Department of Haematology and Oncology, Würzburg University Medical Center, Oberdürrbacher Straße 6, 97080, Würzburg, Germany.
University Hospital of Salamanca-Instituto de Investigación Biomédica de Salamanca, Salamanca, Spain.
BMC Cancer. 2021 Jun 2;21(1):659. doi: 10.1186/s12885-021-08325-2.
BACKGROUND: In the phase III ALCYONE trial, daratumumab plus bortezomib/melphalan/prednisone (D-VMP) significantly improved overall response rate and progression-free status compared with VMP alone in transplant-ineligible patients with newly diagnosed multiple myeloma (NDMM). Here, we present patient-reported outcomes (PROs) from ALCYONE. METHODS: The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item (EORTC QLQ-C30) and EuroQol 5-dimensional descriptive system (EQ-5D-5L) questionnaire were administered at baseline, every 3 months (year 1) and every 6 months (until progression). Treatment effects were assessed using a repeated-measures, mixed-effects model. RESULTS: Compliance with PRO assessments was comparable at baseline (> 90%) and throughout study (> 76%) for both treatment groups. Improvements from baseline were observed in both groups for EORTC QLQ-C30 Global Health Status (GHS), most functional scales, symptom scales and EQ-5D-5L visual analog scale (VAS). Between-group differences were significant for GHS (p = 0.0240) and VAS (p = 0.0160) at month 3. Improvements in pain were clinically meaningful in both groups at all assessment time points. Cognitive function declined in both groups, but the magnitude of the decline was not clinically meaningful. CONCLUSIONS: Patients with transplant-ineligible NDMM demonstrated early and continuous improvements in health-related quality of life, including improvements in functioning and symptoms, following treatment with D-VMP or VMP. TRIAL REGISTRATION: ClinicalTrials.gov identifier NCT02195479 , registered September 21, 2014.
背景:在 III 期 ALCYONE 试验中,与单独使用 VMP 相比,达雷妥尤单抗联合硼替佐米/美法仑/泼尼松(D-VMP)显著提高了不适合移植的新诊断多发性骨髓瘤(NDMM)患者的总体缓解率和无进展生存状态。在这里,我们展示了来自 ALCYONE 的患者报告结果(PRO)。
方法:欧洲癌症研究与治疗组织生存质量问卷核心 30 项(EORTC QLQ-C30)和欧洲五维健康量表(EQ-5D-5L)问卷在基线时、每 3 个月(第 1 年)和每 6 个月(直到进展)进行评估。使用重复测量混合效应模型评估治疗效果。
结果:两组的 PRO 评估的依从性在基线时(>90%)和整个研究期间(>76%)均相似。两组患者的 EORTC QLQ-C30 总体健康状况(GHS)、大多数功能量表、症状量表和 EQ-5D-5L 视觉模拟量表(VAS)均较基线有所改善。在第 3 个月时,GHS(p=0.0240)和 VAS(p=0.0160)两组间差异具有统计学意义。两组患者在所有评估时间点的疼痛均有明显改善。两组的认知功能均下降,但下降幅度无临床意义。
结论:不适合移植的 NDMM 患者在接受 D-VMP 或 VMP 治疗后,在健康相关生活质量方面表现出早期和持续的改善,包括功能和症状的改善。
试验注册:ClinicalTrials.gov 标识符 NCT02195479,注册日期为 2014 年 9 月 21 日。
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