Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients
Background Biomarkers predicting immunotherapy response in metastatic renal cell cancer (mRCC) are lacking. PD-L1 immunohistochemistry is a complementary diagnostic for immune checkpoint inhibitors (ICIs) in mRCC, but has shown minimal clinical utility and is not used in routine clinical practice. M...
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doaj-a9d163d7634140f1b36ef03f7b72ba6d2021-09-24T14:41:24ZengTaylor & Francis GroupOncoImmunology2162-402X2020-01-019110.1080/2162402X.2020.17732001773200Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patientsTian Zhang0Sarabjot Pabla1Felicia L. Lenzo2Jeffrey M. Conroy3Mary K. Nesline4Sean T. Glenn5Antonios Papanicolau-Sengos6Blake Burgher7Vincent Giamo8Jonathan Andreas9Yirong Wang10Wiam Bshara11Katherine G. Madden12Keisuke Shirai13Konstantin Dragnev14Laura J. Tafe15Rajan Gupta16Jason Zhu17Matthew Labriola18Shannon McCall19Daniel J. George20Pooja Ghatalia21Farshid Dayyani22Robert Edwards23Michelle S Park24Rajbir Singh25Robin Jacob26Saby George27Bo Xu28Matthew Zibelman29Razelle Kurzrock30Carl Morrison31Duke UniversityOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncOmniSeq, IncDartmouth-Hitchcock Medical CenterDartmouth-Hitchcock Medical CenterDartmouth-Hitchcock Medical CenterDartmouth-Hitchcock Medical CenterDuke UniversityDuke UniversityDuke UniversityDuke UniversityDuke UniversityFox Chase Cancer CenterUniversity of CaliforniaUniversity of CaliforniaUniversity of CaliforniaMeharry Medical CollegeMeharry Medical CollegeRoswell Park Comprehensive Cancer CenterRoswell Park Comprehensive Cancer CenterFox Chase Cancer CenterMoores Cancer CenterOmniSeq, IncBackground Biomarkers predicting immunotherapy response in metastatic renal cell cancer (mRCC) are lacking. PD-L1 immunohistochemistry is a complementary diagnostic for immune checkpoint inhibitors (ICIs) in mRCC, but has shown minimal clinical utility and is not used in routine clinical practice. Methods Tumor specimens from 56 patients with mRCC who received nivolumab were evaluated for PD-L1, cell proliferation (targeted RNA-seq), and outcome. Results For 56 patients treated with nivolumab as a standard of care, there were 2 complete responses and 8 partial responses for a response rate of 17.9%. Dividing cell proliferation into tertiles, derived from the mean expression of 10 proliferation-associated genes in a reference set of tumors, poorly proliferative tumors (62.5%) were more common than moderately (30.4%) or highly proliferative (8.9%) counterparts. Moderately proliferative tumors were enriched for PD-L1 positive (41.2%), compared to poorly proliferative counterparts (11.4%). Objective response for moderately proliferative (29.4%) tumors was higher than that of poorly (11.4%) proliferative counterparts, but not statistically significant (p = .11). When cell proliferation and negative PD-L1 tumor proportion scores were combined statistically significant results were achieved (p = .048), showing that patients with poorly proliferative and PD-L1 negative tumors have a very low response rate (6.5%) compared to moderately proliferative PD-L1 negative tumors (30%). Conclusions Cell proliferation has value in predicting response to nivolumab in clear cell mRCC patients, especially when combined with PD-L1 expression. Further studies which include the addition of progression-free survival (PFS) along with sufficiently powered subgroups are required to further support these findings.http://dx.doi.org/10.1080/2162402X.2020.1773200nivolumabrenal cell carcinomapd-1pd-l1proliferationki-67 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tian Zhang Sarabjot Pabla Felicia L. Lenzo Jeffrey M. Conroy Mary K. Nesline Sean T. Glenn Antonios Papanicolau-Sengos Blake Burgher Vincent Giamo Jonathan Andreas Yirong Wang Wiam Bshara Katherine G. Madden Keisuke Shirai Konstantin Dragnev Laura J. Tafe Rajan Gupta Jason Zhu Matthew Labriola Shannon McCall Daniel J. George Pooja Ghatalia Farshid Dayyani Robert Edwards Michelle S Park Rajbir Singh Robin Jacob Saby George Bo Xu Matthew Zibelman Razelle Kurzrock Carl Morrison |
spellingShingle |
Tian Zhang Sarabjot Pabla Felicia L. Lenzo Jeffrey M. Conroy Mary K. Nesline Sean T. Glenn Antonios Papanicolau-Sengos Blake Burgher Vincent Giamo Jonathan Andreas Yirong Wang Wiam Bshara Katherine G. Madden Keisuke Shirai Konstantin Dragnev Laura J. Tafe Rajan Gupta Jason Zhu Matthew Labriola Shannon McCall Daniel J. George Pooja Ghatalia Farshid Dayyani Robert Edwards Michelle S Park Rajbir Singh Robin Jacob Saby George Bo Xu Matthew Zibelman Razelle Kurzrock Carl Morrison Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients OncoImmunology nivolumab renal cell carcinoma pd-1 pd-l1 proliferation ki-67 |
author_facet |
Tian Zhang Sarabjot Pabla Felicia L. Lenzo Jeffrey M. Conroy Mary K. Nesline Sean T. Glenn Antonios Papanicolau-Sengos Blake Burgher Vincent Giamo Jonathan Andreas Yirong Wang Wiam Bshara Katherine G. Madden Keisuke Shirai Konstantin Dragnev Laura J. Tafe Rajan Gupta Jason Zhu Matthew Labriola Shannon McCall Daniel J. George Pooja Ghatalia Farshid Dayyani Robert Edwards Michelle S Park Rajbir Singh Robin Jacob Saby George Bo Xu Matthew Zibelman Razelle Kurzrock Carl Morrison |
author_sort |
Tian Zhang |
title |
Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients |
title_short |
Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients |
title_full |
Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients |
title_fullStr |
Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients |
title_full_unstemmed |
Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients |
title_sort |
proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients |
publisher |
Taylor & Francis Group |
series |
OncoImmunology |
issn |
2162-402X |
publishDate |
2020-01-01 |
description |
Background Biomarkers predicting immunotherapy response in metastatic renal cell cancer (mRCC) are lacking. PD-L1 immunohistochemistry is a complementary diagnostic for immune checkpoint inhibitors (ICIs) in mRCC, but has shown minimal clinical utility and is not used in routine clinical practice. Methods Tumor specimens from 56 patients with mRCC who received nivolumab were evaluated for PD-L1, cell proliferation (targeted RNA-seq), and outcome. Results For 56 patients treated with nivolumab as a standard of care, there were 2 complete responses and 8 partial responses for a response rate of 17.9%. Dividing cell proliferation into tertiles, derived from the mean expression of 10 proliferation-associated genes in a reference set of tumors, poorly proliferative tumors (62.5%) were more common than moderately (30.4%) or highly proliferative (8.9%) counterparts. Moderately proliferative tumors were enriched for PD-L1 positive (41.2%), compared to poorly proliferative counterparts (11.4%). Objective response for moderately proliferative (29.4%) tumors was higher than that of poorly (11.4%) proliferative counterparts, but not statistically significant (p = .11). When cell proliferation and negative PD-L1 tumor proportion scores were combined statistically significant results were achieved (p = .048), showing that patients with poorly proliferative and PD-L1 negative tumors have a very low response rate (6.5%) compared to moderately proliferative PD-L1 negative tumors (30%). Conclusions Cell proliferation has value in predicting response to nivolumab in clear cell mRCC patients, especially when combined with PD-L1 expression. Further studies which include the addition of progression-free survival (PFS) along with sufficiently powered subgroups are required to further support these findings. |
topic |
nivolumab renal cell carcinoma pd-1 pd-l1 proliferation ki-67 |
url |
http://dx.doi.org/10.1080/2162402X.2020.1773200 |
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