Katz Daniela, Boonsirikamchai Piyaporn, Choi Haeson, Lazar Alexander J, Wang Wei-Lein, Xiao Lianchun, Park Min S, Ravi Vinod, Benjamin Robert S, Araujo Dejka M
Department of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Clin Sarcoma Res. 2012 Jan 24;2(1):2. doi: 10.1186/2045-3329-2-2.
Myxoid liposarcoma (MLS) is a soft tissue sarcoma with adipocytic differentiation characterized by a unique chromosome rearrangement, t(12;16)(q13;p11). The exact efficacy of chemotherapy in MLS has not been clearly established.
We retrospectively analyzed the records of 37 histologically confirmed MLS patients who were treated at the University of Texas MD Anderson Cancer Center from January 2000 to December 2009 with doxorubicin 75-90 mg/m2 over 72 hours combined with ifosfamide 10 gm/m2 in the first-line setting. Response was assessed using RECIST and Choi criteria. The Kaplan-Meier method and log-rank test was used to estimate clinical outcomes.
The median follow-up period was 50.1 months. The overall response rates were 43.2% using RECIST and 86.5% using the Choi criteria. The 5-year disease-free survival rate was 90% for patients with resectable tumors. Median time to progression and overall survival time for the advanced-disease group were 23 and 31.1 months, respectively.
Our study demonstrates that doxorubicin-ifosfamide combination therapy has a role in the treatment of MLS. The Choi criteria may be more sensitive in evaluating response to chemotherapy in MLS.
黏液样脂肪肉瘤(MLS)是一种具有脂肪细胞分化的软组织肉瘤,其特征为独特的染色体重排,即t(12;16)(q13;p11)。化疗在MLS中的确切疗效尚未明确确立。
我们回顾性分析了2000年1月至2009年12月在德克萨斯大学MD安德森癌症中心接受治疗的37例经组织学确诊的MLS患者的记录,这些患者在一线治疗中接受了72小时内阿霉素75 - 90 mg/m²联合异环磷酰胺10 gm/m²的治疗。使用RECIST和Choi标准评估反应。采用Kaplan-Meier方法和对数秩检验来估计临床结局。
中位随访期为50.1个月。使用RECIST标准的总反应率为43.2%,使用Choi标准的总反应率为86.5%。可切除肿瘤患者的5年无病生存率为90%。晚期疾病组的中位进展时间和总生存时间分别为23个月和31.1个月。
我们的研究表明阿霉素 - 异环磷酰胺联合治疗在MLS治疗中具有作用。Choi标准在评估MLS化疗反应方面可能更敏感。