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小细胞肺癌中的异常止血

Abnormal haemostasis in small cell lung cancer.

作者信息

Milroy R, Douglas J T, Campbell J, Carter R, Lowe G D, Banham S W

机构信息

Department of Respiratory Medicine, University Department of Medicine, Royal Infirmary, Glasgow.

出版信息

Thorax. 1988 Dec;43(12):978-81. doi: 10.1136/thx.43.12.978.

Abstract

Disorders of haemostasis and altered platelet activity have been documented in patients with malignant disease but their relation to response to treatment and prognosis are not known. Thrombin activity (fibrinopeptide A (FpA), plasmin mediated fibrinolysis (B beta 15-42) antigen), and platelet alpha granule release (beta thromboglobulin) were studied in 37 patients with small cell lung cancer to find out whether these indices show a relationship to chemoresponse. There was evidence of considerably increased thrombin activity, with a median fibrinopeptide A concentration of 13.2 (normal less than 4) pmol/ml, but only modestly increased fibrinolysis, with a median B beta 14-42 antigen concentration of 5.6 (normal less than 3) pmol/ml. Thus the ratio of fibrinopeptide A to B beta 15-42 concentration (FpA:B beta) was raised, with a median value of 2.2 (normal less than 1.33). In addition, 57% of patients had increased platelet alpha granule release, the median beta thromboglobulin concentration being 50 (normal less than 50) ng/ml. There was a significant association between increased thrombin generation and lack of response to chemotherapy. Furthermore, non-responders had higher FpA:B beta ratios. The same haemostatic markers were studied in nine patients who have been in complete remission for at least two years after chemotherapy for small cell lung cancer. There was a significant difference in thrombin activity and also in the ratio of thrombin activity to lysis between the pretreatment group and the group of two year survivors. Lack of response to chemotherapy appears to be related to increased thrombin activity. Such an association has not previously been reported in patients with malignant disease.

摘要

恶性疾病患者存在止血功能紊乱和血小板活性改变的情况,但它们与治疗反应和预后的关系尚不清楚。对37例小细胞肺癌患者的凝血酶活性(纤维蛋白肽A(FpA)、纤溶酶介导的纤维蛋白溶解(Bβ15 - 42)抗原)和血小板α颗粒释放(β - 血小板球蛋白)进行了研究,以确定这些指标是否与化疗反应相关。有证据表明凝血酶活性显著增加,纤维蛋白肽A浓度中位数为13.2(正常小于4)pmol/ml,但纤维蛋白溶解仅适度增加,Bβ14 - 42抗原浓度中位数为5.6(正常小于3)pmol/ml。因此,纤维蛋白肽A与Bβ15 - 42浓度之比(FpA:Bβ)升高,中位数为2.2(正常小于1.33)。此外,57%的患者血小板α颗粒释放增加,β - 血小板球蛋白浓度中位数为50(正常小于50)ng/ml。凝血酶生成增加与化疗无反应之间存在显著关联。此外,无反应者的FpA:Bβ比值更高。对9例小细胞肺癌化疗后至少两年完全缓解的患者进行了相同的止血指标研究。预处理组和两年存活组之间在凝血酶活性以及凝血酶活性与溶解比值方面存在显著差异。化疗无反应似乎与凝血酶活性增加有关。这种关联在恶性疾病患者中此前尚未见报道。

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