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Peer-reviewedCC BY 4.0Frontiers in Oncology

Prognostic associations of PD-L1 expression and BAP1 loss in pleural mesothelioma: a retrospective single-center cohort from Colombia

6 affiliations
  1. 1Departamento de Oncología, Instituto Nacional de Cancerología
  2. 2Departamento de Cirugía de Tórax, Instituto Nacional de Cancerología y Fundación CTIC
  3. 3Departamento de Oncología, Clínica Universitaria Colombia, Fundación Universitaria Sanitas
  4. 4Departamento de Estadística, Instituto Nacional de Cancerología
  5. 5Departamento de Patología Oncologica, Instituto Nacional de Cancerología
  6. 6Instituto de Investigación, Universidad FUCS.

Abstract

Background: Evidence on the prognostic associations of programmed death-ligand 1 (PD-L1) and BRCA1-associated protein 1 (BAP1) in pleural mesothelioma (PM) remains inconsistent, and joint data from Latin American cohorts are limited. We evaluated these biomarkers in a Colombian cohort.

Methods: This retrospective single-center cohort included adults with histologically confirmed PM treated at the Instituto Nacional de Cancerología, Bogotá, from January 2011 through December 2023. PD-L1 was quantified using tumor proportion score (TPS), with ≥1% as the primary threshold; BAP1 was classified as retained or lost by nuclear immunoreactivity. Overall survival (OS) was measured from pathologic diagnosis to death. Event-free survival (EFS) was measured from diagnosis to first documented progression or death; patients without an event were censored at last contact. Kaplan–Meier methods and separate multivariable Cox models were used.

Results: Sixty-seven patients were included; 60/67 (89.6%) had locally advanced or metastatic disease. PD-L1 TPS ≥1% was present in 26/67 (38.8%), and BAP1 loss in 47/61 evaluable tumors (77.0%). All 67 patients died. Median OS was 9.20 months (95% CI, 6.11–14.13), and median EFS was 6.51 months (95% CI, 5.49–9.13). PD-L1 TPS ≥1% was not clearly associated with OS (adjusted HR, 1.03; 95% CI, 0.57–1.86) or EFS (adjusted HR, 1.11; 95% CI, 0.62–2.00). BAP1 loss also showed no clear adjusted association with OS (HR, 1.57; 95% CI, 0.78–3.16) or EFS (HR, 1.65; 95% CI, 0.82–3.33).

Conclusions: Neither PD-L1 TPS ≥1% nor BAP1 loss showed a clear adjusted association with survival. These jointly measured estimates extend the evidence from an underrepresented Latin American population but require external validation; the exploratory ≥5% and ≥10% analyses were based on only 14 and 7 patients, respectively.

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BibTeX
@article{bruges2026prognostic,
  title = {{Prognostic associations of PD-L1 expression and BAP1 loss in pleural mesothelioma: a retrospective single-center cohort from Colombia}},
  author = {Ricardo Brugés and Carlos Carvajal and Angela Luna-Meza and Marcela Núñez and Alejandra Navarrete and Rafael Parra-Medina},
  journal = {Frontiers in Oncology},
  year = {2026},
  month = oct,
  doi = {10.3389/fonc.2026.1920798},
  url = {https://www.frontiersin.org/articles/10.3389/fonc.2026.1920798/full},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Prognostic associations of PD-L1 expression and BAP1 loss in pleural mesothelioma: a retrospective single-center cohort from Colombia
AU  - Ricardo Brugés
AU  - Carlos Carvajal
AU  - Angela Luna-Meza
AU  - Marcela Núñez
AU  - Alejandra Navarrete
AU  - Rafael Parra-Medina
PY  - 2026
DA  - 2026/10/14
JO  - Frontiers in Oncology
DO  - 10.3389/fonc.2026.1920798
UR  - https://www.frontiersin.org/articles/10.3389/fonc.2026.1920798/full
AB  - Background: Evidence on the prognostic associations of programmed death-ligand 1 (PD-L1) and BRCA1-associated protein 1 (BAP1) in pleural mesothelioma (PM) remains inconsistent, and joint data from Latin American cohorts are limited. We evaluated these biomarkers in a Colombian cohort.  Methods: This retrospective single-center cohort included adults with histologically confirmed PM treated at the Instituto Nacional de Cancerología, Bogotá, from January 2011 through December 2023. PD-L1 was quantified using tumor proportion score (TPS), with ≥1% as the primary threshold; BAP1 was classified as retained or lost by nuclear immunoreactivity. Overall survival (OS) was measured from pathologic diagnosis to death. Event-free survival (EFS) was measured from diagnosis to first documented progression or death; patients without an event were censored at last contact. Kaplan–Meier methods and separate multivariable Cox models were used.  Results: Sixty-seven patients were included; 60/67 (89.6%) had locally advanced or metastatic disease. PD-L1 TPS ≥1% was present in 26/67 (38.8%), and BAP1 loss in 47/61 evaluable tumors (77.0%). All 67 patients died. Median OS was 9.20 months (95% CI, 6.11–14.13), and median EFS was 6.51 months (95% CI, 5.49–9.13). PD-L1 TPS ≥1% was not clearly associated with OS (adjusted HR, 1.03; 95% CI, 0.57–1.86) or EFS (adjusted HR, 1.11; 95% CI, 0.62–2.00). BAP1 loss also showed no clear adjusted association with OS (HR, 1.57; 95% CI, 0.78–3.16) or EFS (HR, 1.65; 95% CI, 0.82–3.33).  Conclusions: Neither PD-L1 TPS ≥1% nor BAP1 loss showed a clear adjusted association with survival. These jointly measured estimates extend the evidence from an underrepresented Latin American population but require external validation; the exploratory ≥5% and ≥10% analyses were based on only 14 and 7 patients, respectively.
SN  - 2234-943X
ER  -