Patient perspectives on treatment for mantle cell lymphoma and chronic lymphocytic leukemia in Japan.

IF 0.9 Q4 HEMATOLOGY
Toru Kiguchi, Yasushi Hiramatsu, Shuichi Ota, Michihiro Uchiyama, Moe Matsuo, Miyu Okamura, Shimpei Morimoto, Yoshinori Tanizawa, Masaomi Tajimi, Nalin Payakachat
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引用次数: 0

Abstract

The increasing number of treatment options for patients with mantle cell lymphoma (MCL) and chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) in Japan underscores the critical need to comprehend their treatment preferences. In this study, individual semi-structured interviews with 20 Japanese patients with diagnosis of MCL or CLL/SLL were conducted and qualitatively analyzed to elicit concepts important for patients regarding treatment selection. Although effectiveness and safety were imperative for treatment selection, convenience and quality of life were also reported as important attributes. Over the course of their disease journey, patients reported diverse and changing preferences in terms of treatment characteristics. Additionally, there was a discrepancy between their desired and actual levels of involvement in shared decision-making with physicians about treatment choices. Optimal personalized care for better outcomes of patients with MCL and CLL/SLL hinges on healthcare professionals acknowledging individual patient needs and preferences within their cultural, societal and personal context.

日本套细胞淋巴瘤和慢性淋巴细胞白血病患者对治疗的看法。
在日本,套细胞淋巴瘤(MCL)和慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)患者的治疗选择越来越多,这凸显了了解他们治疗偏好的迫切需要。本研究对 20 名确诊为 MCL 或 CLL/SLL 的日本患者进行了个人半结构式访谈,并对访谈内容进行了定性分析,以了解患者在治疗选择方面的重要概念。虽然有效性和安全性是选择治疗的必要条件,但方便性和生活质量也是重要因素。在疾病的治疗过程中,患者对治疗特点的偏好多种多样且不断变化。此外,在与医生共同决策治疗选择方面,患者的期望参与度与实际参与度之间也存在差异。要为 MCL 和 CLL/SLL 患者提供更好的治疗效果,最佳的个性化护理取决于医疗保健专业人员是否承认患者在其文化、社会和个人背景下的个人需求和偏好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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