Defining Ewing and Ewing-like small round cell tumors (SRCT): The need for molecular techniques in their categorization and differential diagnosis. A study of 200 cases

被引:41
作者
Machado, Isidro [1 ]
Navarro, Lara [2 ]
Pellin, Antonio [2 ]
Navarro, Samuel [2 ]
Agaimy, Abbas [3 ]
Tardio, Juan C. [4 ]
Karseladze, Apollon [5 ]
Petrov, Semyon [6 ,7 ]
Scotlandi, Katia [8 ]
Picci, Piero [8 ]
Llombart-Bosch, Antonio [2 ]
机构
[1] Inst Valenciano Oncol FIVO, Dept Pathol, C Gregorio Gea 31, Valencia 46009, Spain
[2] Univ Valencia, Dept Pathol, Valencia, Spain
[3] Univ Erlangen Nurnberg, Inst Pathol, Univ Hosp, Erlangen, Germany
[4] Hosp Univ Fuenlabrada, Dept Pathol, Madrid, Spain
[5] All Canc Ctr, Dept Pathol, Moscow, Russia
[6] Ctr Canc, Dept Pathol, Kazan, Russia
[7] Kazan State Med Univ, Dept Pathol, Kazan, Russia
[8] Rizzoli Inst, Expt Oncol Lab, Bologna, Italy
关键词
Ewing-like tumors; Ewing sarcoma family of tumors; Molecular biology; RT-PCR; SOFT-TISSUE TUMORS; SARCOMA FAMILY; GENE FUSION; CIC-DUX4; TRANSLOCATION; EWSR1; IMMUNOHISTOCHEMISTRY; REARRANGEMENTS; OSTEOSARCOMA; PREVALENCE; TRANSCRIPT;
D O I
10.1016/j.anndiagpath.2016.03.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Differentiation of Ewing sarcoma family of tumors (ESFT) and Ewing-like tumors remains problematic. Certain ESFT with morphological and immunohistochemical (IHC) profiles lack the EWSR1-ETS transcript. To improve diagnostic accuracy we investigated the presence of several specific transcripts in 200 small round cell tumors (SRCT) displaying ESFT morphology and immunophenotype in which EWSR1 FISH analysis was non informative or negative. Design: 200 tumors (formalin-fixed, paraffin-embedded) were analyzed by RT-PCR. All tumors were tested for EWSR1-ETS, EWSR1/WT1, PAX3/7-FOX01 or SYT/SSX transcripts, and the negative tumors were subsequently analyzed for CIC/DUX4, BCOR/CCNB3 and CIC/FOX04 transcripts. Results: 133 (66.5%) ESFT displayed one of the above EWSR1-ETS translocations. Three cases (1.5%) revealed the SYT-SSX transcript for Synovial sarcoma, and one (0.5%) a EWSR1-WT1 transcript for Desmoplastic Small Round Cell tumor. The CIC-DUX4 translocation was found in six Ewing-like tumors (3%) with CD99 positivity. The BCOR-CCNB3 gene fusion was observed in 5 tumors (2.5%) displaying round or spindle cells with strong CCNB3 IHC expression in 3 tumors. Moreover, RT-PCR failed to detect any gene fusion transcripts in 19 tumors (9.5%) and were considered "undifferentiated small round cell sarcoma" (SRCS). Molecular biology results were non informative in 33 SRCTs (16.5%) due to RNA degradation through inadequate fixation and/or decalcification. Conclusion: Our analysis of 200 SRCTs confirms the molecular heterogeneity of neoplasms with ESFT morphology and highlight that molecular studies with RT-PCR including new emerging gene fusion transcripts are mandatory for the diagnosis when EWSR1 FISH is negative or non-informative. The incidence of CIC-DUX4, BCOR-CCNB3 and CIC-FOX04 transcripts was relatively low. A small group of Ewing-like sarcomas or undifferentiated SRCS remains unclassified. Adopting appropriate tissue fixation and processing protocols is important to avoid degradation of fixed/embedded tissue when no frozen tumor is available. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:25 / 32
页数:8
相关论文
共 47 条
  • [41] Distinct Transcriptional Signature and Immunoprofile of CIC-DUX4 Fusion-Positive Round Cell Tumors Compared to EWSR1-Rearranged Ewing Sarcomas: Further Evidence Toward Distinct Pathologic Entities
    Specht, Katja
    Sung, Yun-Shao
    Zhang, Lei
    Richter, Guenther H. S.
    Fletcher, Christopher D.
    Antonescu, Cristina R.
    [J]. GENES CHROMOSOMES & CANCER, 2014, 53 (07) : 622 - 633
  • [42] Sugita S, 2014, AM J SURG PATHOL, V38, P1571, DOI 10.1097/PAS.0000000000000286
  • [43] Ewing-like sarcoma with CIC-DUX4 gene fusion in a patient with neurofibromatosis type 1. A hitherto unreported association
    Tardio, Juan C.
    Machado, Isidro
    Navarro, Lara
    Idrovo, Franklin
    Sanz-Ortega, Julian
    Pellin, Antonio
    Llombart-Bosch, Antonio
    [J]. PATHOLOGY RESEARCH AND PRACTICE, 2015, 211 (11) : 877 - 882
  • [44] Undifferentiated small round cell sarcomas with rare EWS gene fusions -: Identification of a novel EWS-SP3 fusion and of additional cases with the EWS-ETV1 and EWS-FEV Fusions
    Wang, Lu
    Bhargava, Rohit
    Zheng, Tao
    Wexler, Leonard
    Collins, Margaret H.
    Roulston, Diane
    Ladanyi, Marc
    [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2007, 9 (04) : 498 - 509
  • [45] Round Cell Tumors of Bone: An Update on Recent Molecular Genetic Advances
    Wei, Shi
    Siegal, Gene P.
    [J]. ADVANCES IN ANATOMIC PATHOLOGY, 2014, 21 (05) : 359 - 372
  • [46] NKX2.2 is a Useful Immunohistochemical Marker for Ewing Sarcoma
    Yoshida, Akihiko
    Sekine, Shigeki
    Tsuta, Koji
    Fukayama, Masashi
    Furuta, Koh
    Tsuda, Hitoshi
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2012, 36 (07) : 993 - 999
  • [47] Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC-DUX4 fusion gene event
    Yoshimoto, Maisa
    Graham, Cassandra
    Chilton-MacNeill, Susan
    Lee, Eric
    Shago, Mary
    Squire, Jeremy
    Zielenska, Maria
    Somers, Gino R.
    [J]. CANCER GENETICS AND CYTOGENETICS, 2009, 195 (01) : 1 - 11