Liu W F, Huang Z, Gong L H, Yang Y K, Jin T, Deng Z P, Li Y, Hao L, Zhang Q, Ding Y, Niu X H
Department of Orthopedic Oncology Surgery, Beijing Jishuitan Hospital, Peking University, Beijing 100035, China.
Department of Pathology, Beijing Jishuitan Hospital, Peking University, Beijing 100035, China.
Zhonghua Yi Xue Za Zhi. 2019 Oct 8;99(37):2897-2902. doi: 10.3760/cma.j.issn.0376-2491.2019.37.005.
To identify the clinical outcome and prognostic factors of synchronous multicentric osteosarcoma (SMOS). The clinical data of 2 602 conventional osteosarcoma patients admitted to Beijing Jishuitan Hospital from January 1995 to June 2018 were retrospectively analyzed. Finally, 56 (2.1%) cases were confirmed as SMOS according to clinical and imaging database, medical record and pathological results.All epidemiological data of SMOS cases,initial diagnosis time, tumor site, number of lesions, chemotherapy, surgical treatment, alkline phosphatase (AKP),lactate dehydrogenase (LDH) and oncological results were collected in our institution. The Survival rate, comparison of various parameters, univariate analysis and multivariate Cox regression were performed with statistical software. There were 41 males and 15 females enrolled in this research, the median and mean ages were 15 and 18 years (range, 8-50 years) respectively. All of them were multi-site involved, whereas the initial complaints of sites distribution were 32 cases of femur, 13 cases of tibia, 4 cases of humerus, 3 cases of fibula, 2 cases of spine, 1 case of sternum and 1 case of calcaneus. Forty-four of 56 cases performed adjuvant chemotherapy and 31 of them underwent surgical treatment. The mean follow-up time was 15.4 (range, 1-186) months. Thirty-five cases died of disease at the end of the follow-up. The 5-year survival rate was 10.4%. According to the number of lesions stratification, the 2-year survival rates in patients with low (<5 sites) and high (≥5 sites) tumor load was 33.6% and 0, respectively (χ(2)=6.697, 0.010). The 2-year survival rate of chemotherapy and non-chemotherapy patients was 20.8% and 0, respectively (χ(2)=6.998, 0.008), the value of AKP after chemotherapy(median: 272 IU/L) significantly decreased when compared with that at the initial diagnosis (median: 454 U/L) (-3.274, 0.001).The 2-year survival rate in patients with and without standard chemotherapy was 55.6% and 0, respectively (χ(2)=8.798, 0.003). The 2-year survival rate was 25.0% in the surgical group and 0 in the non-surgical group, respectively (χ(2)=7.942, 0.005). Multivariate cox regression analysis with the forward Wald method indicated that standard chemotherapy was the only variable contributor to survival and prognosis of multifocal osteosarcoma. SMOS has low survival rate and poor prognosis. Chemotherapy and surgery can improve the survival rate, standard chemotherapy is an independent prognostic factor.
探讨同步多中心骨肉瘤(SMOS)的临床结局及预后因素。回顾性分析1995年1月至2018年6月在北京积水潭医院收治的2602例传统骨肉瘤患者的临床资料。最终,根据临床和影像数据库、病历及病理结果确诊56例(2.1%)为SMOS。收集了我院SMOS病例的所有流行病学数据、初始诊断时间、肿瘤部位、病灶数量、化疗、手术治疗、碱性磷酸酶(AKP)、乳酸脱氢酶(LDH)及肿瘤学结局。使用统计软件进行生存率计算、各项参数比较、单因素分析及多因素Cox回归分析。本研究共纳入41例男性和15例女性,年龄中位数和平均数分别为15岁和18岁(范围8 - 50岁)。所有患者均为多部位受累,首发部位分布的初始主诉中,股骨32例,胫骨13例,肱骨4例,腓骨3例,脊柱2例,胸骨1例,跟骨1例。56例中有44例进行了辅助化疗,其中31例接受了手术治疗。平均随访时间为15.4(范围1 - 186)个月。随访结束时35例死于疾病。5年生存率为10.4%。根据病灶数量分层,肿瘤负荷低(<5个部位)和高(≥5个部位)的患者2年生存率分别为33.6%和0(χ² = 6.697,P = 0.010)。化疗和未化疗患者的2年生存率分别为20.8%和0(χ² = 6.998,P = 0.008),化疗后AKP值(中位数:272 IU/L)与初始诊断时(中位数:454 U/L)相比显著降低(-3.274,P = 0.001)。接受标准化疗和未接受标准化疗患者的2年生存率分别为55.6%和0(χ² = 8.798,P = 0.003)。手术组和非手术组的2年生存率分别为25.0%和0(χ² = 7.942, P = 0.005)。采用向前Wald法进行多因素Cox回归分析表明,标准化疗是多灶性骨肉瘤生存和预后的唯一变量因素。SMOS生存率低,预后差。化疗和手术可提高生存率,标准化疗是独立的预后因素。