Programmed Death Ligand-1 and Tumor Mutation Burden Testing of Patients With Lung Cancer for Selection of Immune Checkpoint Inhibitor Therapies: Guideline From the College of American Pathologists, Association for Molecular Pathology, International Association for the Study of Lung Cancer, Pulmonary Pathology Society, and LUNGevity Foundation.


Journal

Archives of pathology & laboratory medicine
ISSN: 1543-2165
Titre abrégé: Arch Pathol Lab Med
Pays: United States
ID NLM: 7607091

Informations de publication

Date de publication:
16 Apr 2024
Historique:
accepted: 29 02 2024
medline: 16 4 2024
pubmed: 16 4 2024
entrez: 16 4 2024
Statut: aheadofprint

Résumé

Rapid advancements in the understanding and manipulation of tumor-immune interactions have led to the approval of immune therapies for patients with non-small cell lung cancer. Certain immune checkpoint inhibitor therapies require the use of companion diagnostics, but methodologic variability has led to uncertainty around test selection and implementation in practice. To develop evidence-based guideline recommendations for the testing of immunotherapy/immunomodulatory biomarkers, including programmed death ligand-1 (PD-L1) and tumor mutation burden (TMB), in patients with lung cancer. The College of American Pathologists convened a panel of experts in non-small cell lung cancer and biomarker testing to develop evidence-based recommendations in accordance with the standards for trustworthy clinical practice guidelines established by the National Academy of Medicine. A systematic literature review was conducted to address 8 key questions. Using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach, recommendations were created from the available evidence, certainty of that evidence, and key judgments as defined in the GRADE Evidence to Decision framework. Six recommendation statements were developed. This guideline summarizes the current understanding and hurdles associated with the use of PD-L1 expression and TMB testing for immune checkpoint inhibitor therapy selection in patients with advanced non-small cell lung cancer and presents evidence-based recommendations for PD-L1 and TMB testing in the clinical setting.

Identifiants

pubmed: 38625026
pii: 499926
doi: 10.5858/arpa.2023-0536-CP
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 College of American Pathologists.

Déclaration de conflit d'intérêts

Authors’ disclosures of potential conflicts of interest and author contributions are found in the Appendix at the end of this article.

Auteurs

Lynette M Sholl (LM)

From the Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts (Sholl).

Mark Awad (M)

Lowe Center for Thoracic Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts (Awad).

Upal Basu Roy (U)

Translational Science Research Program, LUNGevity Foundation, Chicago, Illinois (Basu Roy).

Mary Beth Beasley (MB)

the Department of Anatomic Pathology and Clinical Pathology, Mt. Sinai Medical Center, New York, New York (Beasley).

Richard Walter Cartun (RW)

the Department of Anatomic Pathology, Hartford Hospital, Hartford, Connecticut (Cartun).

David M Hwang (DM)

the Department of Laboratory Medicine & Pathobiology, Sunnybrook Health Science Centre, Toronto, Ontario, Canada (Hwang).

Gregory Kalemkerian (G)

the Department of Medical Oncology and Internal Medicine, University of Michigan Health, Ann Arbor (Kalemkerian).

Fernando Lopez-Rios (F)

Pathology Department, Hospital Universitario 12 de Octubre, Madrid, Spain (Lopez-Rios).

Mari Mino-Kenudson (M)

the Department of Pathology, Massachusetts General Hospital, Boston (Mino-Kenudson).

Ajit Paintal (A)

the Department of Pathology, NorthShore University Health System, Evanston, Illinois (Paintal).

Kearin Reid (K)

Governance (Reid) and the Pathology and Laboratory Quality Center for Evidence-based Guidelines (Ventura), College of American Pathologists, Northfield, Illinois.

Lauren Ritterhouse (L)

the Department of Pathology, Foundation Medicine, Cambridge, Massachusetts (Ritterhouse).

Lesley A Souter (LA)

Methodology Consultant, Hamilton, Ontario, Canada (Souter).

Paul E Swanson (PE)

the Department of Laboratory Medicine and Pathology, University of Washington Medical Center, Seattle (Swanson).

Christina B Ventura (CB)

Governance (Reid) and the Pathology and Laboratory Quality Center for Evidence-based Guidelines (Ventura), College of American Pathologists, Northfield, Illinois.

Larissa V Furtado (LV)

the Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee (Furtado).

Classifications MeSH