Prolonged Improvement In Patient Reported Quality Of Life (Qol) Following Tisagenlecleucel Infusion In Adult Patients (Pts) With Relapsed/Refractory (R/R) Diffuse Large B-Cell Lymphoma (Dlbcl): 19-Month Follow-Up (Fu) Of The Juliet Study

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION(2019)

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摘要
BackgroundQuality of life (QoL) is an important endpoint in the JULIET study (NCT02445248), a phase 2 trial evaluating a single infusion of tisagenlecleucel in adult patients (pts) with relapsed/refractory (r/r) diffuse large B-cell lymphoma (DLBCL). Earlier analyses showed improvements in QoL at month (mo) 3 and 6 (Maziarz et al, ASH 2017, EBMT 2018). We report updated JULIET data with extended follow-up (FU; median: 19.3 mo).MethodsPts were aged ≥18 years with r/r DLBCL after ≥2 lines of therapy and either failed or were ineligible for autologous hematopoietic stem cell transplant (SCT). At baseline, mo-3 through mo-24, pts completed the Functional Assessment of Cancer Therapy-Lymphoma (FACT-Lym) and Short Form-36 Health Survey v2 (SF-36). Higher scores indicate better QoL.ResultsOf the 167 enrolled pts, 115 pts were infused with tisagenlecleucel before data cutoff; 96% had previously received ≥2 systemic therapies and 49% had relapsed after SCT. QoL instruments were completed by 108 pts (94%) at baseline, including 50 patients who had complete response (CR) or partial response (PR). Of pts eligible for analysis with CR or PR, 26 and 21 completed the assessments at mo-12 and -18, respectively. Scores of pts with CR or PR (mean change at baseline through mo-18) indicated sustained improvements in all categories (Table 1). Similar trends were observed for SF-36.ConclusionsWith long term FU, pts with r/r DLBCL responding to tisagenlecleucel continue to show sustained improvements in QoL. Quality of life (QoL) is an important endpoint in the JULIET study (NCT02445248), a phase 2 trial evaluating a single infusion of tisagenlecleucel in adult patients (pts) with relapsed/refractory (r/r) diffuse large B-cell lymphoma (DLBCL). Earlier analyses showed improvements in QoL at month (mo) 3 and 6 (Maziarz et al, ASH 2017, EBMT 2018). We report updated JULIET data with extended follow-up (FU; median: 19.3 mo). Pts were aged ≥18 years with r/r DLBCL after ≥2 lines of therapy and either failed or were ineligible for autologous hematopoietic stem cell transplant (SCT). At baseline, mo-3 through mo-24, pts completed the Functional Assessment of Cancer Therapy-Lymphoma (FACT-Lym) and Short Form-36 Health Survey v2 (SF-36). Higher scores indicate better QoL. Of the 167 enrolled pts, 115 pts were infused with tisagenlecleucel before data cutoff; 96% had previously received ≥2 systemic therapies and 49% had relapsed after SCT. QoL instruments were completed by 108 pts (94%) at baseline, including 50 patients who had complete response (CR) or partial response (PR). Of pts eligible for analysis with CR or PR, 26 and 21 completed the assessments at mo-12 and -18, respectively. Scores of pts with CR or PR (mean change at baseline through mo-18) indicated sustained improvements in all categories (Table 1). Similar trends were observed for SF-36. With long term FU, pts with r/r DLBCL responding to tisagenlecleucel continue to show sustained improvements in QoL.
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lymphoma,tisagenlecleucel infusion,dlbcl,b-cell
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