Carrió I, Lopez-Pousa A, Estorch M, Duncker D, Berná L, Torres G, de Andrés L
Department of Nuclear Medicine, Hospital de Sant Pau, Barcelona, Spain.
J Nucl Med. 1993 Sep;34(9):1503-7.
To assess myocardial cell damage due to doxorubicin cardiotoxicity, we prospectively studied 30 patients with sarcomas who were receiving chemotherapy, including doxorubicin. Sixteen patients were treated by continuous infusion over 72 hr and 14 patients were treated by bolus injection. Antimyosin studies and left ventricular ejection fraction (LVEF) measurements were performed before chemotherapy and at intermediate and maximal cumulative doses. Myocardial antimyosin uptake was quantified by a heart-to-lung ratio (HLR). Myocardial antimyosin uptake was observed in all patients at 240-300 mg/m2 when ejection fraction was still maintained. Seven patients presented with a decrease of > or = 10% in absolute ejection fraction units at 420-600 mg/m2. Five of these patients had mild congestive heart failure. All patients who presented with a decrease in LVEF > or = 10% at 420-600 mg/m2 had increased antimyosin uptake with HLR > or = 1.90 at a cumulative dose of 240-300 mg/m2. Patients who were treated with continuous infusion had less antimyosin uptake than those who were treated with bolus administration (mean HLR of 1.70 +/- 0.09 versus HLR of 2.01 +/- 0.16 at a cumulative dose of 240-300 mg/m2, p < 0.01; HLR of 1.86 +/- 0.12 versus HLR of 2.32 +/- 0.34 at a cumulative dose of 420-600 mg/m2, p < 0.01). Two of 16 patients treated by continuous infusion and 5 of 14 patients treated by bolus injection presented with a decrease in ejection fraction > or = 10%. LVEF after chemotherapy in the infusion group was 56% +/- 5% and 48% +/- 8% (p < 0.05) in the bolus group. Antimyosin studies are helpful in the assessment of doxorubicin cardiotoxicity. Intense antimyosin uptake at intermediate cumulative doses identifies patients at risk of cardiotoxicity before ejection fraction deteriorates. Patients with sarcomas treated by continuous infusion present with less antimyosin uptake than those treated with bolus injection, indicating less severe cardiotoxicity.
为评估阿霉素心脏毒性所致的心肌细胞损伤,我们前瞻性地研究了30例接受包括阿霉素在内的化疗的肉瘤患者。16例患者采用72小时持续输注治疗,14例患者采用大剂量注射治疗。在化疗前以及累积剂量达到中等和最大剂量时进行抗肌凝蛋白研究和左心室射血分数(LVEF)测量。通过心-肺比率(HLR)对心肌抗肌凝蛋白摄取进行定量。当射血分数仍维持时,所有患者在累积剂量达到240 - 300mg/m²时均观察到心肌抗肌凝蛋白摄取。7例患者在累积剂量达到420 - 600mg/m²时,绝对射血分数单位下降≥10%。其中5例患者出现轻度充血性心力衰竭。所有在累积剂量达到420 - 600mg/m²时LVEF下降≥10%的患者,在累积剂量为240 - 300mg/m²时,抗肌凝蛋白摄取增加且HLR≥1.90。持续输注治疗的患者比大剂量注射治疗的患者抗肌凝蛋白摄取更少(累积剂量为240 - 300mg/m²时,平均HLR分别为1.70±0.09和2.01±0.16,p<0.01;累积剂量为420 - 600mg/m²时,HLR分别为1.86±0.12和2.32±0.34,p<0.01)。16例持续输注治疗的患者中有2例、14例大剂量注射治疗的患者中有5例出现射血分数下降≥10%。化疗后输注组的LVEF为56%±5%,大剂量注射组为48%±8%(p<0.05)。抗肌凝蛋白研究有助于评估阿霉素心脏毒性。在中等累积剂量时强烈的抗肌凝蛋白摄取可在射血分数恶化前识别出有心脏毒性风险的患者。持续输注治疗的肉瘤患者比大剂量注射治疗的患者抗肌凝蛋白摄取更少,表明心脏毒性较轻。