Questioning the prognostic role of BAP-1 immunohistochemistry in malignant pleural mesothelioma: A single center experience with systematic review and meta-analysis. (August 2020)
- Record Type:
- Journal Article
- Title:
- Questioning the prognostic role of BAP-1 immunohistochemistry in malignant pleural mesothelioma: A single center experience with systematic review and meta-analysis. (August 2020)
- Main Title:
- Questioning the prognostic role of BAP-1 immunohistochemistry in malignant pleural mesothelioma: A single center experience with systematic review and meta-analysis
- Authors:
- Cantini, Luca
Pecci, Federica
Murrone, Alberto
Tomasetti, Marco
Copparoni, Cecilia
Fiordoliva, Ilaria
Morgese, Francesca
Rinaldi, Silvia
Mazzanti, Paola
Rubini, Corrado
Cimadamore, Alessia
Barbisan, Francesca
Giampieri, Riccardo
Scarpelli, Marina
Santarelli, Lory
Berardi, Rossana - Abstract:
- Highlights: Loss of BAP1 nuclear staining has been prevalently described in epithelioid MPM. The prognostic value of BAP1 expression in MPM still represents a matter of debate. BAP1 loss was not independently associated with a different risk of all-cause mortality. Abstract: Introduction: The prognostic role of BRCA1 associated protein-1 (BAP1) expression in malignant pleural mesothelioma (MPM) is a matter of debate. We aimed to clarify whether MPM patients with loss of BAP1 expression have better overall survival (OS) compared to BAP1 positive patients. Methods: BAP1 immunohistochemical staining of tumor samples from 60 MPM patients treated at our institution with first-line chemotherapy was evaluated. A systematic literature search was also performed. Only cohort studies that investigated BAP1 by immunohistochemistry (IHC) and reported hazard ratio (HR) values for OS obtained through multivariate analysis (or adjusted for histotype) were considered. A dataset comprising 638 MPM patients was added to our cohort and included in the meta-analysis. Results: In our cohort, 23 samples (38 %) were BAP1 positive/retained (≥1 %) and 37 samples (62 %) were BAP1 negative/loss. BAP1 loss was associated with epithelioid histotype ( p 0.01). Median OS times were 14.8 months (95 % CI: 10.7–29.3) and 18.1 months (95 % CI: 11.2–25.8) for negative and positive BAP1 expression, respectively ( p 0.2). At multivariate analysis, again no differences were observed among the two groups ( p 0.81).Highlights: Loss of BAP1 nuclear staining has been prevalently described in epithelioid MPM. The prognostic value of BAP1 expression in MPM still represents a matter of debate. BAP1 loss was not independently associated with a different risk of all-cause mortality. Abstract: Introduction: The prognostic role of BRCA1 associated protein-1 (BAP1) expression in malignant pleural mesothelioma (MPM) is a matter of debate. We aimed to clarify whether MPM patients with loss of BAP1 expression have better overall survival (OS) compared to BAP1 positive patients. Methods: BAP1 immunohistochemical staining of tumor samples from 60 MPM patients treated at our institution with first-line chemotherapy was evaluated. A systematic literature search was also performed. Only cohort studies that investigated BAP1 by immunohistochemistry (IHC) and reported hazard ratio (HR) values for OS obtained through multivariate analysis (or adjusted for histotype) were considered. A dataset comprising 638 MPM patients was added to our cohort and included in the meta-analysis. Results: In our cohort, 23 samples (38 %) were BAP1 positive/retained (≥1 %) and 37 samples (62 %) were BAP1 negative/loss. BAP1 loss was associated with epithelioid histotype ( p 0.01). Median OS times were 14.8 months (95 % CI: 10.7–29.3) and 18.1 months (95 % CI: 11.2–25.8) for negative and positive BAP1 expression, respectively ( p 0.2). At multivariate analysis, again no differences were observed among the two groups ( p 0.81). Similarly, the meta-analysis consisting of 698 patients showed no difference in terms of OS according to BAP1 status (HR 1.11; 95 % CI, 0·76-1·61; p 0.60). Conclusions: BAP1 expression is not an independent prognostic factor for MPM patients and it should not be considered without taking into account tumor histotype. Future studies should investigate its predictive role in patients treated with new emerging therapies such as immunotherapy. … (more)
- Is Part Of:
- Lung cancer. Volume 146(2020)
- Journal:
- Lung cancer
- Issue:
- Volume 146(2020)
- Issue Display:
- Volume 146, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 146
- Issue:
- 2020
- Issue Sort Value:
- 2020-0146-2020-0000
- Page Start:
- 318
- Page End:
- 326
- Publication Date:
- 2020-08
- Subjects:
- BAP1 BRCA1 associated protein-1 -- BOR best overall response -- CI confidence interval -- ECOG PS eastern cooperative oncology group perfomance status -- FFPE formalin fixed and paraffin embedded -- Hb hemoglobin -- HR hazard ratio -- IHC immunohistochemistry -- MOOSE meta-analysis of observational studies in epidemiology -- MPM malignant pleural mesothelioma -- mRECIST modified response evaluation criteria in solid tumors -- NA information not available -- NLR neutrophil/lymphocyte ratio -- OS overall survival -- PFS progression-free survival -- PRISMA preferred reporting items for systematic reviews and meta-analyses -- TNM TNM classification of malignant tumors -- WHO World Health Organization
BAP1 -- Mesothelioma -- Immunohistochemistry -- Chemotherapy -- Immunotherapy
Lungs -- Cancer -- Periodicals
Lung Neoplasms -- Abstracts
Lung Neoplasms -- Periodicals
Poumons -- Cancer -- Périodiques
Lungs -- Cancer
Periodicals
Electronic journals
Electronic journals
616.99424 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01695002 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01695002 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01695002 ↗
http://www.lungcancerjournal.info/issues ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.lungcan.2020.06.024 ↗
- Languages:
- English
- ISSNs:
- 0169-5002
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5307.245000
British Library DSC - BLDSS-3PM
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