Trassard M, Le Doussal V, Hacène K, Terrier P, Ranchère D, Guillou L, Fiche M, Collin F, Vilain M O, Bertrand G, Jacquemier J, Sastre-Garau X, Bui N B, Bonichon F, Coindre J M
French Federation of Cancer Centers Sarcoma Group, Paris, France.
J Clin Oncol. 2001 Jan 15;19(2):525-34. doi: 10.1200/JCO.2001.19.2.525.
To identify most significant and therapeutically relevant prognostic factors in adults with localized primary synovial sarcomas (SS) and to confirm the usefulness of the French Federation of Cancer Centers (FNCLCC) grading system, the prognostic impact of which has been already proven in soft tissue sarcomas.
Data on 128 patients with nonmetastatic SS collected from a cooperative database by the FNCLCC Sarcoma Group between 1980 and 1994 were studied retrospectively. Immunohistochemistry was performed at diagnosis in 77 cases (61%). The tumors were classified as biphasic (n = 45), monophasic fibrous (n = 72), and poorly differentiated (n = 10) subtypes. Histologic grade was determined according to the FNCLCC method, and vascular invasion was assessed in every case.
The 5-year disease-specific survival (DSS) rate for this series of patients with localized SS was 62.9% (+/- 9.6% [SD]) with a median follow-up time of 37 months (range, 8 to 141 months). In multivariate analysis, the adverse risk factors associated with decreased DSS were International Union Against Cancer/American Joint Committee on Cancer stage III/IVA disease, male sex, and truncal tumor locations. For metastasis-free survival (MFS), disease stage III/IVA, tumor necrosis, and monophasic subtypes were the major factors associated with a less favorable prognosis. Separately, when not using disease stage, tumor necrosis, and mitotic activity, histologic grade became the most significant prognostic factor for both DSS and MFS. In addition, larger tumors and older patients become associated with a significantly worse prognosis. Independent adverse risk factors for local recurrence-free survival included histologic grade 3 and truncal tumor location.
These data confirm that not all SS present the same severe outcome. High-risk patients identified on the basis of these parameters may qualify for an aggressive treatment approach.
确定局限性原发性滑膜肉瘤(SS)成人患者中最重要且与治疗相关的预后因素,并证实法国癌症中心联合会(FNCLCC)分级系统的实用性,该分级系统在软组织肉瘤中的预后影响已得到证实。
回顾性研究了1980年至1994年间FNCLCC肉瘤小组从合作数据库中收集的128例非转移性SS患者的数据。77例(61%)患者在诊断时进行了免疫组化检查。肿瘤分为双相型(n = 45)、单相纤维型(n = 72)和低分化型(n = 10)亚型。根据FNCLCC方法确定组织学分级,并对每例患者评估血管侵犯情况。
该组局限性SS患者的5年疾病特异性生存率(DSS)为62.9%(±9.6%[标准差]),中位随访时间为37个月(范围8至141个月)。多因素分析显示,与DSS降低相关的不良风险因素为国际抗癌联盟/美国癌症联合委员会III/IVA期疾病、男性和躯干肿瘤部位。对于无转移生存率(MFS),III/IVA期疾病、肿瘤坏死和单相亚型是与预后较差相关的主要因素。另外,不考虑疾病分期、肿瘤坏死和有丝分裂活性时,组织学分级成为DSS和MFS最显著的预后因素。此外,肿瘤较大和年龄较大的患者预后明显较差。局部无复发生存率的独立不良风险因素包括组织学3级和躯干肿瘤部位。
这些数据证实并非所有SS都有同样严重的结局。根据这些参数确定的高危患者可能适合积极的治疗方法。