Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) therapy increases carotid intima-media thickness and plaque score with von Willebrand factor activity elevation in patients with malignant lymphoma.

Naomi Shimizu, Daiji Ngayama, Yasuhiro Watanabe, Takashi Yamaguchi, Shoko Nakamura, Masahiro Ohira, Atsuhito Saiki, Hiroki Onda, Shuhei Yamaoka, Kazuki Abe, Chiaki Nakaseko, Ichiro Tatsuno
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引用次数: 2

Abstract

An increased risk for atherosclerosis has been noted in cancer survivors; however, studies that focus on the risk of atherosclerosis in patients treated with chemotherapy are scarce. Therefore, we evaluated 32 patients who received rituximab, cyclophosphamide, doxorubicin, vincristine and prednisolone (R-CHOP) therapy for B-cell malignant lymphoma by analysing the changes in atherosclerosis. Just before each treatment course, plasma levels of von Willebrand Factor (vWF) activity were evaluated, and carotid ultrasonography was performed at baseline and after the final treatment. Throughout the follow-up period, plasma vWF levels showed significantly transient increased by approximately 20%-40%. Both mean carotid intima-media thickness (IMT) and plaque score (PS) significantly increased during the 36.6 ± 26.0 weeks of observation (mean IMT: 0.724 ± 0.118 to 0.767 ± 0.129 mm; PS: 4.31 ± 3.53 to 4.87 ± 3.88, P < 0.001). Our study suggests that R-CHOP therapy promotes atherosclerosis.

利妥昔单抗、环磷酰胺、阿霉素、长春新碱和强的松龙(R-CHOP)治疗可增加恶性淋巴瘤患者颈动脉内膜-中膜厚度和斑块评分,并伴有血管性血友病因子活性升高。
已经注意到癌症幸存者患动脉粥样硬化的风险增加;然而,关注化疗患者动脉粥样硬化风险的研究很少。因此,我们通过分析动脉粥样硬化的变化,对32例接受利妥昔单抗、环磷酰胺、阿霉素、长春新碱和强的松龙(R-CHOP)治疗的b细胞恶性淋巴瘤患者进行了评估。在每个疗程前,评估血浆血管性血友病因子(vWF)活性水平,并在基线和最终治疗后进行颈动脉超声检查。在整个随访期间,血浆vWF水平显着短暂升高约20%-40%。在36.6±26.0周的观察中,平均颈动脉内膜-中膜厚度(IMT)和斑块评分(PS)均显著升高(平均IMT: 0.724±0.118至0.767±0.129 mm;PS: 4.31±3.53 ~ 4.87±3.88
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