Does Elevated Pre-Treatment Plasma PD-L1 Level Indicate an Increased Tumor Burden and Worse Prognosis in Metastatic Colorectal Cancer?

PD-1 PD-L1 colorectal neoplasms longitudinal survival analysis tumor burden

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
17 Aug 2022
Historique:
received: 25 07 2022
revised: 12 08 2022
accepted: 15 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 27 8 2022
Statut: epublish

Résumé

Programmed death-ligand 1 (PD-L1) and programmed cell death protein 1 (PD-1) have been reported as possibly favorable prognostic factors in colorectal cancer (CRC). However, their longitudinal effect is unknown. A pilot study was performed to investigate whether baseline PD-1/PD-L1 levels are associated with further laboratory changes and/or shorter survival. A total of 506 laboratory measurements from 37 metastatic CRC patients were analyzed. The baseline plasma PD-1 and PD-L1 levels were 27.73 ± 1.20 pg/mL and 16.01 ± 1.09 pg/mL, respectively. Disease progression ( Abnormal levels of laboratory parameters and intensified tumor burden can be expected if elevated baseline plasma PD-1/PD-L1 levels are found.

Sections du résumé

BACKGROUND BACKGROUND
Programmed death-ligand 1 (PD-L1) and programmed cell death protein 1 (PD-1) have been reported as possibly favorable prognostic factors in colorectal cancer (CRC). However, their longitudinal effect is unknown.
METHODS METHODS
A pilot study was performed to investigate whether baseline PD-1/PD-L1 levels are associated with further laboratory changes and/or shorter survival.
RESULTS RESULTS
A total of 506 laboratory measurements from 37 metastatic CRC patients were analyzed. The baseline plasma PD-1 and PD-L1 levels were 27.73 ± 1.20 pg/mL and 16.01 ± 1.09 pg/mL, respectively. Disease progression (
CONCLUSIONS CONCLUSIONS
Abnormal levels of laboratory parameters and intensified tumor burden can be expected if elevated baseline plasma PD-1/PD-L1 levels are found.

Identifiants

pubmed: 36013050
pii: jcm11164815
doi: 10.3390/jcm11164815
pmc: PMC9410536
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : National Research, Development and Innovation Office (Hungary)
ID : NVKP_16-1-2016-0004
Organisme : National Research, Development and Innovation Office (Hungary)
ID : NVKP_16-1-2016-0042
Organisme : Spectrum Radiology for Health Foundation
ID : APC coverage
Organisme : Semmelweis University
ID : APC coverage

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Auteurs

Magdolna Dank (M)

Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.

Dorottya Mühl (D)

Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.

Magdolna Herold (M)

Department of Internal Medicine and Hematology, Semmelweis University, 1088 Budapest, Hungary.

Lilla Hornyák (L)

Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.

Attila Marcell Szasz (AM)

Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.

Zoltan Herold (Z)

Division of Oncology, Department of Internal Medicine and Oncology, Semmelweis University, 1083 Budapest, Hungary.

Classifications MeSH