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在HELIOS研究中,基线时严重受损的复发慢性淋巴细胞白血病/小淋巴细胞淋巴瘤患者接受依鲁替尼联合苯达莫司汀和利妥昔单抗治疗后疲劳、身体功能和幸福感的改善。

Improvement of fatigue, physical functioning, and well-being among patients with severe impairment at baseline receiving ibrutinib in combination with bendamustine and rituximab for relapsed chronic lymphocytic leukemia/small lymphocytic lymphoma in the HELIOS study.

作者信息

Cramer Paula, Fraser Graeme, Santucci-Silva Rodrigo, Grosicki Sebastian, Dilhuydy Marie-Sarah, Janssens Ann, Loscertales Javier, Rule Simon, Goy Andre, Traina Shana, Chan Eric K H, Diels Joris, Sengupta Nishan, Mahler Michelle, Salman Mariya, Howes Angela, Chanan-Khan Asher

机构信息

a Department I of Internal Medicine and Center of Integrated Oncology Cologne-Bonn , German CLL Study Group, University Hospital Cologne , Cologne , Germany.

b Juravinski Cancer Centre, McMaster University , Hamilton , ON , Canada.

出版信息

Leuk Lymphoma. 2018 Sep;59(9):2075-2084. doi: 10.1080/10428194.2017.1416364. Epub 2018 Jan 3.

Abstract

Health-related quality of life (HRQoL) is an important endpoint, especially in clinical trials for malignancies with a long course of disease, such as chronic lymphocytic leukemia (CLL). Patient-reported outcomes were examined in the randomized, double-blind, placebo-controlled HELIOS study to assess the impact of treatment with the Bruton's tyrosine kinase inhibitor ibrutinib, added to bendamustine plus rituximab (BR) background therapy. Measures included FACIT-Fatigue, EORTC QLQ-C30, QLQ-CLL16, and EQ-5D-5L. Of 578 patients enrolled, 540 (93%) provided FACIT-Fatigue responses at baseline. Most had only a moderate degree of impairment at baseline; mean values did not appear to change over time in either treatment arm, suggesting that adding ibrutinib to BR did not impact health-related quality of life. However, post-hoc analyses showed that subgroups of patients with the worst fatigue, physical functional status, and well-being at baseline had greater improvements in these outcomes with ibrutinib plus BR treatment versus placebo.

摘要

健康相关生活质量(HRQoL)是一个重要的终点指标,尤其在诸如慢性淋巴细胞白血病(CLL)等病程较长的恶性肿瘤临床试验中。在随机、双盲、安慰剂对照的HELIOS研究中,对患者报告的结局进行了检查,以评估在苯达莫司汀加利妥昔单抗(BR)基础治疗中添加布鲁顿酪氨酸激酶抑制剂依鲁替尼的治疗效果。测量指标包括功能性评估癌症治疗-疲劳量表(FACIT-Fatigue)、欧洲癌症研究与治疗组织生活质量核心问卷(EORTC QLQ-C30)、QLQ-CLL16和EQ-5D-5L。在入组的578例患者中,540例(93%)在基线时提供了FACIT-Fatigue量表的反应。大多数患者在基线时仅有中度损伤;两个治疗组的平均值似乎均未随时间变化,这表明在BR治疗中添加依鲁替尼不会影响健康相关生活质量。然而,事后分析显示,与安慰剂相比,基线时疲劳、身体功能状态和幸福感最差的患者亚组在接受依鲁替尼加BR治疗后,这些结局有更大改善。

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