Evidence map›Paper›PMID 33024921›Full record

ArticleHepatology communications2020

Hepatocellular Carcinoma-Circulating Tumor Cells Expressing PD-L1 Are Prognostic and Potentially Associated With Response to Checkpoint Inhibitors.

Paul Winograd, Shuang Hou, Colin M Court, Yi-Te Lee, Pin-Jung Chen, Yazhen Zhu, Saeed Sadeghi, Richard S Finn, Pai-Chi Teng, Jasmin J Wang and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Hepatology communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05810402 (Liver Cancer and Immunotherapy), which is not on this map. Cited by 81 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 3 pooled it
4.7field-weighted citation impact, top 4% 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.

NCT05810402 narecruitingnot on this mapstarted 2023, after this paper: background citation

Liver Cancer and Immunotherapy : Clinical Relevance of LIquid BioPSY

TypeinterventionalSponsorUniversity Hospital, MontpellierRan2023 to 2027Enrolled60ConditionsHepatocellular Carcinoma, BCLC Stage B Hepatocellular Carcinoma, BCLC Stage C Hepatocellular Carcinoma, Immune Checkpoint InhibitorArmsLiquid Biopsy
3 · Its place in the literature

Who cites it

81 citing papers in PubMed, 3 syntheses or guidelines pooled it, 99 citations in OpenAlex.

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21 more citing papers are in PubMed but not listed here.

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

16 authors at 3 institutions in 1 country.

Paul WinogradDepartment of Surgery University of California Los Angeles Los Angeles CA.
Shuang HouDepartment of Surgery University of California Los Angeles Los Angeles CA.
Colin M CourtDepartment of Surgery University of California Los Angeles Los Angeles CA.ORCID https://orcid.org/0000-0002-9357-8957
Yi-Te LeeDepartment of Molecular and Medical Pharmacology University of California Los Angeles Los Angeles CA.
Pin-Jung ChenDepartment of Molecular and Medical Pharmacology University of California Los Angeles Los Angeles CA.ORCID https://orcid.org/0000-0002-5923-5299
Yazhen ZhuDepartment of Molecular and Medical Pharmacology University of California Los Angeles Los Angeles CA.
Saeed SadeghiDivision of Hematology/Oncology Department of Medicine University of California Los Angeles Los Angeles CA.
Richard S FinnDivision of Hematology/Oncology Department of Medicine University of California Los Angeles Los Angeles CA.
Pai-Chi TengUrologic Oncology Program Cedars-Sinai Medical Center Cedars-Sinai Cancer Centere Los Angeles CA.
Jasmin J WangUrologic Oncology Program Cedars-Sinai Medical Center Cedars-Sinai Cancer Centere Los Angeles CA.
Zhicheng ZhangDepartment of Molecular and Medical Pharmacology University of California Los Angeles Los Angeles CA.
Hongtao LiuDepartment of Molecular and Medical Pharmacology University of California Los Angeles Los Angeles CA.
Ronald W BusuttilDepartment of Surgery University of California Los Angeles Los Angeles CA.ORCID https://orcid.org/0000-0001-8157-1531
James S TomlinsonDepartment of Surgery University of California Los Angeles Los Angeles CA.
Hsian-Rong TsengDepartment of Molecular and Medical Pharmacology University of California Los Angeles Los Angeles CA.
Vatche G AgopianDepartment of Surgery University of California Los Angeles Los Angeles CA.ORCID https://orcid.org/0000-0003-0130-9838
University of California, Los Angeles · USCalifornia NanoSystems Institute · USCedars-Sinai Medical Center · US

Funding

HCC EV Digital Scoring Assay for assessing treatment response in HCC patientsR01CA253651 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AGOPIAN, VATCHE, TSENG, HSIAN-RONG · 2020 to 2024
$3.3M
Integrated analysis of HCC CTCs for Liver Transplant Candidate SelectionR01CA246304 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AGOPIAN, VATCHE, TSENG, HSIAN-RONG · 2020 to 2024
$2.8M
Thermoresponsive NanoVelcro CTC Purification System for Prostate Cancer ProfilingU01CA198900 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI POSADAS, EDWIN MELENCIO, TSENG, HSIAN-RONG · 2015 to 2019
$2.4M
Analysis of HCC CTC Phenotype for Liver Transplant Candidate SelectionR21CA216807 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AGOPIAN, VATCHE · 2018 to 2019
$368k
NCI NIH HHS R01 CA246304NCI NIH HHS R01 CA253651NCI NIH HHS R21 CA216807NCI NIH HHS U01 CA198900
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a leading cause of mortality. Checkpoint inhibitors of programmed cell death protein-1 (PD-1) and programmed death-ligand 1 (PD-L1) have shown great efficacy, but lack biomarkers that predict response. Circulating tumor cells (CTCs) have promise as a liquid-biopsy biomarker; however, data on HCC CTCs expressing PD-L1 have not been reported. We sought to detect PD-L1-expressing HCC-CTCs and investigated their role as a prognostic and predictive biomarker. Using an antibody-based platform, CTCs were enumerated/phenotyped from a prospective cohort of 87 patients with HCC (49 early-stage, 22 locally advanced, and 16 metastatic), 7 patients with cirrhosis, and 8 healthy controls. Immunocytochemistry identified total HCC CTCs (4',6-diamidino-2-phenylindole-positive [DAPI+]/cytokeratin-positive [CK+]/clusters of differentiation 45-negative [CD45-]) and a subpopulation expressing PD-L1 (DAPI+/CK+/PD-L1+/CD45-). PD-L1+ CTCs were identified in 4 of 49 (8.2%) early-stage patients, but 12 of 22 (54.5%) locally advanced and 15 of 16 (93.8%) metastatic patients, accurately discriminating early from locally advanced/metastatic HCC (sensitivity = 71.1%, specificity = 91.8%, area under the receiver operating characteristic curve = 0.807;

Identifiers

PMID33024921
PMCPMC7527695
OpenAlexW3047541887

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.