4.2 Article

Impact of hypoalbuminemia on the prognosis of relapsed/refractory B-cell lymphoma treated with axicabtagene ciloleucel

Journal

EUROPEAN JOURNAL OF HAEMATOLOGY
Volume 107, Issue 1, Pages 48-53

Publisher

WILEY
DOI: 10.1111/ejh.13609

Keywords

chimeric antigen receptor T cell; cytokine release syndrome; diffuse large B‐ cell lymphoma; neurotoxicity; serum albumin

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This retrospective analysis of 81 patients treated with axi-cel showed that 22.8% had hypoalbuminemia. Results indicated that axi-cel therapy appeared to overcome the adverse prognostic impact of hypoalbuminemia on overall survival and progression-free survival in these patients. Further large multicenter clinical studies are needed to validate these findings.
Introduction Hypoalbuminemia is a known adverse prognostic factor in lymphomas. Yet, it is unknown if axicabtagene ciloleucel (axi-cel) overcomes the adverse prognostic impact of hypoalbuminemia in relapsed/refractory large B-cell lymphoma. Methods We conducted a retrospective analysis across three Mayo Clinic centers to assess the relationship of hypoalbuminemia (defined as a serum albumin (SA) levels <= 3.5 g/dL) on outcomes of patients treated with axi-cel. Results This analysis included 81 patients. Two patients had no available SA levels preceding axi-cel infusion. Eighteen patients (22.8%) had hypoalbuminemia with a median SA of 3.3 g/dL. Patients with normal SA had a statistically higher ORR than those without hypoalbuminemia (P = .018). There was no difference in 1-year PFS and OS between the group with hypoalbuminemia and the group with normal SA levels (48% vs 49%, P = .81) and (74% vs 73%, P = .97), respectively. There was no difference in the severity or median duration of cytokine release syndrome or neurotoxicity between the two groups. Conclusion Notwithstanding the limitations related to the relatively small sample size, axi-cel therapy appears to overcome the adverse effect of hypoalbuminemia on OS and PFS. Large multicenter clinical studies are certainly needed to validate these findings.

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