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Editorial comment on: Platelet microparticles: a potential predictive factor of survival in hormone-refractory prostate cancer patients treated with docetaxel-based chemotherapy.

机译:社论评论:血小板微粒:接受基于多西他赛的化疗的激素难治性前列腺癌患者生存的潜在预测因素。

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Platelet activation results in the production of platelet microparticles (PMPs) and has been found to be increased in several types of cancer. PMPs are suggested to be useful in a number of basic and preclinical papers. The study by Helley et al [1] found that hormone refractory prostate cancer patients treated with docetaxel showing PMP levels above the median had a significantly lower overall survival. PMPs presumably reflect microthrombosis, a finding that seems to be commonly seen in prostate cancer. Although the topic of this report is of interest to urologists and scientists who work in the field of prostate cancer research, there is no "major impact on treatment", and the study shows a biologic association resulting in a negative study since PMPs were not independently associated with overall survival in multivariate analysis. In addition, the study series is of value because it is prospective, but limited in size because it includes only 43 cases recruited over a period of 5 years. This represents a major limitation, and the paper should be considered as a preliminary data report. Adding more cases to the reported series would thus add strength to the paper in terms of clinical value. Finally, although the authors suggest that therapies targeting PMPs may be useful, it is not clear whether they contribute to disease progression or are only a marker of disease extension and ongoing thrombosis. In summary, this study represents a limited advance that is consistent with previous data and suggests that PMPs or other markers of ongoing thrombosis might be indicators of disease burden; nonetheless, the potential value of PMP as an independent marker remains unclear. The data reported by Helley et al [1] underscore the need for more studies with appropriate sample size confirming the suggested clinical potential of PMP formation in hormone refractory prostate cancer patients.
机译:血小板活化导致血小板微粒(PMP)的产生,并且已发现在几种类型的癌症中血小板活化都会增加。建议将PMP用于许多基础和临床前论文中。 Helley等[1]的研究发现,多西他赛治疗的激素难治性前列腺癌患者的PMP水平高于中位数,其总生存期明显降低。 PMP可能反映了微血栓形成,这一发现似乎在前列腺癌中很常见。尽管本报告的主题对从事前列腺癌研究领域的泌尿科医师和科学家很感兴趣,但没有“对治疗的重大影响”,并且该研究表明生物学关联导致了阴性研究,因为PMP并非独立存在与多因素分析中的总体生存率相关。此外,该研究系列具有前瞻性,但具有一定的价值,但规模有限,因为它仅包括5年内招募的43例病例。这是一个主要限制,因此该论文应被视为初步数据报告。因此,在报告的系列中增加更多病例将增加临床价值。最后,尽管作者建议靶向PMP的疗法可能有用,但尚不清楚它们是否有助于疾病进展或仅是疾病扩展和持续血栓形成的标志。总而言之,这项研究的进展有限,与先前的数据相符,并表明PMPs或其他正在进行的血栓形成标志可能是疾病负担的指标。尽管如此,PMP作为独立标志物的潜在价值仍不清楚。 Helley等[1]报告的数据强调需要进行更多研究,并采用适当的样本量,以确认激素抵抗性前列腺癌患者中PMP形成的临床潜力。

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