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5-氟尿嘧啶可诱导动脉血管收缩。

5-Fluorouracil induces arterial vasocontractions.

作者信息

Südhoff T, Enderle M-D, Pahlke M, Petz C, Teschendorf C, Graeven U, Schmiegel W

机构信息

Department of Internal Medicine, Ruhr-University Bochum, Knappschaftskrankenhaus, Bochum, Germany.

出版信息

Ann Oncol. 2004 Apr;15(4):661-4. doi: 10.1093/annonc/mdh150.

Abstract

BACKGROUND

From 2% to 10% of cancer patients treated with 5-fluorouracil (5-FU) will develop symptomatic cardiotoxicity. Nevertheless, the underlying pathophysiology is mostly unknown.

PATIENTS AND METHODS

We investigated the influence of intravenous chemotherapy (CTX) on the diameter of the brachial artery using high resolution ultrasound in patients with malignant tumors, mostly gastrointestinal cancer. Cytostatic drugs included 30 cases with 5-FU and 30 cases with non-5-FU CTX (cis/carboplatin, anthracycline and cyclophosphamide). In addition, plasma levels of big endothelin were assessed prior to and after CTX.

RESULTS

Fifteen of 30 patients (50%) showed a contraction of the brachial artery after the end of 5-FU application (median 11%, range 4.3-18.5), whereas no single contraction was noticed in 30 patients following non-5-FU-based CTX. Vessel tonus generally normalized within 30 min after stopping 5-FU. Five patients positive for 5-FU associated vessel contraction were repeatedly exposed to 5-FU. Vessel contractions reoccurred in 86% (18/21) of these administrations. When patients with 5-FU bolus application were pre-treated with glyceroltrinitrate no contraction of the brachial artery was detected in five out of five occasions. There was a trend towards increased big endothelin plasma levels after 5-FU application (median 1.52 versus 1.99 fmol/ml; P = 0.07), whereas big endothelin levels remained unchanged after non-5-FU CTX (1.83 versus 1.83 fmol/ml; P = 0.99).

CONCLUSIONS

Application of 5-FU is commonly accompanied by arterial vessel contractions, which is likely to represent the first step in 5-FU-induced cardiotoxicity. 5-FU-associated vessel contractions were highly reproducible on re-exposure and were in the case of bolus application completely preventable by glyceroltrinitrate.

摘要

背景

接受5-氟尿嘧啶(5-FU)治疗的癌症患者中有2%至10%会出现有症状的心脏毒性。然而,其潜在的病理生理学机制大多未知。

患者与方法

我们使用高分辨率超声研究了静脉化疗(CTX)对恶性肿瘤患者(主要是胃肠道癌)肱动脉直径的影响。细胞毒性药物包括30例使用5-FU的患者和30例使用非5-FU CTX(顺铂/卡铂、蒽环类药物和环磷酰胺)的患者。此外,在CTX治疗前后评估血浆大内皮素水平。

结果

30例患者中有15例(50%)在5-FU应用结束后出现肱动脉收缩(中位数为11%,范围为4.3 - 18.5),而在接受非5-FU基础CTX治疗的30例患者中未观察到单一收缩情况。停止使用5-FU后,血管张力通常在30分钟内恢复正常。5例5-FU相关血管收缩阳性的患者再次接受5-FU治疗。在这些给药中,86%(18/21)出现血管收缩复发。当5-FU推注给药的患者预先用硝酸甘油治疗时,5次中有5次未检测到肱动脉收缩。5-FU应用后血浆大内皮素水平有升高趋势(中位数为1.52对1.99 fmol/ml;P = 0.07),而非5-FU CTX后大内皮素水平保持不变(1.83对1.83 fmol/ml;P = 0.99)。

结论

5-FU的应用通常伴随着动脉血管收缩,这可能是5-FU诱导心脏毒性的第一步。5-FU相关的血管收缩在再次暴露时具有高度可重复性,并且在推注给药的情况下可通过硝酸甘油完全预防。

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