IDENTIFYING RISK FACTORS FOR TREATMENT FAILURE IN B-CELL CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS RECEIVING BENDAMUSTINE±RITUXIMAB THERAPY

I. Drabovska, G. Maslova
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Abstract

Introduction. The initial assessment of prognosis is of particular importance in determining the management of patients with B-cell chronic lymphocytic leukemia and the choice of specific therapy. The aim is to analyze the risk factors for failure to achieve a complete response to the bendamustine±rituximab treatment regimen in patients with B-cell chronic lymphocytic leukemia. Materials and methods. Twenty-two patients undergoing treatment for B-cell chronic lymphocytic leukemia (B-CLL) progression were included in the study. Response to treatment was assessed on the 56th day, categorized as complete, partial, or no response. Patients were divided into three groups based on their response: group I (n=6) included patients who showed a complete response after receiving bendamustine±rituximab; group II (n=11) included patients who achieved a partial response; and group III (n=5) consisted of patients with no response. Risk factors for chemotherapy resistance, as well as general and biochemical blood counts, were evaluated and subjected to statistical analysis. Results: Stage III (C) and IV (C) according to the Rai, Binet classification were recorded in 33.2% of patients with a complete response to chemotherapy, in 36.4% of patients with a partial response to chemotherapy, and in 60% of patients with no response to specific treatment. A decrease in hemoglobin level below 100 g/L was recorded only in patients with a partial response and no response, namely in 4 (36%) patients of group II and 1 (20%) patient of group III. On day 56, in patients of group II who received a partial response, there was a direct correlation between the level of leukocytes in the hemogram and the activity of aspartate aminotransferase (r=0.71; p=0.01) and the content of total bilirubin (r=0.63; p=0.03) in the biochemical blood test. After 2 courses of chemotherapy in patients of group III, a direct correlation of high strength between the level of leukocytes in the hemogram and the activity of aspartate aminotransferase (r=0.93; p=0.02) and alanine aminotransferase (r=0.93; p=0.02) in the biochemical blood test was found. The bendamustine±rituximab chemotherapy regimen has a high safety profile.
确定接受苯达莫司汀±利妥昔单抗治疗的 b 细胞慢性淋巴细胞白血病患者治疗失败的风险因素
导言对预后的初步评估对于确定 B 细胞慢性淋巴细胞白血病患者的治疗方案和特定疗法的选择尤为重要。本文旨在分析 B 细胞慢性淋巴细胞白血病患者在接受苯达莫司汀±利妥昔单抗治疗方案后未能获得完全应答的风险因素。材料与方法研究纳入了22名正在接受治疗的B细胞慢性淋巴细胞白血病(B-CLL)进展期患者。治疗反应在第 56 天进行评估,分为完全反应、部分反应或无反应。根据患者的反应分为三组:I组(6人)包括接受苯达莫司汀±利妥昔单抗治疗后出现完全反应的患者;II组(11人)包括出现部分反应的患者;III组(5人)包括无反应的患者。对化疗耐药的风险因素以及一般和生化血液计数进行了评估和统计分析。结果根据 Rai 和 Binet 的分类,33.2% 的患者对化疗完全有反应,36.4% 的患者对化疗部分有反应,60% 的患者对特定治疗无反应,均为 III 期(C)和 IV 期(C)。只有部分反应和无反应患者的血红蛋白水平下降到 100 克/升以下,即第二组的 4 名患者(36%)和第三组的 1 名患者(20%)。第 56 天,在获得部分应答的 II 组患者中,血液图中的白细胞水平与血液生化检验中的天冬氨酸氨基转移酶活性(r=0.71;p=0.01)和总胆红素含量(r=0.63;p=0.03)之间存在直接相关性。第三组患者经过两个疗程的化疗后,发现血象中的白细胞水平与血液生化检验中的天冬氨酸氨基转移酶活性(r=0.93;p=0.02)和丙氨酸氨基转移酶(r=0.93;p=0.02)之间存在高度的直接相关性。苯达莫司汀±利妥昔单抗化疗方案具有较高的安全性。
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