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首页> 外文期刊>Pathology oncology research: POR >Effectiveness of the Combination of Rituximab and Standard Chemotherapeutic Regimens in Previously Untreated Patients with Chronic Lymphocytic Leukaemia in Real-Life: Results from a Noninterventional Study (CILI Study)
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Effectiveness of the Combination of Rituximab and Standard Chemotherapeutic Regimens in Previously Untreated Patients with Chronic Lymphocytic Leukaemia in Real-Life: Results from a Noninterventional Study (CILI Study)

机译:Rituximab和标准化学治疗方案组合在现实生活中慢性淋巴细胞白血病中的慢性淋巴细胞白血病患者组合的有效性:非行动研究的结果(CILI研究)

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Chronic lymphocytic leukemia (CLL) is one of the most common haematological malignancies exhibiting remarkable heterogeneity in clinical course. Rituximab added to standard chemotherapy has been proven to increase response rate and eventually survival among previously untreated CLL patients. CILI was an open-label, non-randomized, single arm, multicentric, observational study aimed to collect real-life effectiveness data for rituximab used according to the current label in combination with standard chemotherapy in previously untreated CLL patients. Overall response rates (ORR) in the entire study population as well as in various subgroups were estimated. Adverse events were recorded during the entire course of the study. A total number of 150 patients were enrolled by 15 Hungarian study sites. Out of these, 82 patients received 6cycles of rituximab containing treatment. Overall response rates of 88.24% (CI95%: 81.6 93.12%) and 94.59% (CI95%: 86.73 98.51%) were recorded in the intent-to-treat (ITT) and per-protocol (PP) populations, respectively. In both study populations, somewhat higher ORR was observed in patients aged 65years. Subgroups defined according to either chromosomal aberrations (presence of 11q and 17p deletions) showed apparently high ORRs, though these rates were most probably biased by low patient numbers. 144 adverse events were reported during the study, of which 15 AEs were considered to be related to the administration of rituximab. Analyses of the efficacy variables have revealed comparable results to those previously reported by controlled clinical trials.
机译:慢性淋巴细胞白血病(CLL)是最常见的血液恶性肿瘤之一,在临床过程中表现出显着的异质性之一。已被证明加入到标准化疗的Rituximab以增加响应率,最终在预处理的CLL患者中生存。 Cili是一个开放标签,非随机化,单臂,多中心,观察研究,旨在收集根据当前标签使用的Rituximab的现实效力数据,与预先治疗的CLL患者的标准化疗组合使用。估计整个研究人群以及各个亚组的整体反应率(ORR)均估计。在整个研究过程中记录不良事件。 150名患者的总数均由15名匈牙利学习地点注册。其中82名患者接受了含有治疗的6辆菌根治疗。在意图(ITT)和每协定(PP)群体中,记录了88.24%(CI95%:81.6 93.12%)和94.59%(CI95%:86.73 98.51%)。在两个研究人群中,65年患者的患者观察到稍微较高的ORR。根据任一染色体像差(11Q和17P缺失)定义的亚组显然是高的orrs,尽管这些速率最可能被低患者数偏压。在该研究期间报道了144例不良事件,其中15 AES被认为与Rituximab的给药有关。疗效变量的分析揭示了对照临床试验先前报道的结果。

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