Outcomes and Prognostic Factors for Ewing-Family Tumors of the Extremities

被引:29
作者
Biswas, Bivas [1 ]
Rastogi, Shishir [2 ]
Khan, S. A. [2 ]
Mohanti, B. K. [3 ]
Sharma, D. N. [3 ]
Sharma, M. C. [4 ]
Mridha, A. R. [4 ]
Bakhshi, Sameer [1 ]
机构
[1] All India Inst Med Sci, Dept Med Oncol, Dr BR Ambedkar Inst Rotary Canc Hosp, New Delhi 110029, India
[2] All India Inst Med Sci, Dept Orthoped, Dr BR Ambedkar Inst Rotary Canc Hosp, New Delhi 110029, India
[3] All India Inst Med Sci, Dept Radiotherapy, Dr BR Ambedkar Inst Rotary Canc Hosp, New Delhi 110029, India
[4] All India Inst Med Sci, Dept Pathol, Dr BR Ambedkar Inst Rotary Canc Hosp, New Delhi 110029, India
关键词
PRIMITIVE NEUROECTODERMAL TUMOR; SARCOMA FAMILY; NEOADJUVANT CHEMOTHERAPY; RADIATION-THERAPY; BONE; ADJUVANT; EXPERIENCE; CESS-86;
D O I
10.2106/JBJS.M.00411
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: There are few published studies describing the clinical results of patients uniformly treated for a Ewing-family tumor of an extremity. Methods: We performed a review of patients who had received uniform treatment consisting of neoadjuvant chemotherapy, surgery and/or radiation therapy as local treatment, and then adjuvant chemotherapy from June 2003 to November 2011 at a single institution. Results: There were 158 patients included in the study. The median age was fifteen years. Sixty-nine (44%) of the patients had metastatic disease at presentation. Fifty-seven patients underwent surgery, and forty-one received radical radiation therapy following neoadjuvant chemotherapy. After a median of 24.3 months (range, 1.6 to ninety-seven months) of follow-up, the five-year event-free survival, overall survival, and local control rates (and standard error) were 24.1% +/- 4.3%, 43.5% +/- 6%, and 55% +/- 6.8%, respectively, for the entire cohort and 36.4% 6.2%, 57.6% 7.4%, and 58.2% +/- 7.9%, respectively, for patients without metastases. In the multivariate analysis, metastases predicted inferior. event-free survival (p = 0.02) and overall survival (p = 0.03) rates in the entire cohort, whereas radical radiation therapy predicted an inferior local control rate in the entire cohort (p = 0.001) and in patients without metastases (p = 0.04). In the group with localized disease, there was no difference between the patients who received radical radiation therapy and those who underwent surgery with regard to tumor diameter (p = 0.8) or post-neoadjuvant chemotherapy response (p = 0.1). A white blood cell count (WBC) of >11 x 10(9)/L predicted inferior event-free survival (p = 0.005) and local control (p = 0.02) rates for patients without metastases. Conclusions: To our knowledge, this is the largest study on extremity Ewing-family tumors. treated with uniform chemotherapy and either surgical resection or radical radiation therapy in Asia. All possible efforts should be made to resect a primary tumor after neoadjuvant chemotherapy, as radical radiation therapy alone results in a poor local control rate despite a good post-neoadjuvant chemotherapy response. Patients without metastases but With a high WBC had inferior event-free survival and local control rates and may require more aggressive therapy. Level of Evidence: Therapeutic Level IV. See Instructions for Authors for a complete description of levels of evidence.
引用
收藏
页码:841 / 849
页数:9
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