化学免疫疗法
医学
内科学
肿瘤科
细胞因子释放综合征
淋巴瘤
弥漫性大B细胞淋巴瘤
胃肠病学
免疫疗法
美罗华
癌症
嵌合抗原受体
作者
Frederick L. Locke,Olalekan O. Oluwole,John Kuruvilla,Catherine Thieblemont,Franck Morschhauser,Gilles Salles,Steven P. Rowe,Saran Vardhanabhuti,Joshua D. Winters,Simone Filosto,Christina To,Paul Cheng,Marco Schupp,Ronald L. Korn,Marie José Kersten
出处
期刊:Blood
[American Society of Hematology]
日期:2024-04-01
卷期号:143 (24): 2464-2473
被引量:4
标识
DOI:10.1182/blood.2023021620
摘要
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.
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