
PETAL Consortium Survival Prognosticators and How Inflammation Impacts Hematopoiesis
From Blood Podcast by American Society of Hematology
March 5, 2026 · 13 min · Season 11
About this episode
This episode features an interview discussing the prognostic significance of early relapse in T-cell lymphomas and the impact of inflammation on hematopoiesis.
In this week's episode, Blood associate editor Dr. Laura Michaelis interviews Drs. Mark Sorial and Emmanuelle Passegue on their articles published in volume 147 issue 7 of Blood . Dr. Sorial discusses " Early time to relapse as a survival prognosticator in nodal mature T-cell lymphomas: results from the PETAL consortium " where he and his team evaluated the prognostic significance of early relapse in a large retrospective cohort. They report a time to relapse of <12 months as a strong predictive factor independent of the prognostic index for T-cell lymphoma and histology, with results validated in 2 independent cohorts. Dr. Emmanuelle Passegue discusses " Inflammation perturbs hematopoiesis by remodeling specific compartments of the bone marrow niche ". Using a combination of single-cell RNA sequencing profiling and flow cytometry, the team characterized the bone marrow niche compartments in mice subjected to inflammation. They show that inter-feron-mediated inflammation preferentially targets central marrow leptin receptor–expressing mesenchymal cells, triggering cytokine release that affects monocyte dynamics in the bone marrow microenvironment.
People in this episode
Host: Dr. Laura Michaelis
Guests: Dr. Mark Sorial, Dr. Emmanuelle Passegue
Topics covered
- prognostic significance
- inflammation
- hematopoiesis
- T-cell lymphomas
- bone marrow niche
- single-cell RNA sequencing
Keywords
- T-cell lymphomas
- early relapse
- inflammation
- hematopoiesis
- bone marrow
- cytokine release
- single-cell RNA sequencing
Mentioned in this episode
Organizations: PETAL consortium
Books & works: Early time to relapse as a survival prognosticator in nodal mature T-cell lymphomas: results from the PETAL consortium, Blood
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