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去分化低度恶性骨肉瘤与传统骨肉瘤的临床比较。

A clinical comparison between dedifferentiated low-grade osteosarcoma and conventional osteosarcoma.

机构信息

Department of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan; Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.

Department of Musculoskeletal Oncology, National Cancer Center Hospital, Tokyo, Japan; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Bone Joint J. 2019 Jun;101-B(6):745-752. doi: 10.1302/0301-620X.101B6.BJJ-2018-1207.R1.

Abstract

AIMS

The purpose of this study was to clarify the clinical behaviour, prognosis, and optimum treatment of dedifferentiated low-grade osteosarcoma (DLOS) diagnosed based on molecular pathology.

PATIENTS AND METHODS

We retrospectively reviewed 13 DLOS patients (six men, seven women; median age 32 years (interquartile range (IQR) 27 to 38)) diagnosed using the following criteria: the histological coexistence of low-grade and high-grade osteosarcoma components in the lesion, and positive immunohistochemistry of mouse double minute 2 homolog (MDM2) and cyclin-dependent kinase 4 (CDK4) associated with MDM2 amplification. These patients were then compared with 51 age-matched consecutive conventional osteosarcoma (COS) patients (33 men, 18 women; median age 25 years (IQR 20 to 38)) regarding their clinicopathological features.

RESULTS

The five-year overall survival (OAS) rates in the DLOS and COS patients were 85.7% and 77.1% (p = 0.728), respectively, and the five-year progression-free survival (PFS) rates were 57.7% and 44.9% (p = 0.368), respectively. A total of 12 DLOS patients received chemotherapy largely according to regimens for COS. Among the nine cases with a histological evaluation after chemotherapy, eight showed a poor response, and seven of these had a necrosis rate of < 50%. One DLOS patient developed local recurrence and five developed distant metastases.

CONCLUSION

Based on our study of 13 DLOS cases that were strictly defined by histological and molecular means, DLOS showed a poorer response to a standard chemotherapy regimen than COS, while the clinical outcomes were not markedly different. Cite this article: 2019;101-B:745-752.

摘要

目的

本研究旨在阐明基于分子病理学诊断的去分化低度恶性骨肉瘤(DLOS)的临床行为、预后和最佳治疗方法。

患者和方法

我们回顾性分析了 13 例 DLOS 患者(6 名男性,7 名女性;中位年龄 32 岁(四分位距 27 至 38)),其诊断标准为:病变中存在低度和高度骨肉瘤成分的组织学共存,以及鼠双微体 2 同源物(MDM2)和细胞周期蛋白依赖性激酶 4(CDK4)的免疫组织化学阳性,与 MDM2 扩增相关。然后,将这些患者与 51 例年龄匹配的连续常规骨肉瘤(COS)患者(33 名男性,18 名女性;中位年龄 25 岁(四分位距 20 至 38))进行比较,比较其临床病理特征。

结果

DLOS 和 COS 患者的 5 年总生存率(OAS)分别为 85.7%和 77.1%(p = 0.728),5 年无进展生存率(PFS)分别为 57.7%和 44.9%(p = 0.368)。12 例 DLOS 患者根据 COS 的化疗方案接受了化疗。在 9 例化疗后进行组织学评估的病例中,8 例显示化疗反应差,其中 7 例的坏死率<50%。1 例 DLOS 患者发生局部复发,5 例发生远处转移。

结论

根据我们对 13 例严格通过组织学和分子手段定义的 DLOS 病例的研究,DLOS 对标准化疗方案的反应不如 COS 好,而临床结果并无明显差异。

参考文献:2019;101-B:745-752.

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