作者
Ajay Subramanian,Neda Nemat‐Gorgani,Timothy J. Ellis-Caleo,David G.P. van IJzendoorn,Timothy J. Sears,Anish Somani,Bogdan Luca,Maggie Zhou,Martina Bradić,Ileana A. Torres,Eniola Oladipo,Christin New,Deborah Kenney,Raffi S. Avedian,Robert Steffner,Michael S. Binkley,David G. Mohler,William D. Tap,Sandra P. D’Angelo,Matt van de Rijn,Kristen N. Ganjoo,Nam Q. Bui,Gregory W. Charville,Aaron M. Newman,Everett J. Moding
摘要
Characterization of the diverse malignant and stromal cell states that make up soft tissue sarcomas and their correlation with patient outcomes has proven difficult using fixed clinical specimens. Here, we employed EcoTyper, a machine-learning framework, to identify the fundamental cell states and cellular ecosystems that make up sarcomas on a large scale using bulk transcriptomes with clinical annotations. We identified and validated 23 sarcoma-specific, transcriptionally defined cell states, many of which were highly prognostic of patient outcomes across independent datasets. We discovered three conserved cellular communities or ecotypes associated with underlying genomic alterations and distinct clinical outcomes. We show that one ecotype defined by tumor-associated macrophages and epithelial-like malignant cells predicts response to immune-checkpoint inhibition but not chemotherapy and validate our findings in an independent cohort. Our results may enable identification of patients with soft tissue sarcomas who could benefit from immunotherapy and help develop new therapeutic strategies. Subramanian et al. use the EcoTyper machine-learning framework to characterize the tumor, immune and stromal cell states and ecosystems that comprise sarcomas.