Biological Rationale for Peripheral Blood Cell-Derived Inflammatory Indices and Related Prognostic Scores in Patients with Advanced Non-Small-Cell Lung Cancer.

Immune-checkpoint inhibitors Immunotherapy Inflammatory index Non-small-cell lung cancer Peripheral blood Prognostic Score

Journal

Current oncology reports
ISSN: 1534-6269
Titre abrégé: Curr Oncol Rep
Pays: United States
ID NLM: 100888967

Informations de publication

Date de publication:
12 2022
Historique:
accepted: 16 09 2022
pubmed: 19 10 2022
medline: 6 12 2022
entrez: 18 10 2022
Statut: ppublish

Résumé

To describe the biological rationale of peripheral blood cells (PBC)-derived inflammatory indexes and assess the related prognostic scores for patients with advanced non-small cell lung cancer (aNSCLC) treated with immune-checkpoint inhibitors (ICI). Inflammatory indexes based on PBC may indicate a pro-inflammatory condition affecting the immune response to cancer. The lung immune prognostic index (LIPI), consisting of derived neutrophils-to-lymphocyte ratio (NLR) and lactate dehydrogenase, is a validated prognostic tool, especially for pretreated aNSCLC patients, where the combination of NLR and PD-L1 tumour expression might also be predictive of immunotherapy benefit. In untreated high-PD-L1 aNSCLC patients, the Lung-Immune-Prognostic score (LIPS), including NLR, ECOG PS and concomitant steroids, is prognostic, and its modified version might indicate patients with favourable outcomes despite an ECOG PS of 2. NLR times platelets (i.e., SII), included in the NHS-Lung score, might improve the prognostication for combined chemoimmunotherapy. PBC-derived inflammatory indexes and related scores represent accurate, reproducible and non-expensive prognostic tools with clinical and research utility.

Identifiants

pubmed: 36255605
doi: 10.1007/s11912-022-01335-8
pii: 10.1007/s11912-022-01335-8
doi:

Substances chimiques

B7-H1 Antigen 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1851-1862

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Auteurs

Giuseppe Luigi Banna (GL)

Portsmouth Hospitals University NHS Trust, Portsmouth, UK. giuseppe.banna@nhs.net.

Alex Friedlaender (A)

Department of Oncology, Clinique Générale Beaulieu, Geneva, Switzerland.
Department of Oncology, University Hospital of Geneva, Geneva, Switzerland.

Marco Tagliamento (M)

Department of Internal Medicine and Medical Specialties (Di.M.I.), University of Genoa, Genoa, Italy.

Veronica Mollica (V)

Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138, Bologna, Italy.

Alessio Cortellini (A)

Division of Cancer, Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.

Sara Elena Rebuzzi (SE)

Department of Internal Medicine and Medical Specialties (Di.M.I.), University of Genoa, Genoa, Italy.
Medical Oncology Unit, Ospedale San Paolo, Savona, Italy.

Arsela Prelaj (A)

Medical Oncology Department 1, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy.
Department of Electronics, Information, and Bioengineering, Politecnico di Milano, Milan, Italy.

Abdul Rafeh Naqash (AR)

Medical Oncology/TSET Phase 1 Program, Stephenson Cancer Center, University of Oklahoma, Oklahoma City, OK, USA.

Edouard Auclin (E)

Medical Oncology, Hôpital Européen Georges Pompidou, AP-HP, Université Paris Cité, Paris, France.

Lucia Garetto (L)

Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.

Laura Mezquita (L)

Medical Oncology Department, Hospital Clinic of Barcelona, Barcelona, Spain.
Laboratory of Translational Genomics and Targeted Therapies in Solid Tumors, IDIBAPS, Barcelona, Spain.
Department of Medicine, University of Barcelona, Barcelona, Spain.

Alfredo Addeo (A)

Department of Oncology, University Hospital of Geneva, Geneva, Switzerland.

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Classifications MeSH