Departments of Bone and Soft Tissue Tumor, Tianjin Medical University Cancer Institute & Hospital, Tianjin, 300060, People's Republic of China.
National Clinical Research Center of Cancer, Tianjin Medical University Cancer Institute & Hospital, Tianjin, 300060, People's Republic of China.
Sci Rep. 2019 Mar 18;9(1):4816. doi: 10.1038/s41598-019-41089-1.
Extraskeletal osteosarcoma (ESOS) is an extremely rare malignancy with poor prognosis, accounting for 2-4% of all osteogenic sarcomas. The purpose of this study was to examine the oncological outcomes of this disease related to surgical treatment and/or combined adjuvant therapies and to analyze the associated prognostic factors in ESOS. From January 1990 to June 2016, 22 patients with primary ESOS were analyzed in this retrospective study. Overall survival (OS) and progression-free survival (PFS) rates were calculated by Kaplan-Meier methods and compared with log-rank test. 22 patients were diagnosed with ESOS, 19 showed localized diseases and 3 presented with metastatic lesions. The median age at diagnosis was 55.5 years. Surgery resection was performed for all patients, 18 of whom received adjuvant chemotherapy. The median follow-up time was 48.5 months. There were 10 cases of recurrence and 9 patients developed new metastases. The 5-year OS rate for all patients was 58%. For localized cohort, the 5-year OS rate was 62%, and the 3-year PFS rate was 31% with a median PFS of 16 months. Univariate analysis of related prognosis factors showed that larger size of tumor (>5.5 cm) and higher histologic grade emerged as significant factors associated with worse OS. The addition of combination chemotherapy has no effect found on OS or PFS in this study. In summary, for patients who presented with ESOS, larger tumor size and higher histologic grade indicate a lower OS rate. The combination chemotherapy does not improve the OS or PFS.
骨外骨肉瘤(ESOS)是一种罕见的恶性肿瘤,预后差,占所有成骨肉瘤的 2-4%。本研究旨在研究与手术治疗和/或联合辅助治疗相关的这种疾病的肿瘤学结果,并分析 ESOS 中的相关预后因素。在这项回顾性研究中,分析了 1990 年 1 月至 2016 年 6 月期间的 22 例原发性 ESOS 患者。通过 Kaplan-Meier 方法计算总生存率(OS)和无进展生存率(PFS),并采用对数秩检验进行比较。22 例患者被诊断为 ESOS,19 例表现为局限性疾病,3 例表现为转移性病变。诊断时的中位年龄为 55.5 岁。所有患者均行手术切除,18 例患者接受辅助化疗。中位随访时间为 48.5 个月。有 10 例复发,9 例出现新的转移。所有患者的 5 年 OS 率为 58%。对于局限性队列,5 年 OS 率为 62%,3 年 PFS 率为 31%,中位 PFS 为 16 个月。相关预后因素的单因素分析表明,肿瘤较大(>5.5cm)和组织学分级较高是与 OS 较差相关的显著因素。本研究中,联合化疗对 OS 或 PFS 无影响。综上所述,对于患有 ESOS 的患者,肿瘤越大、组织学分级越高,OS 率越低。联合化疗并不能提高 OS 或 PFS。