Syreon Research Institute, Budapest, Hungary.
Department of Transfusion Medicine, Semmelweis University, Budapest, Hungary.
Expert Rev Hematol. 2022 Mar;15(3):273-284. doi: 10.1080/17474086.2022.2042246. Epub 2022 Feb 24.
In chronic lymphocytic leukemia (CLL), therapy-related cytotoxicity and the resulting immunodeficiency are thought to contribute to the development of secondary primary malignancies (SPM). Here, we analyzed clinical trial data on the occurrence of SPM following chemo-immunotherapy (CIT) regimens in treatment-naïve CLL patients.
A systematic literature search was conducted covering multiple databases between 2003 and 2019. Data from relevant clinical trials on the proportion of patients with SPMs were extracted. Then, the number of SPM patients/person-years was calculated by taking into account the trials' follow-up time. Finally, a random-effects meta-analysis to pool the rates from individual studies was performed.
We identified 22 studies reporting SPM data available for analysis. Random-effects meta-analysis estimated that the number of SPM patients/1000 person-years was 24 (95%CI: 19-29). Results from trials with cancer-specific data indicated 19 (95%CI: 14-26) solid and 9 (95%CI: 6-12) hematological SPM patients/1000 person-years. These estimations did not change significantly when sub-groups were analyzed by CIT regimens.
Although pooling data with the intention to analyze adverse event rates is challenging, our study concluded that for CIT regimens, SPM should be considered an important adverse outcome. Different regimens showed similar trends; however, other clinical and demographic factors also have profound impact.
在慢性淋巴细胞白血病(CLL)中,治疗相关的细胞毒性和由此产生的免疫缺陷被认为是导致继发性原发性恶性肿瘤(SPM)发展的原因。在这里,我们分析了针对初治 CLL 患者接受化疗免疫治疗(CIT)方案后 SPM 发生的临床试验数据。
系统检索了 2003 年至 2019 年多个数据库中的文献。提取了相关临床试验中 SPM 患者比例的数据。然后,考虑到试验的随访时间,通过计算 SPM 患者/人年数来计算 SPM 患者人数。最后,对来自个体研究的比率进行了随机效应荟萃分析。
我们确定了 22 项报告 SPM 数据的研究可供分析。随机效应荟萃分析估计,每 1000 人年 SPM 患者人数为 24(95%CI:19-29)。来自具有癌症特异性数据的试验结果表明,每 1000 人年有 19 例(95%CI:14-26)实体瘤和 9 例(95%CI:6-12)血液系统 SPM 患者。当按 CIT 方案对亚组进行分析时,这些估计值没有显著变化。
尽管有意分析不良事件发生率进行数据合并具有挑战性,但我们的研究得出结论,对于 CIT 方案,SPM 应被视为一个重要的不良结局。不同的方案显示出相似的趋势;然而,其他临床和人口统计学因素也有深远的影响。