Karnofsky Performance Status and quality of life in patients with relapsed or refractory primary CNS lymphoma from a phase I/II study of tirabrutinib
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- Yoshiki Arakawa
- Department of Neurosurgery, Kyoto University Graduate School of Medicine , Kyoto , Japan
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- Yoshitaka Narita
- Department of Neurosurgery and Neuro-Oncology, National Cancer Center Hospital , Tokyo , Japan
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- Motoo Nagane
- Department of Neurosurgery, Kyorin University Faculty of Medicine , Tokyo , Japan
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- Kazuhiko Mishima
- Department of Neuro-Oncology/Neurosurgery, Saitama Medical University International Medical Center , Saitama , Japan
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- Yasuhito Terui
- Department of Hematology and Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research , Tokyo , Japan
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- Hajime Yonezawa
- Department of Neurosurgery, Kagoshima University Hospital , Kagoshima , Japan
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- Katsunori Asai
- Department of Neurosurgery, Osaka International Cancer Institute , Osaka , Japan
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- Noriko Fukuhara
- Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine , Miyagi , Japan
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- Kazuhiko Sugiyama
- Department of Clinical Oncology & Neuro-Oncology Program, Hiroshima University Hospital , Hiroshima , Japan
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- Naoki Shinojima
- Department of Neurosurgery, Kumamoto University Hospital , Kumamoto , Japan
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- Arata Aoi
- Ono Pharmaceutical Co, Ltd , Osaka , Japan
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- Ryo Nishikawa
- Department of Neuro-Oncology/Neurosurgery, Saitama Medical University International Medical Center , Saitama , Japan
説明
<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>Tirabrutinib, a second-generation inhibitor of Bruton’s tyrosine kinase, was approved in March 2020 for the treatment of relapsed or refractory primary central nervous system lymphoma (r/r PCNSL) based on phase I/II studies in Japan. We previously reported the overall response rate and safety profile. We describe Karnofsky Performance Status (KPS) and the quality of life (QoL) in patients with r/r PCNSL receiving tirabrutinib based on more than 1-year follow-up data.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>Patients with r/r PCNSL, age ≥20 years, and KPS ≥70 were treated with tirabrutinib once daily at a dose of 320, 480, or 480 mg under fasted conditions. QoL was assessed using questionnaires issued by the European Organization for Research and Treatment of Cancer (EORTC), namely EORTC QLQ-C30, EORTC QLQ-BN20, and EuroQol 5 dimensions 3-level (EQ-5D-3L) along with KPS.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Forty-four patients (mean age, 60 years [range 29–86]) were enrolled. The median follow-up period was 14.9 months (range, 1.4–27.7). The median KPS of the patients at baseline was 80.0 (range, 70–100), and this remained constant during the treatment. The global health status/QoL in the QLQ-C30 showed significant improvements from baseline through cycles 3–17 and remained relatively constant thereafter until cycle 23. Improvements were also seen in emotional functioning and constipation in the QLQ-C30 segments. Other items of QLQ-C30 and QLQ-BN20, EQ-5D visual analog scales, and EQ-5D index were maintained during the treatment.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Tirabrutinib generally maintains KPS and QoL scores with some improvements in specific QoL items in patients with r/r PCNSL.</jats:p> </jats:sec>
収録刊行物
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- Neuro-Oncology Advances
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Neuro-Oncology Advances 5 (1), vdad109-, 2023-01-01
Oxford University Press (OUP)

