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