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Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome
The morphologic spectrum of type 1 papillary renal cell carcinoma (PRCC) is not well-defined, since a significant proportion of cases have mixed type 1 and 2 histology. We analyzed 199 cases of PRCC with any (even if focal) type 1 features, with a median follow-up of 12 years, to identify clinicopat...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177523/ https://www.ncbi.nlm.nih.gov/pubmed/34949764 http://dx.doi.org/10.1038/s41379-021-00990-9 |
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author | Murugan, Paari Jia, Liwei Dinatale, Renzo G. Assel, Melissa Benfante, Nicole Al-Ahmadie, Hikmat A Fine, Samson W. Gopalan, Anuradha Sarungbam, Judy Sirintrapun, S. Joseph Hakimi, A. Ari Russo, Paul Chen, Ying-Bei Tickoo, Satish K. Reuter, Victor E. |
author_facet | Murugan, Paari Jia, Liwei Dinatale, Renzo G. Assel, Melissa Benfante, Nicole Al-Ahmadie, Hikmat A Fine, Samson W. Gopalan, Anuradha Sarungbam, Judy Sirintrapun, S. Joseph Hakimi, A. Ari Russo, Paul Chen, Ying-Bei Tickoo, Satish K. Reuter, Victor E. |
author_sort | Murugan, Paari |
collection | PubMed |
description | The morphologic spectrum of type 1 papillary renal cell carcinoma (PRCC) is not well-defined, since a significant proportion of cases have mixed type 1 and 2 histology. We analyzed 199 cases of PRCC with any (even if focal) type 1 features, with a median follow-up of 12 years, to identify clinicopathological features associated with outcome. Ninety-five tumors (48%) of the cohort contained some type 2 component (median amount: 25%; IQR: 10%, 70%). As a group they showed high rates of progression-free (PFS) and cancer-specific survival (CSS). Tumor size, mitotic rate, lymphovascular invasion, sarcomatoid differentiation, sheet-like architecture, and lack of tumor circumscription were significantly associated with CSS (p≤0.015) on univariate analysis. While predominant WHO/ISUP nucleolar grade was associated with PFS (p=0.013) and CSS (p=0.030), the presence of non-predominant (<50%) nucleolar grade did not show association with outcome (p=0.7). PFS and CSS showed no significant association with the presence or the amount of type 2 morphology. We compared the molecular alterations in paired type 1 and type 2 areas in a subset of 22 cases with mixed type 1 and 2 features and identified 12 recurrently mutated genes including TERT, ARID1A, KDM6A, KMT2D, NFE2L2, MET, APC, and TP53. Among 78 detected somatic mutations, 61 (78%) were shared between the paired type 1 and type 2 areas. Copy number alterations, including chromosome 7 and 17 gains, were similar between type 1 and 2 areas. These findings support that type 2 features in a PRCC with mixed histology represent either morphologic variance or clonal evolution. Our study underscores the notion that PRCC with any classic type 1 regions is best considered as type 1 PRCC and assigned the appropriate WHO/ISUP nucleolar grade. It provides additional evidence that type 2 PRCC as a separate category should be re-assessed and likely needs to be abandoned. |
format | Online Article Text |
id | pubmed-9177523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-91775232022-06-23 Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome Murugan, Paari Jia, Liwei Dinatale, Renzo G. Assel, Melissa Benfante, Nicole Al-Ahmadie, Hikmat A Fine, Samson W. Gopalan, Anuradha Sarungbam, Judy Sirintrapun, S. Joseph Hakimi, A. Ari Russo, Paul Chen, Ying-Bei Tickoo, Satish K. Reuter, Victor E. Mod Pathol Article The morphologic spectrum of type 1 papillary renal cell carcinoma (PRCC) is not well-defined, since a significant proportion of cases have mixed type 1 and 2 histology. We analyzed 199 cases of PRCC with any (even if focal) type 1 features, with a median follow-up of 12 years, to identify clinicopathological features associated with outcome. Ninety-five tumors (48%) of the cohort contained some type 2 component (median amount: 25%; IQR: 10%, 70%). As a group they showed high rates of progression-free (PFS) and cancer-specific survival (CSS). Tumor size, mitotic rate, lymphovascular invasion, sarcomatoid differentiation, sheet-like architecture, and lack of tumor circumscription were significantly associated with CSS (p≤0.015) on univariate analysis. While predominant WHO/ISUP nucleolar grade was associated with PFS (p=0.013) and CSS (p=0.030), the presence of non-predominant (<50%) nucleolar grade did not show association with outcome (p=0.7). PFS and CSS showed no significant association with the presence or the amount of type 2 morphology. We compared the molecular alterations in paired type 1 and type 2 areas in a subset of 22 cases with mixed type 1 and 2 features and identified 12 recurrently mutated genes including TERT, ARID1A, KDM6A, KMT2D, NFE2L2, MET, APC, and TP53. Among 78 detected somatic mutations, 61 (78%) were shared between the paired type 1 and type 2 areas. Copy number alterations, including chromosome 7 and 17 gains, were similar between type 1 and 2 areas. These findings support that type 2 features in a PRCC with mixed histology represent either morphologic variance or clonal evolution. Our study underscores the notion that PRCC with any classic type 1 regions is best considered as type 1 PRCC and assigned the appropriate WHO/ISUP nucleolar grade. It provides additional evidence that type 2 PRCC as a separate category should be re-assessed and likely needs to be abandoned. 2022-06 2021-12-23 /pmc/articles/PMC9177523/ /pubmed/34949764 http://dx.doi.org/10.1038/s41379-021-00990-9 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms |
spellingShingle | Article Murugan, Paari Jia, Liwei Dinatale, Renzo G. Assel, Melissa Benfante, Nicole Al-Ahmadie, Hikmat A Fine, Samson W. Gopalan, Anuradha Sarungbam, Judy Sirintrapun, S. Joseph Hakimi, A. Ari Russo, Paul Chen, Ying-Bei Tickoo, Satish K. Reuter, Victor E. Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome |
title | Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome |
title_full | Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome |
title_fullStr | Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome |
title_full_unstemmed | Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome |
title_short | Papillary Renal Cell Carcinoma: A Single Institutional Study of 199 Cases Addressing Classification, Clinicopathologic and Molecular Features, and Treatment Outcome |
title_sort | papillary renal cell carcinoma: a single institutional study of 199 cases addressing classification, clinicopathologic and molecular features, and treatment outcome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177523/ https://www.ncbi.nlm.nih.gov/pubmed/34949764 http://dx.doi.org/10.1038/s41379-021-00990-9 |
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