4.6 Article

Effect of lisocabtagene maraleucel on HRQoL and symptom severity in relapsed/refractory large B-cell lymphoma

Journal

BLOOD ADVANCES
Volume 5, Issue 8, Pages 2245-2255

Publisher

ELSEVIER
DOI: 10.1182/bloodadvances.2020003503

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Funding

  1. Bristol Myers Squibb
  2. Juno Therapeutics, a Bristol Myers Squibb Company

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The study found that treatment with lisocabtagene maraleucel (liso-cel) could significantly improve the overall health status and quality of life of patients with relapsed/refractory LBCL, particularly showing clinically meaningful improvements in fatigue. For treatment responders, the improvement in global health status/quality of life was more significant.
CD19-directed chimeric antigen receptor (CAR) T-cell therapy has shown efficacy as a thirdline or later treatment in patients with relapsed/refractory large B-cell lymphoma (LBCL). Using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) and the EuroQol 5-Dimension 5-Level (EQ-5D-5L) questionnaire, we evaluated the impact of CAR T-cell treatment with lisocabtagene maraleucel (liso-cel) on health-related quality of life (HRQoL) and symptoms in patients with relapsed/refractory LBCL in the ongoing, open-label, nonrandomized TRANSCEND NHL 001 trial. Clinically meaningful improvement was observed in EORTC QLQ-C30 scores for global health status/QoL, based on a minimally important difference of 10 points at 2 to 18 months after liso-cel infusion. There were no clinically meaningful changes in physical functioning and pain, whereas clinically meaningful improvements were observed in fatigue at 2, 12, and 18 months. The proportion of patients with clinically meaningful improvement in global health status/QoL was generally higher for treatment responders than for nonresponders. A trend toward decreased mean EQ-5D-5L index scores was observed at 1 month after liso-cel infusion, followed by subsequent increases through 18 months. Mean EQ-5D-SL visual analog scale scores increased from 2 through 18 months. In summary, patients with relapsed/refractory LBCL treated with liso-cel had early, sustained, and clinically meaningful improvements in HRQoL and symptoms that correlated with antitumor activity.

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