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Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition
BACKGROUND: Renal medullary carcinoma is one of the rarest malignancies arising from the kidney. Despite various aggressive therapeutic regimens, mortality remains significantly high (95%) with a median overall survival of 5 months. Furthermore, the scarcity of this malignancy renders randomized cli...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557570/ https://www.ncbi.nlm.nih.gov/pubmed/28807004 http://dx.doi.org/10.1186/s40425-017-0267-9 |
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author | Sodji, Quaovi Klein, Kandy Sravan, Kavuri Parikh, Jigarkumar |
author_facet | Sodji, Quaovi Klein, Kandy Sravan, Kavuri Parikh, Jigarkumar |
author_sort | Sodji, Quaovi |
collection | PubMed |
description | BACKGROUND: Renal medullary carcinoma is one of the rarest malignancies arising from the kidney. Despite various aggressive therapeutic regimens, mortality remains significantly high (95%) with a median overall survival of 5 months. Furthermore, the scarcity of this malignancy renders randomized clinical trials impossible. We examined the expression of programmed death ligand 1 (PD-L1) in two new renal medullary carcinoma cases, investigated their responses to the PD-L1 inhibitor nivolumab and explored the predictive role of the rate of PD-L1 expression in such response. CASE PRESENTATION: Two African-American patients (male and female) with sickle cell trait who presented to our center with hematuria and flank pain were diagnosed with metastatic renal medullary carcinoma. PD-L1 was expressed at rate of 25% and 60% in patient 1 and 2 respectively. Following nephrectomy, they were started on nivolumab. Patient 1 initially responded to the treatment with regression of metastatic lesions. However, following this early response, patient 1 who has been receiving nivolumab for more than 15 months, was noted to have a disease progression. Patient 2 had disease progression after 3 months of nivolumab therapy. CONCLUSIONS: Although PD-L1 is expressed in these patients with renal medullary carcinoma, response to nivolumab was only observed in patient 1 whose tumor has the lowest rate of PD-L1 expression. This may suggest that in RMC, response to PD-L1 inhibition therapy may not correlate with the rate of PD-L1 expression. |
format | Online Article Text |
id | pubmed-5557570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55575702017-08-16 Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition Sodji, Quaovi Klein, Kandy Sravan, Kavuri Parikh, Jigarkumar J Immunother Cancer Case Report BACKGROUND: Renal medullary carcinoma is one of the rarest malignancies arising from the kidney. Despite various aggressive therapeutic regimens, mortality remains significantly high (95%) with a median overall survival of 5 months. Furthermore, the scarcity of this malignancy renders randomized clinical trials impossible. We examined the expression of programmed death ligand 1 (PD-L1) in two new renal medullary carcinoma cases, investigated their responses to the PD-L1 inhibitor nivolumab and explored the predictive role of the rate of PD-L1 expression in such response. CASE PRESENTATION: Two African-American patients (male and female) with sickle cell trait who presented to our center with hematuria and flank pain were diagnosed with metastatic renal medullary carcinoma. PD-L1 was expressed at rate of 25% and 60% in patient 1 and 2 respectively. Following nephrectomy, they were started on nivolumab. Patient 1 initially responded to the treatment with regression of metastatic lesions. However, following this early response, patient 1 who has been receiving nivolumab for more than 15 months, was noted to have a disease progression. Patient 2 had disease progression after 3 months of nivolumab therapy. CONCLUSIONS: Although PD-L1 is expressed in these patients with renal medullary carcinoma, response to nivolumab was only observed in patient 1 whose tumor has the lowest rate of PD-L1 expression. This may suggest that in RMC, response to PD-L1 inhibition therapy may not correlate with the rate of PD-L1 expression. BioMed Central 2017-08-15 /pmc/articles/PMC5557570/ /pubmed/28807004 http://dx.doi.org/10.1186/s40425-017-0267-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Sodji, Quaovi Klein, Kandy Sravan, Kavuri Parikh, Jigarkumar Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition |
title | Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition |
title_full | Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition |
title_fullStr | Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition |
title_full_unstemmed | Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition |
title_short | Predictive role of PD-L1 expression in the response of renal Medullary carcinoma to PD-1 inhibition |
title_sort | predictive role of pd-l1 expression in the response of renal medullary carcinoma to pd-1 inhibition |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557570/ https://www.ncbi.nlm.nih.gov/pubmed/28807004 http://dx.doi.org/10.1186/s40425-017-0267-9 |
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