BAP1 Loss by Immunohistochemistry Predicts Improved Survival to First-Line Platinum and Pemetrexed Chemotherapy for Patients With Pleural Mesothelioma: A Validation Study.
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Australia
/ epidemiology
Humans
Immunohistochemistry
Lung Neoplasms
/ pathology
Mesothelioma
/ pathology
Mesothelioma, Malignant
Pemetrexed
/ therapeutic use
Platinum
/ therapeutic use
Pleural Neoplasms
/ pathology
Tumor Suppressor Proteins
Ubiquitin Thiolesterase
BAP1
Chemotherapy
Pemetrexed
Pleural mesothelioma
Predictive biomarkers
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
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
921-930Commentaires et corrections
Type : CommentIn
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2022 International Association for the Study of Lung Cancer. All rights reserved.