Evaluating the Soft Tissue Sarcoma Paradigm for the Local Management of Extraskeletal Ewing Sarcoma

被引:8
作者
Boyce-Fappiano, David [1 ]
Guadagnolo, B. Ashleigh [1 ]
Ratan, Ravin [2 ]
Wang, Wei-Lien [3 ]
Wagner, Michael J. [6 ]
Patel, Shreyaskumar [2 ]
Livingston, John A. [2 ]
Lin, Patrick P. [4 ]
Diao, Kevin [1 ]
Mitra, Devarati [1 ]
Farooqi, Ahsan [1 ]
Lazar, Alexander J. [3 ]
Roland, Christina L. [5 ]
Bishop, Andrew J. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, 1515 Holcombe Blvd,Unit 0097, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Sarcoma Med Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Orthoped Surg, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[6] Univ Washington, Div Med Oncol, Seattle, WA 98195 USA
关键词
Extraskeletal Ewing sarcoma; Sarcoma; Local therapy; Radiation therapy; PRIMITIVE NEUROECTODERMAL TUMOR; RADIATION-THERAPY; PROGNOSTIC-SIGNIFICANCE; STANDARD CHEMOTHERAPY; DEFINITIVE SURGERY; MULTIMODAL THERAPY; SYSTEMIC THERAPY; RANDOMIZED-TRIAL; FAMILY; BONE;
D O I
10.1002/onco.13616
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives We reviewed our experience treating patients with localized extraskeletal Ewing sarcoma (EES) to determine optimal local management strategies for this rare disease. Methods 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. Results 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). Conclusion 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. Implications for Practice 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.
引用
收藏
页码:250 / 260
页数:11
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