1. Academic Validation
  2. SPEN loss drives extra-follicular diffuse large B cell lymphoma with female-specific lethality and therapeutic vulnerabilities

SPEN loss drives extra-follicular diffuse large B cell lymphoma with female-specific lethality and therapeutic vulnerabilities

  • Cancer Discov. 2026 Apr 21:10.1158/2159-8290.CD-25-1458. doi: 10.1158/2159-8290.CD-25-1458.
Benedikt Pelzer 1 Cem Meydan 2 Isaac M Spiegel 3 Ioannis Karagiannidis 2 Min Xia 2 Matt Teater 2 Emma M Welter 4 Zowie E Searcy 4 Laura K Hilton 5 Darko Barisic 3 Amos Fong 6 Pengyan Fa 3 Shenon Sethi 7 Irem S Isgor 7 Jessie J Fielding 8 Alireza Karbalayghareh 7 Colin S Burdette 3 Sravya Tumuluru 2 Sonia M Debek 3 Sunjae Lee 3 Ramon Massoni-Badosa 3 Ceyda Durmaz 9 Eralda Salataj 10 Prasath Pararajalingam 11 Zhengming Chen 12 Richard J Pelzl 13 Sanket Shah 3 Martin A Rivas 14 Kenneth B Hoehn 8 Coraline Mlynarczyk 15 Hannah M Isles 3 Xiang Wang 2 Ahmet Dogan 16 Kojo S J Elenitoba-Johnson 16 David W Scott 17 Kostiantyn Dreval 18 Ryan D Morin 19 Christina S Leslie 16 Rishi Puri 20 Jacob B Geri 9 Christopher R Chin 2 Amy Chadburn 2 Christopher E Mason 2 Hans Christian Reinhardt 21 Montserrat C Anguera 4 Wendy Béguelin 22 Leandro Venturutti 23 Ari M Melnick 2
Affiliations

Affiliations

  • 1 Weill Cornell Medicine New York City United States.
  • 2 Weill Cornell Medicine New York, NY United States.
  • 3 Weill Cornell Medicine New York City, NY United States.
  • 4 University of Pennsylvania Philadelphia, PA United States.
  • 5 BC Cancer Agency Vancouver, BC Canada.
  • 6 British Columbia Cancer Vancouver, British Columbia Canada.
  • 7 Memorial Sloan Kettering Cancer Center New York City, NY United States.
  • 8 Dartmouth College Hanover, NH United States.
  • 9 Weill Cornell Medicine United States.
  • 10 Memorial Sloan Kettering Cancer Center New York, New York United States.
  • 11 Memorial Sloan Kettering Cancer Center New York City, New York United States.
  • 12 Weill Cornell Medicine New York United States.
  • 13 University of Erlangen-Nuremberg Erlangen, Bavaria Germany.
  • 14 University of Miami Miami, FL United States.
  • 15 Yale University New Haven, CT United States.
  • 16 Memorial Sloan Kettering Cancer Center New York, NY United States.
  • 17 British Columbia Cancer Agency Vancouver Canada.
  • 18 BC Cancer Research Centre Vancouver Canada.
  • 19 Simon Fraser University Burnaby, British Columbia Canada.
  • 20 Cornell University Ithaca, NY United States.
  • 21 University Hospital Essen Essen Germany.
  • 22 Weill Cornell Medicine New York, New York United States.
  • 23 University of British Columbia Vancouver, British Columbia Canada.
Abstract

Diffuse large B-cell lymphomas (DLBCL) are genetically and phenotypically heterogeneous, making diagnosis and treatment challenging. Current models suggest DLBCL derive from follicular B cells engaged in adaptive immune responses. By studying co-occurring truncating mutations in SPEN and NOTCH2 in the BN2-DLBCL subtype, our data suggest a previously unrecognized extra-follicular trajectory. Using animal models and human specimens, we find this cooperative mutational axis supports expansion of putative clonal precursors with features of marginal zone, memory and a distinct, autoimmune B-cell-like state. This trajectory is associated with sex-biased outcomes: female patients and mice exhibit reduced survival compared to males in our cohorts. Further analysis links this disparity to enhanced X-chromosome-linked expression and functionality of Toll-like Receptor signaling. We show that IRAK inhibition represents a potential sex-specific therapeutic strategy in preclinical models. These findings support a distinct developmental origin for BN2-DLBCL and identify a high-risk female population with actionable targets for precision therapy.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-111101
    98.07%, IRAK4 Inhibitor