环磷酰胺、阿霉素、长春新碱和强的松/泼尼松(CHOP)化疗方案对非霍奇金淋巴瘤患者左室收缩功能和心脏结构异常的影响

IF 2.1 Q3 ONCOLOGY
Imanita Septianda, Mochamad Yusuf Alsagaff, Budi Susetyo Pikir, Ami Ashariati, Muhamad Robiul Fuadi, Fatimah Zahra
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引用次数: 0

摘要

背景:环磷酰胺、阿霉素、长春新碱和泼尼松/泼尼松(CHOP)方案是侵袭性非霍奇金淋巴瘤(NHL)的标准治疗方案,有效但与化疗诱导的心脏毒性(CDIC)相关,如心力衰竭和左心室功能障碍。阿霉素等蒽环类药物是CDIC的关键因素。本研究探讨了接受CHOP治疗且阿霉素累计剂量≥250mg /m2的NHL患者左心室功能障碍和结构异常,旨在提高CDIC的早期发现,指导及时的心脏保护干预。方法:这项前瞻性队列研究于2023年6月至10月在泗水Soetomo博士地区总医院进行。我们纳入了年龄在18-60岁的任何阶段的NHL患者,接受CHOP方案治疗,其中累计阿霉素剂量≥250mg /m2,完成至少4个化疗周期,基线左室射血分数(LVEF)≥50%,超声心动图窗口质量良好。数据收集自医疗记录、生化试验和超声心动图。采用Wilcoxon检验和配对t检验进行统计分析。主要终点是心功能,通过化疗后LVEF降低、左心室应变增加、新的结构异常、高敏感性(HS)肌钙蛋白和NT-proBNP水平升高来评估。结果:共纳入32例患者,年龄46.62±16.64岁,以颈区和2期NHL最为常见。化疗前后各项指标均有显著差异。结论:CHOP方案存在NHL患者亚临床心功能障碍和结构异常的显著风险,累积阿霉素剂量是关键因素。使用GLS和NT-proBNP等敏感生物标志物进行早期检测对于识别心脏毒性和及时干预至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of cyclophospamide, doxorubicin, vincristine and prednisone/prednisolone (CHOP) chemotherapy regimens on left ventricular systolic function and cardiac structural abnormalities in non-Hodgkin lymphoma patients.

Background: The cyclophospamide, doxorubicin, vincristine, and prednisone/prednisolone (CHOP) regimen, a standard treatment for aggressive non-Hodgkin lymphoma (NHL), is effective but linked to chemotherapy-induced cardiotoxicity (CDIC), such as heart failure and left ventricular dysfunction. Anthracyclines like doxorubicin are key contributors to CDIC. This study examines left ventricular dysfunction and structural abnormalities in NHL patients receiving CHOP therapy with cumulative doxorubicin doses ≥ 250 mg/m2, aiming to improve early CDIC detection and guide timely cardioprotective interventions.

Methods: This prospective cohort study was conducted at Dr. Soetomo Regional General Hospital, Surabaya, from June to October 2023. We included NHL patients aged 18-60 years at any stage, treated with CHOP regimens containing cumulative doxorubicin doses ≥ 250 mg/m2, who completed at least four chemotherapy cycles, had baseline left ventricular ejection fraction (LVEF) ≥ 50%, and good echocardiographic window quality. Data were collected from medical records, biochemical tests, and echocardiography. Wilcoxon and paired T-tests were used for statistical analyses. The primary outcome was cardiac function, evaluated by reductions in LVEF, increased left ventricular strain, new structural abnormalities, and elevated high-sensitivity (HS) troponin and NT-proBNP levels post-chemotherapy.

Results: A total of 32 patients, aged 46.62 ± 16.64 years, were included, with the colli region and stage 2 NHL being the most common. Significant differences were observed in all parameters between pre- and post-chemotherapy. LVEF decreased by - 2.40% ± 1.79 (p < 0.001), while global longitudinal strain (GLS) declined by 2.25 ± 1.36 (p < 0.001). HS troponin I levels showed a significant increase of 17.27 ± 36.29 (p < 0.001), and NT-proBNP levels rose by 321.23 ± 85.34 (p < 0.001). The study also identified a higher risk of cardiotoxicity in patients over 50 years of age.

Conclusion: The CHOP regimen poses significant risks of subclinical cardiac dysfunction and structural abnormalities in NHL patients, with cumulative doxorubicin dosage being a key contributor. Early detection using sensitive biomarkers like GLS and NT-proBNP is crucial for identifying cardiotoxicity and enabling timely interventions.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
46
审稿时长
11 weeks
期刊介绍: As the official publication of the National Cancer Institute, Cairo University, the Journal of the Egyptian National Cancer Institute (JENCI) is an open access peer-reviewed journal that publishes on the latest innovations in oncology and thereby, providing academics and clinicians a leading research platform. JENCI welcomes submissions pertaining to all fields of basic, applied and clinical cancer research. Main topics of interest include: local and systemic anticancer therapy (with specific interest on applied cancer research from developing countries); experimental oncology; early cancer detection; randomized trials (including negatives ones); and key emerging fields of personalized medicine, such as molecular pathology, bioinformatics, and biotechnologies.
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