence of TP53 mutation was lower in MOB (43%), than in expansile (58%) and infiltrative MOC (71%). Our results confirm that in MOC, the expansile pattern of invasion is associated with a better prognosis than extensive (> 5 mm) infiltrative-type pattern of invasion. No specific or sensitive molecular profile might help in the differential diagnosis of mucinous ovarian tumors.
各种类型的黏液性卵巢肿瘤在形态学上的鉴别具有重要的预后意义,但可能具有挑战性。我们的研究目的是描述黏液性卵巢肿瘤形态学诊断的观察者间可重复性,评估可能的诊断差异的临床相关性,并确定与组织学类型相关的分子异常。79 例卵巢黏液性交界性肿瘤(MOB)和扩张型或浸润型癌(MOC)由两名妇科病理学家独立进行回顾性分析。对 32 例病例进行了分子分析。两名病理学家之间的一致性达到了 67 例(k:0.78)。主要的分歧(8/12)在于评估核分级 3 级或在 otherwise典型的膨胀型 MOC 中微浸润灶(<5mm)。我们的随访分析显示,浸润型 MOC 的总生存(OS)(p<0.0024)和无进展生存(PFS)(p=0.0060)低于 MOB 和扩张型 MOC。在 otherwise典型的膨胀型 MOC 中存在核分级 3 级或微浸润型浸润模式的微灶(<5mm),与不具有这些特征的膨胀型 MOC 相比,并不改变预后,在 OS(p<0.0028)和 PFS(p=0.0074)方面。KRAS 突变在 MOB 中更为常见(71%),而在扩张型(50%)和浸润型 MOC(14%)中则较少见。相比之下,TP53 突变在 MOB 中的发生率较低(43%),而在扩张型(58%)和浸润型 MOC(71%)中则较高。我们的研究结果证实,在 MOC 中,扩张型浸润模式与较好的预后相关,而广泛的(>5mm)浸润型浸润模式则预后较差。没有特定或敏感的分子谱可能有助于黏液性卵巢肿瘤的鉴别诊断。