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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Main Authors: 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
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:OncoImmunology
Subjects:
Online Access:http://dx.doi.org/10.1080/2162402X.2020.1773200
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spelling 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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