Delta-Like Protein 3 Expression in Paired Chemonaive and Chemorelapsed Small Cell Lung Cancer Samples.

chemonaive chemorelapsed delta-like protein 3 paired small cell lung cancer

Journal

Frontiers in medicine
ISSN: 2296-858X
Titre abrégé: Front Med (Lausanne)
Pays: Switzerland
ID NLM: 101648047

Informations de publication

Date de publication:
2021
Historique:
received: 01 07 2021
accepted: 23 08 2021
entrez: 25 10 2021
pubmed: 26 10 2021
medline: 26 10 2021
Statut: epublish

Résumé

Rovalpituzumab tesirine (Rova-T), an antibody-drug conjugate directed against Delta-like protein 3 (DLL3), is under development for patients with small cell lung cancer (SCLC). DLL3 is expressed on the majority of SCLC samples. Because SCLC is rarely biopsied in the course of disease, data regarding DLL3 expression in relapses is not available. The aim of this study was to investigate the expression of DLL3 in chemorelapsed (but untreated with Rova-T) SCLC samples and compare the results with chemonaive counterparts. Two evaluation methods to assess DLL3 expression were explored. Additionally, we assessed if DLL3 expression of chemorelapsed and/or chemonaive samples has prognostic impact and if it correlates with other clinicopathological data. The study included 30 paired SCLC samples, which were stained with an anti DLL3 antibody. DLL3 expression was assessed using tumor proportion score (TPS) and H-score and was categorized as DLL3 low (TPS < 50%, H-score ≤ 150) and DLL3 high (TPS ≥ 50%, H-score > 150). Expression data were correlated with clinicopathological characteristics. Kaplan-Meier curves were used to illustrate overall survival (OS) depending on DLL3 expression in chemonaive and chemorelapsed samples, respectively, and depending on dynamics of expression during course of therapy. DLL3 was expressed in 86.6% chemonaive and 80% chemorelapsed SCLC samples without significant differences between the two groups. However, the extent of expression varied in a substantial proportion of pairs (36.6% with TPS, 43.3% with H-score), defined as a shift from low to high or high to low expression. TPS and H-score provided comparable results. There were no profound correlations with clinicopathological data. Survival analysis revealed a trend toward a more favorable OS in DLL low-expressing chemonaive SCLC (

Identifiants

pubmed: 34692726
doi: 10.3389/fmed.2021.734901
pmc: PMC8531433
doi:

Types de publication

Journal Article

Langues

eng

Pagination

734901

Informations de copyright

Copyright © 2021 Kuempers, Jagomast, Krupar, Paulsen, Heidel, Ribbat-Idel, Idel, Märkl, Anlauf, Berezowska, Tiemann, Bösmüller, Fend, Kalsdorf, Bohnet, Dreyer, Sailer, Kirfel and Perner.

Déclaration de conflit d'intérêts

SP is a consultant of Ventana, Roche, Novartis, Astellar, Astrazeneca, Bristol-Myers Squibb, Merck Serono and MSD. JK is a consultant of Roche, Novartis, BMS and MSD. BM received an honorary from AbbVie for a one-time consulting activity. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Christiane Kuempers (C)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Tobias Jagomast (T)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Rosemarie Krupar (R)

Pathology, Research Center Borstel-Leibniz Lung Center, Borstel, Germany.

Finn-Ole Paulsen (FO)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.
Department of Oncology, Hematology and Bone Marrow Transplantation With Division of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Carsten Heidel (C)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Julika Ribbat-Idel (J)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Christian Idel (C)

Department of Otorhinolaryngology, Luebeck, University of Luebeck and University Hospital Schleswig-Holstein, Luebeck, Germany.

Bruno Märkl (B)

Medical Faculty, General Pathology and Molecular Diagnostics, University Augsburg, Augsburg, Germany.

Martin Anlauf (M)

Institute of Pathology, Cytology and Molecular Pathology Limburg, Limburg, Germany.

Sabina Berezowska (S)

Department of Laboratory Medicine and Pathology, Institute of Pathology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Institute of Pathology, University of Bern, Bern, Switzerland.

Markus Tiemann (M)

Institute for Hematopathology, Hamburg, Germany.

Hans Bösmüller (H)

Institute of Pathology and Neuropathology University Hospital Tuebingen, Tuebingen, Germany.

Falko Fend (F)

Institute of Pathology and Neuropathology University Hospital Tuebingen, Tuebingen, Germany.

Barbara Kalsdorf (B)

Medical Clinic, Research Center Borstel-Leibniz Lung Center, Borstel, Germany.

Sabine Bohnet (S)

Department of Pulmonology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Eva Dreyer (E)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Verena Sailer (V)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Jutta Kirfel (J)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.

Sven Perner (S)

Institute of Pathology, Luebeck, University Hospital Schleswig-Holstein, Luebeck, Germany.
Pathology, Research Center Borstel-Leibniz Lung Center, Borstel, Germany.
Airway Research Center North (ARCN), Member of the German Center for Lung Research (DZL), Borstel, Germany.

Classifications MeSH