晚期胃肠道间质瘤患者伊马替尼治疗后血红蛋白水平变化的预测意义。

IF 0.8
Burhan Safakoglu, Tulay Kus, Gokmen Aktas
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引用次数: 0

摘要

目的:探讨伊马替尼治疗晚期胃肠道间质瘤(GIST)后血红蛋白降低的预测价值。研究设计:回顾性观察性研究。研究地点和时间:2021年7月至2024年2月,土耳其加济安泰普加济安泰普医疗点私立医院肿瘤科。方法:该研究纳入了79例经伊马替尼治疗后诊断为晚期GIST的患者。收集患者的年龄、性别、肿瘤位置、转移部位、转移部位数量、治疗前初始分期等综合临床信息,并测量患者在伊马替尼治疗前和治疗后1-3个月的血液学参数。分析血液学参数的变化,并采用Kaplan-Meier法评估临床变量与无病生存期(DFS)和总生存期(OS)的关系。结果:伊马替尼治疗后,35例患者(44.3%)出现血红蛋白水平下降。血红蛋白水平降低的患者比没有下降的患者表现出更好的无进展生存期(PFS)[43.0个月(31.5-54.5)对22.0个月(14.9-29.1)];结论:伊马替尼治疗后血红蛋白水平降低是晚期GIST患者的预测靶毒性。关键词:GIST,伊马替尼治疗,靶毒性,预测标志物,贫血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive Significance of Changes in Haemoglobin Level Following Imatinib Treatment in Patients with Advanced Gastrointestinal Stromal Tumour.

Objective: To evaluate the predictive value of haemoglobin decrease following imatinib treatment in patients with advanced gastro- intestinal stromal tumours (GIST).

Study design: An retrospective observational study. Place and Duration of the Study: Department of Medical Oncology, Gaziantep Medical Point Private Hospital, Gaziantep, Turkiye, between July 2021 and February 2024.

Methodology: The study included 79 patients diagnosed with advanced GIST following imatinib therapy. Comprehensive clinical information, such as age, gender, tumour location, sites of metastasis, number of metastatic sites, and initial staging before treatment, was collected, and haematological parameters were measured both prior to and 1-3 months after starting imatinib. Changes in haematological parameters were analysed, and the relationship between clinical variables and both disease-free survival (DFS) and overall survival (OS) was assessed using the Kaplan-Meier method.

Results: Post-imatinib treatment, 35 patients (44.3%) experienced a decrease in haemoglobin levels. Those with reduced haemoglobin levels exhibited better progression-free survival (PFS) compared to those without a decline [43.0 months (31.5-54.5) vs. 22.0 months (14.9-29.1); p <0.001]. No significant predictive associations for PFS were identified with changes in other haematological parameters. Multivariate analysis revealed that only a decrease in haemoglobin values remained an independent predictive factor, even after adjusting for tumour localisation [2.5 (1.3-4.7); p = 0.004]. Conversely, concerning the overall survival (OS), neither the decrease in haemoglobin levels nor other haematological and clinical parameters demonstrated statistical significance following imatinib treatment.

Conclusion: Decreased haemoglobin levels following imatinib treatment is a predictive on-target toxicity in patients with advanced GIST.

Key words: GIST, Imatinib treatment, On-target toxicity, Predictive marker, Anaemia.

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