Departments of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Departments of Sarcoma Medical Oncology, , The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Oncologist. 2021 Mar;26(3):250-260. doi: 10.1002/onco.13616. Epub 2020 Dec 14.
We reviewed our experience treating patients with localized extraskeletal Ewing sarcoma (EES) to determine optimal local management strategies for this rare disease.
Sixty patients with localized EES treated at our institution between 1994 and 2018 were reviewed. The Kaplan-Meier method was used to estimates disease outcomes.
The median follow-up time was 74 months (interquartile range [IQR], 17-121). Half the patients (n = 30) received combined-modality local therapy (CMT) with both surgery and radiation therapy (RT), whereas the other half received single-modality local therapy (SMT) with either surgery or RT. All patients received chemotherapy. The 5-year overall survival was 76%. Twenty-two patients (37%) developed recurrence at a median time of 15 months (IQR, 5-56 months) resulting in 3-year progression-free survival (PFS) of 65%. On univariate analysis, the use of both neoadjuvant and adjuvant chemotherapy was associated with improved 5-year PFS (71% vs. 50%, p = .04) compared with those who received one or the other. Furthermore, 11 patients (18%) developed local recurrences at a median time of 14 months (IQR, 2-19 months), resulting in a 5-year local control (LC) rate of 77%. Use of CMT was not associated with improved LC (83% vs. 72% SMT, p = .41). Also, use of CMT was the only factor associated with poorer disease-specific survival (vs. SMT; hazard ratio, 3.4; p = .047; 95% confidence interval, 1.01-11.4).
For patients with EES, CMT was not associated with a decreased rate of local relapse. These data suggest that SMT alone may be sufficient for LC in select patients. A multi-institutional collaborative effort should be considered to validate these findings.
Extraskeletal Ewing sarcoma is a rare chemosensitive sarcoma whose clinical course more closely follows Ewing sarcoma of bone rather than that of other soft tissue sarcomas. Based on this study, combined-modality local therapy did not confer a local control advantage compared with single-modality local therapy. Therefore, single-modality local therapy is likely adequate in select patients with favorable disease features, which has the advantage of ensuring prompt administration of systemic therapy. A multi-institutional collaborative effort is warranted to determine which patients may benefit from de-escalated local therapy.
我们回顾了治疗局部骨外尤因肉瘤(EES)患者的经验,以确定这种罕见疾病的最佳局部治疗策略。
我们回顾了 1994 年至 2018 年期间在我院治疗的 60 例局部 EES 患者。采用 Kaplan-Meier 法估计疾病结局。
中位随访时间为 74 个月(四分位距 [IQR],17-121)。一半的患者(n=30)接受了手术联合放化疗(CMT)的联合局部治疗,而另一半患者接受了手术或放化疗的单一局部治疗(SMT)。所有患者均接受化疗。5 年总生存率为 76%。22 例患者(37%)在中位时间 15 个月(IQR,5-56 个月)时复发,导致 3 年无进展生存率(PFS)为 65%。单因素分析显示,与仅使用新辅助化疗或辅助化疗相比,同时使用新辅助化疗和辅助化疗的患者 5 年 PFS 提高(71%比 50%,p=0.04)。此外,11 例患者(18%)在中位时间 14 个月(IQR,2-19 个月)时发生局部复发,导致 5 年局部控制率(LC)为 77%。CMT 的使用与 LC 无改善相关(CMT 组为 83%,SMT 组为 72%,p=0.41)。此外,CMT 的使用是唯一与较差的疾病特异性生存率相关的因素(与 SMT 相比;风险比,3.4;p=0.047;95%置信区间,1.01-11.4)。
对于 EES 患者,CMT 并不能降低局部复发率。这些数据表明,在某些患者中,单独使用 SMT 可能足以实现 LC。应考虑开展多机构合作研究,以验证这些发现。
骨外尤因肉瘤是一种罕见的化疗敏感肉瘤,其临床过程更接近骨尤因肉瘤,而不是其他软组织肉瘤。基于这项研究,与单一局部治疗相比,联合局部治疗并未带来局部控制优势。因此,对于具有良好疾病特征的患者,单一局部治疗可能就足够了,这具有确保及时进行全身治疗的优势。有必要开展多机构合作研究,以确定哪些患者可能受益于降级的局部治疗。