Rhabdoid tumor: the Irish experience 1986–2013

• Published in: Cancer genetics 2014-09, Vol.207 (9), p.398-402
• Main Authors: Uwineza, Alice, Gill, Harinder, Buckley, Patrick, Owens, Cormac, Capra, Michael, O'Sullivan, Catriona, McDermott, Michael, Brett, Francesca, Farrell, Michael, Pears, Jane, O'Sullivan, Maureen J
• Format: Article
• Language: English
• Subjects: Adolescent; Base Sequence; Central Nervous System Neoplasms - classification; Central Nervous System Neoplasms - genetics; Central Nervous System Neoplasms - pathology; Child; Child, Preschool; Chromosomal Proteins, Non-Histone - genetics; DNA-Binding Proteins - genetics; Female; Hematology, Oncology and Palliative Medicine; Humans; Infant; Infant, Newborn; Ireland; Irish; Karyotype; Kidney Neoplasms - classification; Kidney Neoplasms - genetics; Kidney Neoplasms - mortality; Male; Medical Education; Neoplasm Recurrence, Local - pathology; pediatric; Rhabdoid tumor; Rhabdoid Tumor - classification; Rhabdoid Tumor - genetics; Rhabdoid Tumor - pathology; Sequence Deletion; SMARCB1; SMARCB1 Protein; Survival Rate; Teratoma - classification; Teratoma - genetics; Teratoma - pathology; Transcription Factors - genetics
• ISSN: 2210-7762; 2210-7770
• DOI: 10.1016/j.cancergen.2014.05.015

Nomenclature for the three recognized forms of rhabdoid tumor reflect their anatomic localization and include malignant rhabdoid tumor of the kidney (MRTK), extrarenal extracranial rhabdoid tumor (EERT), and atypical teratoid rhabdoid tumor (ATRT) involving the central nervous system. A strikingly simple karyotype belies the fact that rhabdoid tumors are among the most lethal human cancers, and now early strides are beginning to elucidate their molecular pathogenesis. Rhabdoid tumors are largely confined to the pediatric population, where they occur preferentially during infancy. Given the rarity of this tumor, international consensus on best treatment has only recently been achieved in conjunction with the establishment of the European Rhabdoid Tumor Registry. Between 1986 and 2013, 25 pediatric patients were diagnosed with rhabdoid tumor in the Republic of Ireland. Of these patients, 13 presented with ATRT, eight had MRTK, and four had EERT. The mean age at diagnosis was 38.8 months, with an equal sex incidence. Because of the lack of a standardized treatment strategy for rhabdoid tumors, these patients have been treated largely according to anatomic site, based on sarcoma, renal, or brain tumor protocols contemporary to their diagnoses. Of the patients, 84% received chemotherapy, 80% underwent surgery, and 44% had radiation therapy. The outcome overall was poor, independent of anatomic location. The overall survival rate was 24%, and mean time to death was just under 9 months.