Day 30 SUVmax predicts progression in patients with lymphoma achieving PR/SD after CAR T-cell therapy

Author:

Al Zaki Ajlan1,Feng Lei2,Watson Grace1,Ahmed Sairah A.1ORCID,Mistry Haleigh1,Nastoupil Loretta J.1,Hawkins Misha1,Nair Ranjit1,Iyer Swaminathan P.1,Lee Hun J.1,Steiner Raphael E.1ORCID,Flowers Christopher R.1,Shpall Elizabeth J.3,Kebriaei Partow3,Neelapu Sattva S.1ORCID,Westin Jason R.1ORCID,Strati Paolo1

Affiliation:

1. Department of Lymphoma and Myeloma,

2. Department of Biostatistics, and

3. Department of Stem Cell Transplantation, The University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

Abstract About 70% of patients with large B-cell lymphoma (LBCL) who are treated with axicabtagene ciloleucel (axi-cel) and who achieve a partial response (PR) or stable disease (SD) on the day 30 (D30) positron emission tomography (PET)–computed tomography (CT) scan progress; however, the factors that are predictive of progression are unknown. This a retrospective study of patients with LBCL who were treated with axi-cel at MD Anderson Cancer Center between January of 2018 and February of 2021. Among 50 patients with D30 PR/SD, 13 (26%) converted to a complete response (CR). Among 95 patients with a D30 CR, 72 (76%) remained in CR. On univariate analysis, the only day −5 characteristic associated with conversion from D30 PR/SD to subsequent CR was a higher platelet count (P = .05). The only D30 factor associated with conversion from D30 PR/SD to subsequent CR was a lower maximum standardized uptake volume (SUVmax; P < .001); all patients with D30 SUVmax ≥ 10 progressed. After a median follow-up of 12 months, no significant difference in median progression-free survival was observed between patients who converted from D30 PR/SD to subsequent CR and those who had been in CR since D30 (P = .19). Novel predictive and prognostic markers based on tissue biopsy and noninvasive diagnostic assays are needed to more effectively identify these patients and characterize the biology of their residual disease.

Publisher

American Society of Hematology

Subject

Hematology

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