Blood platelet RNA profiles do not enable for nivolumab response prediction at baseline in patients with non-small cell lung cancer.

Blood platelets RNA-sequencing immunotherapy nivolumab

Journal

Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
ISSN: 1423-0380
Titre abrégé: Tumour Biol
Pays: Netherlands
ID NLM: 8409922

Informations de publication

Date de publication:
26 May 2023
Historique:
medline: 4 6 2023
pubmed: 4 6 2023
entrez: 4 6 2023
Statut: aheadofprint

Résumé

Anti-PD-(L)1 immunotherapy has emerged as a promising treatment approach for non-small cell lung cancer (NSCLC), though the response rates remain low. Pre-treatment response prediction may improve patient allocation for immunotherapy. Blood platelets act as active immune-like cells, thereby constraining T-cell activity, propagating cancer metastasis, and adjusting their spliced mRNA content. We investigated whether platelet RNA profiles before start of nivolumab anti-PD1 immunotherapy may predict treatment responses. We performed RNA-sequencing of platelet RNA samples isolated from stage III-IV NSCLC patients before treatment with nivolumab. Treatment response was scored by the RECIST-criteria. Data were analyzed using a predefined thromboSeq analysis including a particle-swarm-enhanced support vector machine (PSO/SVM) classification algorithm. We collected and processed a 286-samples cohort, separated into a training/evaluation and validation series and subjected those to training of the PSO/SVM-classification algorithm. We observed only low classification accuracy in the 107-samples validation series (area under the curve (AUC) training series: 0.73 (95% -CI: 0.63-0.84, n = 88 samples), AUC evaluation series: 0.64 (95% -CI: 0.51-0.76, n = 91 samples), AUC validation series: 0.58 (95% -CI: 0.45-0.70, n = 107 samples)), employing a five-RNAs biomarker panel. We concluded that platelet RNA may have minimally discriminative capacity for anti-PD1 nivolumab response prediction, with which the current methodology is insufficient for diagnostic application.

Sections du résumé

BACKGROUND BACKGROUND
Anti-PD-(L)1 immunotherapy has emerged as a promising treatment approach for non-small cell lung cancer (NSCLC), though the response rates remain low. Pre-treatment response prediction may improve patient allocation for immunotherapy. Blood platelets act as active immune-like cells, thereby constraining T-cell activity, propagating cancer metastasis, and adjusting their spliced mRNA content.
OBJECTIVE OBJECTIVE
We investigated whether platelet RNA profiles before start of nivolumab anti-PD1 immunotherapy may predict treatment responses.
METHODS METHODS
We performed RNA-sequencing of platelet RNA samples isolated from stage III-IV NSCLC patients before treatment with nivolumab. Treatment response was scored by the RECIST-criteria. Data were analyzed using a predefined thromboSeq analysis including a particle-swarm-enhanced support vector machine (PSO/SVM) classification algorithm.
RESULTS RESULTS
We collected and processed a 286-samples cohort, separated into a training/evaluation and validation series and subjected those to training of the PSO/SVM-classification algorithm. We observed only low classification accuracy in the 107-samples validation series (area under the curve (AUC) training series: 0.73 (95% -CI: 0.63-0.84, n = 88 samples), AUC evaluation series: 0.64 (95% -CI: 0.51-0.76, n = 91 samples), AUC validation series: 0.58 (95% -CI: 0.45-0.70, n = 107 samples)), employing a five-RNAs biomarker panel.
CONCLUSIONS CONCLUSIONS
We concluded that platelet RNA may have minimally discriminative capacity for anti-PD1 nivolumab response prediction, with which the current methodology is insufficient for diagnostic application.

Identifiants

pubmed: 37270827
pii: TUB220037
doi: 10.3233/TUB-220037
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Mirte Muller (M)

Department of Thoracic Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Myron G Best (MG)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Neurosurgery, Boelelaan 1117, Amsterdam, the Netherlands.
Cancer Center Amsterdam and Liquid Biopsy Center, Amsterdam, The Netherlands.
Brain Tumor Center Amsterdam, Amsterdam, The Netherlands.

Vincent van der Noort (V)

Department of Biometrics, Netherlands Cancer Institute, Amsterdam, The Netherlands.

T Jeroen N Hiltermann (TJN)

Department of Pulmonary Diseases, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Anna-Larissa N Niemeijer (AN)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Pulmonary Medicine, Boelelaan 1117, Amsterdam, The Netherlands.

Edward Post (E)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Neurosurgery, Boelelaan 1117, Amsterdam, the Netherlands.
Cancer Center Amsterdam and Liquid Biopsy Center, Amsterdam, The Netherlands.
Brain Tumor Center Amsterdam, Amsterdam, The Netherlands.

Nik Sol (N)

Cancer Center Amsterdam and Liquid Biopsy Center, Amsterdam, The Netherlands.
Brain Tumor Center Amsterdam, Amsterdam, The Netherlands.
Department of Neurology, Amsterdam UMC, location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Sjors G J G In 't Veld (SGJG)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Neurosurgery, Boelelaan 1117, Amsterdam, the Netherlands.
Cancer Center Amsterdam and Liquid Biopsy Center, Amsterdam, The Netherlands.
Brain Tumor Center Amsterdam, Amsterdam, The Netherlands.

Tineke Nogarede (T)

Division of Molecular Oncology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Lisanne Visser (L)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Neurosurgery, Boelelaan 1117, Amsterdam, the Netherlands.
Cancer Center Amsterdam and Liquid Biopsy Center, Amsterdam, The Netherlands.
Brain Tumor Center Amsterdam, Amsterdam, The Netherlands.

Robert D Schouten (RD)

Department of Thoracic Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Daan van den Broek (D)

Department of Laboratory Medicine, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Karlijn Hummelink (K)

Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Kim Monkhorst (K)

Department of Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Adrianus J de Langen (AJ)

Department of Thoracic Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Pulmonary Medicine, Boelelaan 1117, Amsterdam, The Netherlands.

Ed Schuuring (E)

Department of Pathology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Egbert F Smit (EF)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Pulmonary Medicine, Boelelaan 1117, Amsterdam, The Netherlands.
Department of Pulmonary Medicine LUMC, Leiden, The Netherlands.

Harry J M Groen (HJM)

Department of Pulmonary Diseases, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Thomas Wurdinger (T)

Amsterdam UMC Location Vrije Universiteit Amsterdam, Department of Neurosurgery, Boelelaan 1117, Amsterdam, the Netherlands.
Cancer Center Amsterdam and Liquid Biopsy Center, Amsterdam, The Netherlands.
Brain Tumor Center Amsterdam, Amsterdam, The Netherlands.

Michel M van den Heuvel (MM)

Department of Thoracic Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Respiratory Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.

Classifications MeSH