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首页> 外文期刊>BJU international >What is the real impact of bone pain on survival in patients with metastatic hormone-refractory prostate cancer treated with docetaxel?
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What is the real impact of bone pain on survival in patients with metastatic hormone-refractory prostate cancer treated with docetaxel?

机译:骨痛对多西他赛治疗的转移性激素难治性前列腺癌患者生存的真正影响是什么?

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摘要

OBJECTIVES: To determine the benefit of starting early chemotherapy with docetaxel (the recommended first-line treatment) for patients with asymptomatic metastatic hormone-refractory prostate cancer (HRPC). PATIENTS AND METHODS: Data were analysed from 145 patients with HRPC treated with chemotherapy between February 2000 and June 2002 in one French centre. Eligible patients were categorized into three groups according to the bone pain at baseline, i.e. minimalo pain, mild, and moderate/severe pain. The primary endpoint was the effect of bone pain on overall survival (OS). RESULTS: Docetaxel was administered to 67% of patients. The risk of death was 1.56 and 2.11 times higher for patients with mild or moderate/severe pain than for those with minimalo pain (P = 0.027). The median (95% confidence interval (CI)) OS was 23.1 (18.5-27.6) and 14.1 (8.9-19.2) months (P = 0.001, log-rank-test) for patients with minimal pain or no pain treated with docetaxel-based chemotherapy compared with mitoxantrone, respectively. The prostate-specific antigen doubling time (PSA-DT) had a significant effect on OS in patients with minimalo pain, with a median of 32.4 and 16.5 months for a PSA-DT of >or=45 and <45 days, respectively (P < 0.001). CONCLUSIONS: Our results suggest that patients with HRPC and minimal or no bone pain could have better survival than those with mild pain or moderate to severe pain, independent of the treatment administered. In addition, patients with HRPC and minimal or no bone pain treated with docetaxel-based chemotherapy have a significantly better OS than those treated with mitoxantrone. The PSA-DT can be useful to identify asymptomatic patients who are candidates for early treatment.
机译:目的:为了确定无症状转移性激素难治性前列腺癌(HRPC)患者开始采用多西他赛(建议的一线治疗)早期化疗的益处。患者与方法:分析了2000年2月至2002年6月在法国一个中心进行的145例接受化学疗法治疗的HRPC患者的数据。根据基线时的骨痛,将符合条件的患者分为三类,即轻度/无痛,轻度和中度/重度疼痛。主要终点是骨痛对总生存期(OS)的影响。结果:67%的患者服用多西他赛。轻度或中度/重度疼痛患者的死亡风险比轻度/无痛患者的死亡风险高1.56倍和2.11倍(P = 0.027)。多西他赛治疗的疼痛最小或无疼痛的患者的中位(95%置信区间(CI))OS为23.1(18.5-27.6)和14.1(8.9-19.2)个月(P = 0.001,对数秩检验)。化疗与米托蒽醌比较。前列腺特异性抗原加倍时间(PSA-DT)对无/无疼痛患者的OS有显着影响,PSA-DT≥45天和<45天的中位时间分别为32.4和16.5个月(P <0.001)。结论:我们的结果表明,HRPC和骨痛极少或无骨痛的患者比轻度或中度至重度疼痛的患者有更好的生存率,而与所给予的治疗无关。此外,以多西他赛为基础的化疗治疗的HRPC患者,骨痛极少或没有,比米托蒽醌治疗的OS明显好。 PSA-DT有助于识别无症状的早期治疗患者。

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