Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases

. 2022 Mar ; 35 (3) : 344-351. [epub] 20210914

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, multicentrická studie, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid34521993
Odkazy

PubMed 34521993
DOI 10.1038/s41379-021-00923-6
PII: S0893-3952(22)00311-8
Knihovny.cz E-zdroje

A distinct renal tumor has recently been described as "high-grade oncocytic renal tumor" and "sporadic renal cell carcinoma with eosinophilic and vacuolated cytoplasm". The Genitourinary Pathology Society (GUPS) consensus proposed a unifying name "eosinophilic vacuolated tumor" (EVT) for this emerging entity. In this multi-institutional study, we evaluated 19 EVTs, particularly their molecular features and mutation profile, using next-generation sequencing. All cases were sporadic and none of the patients had a tuberous sclerosis complex. There were 8 men and 11 women, with a mean age of 47 years (median 50; range 15-72 years). Average tumor size was 4.3 cm (median 3.8 cm; range 1.5-11.5 cm). All patients with available follow-up data (18/19) were alive and without evidence of disease recurrence or progression during the follow-up, ranging from 12 to 198 months (mean 56.3, median 41.5 months). The tumors were well circumscribed, but lacked a well-formed capsule, had nested to solid growth, focal tubular architecture, and showed ubiquitous, large intracytoplasmic vacuoles, round to oval nuclei, and prominent nucleoli. Immunohistochemically, cathepsin K, CD117, CD10, and antimitochondrial antigen were expressed in all cases. Other positive stains included: PAX8, AE1/AE3 and CK18. CK7 was typically restricted only to rare scattered cells. Vimentin, HMB45, melan-A, and TFE3 were negative in all cases. All tumors showed retained SDHB. All cases (19/19) showed non-overlapping mutations of the mTOR pathway genes: TSC1 (4), TSC2 (7), and MTOR (8); one case with MTOR mutation showed a coexistent RICTOR missense mutation. Low mutational rates were found in all samples (ranged from 0 to 6 mutations/Mbp). Microsatellite instability and copy number variations were not found in any of the 17 analyzable cases. EVT represents an emerging renal entity that shows a characteristic and readily identifiable morphology, consistent immunohistochemical profile, indolent behavior, and mutations in either TSC1, TSC2, or MTOR genes.

Cancer Diagnosis and Pathology Group Kolling Institute of Medical Research Royal; North Shore Hospital St Leonards NSW Australia

Caris Life Sciences Phoenix AZ USA

Department of Biology and Medical Genetics 2nd Faculty of Medicine Charles University Prague and Motol University Hospital Prague Czech Republic

Department of Pathology Alfa Medical Bratislava Slovakia

Department of Pathology and Laboratory Medicine Cumming School of Medicine University of Calgary Calgary Alberta Canada

Department of Pathology British Columbia University Vancouver Canada

Department of Pathology Charles University Medical Faculty and Charles University Hospital Plzen Plzen Czech Republic

Department of Pathology Colentina Clinical Hospital Bucharest Romania

Department of Pathology Cruces University Hospital Biocruces Bizkaia Institute Barakaldo Spain

Department of Pathology El Camino Hospital Mountain View CA USA

Department of Pathology Heath Science Centre St John's NL Canada

Department of Pathology Institute Nacional de Cancerologia Mexico City Mexico

Department of Pathology McGill University Montreál QC Canada

Department of Pathology Oklahoma University School of Medicine Oklahoma USA

Department of Pathology School of Medicine University of Alabama Birmingham AL USA

Department of Pathology Sorbonne Université Service d'Anatomie et Cytologie Pathologiques Hôpital Tenon Paris France

Department of Pathology Stradin´s University Riga Latvia

Department of Pathology Tufts Medical Center Boston MA USA

Department of Pathology Universitätsklinikum Hamburg Eppendorf Hamburg Germany

Department of Pathology University Hospital Nitra Nitra Slovakia

Department of Pathology University Hospital Ostrava Ostrava Czech Republic

Department of Pathology University of Erlangen Erlangen Germany

Department of Pathology University of Szeged Szeged Hungary

Department of Pathology University of Toronto Toronto ON Canada

Department of Pathology University of Vienna Vienna Austria

Department of Pathology University of Washington School of Medicine Seattle WA USA

Department of Urology Charles University Medical Faculty and Charles University Hospital Plzen Plzen Czech Republic

Department of Urology University of Erlangen Erlangen Germany

Onco Team Diagnostic Bucharest Romania

Robert J Tomsich Pathology and Laboratory Medicine Institute Cleveland Clinic Cleveland OH USA

University of Sydney Sydney NSW Australia 2006; NSW Health Pathology Department of Anatomical Pathology Royal North Shore Hospital St Leonards NSW Australia

Erratum v

PubMed

Erratum v

PubMed

Zobrazit více v PubMed

He, H. et al. “High-grade oncocytic renal tumor”: morphologic, immunohistochemical, and molecular genetic study of 14 cases. Virchows Arch 473, 725–738 (2018). DOI

Chen, Y. B. et al. Somatic mutations of TSC2 or MTOR characterize a morphologically distinct subset of sporadic renal cell carcinoma with eosinophilic and vacuolated cytoplasm. Am. J. Surg. Pathol. 43, 121–131 (2019). DOI

Trpkov, K. et al. High-grade oncocytic tumour (HOT) of kidney in a patient with tuberous sclerosis complex. Histopathology 75, 440–442 (2019). DOI

Trpkov, K. et al. Novel, emerging and provisional renal entities: The Genitourinary Pathology Society (GUPS) update on renal neoplasia. Mod. Pathol. 34, 1167–1184 (2021). DOI

Gatalica, Z., Xiu, J., Swensen, J. & Vranic, S. Comprehensive analysis of cancers of unknown primary for the biomarkers of response to immune checkpoint blockade therapy. Eur. J. Cancer 94, 179–186 (2018). DOI

Samstein, R. M. et al. Tumor mutational load predicts survival after immunotherapy across multiple cancer types. Nat. Genet 51, 202–206 (2019). DOI

Vanderwalde, A., Spetzler, D., Xiao, N., Gatalica, Z. & Marshall, J. Microsatellite instability status determined by next-generation sequencing and compared with PD-L1 and tumor mutational burden in 11,348 patients. Cancer Med. 7, 746–756 (2018). DOI

Ruder, D. et al. Concomitant targeting of the mTOR/MAPK pathways: novel therapeutic strategy in subsets of RICTOR/KRAS-altered non-small cell lung cancer. Oncotarget 9, 33995–34008 (2018). DOI

Siadat, F. & Trpkov, K. ESC, ALK, HOT and LOT: Three letter acronyms of emerging renal entities knocking on the door of the WHO Classification. Cancers 12, 1 (2020). DOI

Guo, J. et al. Tuberous sclerosis-associated renal cell carcinoma: a clinicopathologic study of 57 separate carcinomas in 18 patients. Am. J. Surg. Pathol. 38, 1457–1467 (2014). DOI

Tjota, M. et al. Eosinophilic renal cell tumors with a TSC and MTOR gene mutations are morphologically and immunohistochemically heterogenous: clinicopathologic and molecular study. Am. J. Surg. Pathol. 44, 943–954 (2020). DOI

Palsgrove, D. N. et al. Eosinophilic solid and cystic (ESC) renal cell carcinomas harbor TSC mutations: Molecular analysis supports an expanding clinicopathologic spectrum. Am. J. Surg. Pathol. 42, 1166–1181 (2018). DOI

Williamson, S. R. et al. Diagnostic criteria for oncocytic renal neoplasms: a survey of urologic pathologists. Hum. Pathol. 63, 149–156 (2017). DOI

Petersson, F. et al. Sporadic hybrid oncocytic/chromophobe tumor of the kidney: a clinicopathologic, histomorphologic, immunohistochemical, ultrastructural, and molecular cytogenetic study of 14 cases. Virchows Arch 456, 355–365 (2010). DOI

Delongchamps, N. B. et al. Hybrid tumour ‘oncocytoma-chromophobe renal cell carcinoma’ of the kidney: a report of seven sporadic cases. BJU Int. 103, 1381–1384 (2009). DOI

Mai, K. T., Dhamanaskar, P., Belanger, E. & Stinson, W. A. Hybrid chromophobe renal cell neoplasm. Pathol. Res. Pr. 201, 385–389 (2005). DOI

Hes, O., Petersson, F., Kuroda, N., Hora, M. & Michal, M. Renal hybrid oncocytic/chromophobe tumors - a review. Histol. Histopathol. 28, 1257–1264 (2013). PubMed

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

Trpkov, K. et al. New developments in existing WHO entities and evolving molecular concepts: the Genitourinary Pathology Society (GUPS) update on renal neoplasia. Mod. Pathol. 34, 1392–1424 (2021). DOI

Alaghehbandan, R., Perez Montiel, D., Luis, A. S. & Hes, O. Molecular genetics of renal cell tumors: a practical diagnostic approach. Cancers 12, 1 (2019). DOI

Tretiakova, M. S. Eosinophilic solid and cystic renal cell carcinoma mimicking epithelioid angiomyolipoma: series of 4 primary tumors and 2 metastases. Hum. Pathol. 80, 65–75 (2018). DOI

Trpkov, K. et al. Eosinophilic, solid, and cystic renal cell carcinoma: Clinicopathologic study of 16 unique, sporadic neoplasms occurring in women. Am. J. Surg. Pathol. 40, 60–71 (2016). DOI

Trpkov, K. et al. Eosinophilic solid and cystic renal cell carcinoma (ESC RCC): Further morphologic and molecular characterization of ESC RCC as a distinct entity. Am. J. Surg. Pathol. 41, 1299–1308 (2017). DOI

Parilla, M. et al. Are sporadic eosinophilic solid and cystic renal cell carcinomas characterized by somatic tuberous sclerosis gene mutations? Am. J. Surg. Pathol. 42, 911–917 (2018). DOI

Shah, R. B. et al. “Renal cell carcinoma with leiomyomatous stroma” harbor somatic mutations of TSC1, TSC2, MTOR, and/or ELOC (TCEB1): Clinicopathologic and molecular characterization of 18 sporadic tumors supports a distinct entity. Am. J. Surg. Pathol. 44, 571–581 (2020). DOI

Schultz, L. et al. Immunoexpression status and prognostic value of mTOR and hypoxia-induced pathway members in primary and metastatic clear cell renal cell carcinomas. Am. J. Surg. Pathol. 35, 1549–1556 (2011). DOI

Kwiatkowski, D. J. et al. Mutations in TSC1, TSC2, and MTOR are associated with response to rapalogs in patients with metastatic renal cell carcinoma. Clin. Cancer Res. 22, 2445–2452 (2016). DOI

Roldan-Romero, J. M. et al. Molecular characterization of chromophobe renal cell carcinoma reveals mTOR pathway alterations in patients with poor outcome. Mod. Pathol. 33, 2580–2590 (2020). DOI

Chaux, A. et al. Dysregulation of the mammalian target of rapamycin pathway in chromophobe renal cell carcinomas. Hum. Pathol. 44, 2323–2330 (2013). DOI

Chen, Y. B. et al. Molecular analysis of aggressive renal cell carcinoma with unclassified histology reveals distinct subsets. Nat. Commun. 7, 13131 (2016). DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...