唐顺, 郭卫, 汤小东, 李大森, 王毅飞. 间叶性软骨肉瘤的外科治疗及预后分析[J]. 中国肿瘤临床, 2013, 40(16): 984-987. DOI: 10.3969/j.issn.1000-8179.20121855
引用本文: 唐顺, 郭卫, 汤小东, 李大森, 王毅飞. 间叶性软骨肉瘤的外科治疗及预后分析[J]. 中国肿瘤临床, 2013, 40(16): 984-987. DOI: 10.3969/j.issn.1000-8179.20121855
Shun TANG, Wei GUO, Xiaodong TANG, Dasen LI, Yifei WANG. Surgical treatment and prognosis of mesenchymal chondrosarcoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 40(16): 984-987. DOI: 10.3969/j.issn.1000-8179.20121855
Citation: Shun TANG, Wei GUO, Xiaodong TANG, Dasen LI, Yifei WANG. Surgical treatment and prognosis of mesenchymal chondrosarcoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 40(16): 984-987. DOI: 10.3969/j.issn.1000-8179.20121855

间叶性软骨肉瘤的外科治疗及预后分析

Surgical treatment and prognosis of mesenchymal chondrosarcoma

  • 摘要:
      目的  通过研究在本中心治疗的27例间叶性软骨肉瘤患者的临床资料,总结其临床特点,治疗及预后情况,探讨间叶性软骨肉瘤临床治疗的合理方案。
      方法  自1997年10月至2011年3月,本院骨肿瘤科共治疗了27例间叶性软骨肉瘤的患者,并对随访的临床资料进行了回顾性研究和统计学相关分析。
      结果  在27例间叶性软骨肉瘤中,包括男性患者9例,女性患者18例,平均年龄30.4岁(14~51岁)。平均随访时间42.6个月(6~104个月)。其中22例为骨来源,5例为软组织来源。除2例患者外,其余25例患者均接受了手术治疗,但其中只有17例达到了广泛性切除的外科边界。16例患者接受了辅助化疗;13例患者接受了局部放疗。随访术后3年和5年的总体生存率分别为65.0%和49.5%。
      结论  间叶性软骨肉瘤是一种少见的骨与软组织的恶性肿瘤,易于出现远期的局部复发和远处转移。对于间叶性软骨肉瘤的治疗需要制定标准化的治疗方案,目前认为外科手术是否能达到广泛切除的外科边界是肿瘤治疗的金标准,辅助化疗及局部放疗是否能够有效控制肿瘤的局部复发和转移,仍需得到进一步确认。

     

    Abstract:
      Objective  To assess the surgical outcome of patients with mesenchymal chondrosarcoma (MCS) treated in our institute. This study was also designed to describe the clinical characteristics, treatment, and outcome of MCS to provide a better understanding of its clinical management.
      Methods  A total of 27 patients with MCS were treated in Peking University People's Hospital, Beijing, China from October 1997 to March 2011. Demographic information and follow-up data were obtained and statistically analyzed.
      Results  Among the 27 patients, 9 were males and 18 were females with a mean age of 30.4 years (ranging from 14 years to 51 years). The median follow-up time was 42.6 months (ranging from 6 months to 104 months). Among the total number of tumor cases, 22 and 5 were detected in bone tissues and extra-skeletal sites, respectively. A total of 25 patients underwent surgery, but only 17 achieved the standard surgical margin of wide excision. Among these patients, 16 and 13 were subjected to chemotherapy and irradiation. The threeand five-year survival rates were 65% and 49.5%, respectively.
      Conclusion  MCS is a rare tumor resulting in morbidity with local recurrences and long-term metastases. In this study, standard multimodal regimens were proposed to treat MCS. The results recommended wide resection with suitable surgical margins as the preferred treatment. However, further studies should be conducted because the information about the benefits of chemotherapy and radiotherapy for the control of local or systemic symptoms of MCS remains insufficient.

     

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