LACE-Bio: Validation of Predictive and/or Prognostic Immunohistochemistry/Histochemistry-based Biomarkers in Resected Non-small-cell Lung Cancer.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
03 2019
Historique:
received: 02 08 2018
revised: 28 09 2018
accepted: 02 10 2018
pubmed: 12 11 2018
medline: 27 6 2019
entrez: 12 11 2018
Statut: ppublish

Résumé

Complete resection of non-small-cell lung cancer (NSCLC) offers the potential for cure after surgery and adjuvant chemotherapy. Patients may not benefit and may experience severe toxicity. There are no validated molecular tools to allow better patient selection. The LACE-Bio (LACE [Lung Adjuvant Cisplatin Evaluation]) project includes 4 trials (International Adjuvant Lung Cancer Trial [IALT], Adjuvant Navelbine International Trialist Association [ANITA], JBR10, and Cancer and Leukemia Group B (CALGB)-9633). Immunohistochemistry biomarkers shown in one trial to have a prognostic/predictive effect on overall survival were tested. The majority of the promising biomarkers could not be validated; the prognostic effect of tumor infiltrating lymphocytes and β-tubulin was confirmed. Potential causes include tissue fixation, storage, the use of tissue microarrays, and varying reagent/antibody batches. Immunohistochemistry assays from single trials may be misleading and require validation before being used for patient selection. LACE-Bio-2 is evaluating potential genomic biomarkers that may allow more precise selection of patients with NSCLC for adjuvant chemotherapy in NSCLC.

Sections du résumé

BACKGROUND
Complete resection of non-small-cell lung cancer (NSCLC) offers the potential for cure after surgery and adjuvant chemotherapy. Patients may not benefit and may experience severe toxicity. There are no validated molecular tools to allow better patient selection.
MATERIALS AND METHODS
The LACE-Bio (LACE [Lung Adjuvant Cisplatin Evaluation]) project includes 4 trials (International Adjuvant Lung Cancer Trial [IALT], Adjuvant Navelbine International Trialist Association [ANITA], JBR10, and Cancer and Leukemia Group B (CALGB)-9633). Immunohistochemistry biomarkers shown in one trial to have a prognostic/predictive effect on overall survival were tested.
RESULTS
The majority of the promising biomarkers could not be validated; the prognostic effect of tumor infiltrating lymphocytes and β-tubulin was confirmed. Potential causes include tissue fixation, storage, the use of tissue microarrays, and varying reagent/antibody batches.
CONCLUSIONS
Immunohistochemistry assays from single trials may be misleading and require validation before being used for patient selection. LACE-Bio-2 is evaluating potential genomic biomarkers that may allow more precise selection of patients with NSCLC for adjuvant chemotherapy in NSCLC.

Identifiants

pubmed: 30414783
pii: S1525-7304(18)30262-6
doi: 10.1016/j.cllc.2018.10.001
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Tubulin 0

Types de publication

Clinical Trial Journal Article Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

66-73.e6

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Lesley Seymour (L)

Canadian Cancer Trials Group, Queen's University, Kingston, Ontario, Canada. Electronic address: lseymour@ctg.queensu.ca.

Gwénaël Le Teuff (G)

Ligue Nationale Contre le Cancer Meta-Analysis Platform, Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, Villejuif, France; Inserm U1018, CESP, Université Paris-Saclay, Université Paris-Sud, UVSQ, Villejuif, France.

Elisabeth Brambilla (E)

Inserm U1209, Institut Albert Bonniot, Département de Pathologie, CHU Hospital Albert Michallon University Grenoble Alpes, Grenoble, France.

Frances A Shepherd (FA)

Departments of Medical Oncology and Hematology (FAS) and Pathology (M-ST), University Health Network, Princess Margaret Cancer Centre, and the University of Toronto, Toronto, Ontario, Canada.

Jean-Charles Soria (JC)

Department of Medicine, Gustave Roussy Cancer Campus, Villejuif, France; Universite Paris-sud, Orsay, France.

Robert Kratzke (R)

Department of Medicine, University of Minnesota, Minneapolis, MN.

Stephen Graziano (S)

SUNY Upstate Medical University, Syracuse, NY.

Jean-Yves Douillard (JY)

Institut de Cancerologie de l'Ouest, Saint Herblain, France.

Rafael Rosell (R)

Catalan Institute of Oncology, Barcelona, Spain.

Anthony Reiman (A)

University of New Brunswick, Saint John, New Brunswick, Canada.

Benjamin Lacas (B)

Ligue Nationale Contre le Cancer Meta-Analysis Platform, Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, Villejuif, France; Inserm U1018, CESP, Université Paris-Saclay, Université Paris-Sud, UVSQ, Villejuif, France.

Beranger Lueza (B)

Ligue Nationale Contre le Cancer Meta-Analysis Platform, Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, Villejuif, France; Inserm U1018, CESP, Université Paris-Saclay, Université Paris-Sud, UVSQ, Villejuif, France.

Sarit Aviel-Ronen (S)

Departments of Medical Oncology and Hematology (FAS) and Pathology (M-ST), University Health Network, Princess Margaret Cancer Centre, and the University of Toronto, Toronto, Ontario, Canada.

Anne McLeer (A)

Inserm U1209, Institut Albert Bonniot, Département de Pathologie, CHU Hospital Albert Michallon University Grenoble Alpes, Grenoble, France.

Thierry Le Chevalier (T)

Department of Medicine, Gustave Roussy Cancer Campus, Villejuif, France.

Robert Pirker (R)

Department of Medicine I, Medical University of Vienna, Vienna, Austria.

Martin Filipits (M)

Institute of Cancer Research, Medical University of Vienna, Vienna, Austria.

Ariane Dunant (A)

Ligue Nationale Contre le Cancer Meta-Analysis Platform, Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, Villejuif, France.

Jean-Pierre Pignon (JP)

Ligue Nationale Contre le Cancer Meta-Analysis Platform, Biostatistics and Epidemiology Unit, Gustave Roussy Cancer Campus, Villejuif, France; Inserm U1018, CESP, Université Paris-Saclay, Université Paris-Sud, UVSQ, Villejuif, France.

Ming-Sound Tsao (MS)

Departments of Medical Oncology and Hematology (FAS) and Pathology (M-ST), University Health Network, Princess Margaret Cancer Centre, and the University of Toronto, Toronto, Ontario, Canada.

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