Cellularity in myxoid liposarcoma: association with tumor immune microenvironment and patient outcomes

Background The identification of high-risk patients with myxoid liposarcoma (MLPS) remains challenging. This study aimed to describe the morphological characteristics of cellularity in MLPS and to characterize the spatial distribution and density of the tumor immune microenvironment (TIME) in MLPS. Patients and methods The morphology of untreated primary MLPS was scored for the percentage of classic, round cell, and transitional tumor components (categorized as type A, B, and C density according to a progressively higher neoplastic cellularity). TIME was evaluated by sampling the area showing the highest immune infiltrate (HI), the highest and lowest neoplastic cellularity, and the tumor border (TB). Results More than one tumor component was present in all patients ( N = 35). Most tumors harbored a classic (32/35; 91.4%) or a transitional component (34/35; 97.1%), with type C density present in 16 of 35 cases (45.7%). A round cell component was detected in 11 cases (11/35, 31.4%). In six patients who developed disease relapse, MLPS was more likely to have either a transitional component type C density, a round cell component, or both ( P = 0.014). TIME analysis showed that HI and TB on healthy tissue areas had the highest enrichment of immune cells, which were more frequently detected in transitional tumor component type C density and round cell component. Conclusions Patients with MLPS featuring a tumor with the round cell component in conjunction with transitional component type C density were at higher risk of disease progression and showed higher infiltrating T cells and tumor-associated macrophages.

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Publication Details

Journal
ESMO rare cancers.
Published
2026-08-26
DOI
https://doi.org/10.1016/j.esmorc.2026.100518
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Cellularity in myxoid liposarcoma: association with tumor immune microenvironment and patient outcomes

Luca Lalli, L. Rivoltini, Silvia Brich, L. Mariani et al.
ESMO rare cancers.
Sarcoma Diagnosis and Treatment
article

Cellularity in myxoid liposarcoma: association with tumor immune microenvironment and patient outcomes

Luca Lalli, L. Rivoltini, Silvia Brich, L. Mariani, M. Barisella, Cesare Soffientini, Paola Collini, Viviana Vallacchi, Alessia Bertolotti, Alessandro Gronchi, G. Dagrada, Stefano Redaelli, Sandro Pasquali, S. Massa, R. Sanfilippo, L. Bergamaschi, C. Fabbroni, E. Di Blasi, E.B. Leone
article en

Abstract

Background The identification of high-risk patients with myxoid liposarcoma (MLPS) remains challenging. This study aimed to describe the morphological characteristics of cellularity in MLPS and to characterize the spatial distribution and density of the tumor immune microenvironment (TIME) in MLPS. Patients and methods The morphology of untreated primary MLPS was scored for the percentage of classic, round cell, and transitional tumor components (categorized as type A, B, and C density according to a progressively higher neoplastic cellularity). TIME was evaluated by sampling the area showing the highest immune infiltrate (HI), the highest and lowest neoplastic cellularity, and the tumor border (TB). Results More than one tumor component was present in all patients ( N = 35). Most tumors harbored a classic (32/35; 91.4%) or a transitional component (34/35; 97.1%), with type C density present in 16 of 35 cases (45.7%). A round cell component was detected in 11 cases (11/35, 31.4%). In six patients who developed disease relapse, MLPS was more likely to have either a transitional component type C density, a round cell component, or both ( P = 0.014). TIME analysis showed that HI and TB on healthy tissue areas had the highest enrichment of immune cells, which were more frequently detected in transitional tumor component type C density and round cell component. Conclusions Patients with MLPS featuring a tumor with the round cell component in conjunction with transitional component type C density were at higher risk of disease progression and showed higher infiltrating T cells and tumor-associated macrophages.

ESMO rare cancers.Vol. 7
Fondazione IRCCS Istituto Nazionale dei Tumori (IT), University of Milano-Bicocca (IT)
Ministero della Salute, Associazione Italiana per la Ricerca sul Cancro
Zero hunger
Openalex Percentile: Top 11%
Sarcoma Diagnosis and Treatment
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