Liu Yen-Ting, Wang Chun-Wei, Hong Ruey-Long, Kuo Sung-Hsin
Division of Radiation Oncology, Department of Oncology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan, R.O.C.
Cancer Research Center, National Taiwan University College of Medicine, Taipei, Taiwan, R.O.C.
Anticancer Res. 2019 Mar;39(3):1355-1364. doi: 10.21873/anticanres.13249.
Adults with rhabdomyosarcoma (RMS) have a worse clinical outcome compared to pediatric cases. In the present study, the failure pattern and clinical outcome of adult patients with RMS who received multimodality treatment at our Institution was assessed.
Data were retrospectively recorded and analyzed from 20 adult patients, aged 19 years or more, who were treated for RMS at our Institution between 2004 and 2015. Disease-free (DFS) and overall (OS) survival after starting treatment were calculated using the Kaplan-Meier method. The relationship of these outcome measures with the following variables was then assessed: Primary site, tumor stage, lymph node involvement, histological subtype, radiotherapy (RT), and duration of chemotherapy.
Sixteen patients had localized RMS, and four had metastatic disease. For the whole patient cohort, the 3-year DFS and OS rates were 20%, and 45%, respectively. Patients with alveolar histological subtype had a better 3-year OS than those with other subtypes (p=0.038). The median OS rates for those with localized and metastatic disease were 53.2 (95% confidence interval(CI)=14.7-91.8) months, and 21.7 (95% CI=0-45.7) months, respectively (p=0.047). In patients with localized RMS, those who received RT (n=13) had a better median DFS (24.6 versus 6.0 months, p=0.009) and OS (53.2 versus 11.4 months, p=0.009) than those who did not (n=3). For patients receiving RT, concurrent chemotherapy with vincristine and cyclophosphamide (n=11) was associated with better 3-year DFS (36.4% versus 0%, p<0.001) and OS (81.8% versus 0%, p<0.001) compared with RT alone (n=2). Administration of chemotherapy for more than 19 weeks significantly correlated with better 3-year DFS (44% versus 0%, p=0.001) and OS (53.3% versus 0%, p<0.001) in those with localized RMS.
In addition to staging and histological subtype, our results indicate that concurrent chemoradiotherapy and longer duration of chemotherapy were associated with significantly improved DFS and OS in adult patients with localized RMS.
与儿童横纹肌肉瘤(RMS)患者相比,成年RMS患者的临床结局更差。在本研究中,评估了在我院接受多模式治疗的成年RMS患者的失败模式和临床结局。
回顾性记录并分析了2004年至2015年间在我院接受RMS治疗的20例19岁及以上成年患者的数据。采用Kaplan-Meier法计算开始治疗后的无病生存期(DFS)和总生存期(OS)。然后评估这些结局指标与以下变量的关系:原发部位、肿瘤分期、淋巴结受累情况、组织学亚型、放疗(RT)和化疗持续时间。
16例患者为局限性RMS,4例有转移性疾病。对于整个患者队列,3年DFS率和OS率分别为20%和45%。肺泡组织学亚型患者的3年OS优于其他亚型患者(p=0.038)。局限性和转移性疾病患者的中位OS分别为53.2(9