标准疗法治疗慢性淋巴细胞白血病患者的长期疗效

Alvarado Ibarra Martha, Mena Zepeda Veronica, Ortiz Zepeda Maricela, A. José, Espitia Ríos Maria, J. A. Rosa, L. Antonio
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引用次数: 0

摘要

本研究的目的是报告本世纪以来,在新药使用之前,我们医院血液科服务中心从前瞻性方案中获得的治疗结果。所有患者均接受了化疗(只有一组近期患者也接受了利妥昔单抗治疗)。所有LCL患者都在国家医疗中心(CMN)“11月20日”的血液学服务中心(ISSSTE)接受治疗。纳入本研究的患者被诊断为LCL,并符合以下标准:持续淋巴细胞增多症超过5×109/L,持续时间超过三个月;典型的淋巴细胞形态,未成熟形态不到10%;具有CD5、CD19、CD 79a、CD 20、CD22、CD23、CD24、CD25+低强度SmIg的B株的免疫表型;骨髓中30%以上的淋巴细胞。从2001年到2016年底,有2’857名患者接受了新的治疗。在这些患者中,61名被诊断为LCL(2.1%)。24名患者在被诊断为LC时患有慢性病;14例2型糖尿病患者;尿毒症4例,心脏病3例;其余为系统性高血压(2)和类风湿性关节炎(1)。直到2004年,一线治疗仅为CL。CF适用于接下来的四年(直到2008年)。最后,CFR一直使用到2016年。只有在没有给予治疗或给予CL或CF治疗时,才会注意到缺乏缓解。CFR的反应最好(p=0.0001)。CL毒性仅发现一次(中性粒细胞减少症)。CF有两起事件:中性粒细胞减少症和全血细胞减少症。CFR与两例全血细胞减少症有关(p=0.52)。在多因素分析中,淋巴细胞白细胞增多是SLP和SG以及骨髓淋巴细胞计数的阴性预测因素。因此,淋巴细胞白细胞增多是最常见的与预测相关的变量。作为肿瘤水平的基准,它可以作为一个可靠的指标,这似乎是合理的。然而,尽管其他作者已经报道了这一发现,但这一发现并不一致。与新的预测数据和新药相比,本文中的变量只有在根据本文中使用的治疗方法使用时才适用。对于新药,将使用新的预测数据。
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Long-term Outcomes in Patients with Chronic Lymphocytic Leukemia Treated with Standard Therapy
The purpose of this study was to report the therapeutic results obtained from prospective protocols at the Hematology Service of our hospital, over the course of this century, before new drugs were used. All patients underwent chemotherapy (only one recent group also received rituximab). All LCL patients taken care of at the Hematology Service of the National Medical Center (CMN) “20 de Noviembre”, ISSSTE. Patients included in this study were diagnosed with LCL and met the following criteria: persistent lymphocytosis above 5 × 109/L, for more than three months; typical lymphocytic morphology, with less than 10% of immature forms; immunophenotype of B strain with CD5, CD19, CD 79a, CD 20, CD22, CD23, CD24, CD25 + low-intensity SmIg; 30%+ lymph cells in the bone marrow. From 2001 to late 2016, 2’857patients were taken care of de novo. Out of these patients, 61 were diagnosed with LCL (2.1%). Twenty-four patients suffered from chronic diseases when LCL was diagnosed; Diabetes Mellitus type 2 in 14 patients; uremia in 4 patients, heart disease in 3 patients; the remaining ones were systemic high blood pressure (2) and rheumatoid arthritis (1). Until 2004, the first-line therapeutic treatment was CL only. CF was applied for the next four years (until 2008). Lastly, CFR is used until 2016. The lack of remission is only noticed when no treatment was administered or CL or CF treatment was administered. The best responses were achieved with CFR (p=0.0001). CL toxicity was found once only (neutropenia). There were two incidents with CF: neutropenia and pancytopenia. CFR was related to two cases of pancytopenia (p= 0.52). In the multivaried analysis, lymphocytic leukocytosis was a negative predictor for SLP and SG and lymph cell count for the bone marrow. Therefore, lymphocytic leukocytosis is the most frequent variable related to the forecast. It seems reasonable that being a benchmark of the neoplastic level it may be used as a reliable indicator. However, this finding has not been consistent, although other authors have reported it. Compared against the new forecasting data and new drugs, the variables herein are applicable only if used as per the treatments used herein. With new drugs, new forecast data are to be used.
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