Axicabtagene ciloleucel vs standard of care in second-line large B-cell lymphoma: outcomes by metabolic tumor volume

Author:

Locke Frederick L.1ORCID,Oluwole Olalekan O.2ORCID,Kuruvilla John3ORCID,Thieblemont Catherine4,Morschhauser Franck5ORCID,Salles Gilles6ORCID,Rowe Steven P.7,Vardhanabhuti Saran8,Winters Joshua8,Filosto Simone8,To Christina8ORCID,Cheng Paul8,Schupp Marco8,Korn Ronald9ORCID,Kersten Marie José10ORCID

Affiliation:

1. 1Department of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL

2. 2Division of Hematology and Oncology, Department of Medicine, Vanderbilt University Cancer Center, Nashville, TN

3. 3Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada

4. 4University of Paris, Hôpital Saint-Louis, Hemato-Oncology, DMU DHI, Paris, France

5. 5Department of Hematology, University of Lille, Centre Hospitalier Universitaire de Lille, Lille, France

6. 6Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

7. 7The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins School of Medicine, Baltimore, MD

8. 8Kite, a Gilead Company, Santa Monica, CA

9. 9Imaging Endpoints, Scottsdale, AZ

10. 10Amsterdam University Medical Center (location University of Amsterdam), Cancer Center Amsterdam, Amsterdam, The Netherlands

Abstract

Abstract Metabolic tumor volume (MTV) assessed using 2-deoxy-2-[18F]fluoro-d-glucose positron emission tomography, a measure of tumor burden, is a promising prognostic indicator in large B-cell lymphoma (LBCL). This exploratory analysis evaluated relationships between baseline MTV (categorized as low [median or less] vs high [greater than median]) and clinical outcomes in the phase 3 ZUMA-7 study (NCT03391466). Patients with LBCL relapsed within 12 months of or refractory to first-line chemoimmunotherapy were randomized 1:1 to axicabtagene ciloleucel (axi-cel; autologous anti-CD19 chimeric antigen receptor T-cell therapy) or standard care (2-3 cycles of chemoimmunotherapy followed by high-dose chemotherapy with autologous stem cell transplantation in patients who had a response). All P values are descriptive. Within high- and low-MTV subgroups, event-free survival (EFS) and progression-free survival (PFS) were superior with axi-cel vs standard care. EFS in patients with high MTV (vs low MTV) was numerically shorter with axi-cel and was significantly shorter with standard care. PFS was shorter in patients with high MTV vs low MTV in both the axi-cel and standard-care arms, and median MTV was lower in patients in ongoing response at data cutoff vs others. Median MTV was higher in patients treated with axi-cel who experienced grade ≥3 neurologic events or cytokine release syndrome (CRS) than in patients with grade 1/2 or no neurologic events or CRS, respectively. Baseline MTV less than or equal to median was associated with better clinical outcomes in patients receiving axi-cel or standard care for second-line LBCL. The trial was registered at www.clinicaltrials.gov as #NCT03391466.

Publisher

American Society of Hematology

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