Cristín Olivares
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Cristín Olivares has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Claudia Cabezas
Unidad de Anatomía Patológica, Hospital “Dr. Guillermo Grant Benavente”, Concepción 4070038, Chile
1 shared publication - Luis Viveros
Departamento de Especialidades, Facultad de Medicina, Universidad de Concepción, Concepción 4070386, Chile
1 shared publication - Mauricio Chandía
Departamento de Medicina, Facultad de Medicina, Universidad de Concepción. Concepción, Chile
1 shared publication - Patricia Alejandra Huerta
Departamento de Salud Pública, Facultad de Medicina, Universidad de Concepción, Concepción 4070386, Chile
1 shared publication - Silvana Vásquez
Servicio de Hematología, Hospital “Dr. Guillermo Grant Benavente”, Concepción 4070038, Chile
1 shared publication
Latest Publications
- Open Access
- 27 February 2026
- Published by MDPI AG in Lymphatics
- Vol. 4 (1) , 14
Role of Flow Cytometry in the Diagnosis of Bone Marrow Involvement by B-Cell Non-Hodgkin Lymphoma: Concordance with Bone Marrow Biopsy and Prognostic Impact
Bone marrow involvement in B-cell non-Hodgkin lymphoma is an adverse prognostic factor; therefore, its detection is necessary at the time of diagnosis and during follow-up. This study evaluates the concordance between flow cytometry (FC) and bone marrow biopsy (BMB) in detecting bone marrow involvement in B-cell non-Hodgkin lymphomas as well as their prognostic relevance in a Chilean cohort. A total of 202 samples from 172 patients with diffuse large B-cell (DLBCL), follicular (FL), marginal-zone (MZL), and mantle cell (MCL) lymphoma were retrospectively analyzed; all patients underwent simultaneous BMB and FC. Bone marrow involvement was identified in 29% of samples via BMB and in 40% via FC, with an overall concordance of 89% (kappa: 0.75), which was lower in mantle cell lymphoma. Eleven percent of cases showed BMB-FC+ discordance, generally associated with low tumor burden. In survival analyses, the BMB+/FC+ group exhibited shorter overall and progression-free survival, and concordant involvement was associated with a higher risk of mortality and progression, particularly among patients with an intermediate or high IPI. Involvement detected exclusively by FC did not have a significant prognostic impact. These findings support the role of FC as a complementary or alternative diagnostic tool in settings with limited resources, improving sensitivity for detecting bone marrow involvement without compromising clinical relevance.
- 27 February 2026
- Published by MDPI AG in Lymphatics
- Vol. 4 (1) , 14
Open AccessRole of Flow Cytometry in the Diagnosis of Bone Marrow Involvement by B-Cell Non-Hodgkin Lymphoma: Concordance with Bone Marrow Biopsy and Prognostic Impact
Bone marrow involvement in B-cell non-Hodgkin lymphoma is an adverse prognostic factor; therefore, its detection is necessary at the time of diagnosis and during follow-up. This study evaluates the concordance between flow cytometry (FC) and bone marrow biopsy (BMB) in detecting bone marrow involvement in B-cell non-Hodgkin lymphomas as well as their prognostic relevance in a Chilean cohort. A total of 202 samples from 172 patients with diffuse large B-cell (DLBCL), follicular (FL), marginal-zone (MZL), and mantle cell (MCL) lymphoma were retrospectively analyzed; all patients underwent simultaneous BMB and FC. Bone marrow involvement was identified in 29% of samples via BMB and in 40% via FC, with an overall concordance of 89% (kappa: 0.75), which was lower in mantle cell lymphoma. Eleven percent of cases showed BMB-FC+ discordance, generally associated with low tumor burden. In survival analyses, the BMB+/FC+ group exhibited shorter overall and progression-free survival, and concordant involvement was associated with a higher risk of mortality and progression, particularly among patients with an intermediate or high IPI. Involvement detected exclusively by FC did not have a significant prognostic impact. These findings support the role of FC as a complementary or alternative diagnostic tool in settings with limited resources, improving sensitivity for detecting bone marrow involvement without compromising clinical relevance.