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Chen, Yue

https://orcid.org/0000-0001-6604-7221

Mayo Clinic

Medical College of Wisconsin

Citations 1

Autologous transplant vs chimeric antigen receptor T-cell therapy for relapsed DLBCL in partial remission
Shadman, Mazyar , Pasquini, Marcelo C. , Ahn, Kwang Woo , Chen, Yue , Turtle, Cameron J. , Hematti, Peiman , Cohen, Jonathon B. , Khimani, Farhad , Ganguly, Siddhartha , Munshi, Pashna N. , Beitinjaneh, Amer , Herrera, Alex F. , Sauter, Craig S. , Kharfan‐Dabaja, Mohamed A. , Pasquini, Marcelo , Herrera, Alex F , Kharfan-Dabaja, Mohamed A , Hamadani, Mehdi , Shadman, Mazyar , Hematti, Peiman , Turtle, Cameron J , Merryman, Reid W. , Yared, Jean A. , Locke, Frederick L. , Ahmed, Nausheen , Reagan, Patrick Michael , Hamadani, Mehdi

Blood | September 27, 2021 | Volume: 139 | Issue: 9 | Pages: 1330-1339

10.1182/blood.2021013289 Get It

Abstract The relative efficacy of autologous hematopoietic cell transplant (auto-HCT) vs chimeric antigen receptor T-cell (CAR-T) therapy in patients with diffuse large B-cell lymphoma (DLBCL) who achieve a partial remission (PR) after salvage chemotherapy is not known. Using the Center for International Blood & Marrow Transplant Research registry database, we identified adult patients with DLBCL who received either an auto-HCT (2013-2019) or CAR-T treatment with axicabtagene ciloleucel (2018-2019) while in a PR by computed tomography or positron emission tomography scan. We compared the clinical outcomes between the 2 cohorts using univariable and multivariable regression models after adjustment for relevant baseline and clinical factors. In the univariable analysis, the 2-year progression-free survival (52% vs 42%; P = .1) and the rate of 100-day nonrelapse mortality (4% vs 2%; P = .3) were not different between the 2 cohorts, but consolidation with auto-HCT was associated with a lower rate of relapse/progression (40% vs 53%; P = .05) and a superior overall survival (OS) (69% vs 47%; P = .004) at 2 years. In the multivariable regression analysis, treatment with auto-HCT was associated with a significantly lower risk of relapse/progression rate (hazard ratio = 1.49; P = .01) and a superior OS (hazard ratio = 1.63; P = .008). In patients with DLBCL in a PR after salvage therapy, treatment with auto-HCT was associated with a lower incidence of relapse and a superior OS compared with CAR-T. These data support the role of auto-HCT as the standard of care in transplant-eligible patients with relapsed DLBCL in PR after salvage therapy.