EWSR1-PATZ1 fusion renal cell carcinoma: a recurrent gene fusion characterizing thyroid-like follicular renal cell carcinoma

. 2021 Oct ; 34 (10) : 1921-1934. [epub] 20210607

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid34099871

Thyroid-like follicular renal cell carcinoma is an uncommon kidney tumor with no distinct molecular alteration described to date. This cohort of eight women with mean and median ages of 45 and 46 years, respectively (range 19-65 years), had unencapsulated, well-circumscribed tumors composed of tightly packed anastomosing follicle-like cysts filled with eosinophilic colloid-like material and lined by cuboidal cells with high nuclear to cytoplasmic ratios, oval to elongated nuclei with perpendicular arrangement toward the lumens, and prominent nuclear overlapping. The stroma between these was minimal with the exception of two tumors. Calcifications and necrosis were absent. Immunohistochemically, the tumors were positive for KRT19 (7/7), PAX8 (5/5), cyclin D1 (6/6), KRT7 (5/7), and AMACR (1/5; focal, weak), and were negative for WT1, TTF1 (transcription termination factor-1), and thyroglobulin. In three of three tumors tested molecularly, EWSR1-PATZ1 fusion was identified by RNA sequencing and confirmed by RT-PCR and Sanger sequencing. Over a follow-up period of 1-7 years, no evidence of recurrence or metastasis has been detected. The EWSR1-PATZ1 fusion has been recognized as a recurrent alteration in a subset of round to spindle cell sarcomas with EWSR1-non-ETS fusions (EWSR1-PATZ1 sarcoma) and in several central nervous system tumors. The finding of an EWSR1-PATZ1 fusion in all three of the thyroid-like follicular renal cell carcinomas for which sufficient tissue was available for genomic profiling provides the first distinct molecular abnormality in thyroid-like follicular renal cell carcinomas, supporting its designation as a distinct diagnostic entity.

Zobrazit více v PubMed

Amin M, Bichal M, Radhakrishman A, Hes O, McKenney JK, Cheville JC. Primary thyroid-like follicular carcinoma of the kidney: a histologically distinctive primary renal epithelial tumor. Mod Pathol. 2004;17:136–7. DOI

Amin MB, Gupta R, Ondrej H, McKenney JK, Michal M, Young AN, et al. Primary thyroid-like follicular carcinoma of the kidney: report of 6 cases of a histologically distinctive adult renal epithelial neoplasm. Am J Surg Pathol. 2009;33:393–400. PubMed DOI

Srigley JR, Delahunt B, Eble JN, Egevad L, Epstein JI, Grignon D, et al. The International Society of Urological Pathology (ISUP) Vancouver classification of renal neoplasia. Am J Surg Pathol. 2013;37:1469–89. PubMed DOI

Moch H, Cubilla AL, Humphrey PA, Reuter VE, Ulbright TM. The 2016 WHO classification of tumours of the urinary system and male genital organs-Part A: renal, penile, and testicular tumours. Eur Urol. 2016;70:93–105. PubMed DOI

Eble JN, Delahunt B. Emerging entities in renal cell neoplasia: thyroid-like follicular renal cell carcinoma and multifocal oncocytoma-like tumours associated with oncocytosis. Pathology. 2018;50:24–36. PubMed DOI

Trpkov K, Hes O. New and emerging renal entities: a perspective post-WHO 2016 classification. Histopathology. 2019;74:31–59. PubMed DOI

Tretiakova MS, Kehr EL, Gore JL, Tykodi SS. Thyroid-like follicular renal cell carcinoma arising within benign mixed epithelial and stromal tumor. Int J Surg Pathol. 2020;28:80–6. PubMed DOI PMC

Brunelli M, Eble JN, Zhang S, Martignoni G, Cheng L. Gains of chromosomes 7, 17, 12, 16, and 20 and loss of Y occur early in the evolution of papillary renal cell neoplasia: a fluorescent in situ hybridization study. Mod Pathol. 2003;16:1053–9. PubMed DOI

Cossu-Rocca P, Eble JN, Zhang S, Bonsib SM, Martignoni G, Brunelli M, et al. Interphase cytogenetic analysis with centromeric probes for chromosomes 1, 2, 6, 10, and 17 in 11 tumors from a patient with bilateral renal oncocytosis. Mod Pathol. 2008;21:498–504. PubMed DOI

Cheng L, Zhang S, Wang L, MacLennan GT, Davidson DD. Fluorescence in situ hybridization in surgical pathology: principles and applications. J Pathol Clin Res. 2017;3:73–99. PubMed DOI PMC

Kadri S, Long BC, Mujacic I, Zhen CJ, Wurst MN, Sharma S, et al. Clinical validation of a next-generation sequencing genomic oncology panel via cross-platform benchmarking against established amplicon sequencing assays. J Mol Diagn. 2017;19:43–56. PubMed DOI

Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009;25:1754–60. PubMed DOI PMC

Mose LE, Wilkerson MD, Hayes DN, Perou CM, Parker JS. ABRA: improved coding indel detection via assembly-based realignment. Bioinformatics. 2014;30:2813–5. PubMed DOI PMC

Li MM, Datto M, Duncavage EJ, Kulkarni S, Lindeman NI, Roy S, et al. Standards and guidelines for the interpretation and reporting of sequence variants in cancer: a joint consensus recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists. J Mol Diagn. 2017;19:4–23. PubMed DOI PMC

Talevich E, Shain AH, Botton T, Bastian BC. CNVkit: genome-wide copy number detection and visualization from targeted DNA sequencing. PLoS Comput Biol. 2016;12:e1004873. PubMed DOI PMC

Parilla M, Alikhan M, Al-Kawaaz M, Patil S, Kadri S, Ritterhouse LL, et al. Genetic underpinnings of renal cell carcinoma with leiomyomatous stroma. Am J Surg Pathol. 2019;43:1135–44. PubMed DOI

Benayed R, Offin M, Mullaney K, Sukhadia P, Rios K, Desmeules P, et al. SvABA: genome-wide detection of structural variants and indels by local assembly. Genome Res. 2018;28:581–91. DOI

Benayed R, Offin M, Mullaney K, Sukhadia P, Rios K, Desmeules P, et al. High yield of RNA sequencing for targetable kinase fusions in lung adenocarcinomas with no mitogenic driver alteration detected by DNA sequencing and low tumor mutation burden. Clin Cancer Res. 2019;25:4712–22. PubMed DOI PMC

de Jesus LE, Fulgencio C, Leve T, Dekermacher S. Thyroid-like follicular carcinoma of the kidney presenting on a 10 year-old prepubertal girl. Int Braz J Urol. 2019;45:834–42. PubMed DOI PMC

Sterlacci W, Verdorfer I, Gabriel M, Mikuz G. Thyroid follicular carcinoma-like renal tumor: a case report with morphologic, immunophenotypic, cytogenetic, and scintigraphic studies. Virchows Arch. 2008;452:91–5. PubMed DOI

Dhillon J, Tannir NM, Matin SF, Tamboli P, Czerniak BA, Guo CC. Thyroid-like follicular carcinoma of the kidney with metastases to the lungs and retroperitoneal lymph nodes. Hum Pathol. 2011;42:146–50. PubMed DOI

Dong L, Huang J, Huang L, Shi O, Liu Q, Chen H, et al. Thyroid-like follicular carcinoma of the kidney in a patient with skull and meningeal metastasis: a unique case report and review of the literature. Medicine (Baltim). 2016;95:e3314. DOI

Jenkins TM, Rosenbaum J, Zhang PJ, Schwartz LE, Nayak A, Cooper K, et al. Thyroid-like follicular carcinoma of the kidney with extensive sarcomatoid differentiation: a case report and review of the literature. Int J Surg Pathol. 2019;27:678–83. PubMed DOI

Chen X, Dou FX, Cheng XB, Guo AT, Shi HY. [Clinicopathologic characteristics of thyroid-like follicular carcinoma of the kidney: an analysis of five cases and review of literature]. Zhonghua Bing Li Xue Za Zhi. 2016;45:687–91. PubMed

Herlitz L, Hes O, Michal M, Tretiakova M, Reyes-Mugica M, Nguyen JK, et al. “Atrophic kidney”-like lesion: clinicopathologic series of 8 cases supporting a benign entity distinct from thyroid-like follicular carcinoma. Am J Surg Pathol. 2018;42:1585–95. PubMed DOI

Mehra R, Smith SC, Divatia M, Amin MB. Emerging entities in renal neoplasia. Surg Pathol Clin. 2015;8:623–56. PubMed DOI

Fanelli GN, Fassan M, Dal Moro F, Soligo M, Munari G, Zattoni F, et al. Thyroid-like follicular carcinoma of the kidney: the mutational profiling reveals a BRAF wild type status. Pathol Res Pr. 2019;215:152532. DOI

Nikiforova MN, Lynch RA, Biddinger PW, Alexander EK, Dorn GW 2nd, Tallini G, et al. RAS point mutations and PAX8-PPAR gamma rearrangement in thyroid tumors: evidence for distinct molecular pathways in thyroid follicular carcinoma. J Clin Endocrinol Metab. 2003;88:2318–26. PubMed DOI

Alaghehbandan R, Michal M, Kuroda N, Hes O. Thyroid-like follicular carcinoma of the kidney: an emerging renal neoplasm with curiously misplaced histologic features. A case report. Int J Surg Pathol. 2017;25:379–80. PubMed DOI

Muscara MJ, Simper NB, Gandia E. Thyroid-like follicular carcinoma of the kidney. Int J Surg Pathol. 2017;25:73–7. PubMed DOI

Delahunt B, Eble JN. Papillary renal cell carcinoma: a clinicopathologic and immunohistochemical study of 105 tumors. Mod Pathol. 1997;10:537–44. PubMed

Tosi AL, de Biase D, Leonardi E, Eusebi V. Thyroid-like metastases to the scalp from a papillary renal cell carcinoma: a case report. Tumori. 2012;98:79e–81e. PubMed DOI

Delahunt B, Eble JN, McCredie MR, Bethwaite PB, Stewart JH, Bilous AM. Morphologic typing of papillary renal cell carcinoma: comparison of growth kinetics and patient survival in 66 cases. Hum Pathol. 2001;32:590–5. PubMed DOI

Ricketts CJ, De Cubas AA, Fan H, Smith CC, Lang M, Reznik E, et al. The Cancer Genome Atlas comprehensive molecular characterization of renal cell carcinoma. Cell Rep. 2018;23:3698. PubMed DOI

Quddus MB, Pratt N, Nabi G. Chromosomal aberrations in renal cell carcinoma: an overview with implications for clinical practice. Urol Ann. 2019;11:6–14. PubMed DOI PMC

Al-Obaidy KI, Eble JN, Nassiri M, Cheng L, Eldomery MK, Williamson SR, et al. Recurrent KRAS mutations in papillary renal neoplasm with reverse polarity. Mod Pathol. 2020;33:1157–64. PubMed DOI

Speicher MR, Schoell B, du Manoir S, Schrock E, Ried T, Cremer T, et al. Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization. Am J Pathol. 1994;145:356–64. PubMed PMC

Alessandrini L, Fassan M, Gardiman MP, Guttilla A, Zattoni F, Galletti TP, et al. Thyroid-like follicular carcinoma of the kidney: report of two cases with detailed immunohistochemical profile and literature review. Virchows Arch. 2012;461:345–50. PubMed DOI

Chougule A, Bal A, Das A, Nayak B. Thyroid-like follicular renal cell carcinoma: an emerging morphological variant. Pathology. 2014;46:657–60. PubMed DOI

Wu WW, Chu JT, Nael A, Rezk SA, Romansky SG, Shane L. Thyroid-like follicular carcinoma of the kidney in a young patient with history of pediatric acute lymphoblastic leukemia. Case Rep. Pathol. 2014;2014:313974. PubMed PMC

Jung SJ, Chung JI, Park SH, Ayala AG, Ro JY. Thyroid follicular carcinoma-like tumor of kidney: a case report with morphologic, immunohistochemical, and genetic analysis. Am J Surg Pathol. 2006;30:411–5. PubMed DOI

Dawane R, Grindstaff A, Parwani AV, Brock T, White WM, Nodit L. Thyroid-like follicular carcinoma of the kidney: one case report and review of the literature. Am J Clin Pathol. 2015;144:796–804. PubMed DOI

Le Loarer F, Szuhai K, Tirode F. Round cell sarcoma with EWSR1-non ETS fusions. In: Antonescu CR, Bovee J, Bridge JA, Cunha IW, Dei Tos AP, Flanagan A, et al., editors. WHO classification of tumours of soft tissue and bone, 5th edition. Lyon, France: IARC Press; 2020. p. 326–9.

Qaddoumi I, Orisme W, Wen J, Santiago T, Gupta K, Dalton JD, et al. Genetic alterations in uncommon low-grade neuroepithelial tumors: BRAF, FGFR1, and MYB mutations occur at high frequency and align with morphology. Acta Neuropathol. 2016;131:833–45. PubMed DOI PMC

Johnson A, Severson E, Gay L, Vergilio JA, Elvin J, Suh J, et al. Comprehensive genomic profiling of 282 pediatric low- and high-grade gliomas reveals genomic drivers, tumor mutational burden, and hypermutation signatures. Oncologist. 2017;22:1478–90. PubMed DOI PMC

Alvarez-Breckenridge C, Miller JJ, Nayyar N, Gill CM, Kaneb A, D’Andrea M, et al. Clinical and radiographic response following targeting of BCAN-NTRK1 fusion in glioneuronal tumor. NPJ Precis Oncol. 2017;1:5. PubMed DOI PMC

Siegfried A, Rousseau A, Maurage CA, Pericart S, Nicaise Y, Escudie F, et al. EWSR1-PATZ1 gene fusion may define a new glioneuronal tumor entity. Brain Pathol. 2019;29:53–62. PubMed DOI

ridge JA, Sumegi J, Druta M, Bui MM, Henderson-Jackson E, Linos K, et al. Clinical, pathological, and genomic features of EWSR1-PATZ1 fusion sarcoma. Mod Pathol. 2019;32:1593–604. DOI

Watson S, Perrin V, Guillemot D, Reynaud S, Coindre JM, Karanian M, et al. Transcriptomic definition of molecular subgroups of small round cell sarcomas. J Pathol. 2018;245:29–40. PubMed DOI

Cantile M, Marra L, Franco R, Ascierto P, Liguori G, De Chiara A, et al. Molecular detection and targeting of EWSR1 fusion transcripts in soft tissue tumors. Med Oncol. 2013;30:412. PubMed DOI PMC

Fedele M, Crescenzi E, Cerchia L. The POZ/BTB and AT-hook-containing Zinc finger 1 (PATZ1) transcription regulator: physiological functions and disease involvement. Int J Mol Sci. 2017;18:2524.

Zhu B, Poeta ML, Costantini M, Zhang T, Shi J, Sentinelli S, et al. The genomic and epigenomic evolutionary history of papillary renal cell carcinomas. Nat Commun. 2020;11:3096. PubMed DOI PMC

Argani P, Lewin JR, Edmonds P, Netto GJ, Prieto-Granada C, Zhang L, et al. Primary renal sclerosing epithelioid fibrosarcoma: report of 2 cases with EWSR1-CREB3L1 gene fusion. Am J Surg Pathol. 2015;39:365–73. PubMed DOI PMC

Ertoy Baydar D, Kosemehmetoglu K, Aydin O, Bridge JA, Buyukeren B, Aki FT. Primary sclerosing epithelioid fibrosarcoma of kidney with variant histomorphologic features: report of 2 cases and review of the literature. Diagn Pathol. 2015;10:186. PubMed DOI PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...