BAP1 Loss by Immunohistochemistry Predicts Improved Survival to First-Line Platinum and Pemetrexed Chemotherapy for Patients With Pleural Mesothelioma: A Validation Study.


Journal

Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235

Informations de publication

Date de publication:
07 2022
Historique:
received: 13 02 2022
revised: 09 04 2022
accepted: 15 04 2022
pubmed: 1 5 2022
medline: 29 6 2022
entrez: 30 4 2022
Statut: ppublish

Résumé

Pleural mesothelioma (PM) is an aggressive malignancy with no identified predictive biomarkers. We assessed whether tumor BAP1 status is a predictive biomarker for survival in patients receiving first-line combination platinum and pemetrexed therapy. PM cases (n = 114) from Aalborg, Denmark, were stained for BAP1 on tissue microarrays. Demographic, clinical, and survival data were extracted from registries and medical records. Surgical cases were excluded. BAP1 status was associated with overall survival (OS) by Cox regression and Kaplan-Meier methods. Results were validated in an independent cohort from Perth, Australia (n = 234). BAP1 loss was found in 62% and 60.3% of all Danish and Australian samples, respectively. BAP1 loss was an independent predictor of OS in multivariate analyses corrected for histological subtype, performance status, age, sex, and treatment (hazard ratio = 2.49, p < 0.001, and 1.48, p = 0.01, respectively). First-line platinum and pemetrexed-treated patients with BAP1 loss had significantly longer median survival than those with retained BAP1 in both the Danish (20.1 versus 7.3 mo, p < 0.001) and Australian cohorts (19.6 versus 11.1 mo, p < 0.01). Survival in patients with BAP1 retained and treated with platinum and pemetrexed was similar as in those with best supportive care. There was a higher OS in patients with best supportive care with BAP1 loss, but it was significant only in the Australian cohort (16.8 versus 8.3 mo, p < 0.01). BAP1 is a predictive biomarker for survival after first-line combination platinum and pemetrexed chemotherapy and a potential prognostic marker in PM. BAP1 in tumor is a promising clinical tool for treatment stratification.

Identifiants

pubmed: 35489694
pii: S1556-0864(22)00210-6
doi: 10.1016/j.jtho.2022.04.008
pii:
doi:

Substances chimiques

BAP1 protein, human 0
Tumor Suppressor Proteins 0
Pemetrexed 04Q9AIZ7NO
Platinum 49DFR088MY
Ubiquitin Thiolesterase EC 3.4.19.12

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

921-930

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2022 International Association for the Study of Lung Cancer. All rights reserved.

Auteurs

Amber Louw (A)

Department of Anatomical Pathology, PathWest Laboratory Medicine, QEII Medical Centre, Perth, Australia; School of Medical and Health Sciences, Edith Cowan University, Perth, Australia; Institute for Respiratory Health, Perth, Australia; National Centre for Asbestos Related Disease, University of Western Australia, Perth, Australia.

Vasiliki Panou (V)

Department of Respiratory Medicine, Odense University Hospital, Odense, Denmark; Department of Respiratory Diseases, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.

Weronika Maria Szejniuk (WM)

Department of Oncology & Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University Hospital, Aalborg, Denmark.

Christos Meristoudis (C)

Institute of Pathology, Aalborg University Hospital, Aalborg, Denmark.

Siaw Ming Chai (SM)

Department of Anatomical Pathology, PathWest Laboratory Medicine, QEII Medical Centre, Perth, Australia.

Chris van Vliet (C)

Department of Anatomical Pathology, PathWest Laboratory Medicine, QEII Medical Centre, Perth, Australia.

Y C Gary Lee (YCG)

Institute for Respiratory Health, Perth, Australia; Department of Respiratory Medicine, Sir Charles Gairdner Hospital, Perth, Australia; Medical School, University of Western Australia, Perth, Australia.

Ian M Dick (IM)

National Centre for Asbestos Related Disease, University of Western Australia, Perth, Australia.

Tina Firth (T)

Institute for Respiratory Health, Perth, Australia; National Centre for Asbestos Related Disease, University of Western Australia, Perth, Australia.

Louise Andersen Lynggaard (LA)

Institute of Pathology, Aalborg University Hospital, Aalborg, Denmark.

Azadeh Birbaneh Asghari (AB)

Institute of Pathology, Aalborg University Hospital, Aalborg, Denmark.

Mogens Vyberg (M)

Center for RNA Medicine, Department of Clinical Medicine, Aalborg University, Copenhagen, Denmark.

Johnni Hansen (J)

Danish Cancer Society, Research Center, Copenhagen, Denmark.

Jenette Creaney (J)

Institute for Respiratory Health, Perth, Australia; National Centre for Asbestos Related Disease, University of Western Australia, Perth, Australia; Department of Respiratory Medicine, Sir Charles Gairdner Hospital, Perth, Australia. Electronic address: jenette.creaney@uwa.edu.au.

Oluf Dimitri Røe (OD)

Department of Oncology & Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University Hospital, Aalborg, Denmark; Department of Oncology, Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway; Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

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Classifications MeSH