Bo A Wan, Shabbir M H Alibhai, Lisa Chodirker, Lee Mozessohn, Michelle Geddes, Nancy Zhu, Amy M Trottier, Eve St-Hilaire, Nicholas Finn, Brian Leber, Dina Khalaf, Grace Christou, Mitchell Sabloff, Heather A Leitch, April Shamy, Karen W L Yee, John Storring, Thomas J Nevill, Brett L Houston, Mohamed Elemary, Robert Delage, Anne Parmentier, Mohammad Siddiqui, Alexandre Mamedov, Liying Zhang, Rena Buckstein
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引用次数: 0
摘要
骨髓增生异常综合征(MDSs)治疗的重点是改善受贫血和输血依赖(TD)影响的生活质量(QOL)。我们利用 MDS-CAN 登记研究了输血状态的变化--从输血依赖(TD)到输血独立(TI)(A 组)或反之(B 组),以及维持 TD(C 组)或 TI(D 组)--对 1120 名 MDS 患者的 OS 和 QOL 有何影响。分析结果表明,保持 TI 的患者的 OS 较好,保持 TD 的患者的 OS 较差,发生变化的患者的 OS 中等。在 656 名接受治疗的患者中,A 组(n = 54)的 QOL 有所改善,身体和社会功能评分呈改善趋势。B 组(n = 151)在改用 TD 后,整体 QOL 指标有所下降,尤其是在疲劳、身体、角色和社会功能方面。C 组的疲劳状况明显恶化,而 D 组在多个 QOL 方面的下降幅度较小。在 MDS 中实现 TI 与改善 QOL 相关,而恢复到 TD 会更明显地恶化总体 QOL 和功能评分。
Improvement in quality of life in MDS patients who become transfusion independent after treatment.
Myelodysplastic syndromes (MDSs) treatment focuses on improving quality of life (QOL), affected by anemia and transfusion dependence (TD). Using the MDS-CAN registry, we studied how changes in transfusion status - TD to transfusion independence (TI) (group A), or vice versa (group B), and maintaining TD (group C) or TI (group D) - affected OS and QOL in 1120 MDS patients. Analysis showed superior OS for those remaining TI, poorer for those remaining TD, and intermediate for those with changes. Among 656 treated patients, group A (n = 54) showed improved QOL, with trends toward improved physical and social function scores. Group B (n = 151) experienced declines in global QOL measures after switching to TD, particularly in fatigue and physical, role, and social functioning. Group C had notable fatigue worsening, while group D showed milder declines across multiple QOL aspects. Achieving TI in MDS correlates with improved QOL, whereas reverting to TD more significantly worsens overall QOL and function scores.
期刊介绍:
Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor