Best practices and recommendations for grossing and reporting of post-immunotherapy nephrectomy specimens: a single-institution experience of 70 cases
The gross handling of and reporting of renal cell carcinoma in the setting of neoadjuvant immune checkpoint inhibitor therapy presents unique challenges, and there is little known about the spectrum of histologic changes that can be seen in this setting. We studied 70 cases of RCC, status post immun...
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Published in | Diagnostic histopathology (Oxford, England : 2008) Vol. 30; no. 5; pp. 275 - 281 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
01.05.2024
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Abstract | The gross handling of and reporting of renal cell carcinoma in the setting of neoadjuvant immune checkpoint inhibitor therapy presents unique challenges, and there is little known about the spectrum of histologic changes that can be seen in this setting. We studied 70 cases of RCC, status post immunotherapy and nephrectomy at our institute and devised a standardized grossing protocol to help assess pathologic response. Our protocol includes sampling a complete cross section of the largest diameter of tumor with additional sections from areas of gross extrarenal involvement. Percentage of necrosis is calculated by assessing gross and microscopic necrosis and reporting an approximate average. Common histologic changes included fibrosis, myxoid change, necrosis and a chronic inflammatory infiltrate. Additionally, we found a discrepancy between the gross and the microscopic stages in 15 cases and all cases were of a lower pathologic stage than was suggested by the gross examination. We conclude that conventional staging guidelines may not apply to this unique cohort of cases, as using the gross estimate of tumor can falsely overestimate residual tumor burden. It is our recommendation to only assign a pathologic stage based on the location of the viable microscopic tumor. Before downstaging a tumor with grossly visible tumor outside the kidney, extensive sampling should be done in these areas to exclude microscopic tumor involvement. |
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AbstractList | The gross handling of and reporting of renal cell carcinoma in the setting of neoadjuvant immune checkpoint inhibitor therapy presents unique challenges, and there is little known about the spectrum of histologic changes that can be seen in this setting. We studied 70 cases of RCC, status post immunotherapy and nephrectomy at our institute and devised a standardized grossing protocol to help assess pathologic response. Our protocol includes sampling a complete cross section of the largest diameter of tumor with additional sections from areas of gross extrarenal involvement. Percentage of necrosis is calculated by assessing gross and microscopic necrosis and reporting an approximate average. Common histologic changes included fibrosis, myxoid change, necrosis and a chronic inflammatory infiltrate. Additionally, we found a discrepancy between the gross and the microscopic stages in 15 cases and all cases were of a lower pathologic stage than was suggested by the gross examination. We conclude that conventional staging guidelines may not apply to this unique cohort of cases, as using the gross estimate of tumor can falsely overestimate residual tumor burden. It is our recommendation to only assign a pathologic stage based on the location of the viable microscopic tumor. Before downstaging a tumor with grossly visible tumor outside the kidney, extensive sampling should be done in these areas to exclude microscopic tumor involvement. |
Author | Sharma, Padmanee Brennan, Patrick M Tamboli, Pheroze Rohra, Prih Peshoff, Mekenzie M Hwang, Michael J Rao, Priya Sircar, Kanishka Alkamachi, Bassam Monge, Bryan M |
Author_xml | – sequence: 1 givenname: Michael J surname: Hwang fullname: Hwang, Michael J – sequence: 2 givenname: Patrick M surname: Brennan fullname: Brennan, Patrick M – sequence: 3 givenname: Bryan M surname: Monge fullname: Monge, Bryan M – sequence: 4 givenname: Bassam surname: Alkamachi fullname: Alkamachi, Bassam – sequence: 5 givenname: Prih surname: Rohra fullname: Rohra, Prih – sequence: 6 givenname: Mekenzie M surname: Peshoff fullname: Peshoff, Mekenzie M – sequence: 7 givenname: Padmanee surname: Sharma fullname: Sharma, Padmanee – sequence: 8 givenname: Kanishka surname: Sircar fullname: Sircar, Kanishka – sequence: 9 givenname: Pheroze surname: Tamboli fullname: Tamboli, Pheroze – sequence: 10 givenname: Priya surname: Rao fullname: Rao, Priya |
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after preoperative chemoradiotherapy for rectal cancer publication-title: J Clin Oncol doi: 10.1200/JCO.2005.02.1329 contributor: fullname: Rodel – volume: 14 start-page: 62 year: 2012 ident: 10.1016/j.mpdhp.2024.02.002_bib22 article-title: Clinical implications of acellular mucin pools in resected rectal cancer with pathological complete response to neoadjuvant chemoradiation publication-title: Colorectal Dis doi: 10.1111/j.1463-1318.2010.02532.x contributor: fullname: de Campos-Lobato – volume: 378 start-page: 1976 year: 2018 ident: 10.1016/j.mpdhp.2024.02.002_bib17 article-title: Neoadjuvant PD-1 blockade in resectable lung cancer publication-title: N Engl J Med doi: 10.1056/NEJMoa1716078 contributor: fullname: Forde – volume: 29 start-page: 1861 year: 2018 ident: 10.1016/j.mpdhp.2024.02.002_bib25 article-title: Pathological assessment of resection specimens after neoadjuvant therapy for metastatic melanoma publication-title: Ann Oncol doi: 10.1093/annonc/mdy226 contributor: 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Title | Best practices and recommendations for grossing and reporting of post-immunotherapy nephrectomy specimens: a single-institution experience of 70 cases |
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