BCR::ABL1数字PCR选择CML患者临床队列的无治疗缓解结果

IF 2.3 3区 医学 Q2 HEMATOLOGY
C. Kockerols, P. J. M. Valk, P. Hogenbirk, I. Geelen, N. M. A. Blijlevens, J. J. W. M. Janssen, M. Hoogendoorn, S. Kersting, S. K. Klein, L. G. M. Daenen, M. Donker, P. A. W. te Boekhorst, K.-S. G. Jie, M. Corsten, M. J. Cruijsen, H. Levenga, W. M. Smit, M.-D. Levin, E. de Jongh, S. de Jonge, A. J. Vlot, M. F. Durian, J. J. Zwaginga, M. Mohlmann, T. J. Wustman, R. Blommers, J. J. Cornelissen, P. E. Westerweel, Collaborating Authors
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引用次数: 0

摘要

在 TKI 治疗期间达到稳定的深度分子反应的患者中,约有 40%-60% 在停用 TKI 后会保持缓解状态,称为无治疗缓解(TFR)。TKI 停药前通过 BCR::ABL1 数字 PCR 评估的分子反应深度已证明其作为 TFR 可靠预测参数的重要性。临床适用的预测临界值为 0.0023%IS,该临界值已被确立并通过外部验证。在本研究中,BCR::ABL1 数字 PCR 作为同类检测中最灵敏、最稳定的检测方法,在荷兰作为 TFR 预测工具进行了调查,并评估了其对低于上述临界值停止 TKI 治疗的预测价值。前瞻性评估的主要终点是 12 个月后的分子复发(MolR,BCR::ABL1 > 0.1%IS)。总计纳入了67例低于设定的BCR::ABL1数字PCR临界值的停药患者。总的 MolR 概率为 50%(95% CI,36%-62%)。在 38 例患者中,治疗时间超过 6 年(通常建议在尝试 TFR 之前的理想治疗时间)的 MolR 概率降至 36%(95% CI,18%-50%)。尝试早期停用 TKI 的患者(治疗时间少于 6 年)的 MolR 概率高达 76%(95% CI,65%-89%)。BCR::ABL1 数字 PCR 成功应用于荷兰临床实践。我们的研究表明,在 BCR::ABL1 数字 PCR 结果较低的患者中,TKI 治疗总疗程为 6 年或 6 年以上仍与较低的 MolR 率相关,一般应继续治疗。在治疗时间超过 6 年的患者中,BCR::ABL1 数字 PCR 能够识别出 TFR 成功概率较高的停药候选者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Treatment-Free Remission Outcomes in a BCR::ABL1 Digital PCR Selected Clinical Cohort of CML Patients

Treatment-Free Remission Outcomes in a BCR::ABL1 Digital PCR Selected Clinical Cohort of CML Patients

Approximately 40%–60% of patients reaching a stable deep molecular response during TKI treatment will maintain a state of remission after TKI discontinuation, denoted as treatment-free remission (TFR). Depth of molecular response assessed by BCR::ABL1 digital PCR prior to TKI discontinuation has demonstrated its significance as a reliable predictive parameter for TFR. A clinically applicable prediction cutoff of 0.0023%IS has been established and externally validated. In this study, BCR::ABL1 digital PCR, as most sensitive and stable assay of its kind, was investigated as a TFR prediction tool in the Netherlands, and evaluated for its predictive value to stop TKI treatment below the aforementioned cutoff. The primary endpoint of molecular recurrence (MolR, BCR::ABL1 > 0.1%IS) at 12 months was prospectively assessed. Overall, 67 discontinued patients below the set BCR::ABL1 digital PCR cutoff were included. The overall MolR probability was 50% (95% CI, 36%–62%). In 38 patients treated for more than 6 years as commonly recommended as desirable treatment duration before TFR attempt, the MolR probability dropped to 36% (95% CI, 18%–50%). Patients attempting an early TKI discontinuation (treated for less than 6 years) had a high MolR probability of 76% (95% CI, 65%–89%). BCR::ABL1 digital PCR was successfully used in Dutch clinical practice. Our study indicates that in patients with a low BCR::ABL1 digital PCR result, a total TKI treatment duration of six or more years remains associated with a lower MolR rate and should generally be pursued. In patients treated for more than 6 years, BCR::ABL1 digital PCR was capable to identify stop candidates with a higher probability of TFR success.

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来源期刊
CiteScore
5.50
自引率
0.00%
发文量
168
审稿时长
4-8 weeks
期刊介绍: European Journal of Haematology is an international journal for communication of basic and clinical research in haematology. The journal welcomes manuscripts on molecular, cellular and clinical research on diseases of the blood, vascular and lymphatic tissue, and on basic molecular and cellular research related to normal development and function of the blood, vascular and lymphatic tissue. The journal also welcomes reviews on clinical haematology and basic research, case reports, and clinical pictures.
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