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Treatment with beta-blockers and reduced disease progression in patients with thick melanoma.

机译:β受体阻断剂治疗和减少疾病进展在厚厚的黑素瘤患者。

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Preclinical evidence shows that beta-adrenoceptor antagonists (beta-blockers) inhibit tumor and metastasis progression in animal models of melanoma. We hypothesized that the use of beta-blockers for concomitant diseases is associated with a reduced risk of progression of thick (Breslow thickness >1 mm) malignant melanoma. Two patient subgroups were identified from the medical records of 121 consecutive patients with a thick melanoma. Of these, 30 patients had been prescribed beta-blockers for 1 year or more (treated subgroup), whereas the other 91 were untreated. After a median follow-up time of 2.5 years, tumor progression was observed in 3.3% of the treated subgroup and in 34.1% of the untreated subgroup. The Cox model on progression indicated a 36% (95% confidence interval, 11%-54%) (P = .002) risk reduction for each year of beta-blocker use. No deaths were observed in the treated group, whereas in the untreated group 24 patients died. To our knowledge, the present study suggests for the first time that exposure to beta-blockers for 1 year or more is associated with a reduced risk of progression of thick malignant melanoma, indicating the need for larger epidemiological studies and randomized clinical trials.
机译:临床证据显示beta-adrenoceptor拮抗剂(β受体阻断剂)抑制肿瘤转移动物模型的发展黑素瘤。伴随疾病的β受体阻断剂与发展的风险降低有关厚(‘厚度> 1毫米)恶性的黑素瘤。连续从121年的医疗记录厚厚的黑素瘤患者。病人被规定为1β受体阻断剂年或以上(治疗组),而其他91人未经处理的。时间2.5年,观察肿瘤恶化在治疗组的3.3%和34.1%未经处理的子群。进展表明36%(95%置信区间,11% - -54%)(P = .002)降低风险每年的β受体阻滞剂使用。观察治疗组,而在治疗组24例死亡。知识,目前的研究表明第一次接触为1β受体阻断剂年或一年以上的风险降低相关厚的恶性黑素瘤,表明大流行病学的必要性研究和随机临床试验。

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