Blood Neoplasia最新文献

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KIR3DL1-HLA-Bw status in CML is associated with achievement of TFR: the POKSTIC trial, a multicenter observational study CML 中的 KIR3DL1-HLA-Bw 状态与 TFR 的实现有关:多中心观察研究 POKSTIC 试验
Blood Neoplasia Pub Date : 2024-03-01 DOI: 10.1016/j.bneo.2024.100001
Hiroshi Ureshino , Yasunori Ueda , Shin Fujisawa , Kensuke Usuki , Hideo Tanaka , Masaya Okada , Shugo Kowata , Kazunori Murai , Asao Hirose , Motohiro Shindo , Takashi Kumagai , Tomoharu Takeoka , Kazuharu Kamachi , Keisuke Kidoguchi , Takero Shindo , Satoshi Iyama , Junki Inamura , Takafumi Nakao , Tsutomu Kobayashi , Eri Kawata , Shinya Kimura
{"title":"KIR3DL1-HLA-Bw status in CML is associated with achievement of TFR: the POKSTIC trial, a multicenter observational study","authors":"Hiroshi Ureshino ,&nbsp;Yasunori Ueda ,&nbsp;Shin Fujisawa ,&nbsp;Kensuke Usuki ,&nbsp;Hideo Tanaka ,&nbsp;Masaya Okada ,&nbsp;Shugo Kowata ,&nbsp;Kazunori Murai ,&nbsp;Asao Hirose ,&nbsp;Motohiro Shindo ,&nbsp;Takashi Kumagai ,&nbsp;Tomoharu Takeoka ,&nbsp;Kazuharu Kamachi ,&nbsp;Keisuke Kidoguchi ,&nbsp;Takero Shindo ,&nbsp;Satoshi Iyama ,&nbsp;Junki Inamura ,&nbsp;Takafumi Nakao ,&nbsp;Tsutomu Kobayashi ,&nbsp;Eri Kawata ,&nbsp;Shinya Kimura","doi":"10.1016/j.bneo.2024.100001","DOIUrl":"10.1016/j.bneo.2024.100001","url":null,"abstract":"<div><h3>Abstract</h3><p>Achievement of treatment-free remission (TFR) after tyrosine kinase inhibitor (TKI) discontinuation in patients who show a durable deep molecular response (DMR) during TKI treatment of chronic myeloid leukemia in chronic phase (CML-CP) is a therapeutic goal; however, the prognostic factors that predict successful achievement of TFR are unclear. Previously, we reported that killer immunoglobulin-like receptor (<em>KIR)</em> and <em>HLA</em> polymorphisms are associated with achievement of a DMR. Here, we investigated the association between <em>KIR</em> and <em>HLA</em> polymorphisms and TFR. We conducted the POKSTIC (POlymorphisms of Killer immunoglobulin-like receptor, which affect Stop Tyrosine kinase Inhibitor in patients with Chronic myeloid leukemia) trial, a multicenter collaborative observational study that enrolled 76 patients with CML-CP. The median age was 63 years (interquartile range [IQR], 49-70). Of 76 patients, 42 (56.6%; 95% confidence interval [CI], 47.7-66.8 at 6 months) discontinued TKIs without molecular relapse; the median follow-up time for TFR was 24 months (IQR, 16-64). <em>KIR</em> genotyping and allele typing did not identify risk factors for molecular relapse; however, univariate and multivariate analysis identified the combination of <em>KIR3DL1</em>-<em>HLA-Bw4</em> (an <em>HLA-B</em> allele) as an independent factor for a higher risk of molecular relapse (hazard ratio, 2.206; 95% CI, 1.112-4.376; <em>P</em> = .024). Notably, patients at higher risk of relapse had a significantly lower number of natural killer (NK) cells at TKI discontinuation than the other patients (CD16<sup>+</sup>/CD56<sup>+</sup> NK cells: median 499.63 cells per μL vs 629.17 cells per μL, respectively; <em>P</em> = .049). Thus, <em>KIR3DL1-HLA-Bw</em> status reflects NK cell responses and is associated with TFR. The study is registered with the UMIN Clinical Trials Registry as #UMIN000041798.</p></div>","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2950328024000013/pdfft?md5=4478bc59bb04e478596db505d5a8f1b4&pid=1-s2.0-S2950328024000013-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139819062","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Real-world comparison of daratumumab-based regimens in relapsed/refractory multiple myeloma using health record data 利用健康记录数据对基于达拉单抗的复发性/难治性多发性骨髓瘤治疗方案进行真实世界比较
Blood Neoplasia Pub Date : 2024-03-01 DOI: 10.1016/j.bneo.2024.100003
Benjamin A. Derman , Jacob Ambrose , Laura L. Fernandes , Christina M. Zettler , Eric Hansen , Andrew J. Belli , Ching-Kun Wang
{"title":"Real-world comparison of daratumumab-based regimens in relapsed/refractory multiple myeloma using health record data","authors":"Benjamin A. Derman ,&nbsp;Jacob Ambrose ,&nbsp;Laura L. Fernandes ,&nbsp;Christina M. Zettler ,&nbsp;Eric Hansen ,&nbsp;Andrew J. Belli ,&nbsp;Ching-Kun Wang","doi":"10.1016/j.bneo.2024.100003","DOIUrl":"10.1016/j.bneo.2024.100003","url":null,"abstract":"<div><h3>Abstract</h3><p>Daratumumab (dara)-based triplet therapies are commonly used in the second-line (2L) and third-line (3L) settings in relapsed/refractory multiple myeloma (RRMM), usually in combination with dexamethasone and either bortezomib (dara-Vd), carfilzomib (dara-Kd), or pomalidomide (dara-Pd). We performed a real-world (rw) analysis to directly compare these regimens, to our knowledge, for the first time. This was an observational, retrospective cohort study using COTA’s rw database of patients with MM who have initiated 2L or 3L therapy with dara-Vd, dara-Kd, or dara-Pd. rw time to next treatment (rwTTNT) and rw overall survival (rwOS) were analyzed using the Kaplan-Meier method. Comparative analyses were conducted using a trimmed inverse probability of treatment weighting method to control for potential confounders. A total of 639 patients received a dara-based regimen as either 2L or 3L therapy (dara-Vd, n = 201; dara-Kd, n = 122; and dara-Pd, n = 316). A high proportion had functional (52%) or cytogenetic (26%) high-risk disease; 49% were lenalidomide refractory. Median rwTTNT for dara-Vd was 7.6 months and was 12.9 months for dara-Kd (hazard ratio [HR], 0.70; 95% confidence interval [CI], 0.49-0.99). Similarly, median rwTTNT for dara-Vd was 6.9 months and 15.3 months for dara-Pd (HR, 0.57; 95% CI, 0.43-0.77). Median rwTTNT for dara-Pd was 15.7 months, and for dara-Kd 13.2 months (HR, 1.1; 95% CI, 0.8-1.6). No regimen was associated with superior rwOS. Among patients with RRMM receiving 2L or 3L therapy with a dara-based triplet, dara-Vd was associated with inferior rwTTNT compared with both dara-Kd and dara-Pd. dara-Vd may not be a suitable control arm for most phase 3 studies.</p></div>","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2950328024000037/pdfft?md5=d48c10ab1082c0948b3ca3433ec37ce2&pid=1-s2.0-S2950328024000037-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139873265","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Frequent response monitoring in chronic lymphocytic leukemia clinical trials: what is the value? 慢性淋巴细胞白血病临床试验中的频繁反应监测:价值何在?
Blood Neoplasia Pub Date : 2024-02-15 DOI: 10.1016/j.bneo.2024.100006
Agnes Mattsson , Jeanette Lundin , Tom A. Mulder , Sandra E. Sylvan , Marzia Palma , Lotta Hansson ∗ , Anders Österborg ∗
{"title":"Frequent response monitoring in chronic lymphocytic leukemia clinical trials: what is the value?","authors":"Agnes Mattsson ,&nbsp;Jeanette Lundin ,&nbsp;Tom A. Mulder ,&nbsp;Sandra E. Sylvan ,&nbsp;Marzia Palma ,&nbsp;Lotta Hansson ∗ ,&nbsp;Anders Österborg ∗","doi":"10.1016/j.bneo.2024.100006","DOIUrl":"10.1016/j.bneo.2024.100006","url":null,"abstract":"","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2950328024000062/pdfft?md5=24a77ccdb02c94659b8d09df5fc59fe7&pid=1-s2.0-S2950328024000062-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139880327","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Multiple myeloma-associated DIS3 gene is essential for hematopoiesis but loss of DIS3 is insufficient for myelomagenesis 多发性骨髓瘤相关 DIS3 基因对造血至关重要,但 DIS3 基因缺失不足以导致骨髓瘤形成
Blood Neoplasia Pub Date : 2024-02-01 DOI: 10.1016/j.bneo.2024.100005
Hiroto Ohguchi, Yasuyo Ohguchi, Sho Kubota, Kan Etoh, Ai Hamashima, Shingo Usuki, Takako Yokomizo-Nakano, Jie Bai, Takeshi Masuda, Y. Kawano, Takeshi Harada, Mitsuyoshi Nakao, Takashi Minami, T. Hideshima, Kimi Araki, G. Sashida
{"title":"Multiple myeloma-associated DIS3 gene is essential for hematopoiesis but loss of DIS3 is insufficient for myelomagenesis","authors":"Hiroto Ohguchi, Yasuyo Ohguchi, Sho Kubota, Kan Etoh, Ai Hamashima, Shingo Usuki, Takako Yokomizo-Nakano, Jie Bai, Takeshi Masuda, Y. Kawano, Takeshi Harada, Mitsuyoshi Nakao, Takashi Minami, T. Hideshima, Kimi Araki, G. Sashida","doi":"10.1016/j.bneo.2024.100005","DOIUrl":"https://doi.org/10.1016/j.bneo.2024.100005","url":null,"abstract":"","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139814612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Castleman disease patients report mild COVID-19 symptoms and mount a humoral response to SARS-CoV-2 vaccination 卡斯特曼病患者出现轻微的 COVID-19 症状,并对接种 SARS-CoV-2 疫苗产生体液反应
Blood Neoplasia Pub Date : 2024-02-01 DOI: 10.1016/j.bneo.2024.100002
S. Shyamsundar, S. Pierson, C. Connolly, M. Teles, D. Segev, W. Werbel, F. van Rhee, Corey Casper, Joshua D. Brandstadter, Ariela Noy, D. Fajgenbaum
{"title":"Castleman disease patients report mild COVID-19 symptoms and mount a humoral response to SARS-CoV-2 vaccination","authors":"S. Shyamsundar, S. Pierson, C. Connolly, M. Teles, D. Segev, W. Werbel, F. van Rhee, Corey Casper, Joshua D. Brandstadter, Ariela Noy, D. Fajgenbaum","doi":"10.1016/j.bneo.2024.100002","DOIUrl":"https://doi.org/10.1016/j.bneo.2024.100002","url":null,"abstract":"","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139885906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Frequent response monitoring in chronic lymphocytic leukemia clinical trials: what is the value? 慢性淋巴细胞白血病临床试验中的频繁反应监测:价值何在?
Blood Neoplasia Pub Date : 2024-02-01 DOI: 10.1016/j.bneo.2024.100006
Agnes Mattsson, J. Lundin, T. Mulder, S. E. Sylvan, M. Palma, L. Hansson, Anders Österborg
{"title":"Frequent response monitoring in chronic lymphocytic leukemia clinical trials: what is the value?","authors":"Agnes Mattsson, J. Lundin, T. Mulder, S. E. Sylvan, M. Palma, L. Hansson, Anders Österborg","doi":"10.1016/j.bneo.2024.100006","DOIUrl":"https://doi.org/10.1016/j.bneo.2024.100006","url":null,"abstract":"","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139820587","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Real-world Comparison of Daratumumab-Based Regimens in Relapsed/Refractory Multiple Myeloma Using Health Record Data 利用健康记录数据对基于达拉单抗的复发性/难治性多发性骨髓瘤治疗方案进行真实世界比较
Blood Neoplasia Pub Date : 2024-02-01 DOI: 10.1016/j.bneo.2024.100003
B. Derman, J. Ambrose, L. Fernandes, C. Zettler, E. Hansen, A. Belli, Ching-Kun Wang
{"title":"Real-world Comparison of Daratumumab-Based Regimens in Relapsed/Refractory Multiple Myeloma Using Health Record Data","authors":"B. Derman, J. Ambrose, L. Fernandes, C. Zettler, E. Hansen, A. Belli, Ching-Kun Wang","doi":"10.1016/j.bneo.2024.100003","DOIUrl":"https://doi.org/10.1016/j.bneo.2024.100003","url":null,"abstract":"","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139813452","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
KIR3DL1-HLA-Bw status in CML is associated with achievement of TFR: the POKSTIC Trial, a Multicentre Observational Study CML 中的 KIR3DL1-HLA-Bw 状态与 TFR 的实现有关:多中心观察研究 POKSTIC 试验
Blood Neoplasia Pub Date : 2024-02-01 DOI: 10.1016/j.bneo.2024.100001
H. Ureshino, Yasunori Ueda, Shin Fujisawa, Kensuke Usuki, Hideo Tanaka, Masaya Okada, S. Kowata, Kazunori Murai, Asao Hirose, Motohiro Shindo, Takashi Kumagai, Tomoharu Takeoka, K. Kamachi, K. Kidoguchi, T. Shindo, Satoshi Iyama, J. Inamura, Takafumi Nakao, Tsutomu Kobayashi, E. Kawata, H. Ohkawara, Takayuki Ikezoe, Atsushi Kawaguchi, Shinya Kimura
{"title":"KIR3DL1-HLA-Bw status in CML is associated with achievement of TFR: the POKSTIC Trial, a Multicentre Observational Study","authors":"H. Ureshino, Yasunori Ueda, Shin Fujisawa, Kensuke Usuki, Hideo Tanaka, Masaya Okada, S. Kowata, Kazunori Murai, Asao Hirose, Motohiro Shindo, Takashi Kumagai, Tomoharu Takeoka, K. Kamachi, K. Kidoguchi, T. Shindo, Satoshi Iyama, J. Inamura, Takafumi Nakao, Tsutomu Kobayashi, E. Kawata, H. Ohkawara, Takayuki Ikezoe, Atsushi Kawaguchi, Shinya Kimura","doi":"10.1016/j.bneo.2024.100001","DOIUrl":"https://doi.org/10.1016/j.bneo.2024.100001","url":null,"abstract":"","PeriodicalId":100189,"journal":{"name":"Blood Neoplasia","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139878686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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