Circulating Tumor DNA Assessment of Disease Response in Large B-Cell Lymphoma: Lisocabtagene Maraleucel Versus Autologous Stem Cell Transplantation Standard Therapy

remained significantly associated with EFS after adjusting for positron emission tomography (PET) response, while interaction testing revealed a significant interaction between PET status and treatment arm for EFS. Liso-cel achieved deeper, more durable molecular clearance by ctDNA, consistent with superior EFS and PFS versus ASCT for second-line LBCL treatment. ctDNA-MRD provided prognostic value beyond PET, supporting its role as a complementary biomarker for treatment response and relapse prediction.

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Publication Details

Journal
Journal of Clinical Oncology
Published
2026-04-27
DOI
https://doi.org/10.1200/jco-25-03051
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
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article

Circulating Tumor DNA Assessment of Disease Response in Large B-Cell Lymphoma: Lisocabtagene Maraleucel Versus Autologous Stem Cell Transplantation Standard Therapy

Manali Kamdar, Scott R. Solomon, Ash A. Alizadeh, Koji Izutsu et al.
Journal of Clinical Oncology
Cancer Genomics and Diagnostics
article

Circulating Tumor DNA Assessment of Disease Response in Large B-Cell Lymphoma: Lisocabtagene Maraleucel Versus Autologous Stem Cell Transplantation Standard Therapy

Manali Kamdar, Scott R. Solomon, Ash A. Alizadeh, Koji Izutsu, Pim G. N. J. Mutsaers, Sami Ibrahimi, Mazyar Shadman, Justine Dell’Aringa, Lara Stepan, Leanne Peiser, Alessandro Crotta, Veronika Bachanová, David M. Kurtz, Abood Okal, Jacob J. Chabon, Patrick B. Johnston, Sahar Ansari, Victor A. Chow, Jeremy Abramson, Bertram Glaß, Francisco Hernandez-Ilizaliturri, Ethan G. Thompson, Stephan Mielke, Jon Arnason
article en

Abstract

remained significantly associated with EFS after adjusting for positron emission tomography (PET) response, while interaction testing revealed a significant interaction between PET status and treatment arm for EFS. Liso-cel achieved deeper, more durable molecular clearance by ctDNA, consistent with superior EFS and PFS versus ASCT for second-line LBCL treatment. ctDNA-MRD provided prognostic value beyond PET, supporting its role as a complementary biomarker for treatment response and relapse prediction.

Journal of Clinical Oncology
Northside Hospital (US), Roswell Park Comprehensive Cancer Center (US), University of Minnesota (US), Beth Israel Deaconess Medical Center (US), Karolinska University Hospital (SE), Harvard University (US), Palo Alto University (US), California Institute for Regenerative Medicine (US), University of Washington (US), Erasmus MC (NL), Institute for Stem Cell Biology and Regenerative Medicine (IN), Massachusetts General Hospital (US), Fred Hutch Cancer Center (US), Bristol-Myers Squibb (United States) (US), Mayo Clinic in Arizona (US), Oklahoma State University Oklahoma City (US), University of Colorado Cancer Center (US), Foresight Science & Technology (United States) (US), Helios Hospital Berlin-Buch (DE), Tokyo National Hospital (JP), Bristol-Myers Squibb (Switzerland) (CH), University of Oklahoma (US), University of Colorado Denver (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 8%
Cancer Genomics and Diagnostics
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