A single-center retrospective study of malignant ectomesenchymoma in children

被引:0
作者
Meng, Yiran [1 ]
Su, Yan [2 ]
Zhang, Ge [1 ]
Yang, Wei [3 ]
Li, Zhe [4 ]
Liu, Yuanhu [1 ]
Li, Yanzhen [1 ]
Zhang, Xuexi [1 ]
Liu, Qiaoyin [1 ]
Sun, Nian [1 ]
Liu, Zhiyong [1 ]
Wang, Shengcai [1 ]
Ni, Xin [1 ,4 ]
机构
[1] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Otolaryngol Head & Neck Surg, 56 Nanlishi Rd, Beijing 100045, Peoples R China
[2] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Hematol,Oncol Ctr, 56 Nanlishi Rd, Beijing 100045, Peoples R China
[3] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Surg Oncol, 56 Nanlishi Rd, Beijing 100045, Peoples R China
[4] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Natl Ctr Pediat Canc Surveillance, 56 Nanlishi Rd, Beijing 100045, Peoples R China
关键词
malignant ectomesenchymoma; children; chemotherapy; radiotherapy; surgery;
D O I
10.1093/jjco/hyaf040
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives This study aimed to summarize the clinical and pathological characteristics of Malignant Ectomesenchymoma (MEM) and provide an overview of the available treatment options.Methods A retrospective analysis was conducted on data from 11 children diagnosed with MEM at Beijing Children's Hospital between 2012 and 2023.Results The study included nine male and two female patients, with a median age of 3 years (range, 1.5-11.0 years). The most commonly affected sites were the head and neck (45.6%), followed by the limbs (27.2%) and the pelvis/abdomen (27.2%). Nine children presented with localized MEM, while two had metastatic disease at the time of diagnosis. Among the nine children who underwent surgery, four received a combination of radiotherapy and chemotherapy, while five were treated with chemotherapy alone. Two children received only conservative treatment. The median follow-up period was 5.8 years (range, 0.7-12.3 years). Children who received both radiotherapy and chemotherapy had a significantly lower relapse rate compared to those treated with chemotherapy alone (2/6 vs. 5/5, P = 0.046). Additionally, children with FOXO1(+) tumors had lower survival rates than those with FOXO1(-) tumors (0/2 vs. 7/8). The 5-year overall survival rate was 79%, while the event-free survival rate was 14%.Conclusions Combining chemotherapy with local treatments such as surgery and radiotherapy can improve the prognosis for children with MEM. Radiotherapy may be beneficial in reducing the incidence of adverse effects in patients with MEM. This study of 11 children with MEM analyzed clinical characteristics, treatments (including surgery, radiotherapy and chemotherapy) and outcomes. The results showed that combined radiotherapy may reduce the recurrence rate.
引用
收藏
页码:621 / 625
页数:5
相关论文
共 16 条
[1]   Prognostic factors in children undergoing salvage surgery for bladder/prostate rhabdomyosarcoma [J].
Angelini, Lorenzo ;
Bisogno, Gianni ;
Alaggio, Rita ;
Scarzello, Giovanni ;
Santoro, Luisa ;
Zanetti, Ilaria ;
Scagnellato, Angela ;
Basso, Eleonora ;
D'Angelo, Paolo ;
Ferrari, Andrea ;
Castagnetti, Marco .
JOURNAL OF PEDIATRIC UROLOGY, 2016, 12 (04) :265.e1-265.e8
[2]   Clinicopathologic study of ectomesenchymomas from intergroup rhabdomyosarcoma study groups III and IV [J].
Boué, DR ;
Parham, DM ;
Webber, B ;
Crist, WM ;
Qualman, SJ .
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2000, 3 (03) :290-300
[3]   THE THIRD INTERGROUP RHABDOMYOSARCOMA STUDY [J].
CRIST, W ;
GEHAN, EA ;
RAGAB, AH ;
DICKMAN, PS ;
DONALDSON, SS ;
FRYER, C ;
HAMMOND, D ;
HAYS, DM ;
HERRMANN, J ;
HEYN, R ;
JONES, PM ;
LAWRENCE, W ;
NEWTON, W ;
ORTEGA, J ;
RANEY, RB ;
RUYMANN, FB ;
TEFFT, M ;
WEBBER, B ;
WIENER, E ;
WHARAM, M ;
VIETTI, TJ ;
MAURER, HM .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (03) :610-630
[4]   Malignant ectomesenchymoma in children and adolescents: Report from the Cooperative Weichteilsarkom Studiengruppe (CWS) [J].
Dantonello, Tobias M. ;
Leuschner, Ivo ;
Vokuhl, Christian ;
Gfroerer, Stefan ;
Schuck, Andreas ;
Kube, Stefanie ;
Nathrath, Michaela ;
Bernbeck, Benedikt ;
Kaatsch, Peter ;
Pal, Niklas ;
Ljungman, Gustaf ;
Bielack, Stefan S. ;
Klingebiel, Thomas ;
Koscielniak, Ewa .
PEDIATRIC BLOOD & CANCER, 2013, 60 (02) :224-229
[5]   Malignant Ectomesenchymoma: Series Analysis of a Histologically and Genetically Heterogeneous Tumor [J].
Griffin, Brannan B. ;
Chou, Pauline M. ;
George, David ;
Jennings, Lawrence J. ;
Arva, Nicoleta C. .
INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2018, 26 (03) :200-212
[6]   Ectomesenchymoma: One or two tumors? Case report and review of the literature [J].
Hajivassiliou, CA ;
Carachi, R ;
Simpson, E ;
Patrick, WJA ;
Young, DG .
JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (09) :1351-1355
[7]   Frequent HRAS Mutations in Malignant Ectomesenchymoma: Overlapping Genetic Abnormalities With Embryonal Rhabdomyosarcoma [J].
Huang, Shih-Chiang ;
Alaggio, Rita ;
Sung, Yun-Shao ;
Chen, Chun-Liang ;
Zhang, Lei ;
Kao, Yu-Chien ;
Agaram, Narasimhan P. ;
Wexler, Leonard H. ;
Antonescu, Cristina R. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2016, 40 (07) :876-885
[8]  
KAWAMOTO EH, 1987, CANCER-AM CANCER SOC, V59, P1791, DOI 10.1002/1097-0142(19870515)59:10<1791::AID-CNCR2820591018>3.0.CO
[9]  
2-#
[10]   Malignant ectomesenchymoma in children: The European pediatric Soft tissue sarcoma Study Group experience [J].
Milano, Giuseppe Maria ;
Orbach, Daniel ;
Casanova, Michela ;
Berlanga, Pablo ;
Schoot, Reineke A. ;
Corradini, Nadege ;
Brennan, Bernadette ;
Ramirez-Villar, Gema L. ;
Hjalgrim, Lisa Lyngsie ;
van Noesel, Max M. ;
Alaggio, Rita ;
Ferrari, Andrea .
PEDIATRIC BLOOD & CANCER, 2023, 70 (02)