Clinicodemographic characteristics of extraosseous ewing sarcoma: A comparative meta-analysis of pediatric and adult patients

被引:0
作者
Ghandour, Maher [1 ,2 ]
Semaan, Karl [3 ]
Saad, Eddy [3 ]
Horsch, Axel [1 ]
Abdallah, Ralph [4 ]
Semaan, Doumit [2 ]
机构
[1] Heidelberg Univ Hosp, Orthoped Dept, Heidelberg, Germany
[2] Lebanese Univ, Orthoped Dept, POB 6573-14, Beirut, Lebanon
[3] Univ St Joseph, Med, Beirut, Lebanon
[4] Univ Toronto, Sci, Toronto, ON, Canada
关键词
Extraosseous ewing sarcoma; Pediatric; Children; Extra-skeletal; Adults; Clinical outcomes; PRIMITIVE NEUROECTODERMAL TUMOR; PROGNOSTIC-FACTORS; CLINICAL-FEATURES; EXTRASKELETAL; SKELETAL; OUTCOMES; FAMILY; AGE;
D O I
10.1016/j.jor.2023.09.002
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: Evidence suggests different presentation patterns and prognosis of extraosseous Ewing Sarcoma (EES) based on age. Thus, we carried out this study to test the difference between children and adult EES cases regarding clinicodemographic characteristics and prognosis.Methods: A total of 4 databases were explored yielding 18 relevant studies for data synthesis. Outcomes included the comparison of demographic and clinical characteristics as well as prognosis between children and adults with EES. Log odds ratio (logOR) and its 95% confidence interval (CI) were pooled across studies. Statistical models/ methods were selected based on heterogeneity.Results: Our analysis included a total of 1261 children and 1256 adults. When we compared these two age categories, we did not observe a significant difference in the risk of developing EES [logOR =-0.13; 95% CI:-0.65: 0.39; I2 = 88.42%]. No significant differences regarding gender, tumor location, and size (<= 5 vs. >5 cm), EWSR1 positivity, or management modality. We did not observe significant difference regarding clinical out-comes, such as 5-year overall survival and event-free survival, recurrence, mortality, no evidence of disease, and secondary metastasis.Conclusions: Our findings highlight the absence of an association between the age category of patients and the incidence of EES, as well as its clinical outcomes.
引用
收藏
页码:86 / 92
页数:7
相关论文
共 43 条
  • [1] Clinical Features and Outcomes in Patients with Extraskeletal Ewing Sarcoma
    Applebaum, Mark A.
    Worch, Jennifer
    Matthay, Katherine K.
    Goldsby, Robert
    Neuhaus, John
    West, Daniel C.
    DuBois, Steven G.
    [J]. CANCER, 2011, 117 (13) : 3027 - 3032
  • [2] Ewing's sarcoma
    Balamuth, Naomi J.
    Womer, Richard B.
    [J]. LANCET ONCOLOGY, 2010, 11 (02) : 184 - 192
  • [3] Adults with Ewing's sarcoma primitive neuroectodermal tumor - Adverse effect of older age and primary extraosseous disease on outcome
    Baldini, EH
    Demetri, GD
    Fletcher, CDM
    Foran, J
    Marcus, KC
    Singer, S
    [J]. ANNALS OF SURGERY, 1999, 230 (01) : 79 - 86
  • [4] Clinicopathological characteristics of peripheral primitive neuroectodermal tumour of skin and subcutaneous tissue
    Banerjee, SS
    Agbamu, DA
    Eyden, BP
    Harris, M
    [J]. HISTOPATHOLOGY, 1997, 31 (04) : 355 - 366
  • [5] Updates in the Treatment of Bone Cancer
    Biermann, J. Sybil
    [J]. JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2013, 11 (5.5): : 681 - 683
  • [6] Evaluation of Outcome and Prognostic Factors in Extraosseous Ewing Sarcoma
    Biswas, Bivas
    Shukla, N. K.
    Deo, S. V. S.
    Agarwala, Sandeep
    Sharma, D. N.
    Vishnubhatla, Sreenivas
    Bakhshi, Sameer
    [J]. PEDIATRIC BLOOD & CANCER, 2014, 61 (11) : 1925 - 1931
  • [7] Evaluating the Soft Tissue Sarcoma Paradigm for the Local Management of Extraskeletal Ewing Sarcoma
    Boyce-Fappiano, David
    Guadagnolo, B. Ashleigh
    Ratan, Ravin
    Wang, Wei-Lien
    Wagner, Michael J.
    Patel, Shreyaskumar
    Livingston, John A.
    Lin, Patrick P.
    Diao, Kevin
    Mitra, Devarati
    Farooqi, Ahsan
    Lazar, Alexander J.
    Roland, Christina L.
    Bishop, Andrew J.
    [J]. ONCOLOGIST, 2021, 26 (03) : 250 - 260
  • [8] Carpentieri DF, 2005, ARCH PATHOL LAB MED, V129, P866
  • [9] Bone sarcomas: ESMO-PaedCan-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up
    Casali, P. G.
    Bielack, S.
    Abecassis, N.
    Aro, H. T.
    Bauer, S.
    Biagini, R.
    Bonvalot, S.
    Boukovinas, I.
    Bovee, J. V. M. G.
    Brennan, B.
    Brodowicz, T.
    Martin-Broto, J.
    Brugieres, L.
    Buonadonna, A.
    De Alava, E.
    Dei Tos, A. P.
    Del Muro, X. G.
    Dileo, P.
    Dhooge, C.
    Eriksson, M.
    Fagioli, F.
    Fedenko, A.
    Ferraresi, V.
    Ferrari, A.
    Ferrari, S.
    Frezza, A. M.
    Gaspar, N.
    Gasperoni, S.
    Gelderblom, H.
    Gil, T.
    Grignani, G.
    Gronchi, A.
    Haas, R. L.
    Hassan, B.
    Hecker-Nolting, S.
    Hohenberger, P.
    Issels, R.
    Joensuu, H.
    Jones, R. L.
    Judson, I.
    Jutte, P.
    Kaal, S.
    Kager, L.
    Kasper, B.
    Kopeckova, K.
    Krakorova, D. A.
    Ladenstein, R.
    Le Cesne, A.
    Lugowska, I.
    Merimsky, O.
    [J]. ANNALS OF ONCOLOGY, 2018, 29 : 79 - 95
  • [10] Soft-tissue sarcomas of the extremities in patients of pediatric age
    Casanova, Michela
    Meazza, Cristina
    Gronchi, Alessandro
    Fiore, Marco
    Zaffignani, Elena
    Podda, Marta
    Collini, Paola
    Gandola, Lorenza
    Ferrari, Andrea
    [J]. JOURNAL OF CHILDRENS ORTHOPAEDICS, 2007, 1 (03) : 195 - 203