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首页> 外文期刊>Journal of Rural Medicine >Initial treatment outcome and feasibility of low-dose cabazitaxel against docetaxel- and castration-resistant prostate cancer in a Japanese hospital
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Initial treatment outcome and feasibility of low-dose cabazitaxel against docetaxel- and castration-resistant prostate cancer in a Japanese hospital

机译:低剂量卡泽克克斯对日本医院抗多西紫杉醇和抗阉割前列腺癌的低剂量卡泽特的初步治疗结果及可行性

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Introduction: Cabazitaxel (CBZ) is used worldwide for castration-resistant prostate cancer after docetaxel treatment. In July 2014 the drug was approved in Japan with the same induction dose used for Caucasian patients. In this study, we examined and compared the results of an initial low-dose CBZ treatment in patients admitted to our hospital. Patients and Methods: Between July 2014 and August 2018, sixteen mCRPC patients were enrolled and underwent a low-dose CBZ treatment at our hospital. We compared the results with those of a Japanese metastatic docetaxel- and castration-resistant prostate cancer Phase I study. Results: The median patient age was 77 years (range, 53–84 years). Of the 16 patients, eight (50%) had a lymph node metastasis and 11 (68.8%) had a distant metastasis, 10 of whom had only a bone metastasis. The median dose of CBZ was 30 mg (range, 20–32 mg) and the median number of CBZ cycles was 2.5 (range, 1–18). The PSA level of 9 (56.3%) patients decreased after CBZ treatment, including 4 (25%) who showed a decrease to 50%. The median time interval in which the PSA level decreased was 2 months (range, 1–18 months). The observed adverse events (AE) were neutropenia (31.3%), febrile neutropenia (6.3%), fatigue (43.8%), nausea (18.8%), diarrhea (12.5%), decreased appetite (25%), dysgeusia (6.3%), white blood cell count decrease (43.8%), platelet count decrease (12.3%), and anemia (75%). However, no patient listed an AE as the reason for discontinuing the treatment. Conclusions: Even at a low dose, CBZ could improve the PSA value in patients with CRPC previously treated with docetaxel. Dose reduction and prophylactic administration of sustained G-CSF were also safe treatment options. Further studies involving an introduction period including a modulation of duration and dose are necessary, especially in Japanese patients.
机译:简介:Cabazitaxel(CBZ)在全球范围内用于多西紫杉醇治疗后抵抗前列腺癌。 2014年7月,该药物在日本批准,具有与白种人患者相同的诱导剂量。在这项研究中,我们检查并比较了患者入院的患者初始低剂量CBZ治疗的结果。患者和方法:2014年7月至2018年8月,在我们医院的患者中注册并进行了低剂量CBZ治疗。我们将结果与日本转移性多西紫杉醇和抗阉割前列腺癌阶段进行了比较。结果:中位数患者年龄为77岁(范围,53-84岁)。在16名患者中,八(50%)有淋巴结转移,11例(68.8%)具有远处转移,其中10名只有骨转移。中值的CBZ为30毫克(范围,20-32mg),中位数的CBZ循环循环为2.5(范围,1-18)。 CBZ治疗后9名(56.3%)患者的PSA水平降低,包括4(25%)的降低50%。 PSA水平降低的中位时间间隔为2个月(范围,1-18个月)。观察到的不良事件(AE)是中性粒细胞病(31.3%),发热中性蛋白(6.3%),疲劳(43.8%),恶心(18.8%),腹泻(12.5%),食欲减少(25%),痢疾usia(6.3%) ),白细胞计数降低(43.8%),血小板计数降低(12.3%)和贫血(75%)。然而,没有患者将AE列为终止治疗的原因。结论:即使在低剂量时,CBZ也可以改善先前用多西紫杉醇治疗的CRPC患者的PSA值。减少剂量和预防持续G-CSF的给药也是安全的治疗方案。涉及引入期的进一步研究包括持续时间和剂量调节,特别是在日本患者中。

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