Evidence map›Paper›PMID 32923131›Full record

ArticleOncoimmunology2020

Proliferative potential and response to nivolumab in clear cell renal cell carcinoma patients.

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 and 22 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

32 authors at 8 institutions in 2 countries.

Tian ZhangDepartment of Medicine, Duke University, Durham, NC, USA.
Sarabjot PablaR&D, OmniSeq, Inc, Buffalo, NY, USA.
Felicia L LenzoR&D, OmniSeq, Inc, Buffalo, NY, USA.
Jeffrey M ConroyR&D, OmniSeq, Inc, Buffalo, NY, USA.
Mary K NeslineR&D, OmniSeq, Inc, Buffalo, NY, USA.
Sean T GlennR&D, OmniSeq, Inc, Buffalo, NY, USA.
Antonios Papanicolau-SengosR&D, OmniSeq, Inc, Buffalo, NY, USA.
Blake BurgherR&D, OmniSeq, Inc, Buffalo, NY, USA.
Vincent GiamoR&D, OmniSeq, Inc, Buffalo, NY, USA.
Jonathan AndreasR&D, OmniSeq, Inc, Buffalo, NY, USA.
Yirong WangR&D, OmniSeq, Inc, Buffalo, NY, USA.
Wiam BsharaR&D, OmniSeq, Inc, Buffalo, NY, USA.
Katherine G MaddenDepartment of Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Keisuke ShiraiDepartment of Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Konstantin DragnevDepartment of Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Laura J TafeDepartment of Hematology/Oncology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Rajan GuptaDepartment of Medicine, Duke University, Durham, NC, USA.
Jason ZhuDepartment of Medicine, Duke University, Durham, NC, USA.
Matthew LabriolaDepartment of Medicine, Duke University, Durham, NC, USA.
Shannon McCallDepartment of Medicine, Duke University, Durham, NC, USA.
Daniel J GeorgeDepartment of Medicine, Duke University, Durham, NC, USA.
Pooja GhataliaDepartment of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA, US.
Farshid DayyaniDepartment of Medicine, University of California, Irvine, CA, USA.
Robert EdwardsDepartment of Medicine, University of California, Irvine, CA, USA.
Michelle S ParkDepartment of Medicine, University of California, Irvine, CA, USA.
Rajbir SinghDepartment of Medicine, Meharry Medical College, Nashville, TN, US.
Robin JacobDepartment of Medicine, Meharry Medical College, Nashville, TN, US.
Saby GeorgeDepartment of Pathology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Bo XuDepartment of Pathology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Matthew ZibelmanDepartment of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA, US.
Razelle KurzrockCenter for Personalized Cancer Therapy, Moores Cancer Center, La Jolla, CA, USA.ORCID 0000-0003-4110-1214
Carl MorrisonR&D, OmniSeq, Inc, Buffalo, NY, USA.
IQE (United Kingdom) · GBDuke University · USRoswell Park Comprehensive Cancer Center · USDartmouth–Hitchcock Medical Center · USUniversity of California, Irvine · USFox Chase Cancer Center · USMeharry Medical College · USMoores Cancer Center

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 ( 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.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Renal CellAdultAgedFemaleHumansImmunotherapyMaleMiddle AgedNivolumabProgression-Free SurvivalAntineoplastic Agents, ImmunologicalNivolumabKi-67NivolumabPD-1PD-L1proliferationrenal cell carcinoma

Identifiers

PMID32923131
PMCPMC7458647
OpenAlexW3034482678

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.