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Prognostic significance of grade 3/4 neutropenia in Japanese prostate cancer patients treated with cabazitaxel

机译:卡巴他赛治疗日本前列腺癌患者中度3/4级中性粒细胞减少的预后意义

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摘要

The present study aimed to evaluate the efficacy of cabazitaxel in Japanese patients affected by metastatic castration‐resistant prostate cancer (mCRPC) previously treated with a docetaxel‐containing regimen. In this retrospective study, 41 patients with mCRPC treated with cabazitaxel at Keio University Hospital were retrospectively reviewed. Cabazitaxel at a dose of 20‐25 mg/m² was administered every 3 or 4 weeks. Clinicopathological factors and laboratory data were collected to assess the prognostic factors for overall survival (OS) and progression‐free survival (PFS). An upfront dose‐reduction was required in 52.5% of patients due to their reduced general condition or advanced age. Prophylactic G‐CSF was prescribed to all the patients. Grade ≥3 neutropenia and febrile neutropenia occurred in 21 patients (53.6%) and 3 patients (6.8%), respectively. Treatment was generally well tolerated, with a median of 5 cycles (range 1‐17). Median PFS and OS from the start of cabazitaxel treatment were 4.4 and 15.0 months (95% CI 8.9‐21.2), respectively. Waterfall plot analysis revealed that a prostate‐specific antigen (PSA) decline >50% was noticed in n = 11 patients receiving cabazitaxel (26.8%). Univariate analysis revealed that poor performance status, PSA ≥100 ng/mL prior to cabazitaxel treatment, visceral metastasis, absence of grade 3/4 neutropenia during cabazitaxel therapy and neutrophil‐lymphocyte ratio were significantly associated with shorter overall survival. Multivariate analysis revealed that poor performance status, visceral metastasis, and the absence of grade 3/4 neutropenia during cabazitaxel therapy were the independent prognostic indicators for OS. The practical implication of our results might be to tailor cabazitaxel dosing on the basis of its hematological effects.
机译:本研究旨在评估卡巴他赛在日本患者中的疗效,该患者先前已接受含多西他赛的方案治疗而受到转移性去势抵抗性前列腺癌(mCRPC)的影响。在这项回顾性研究中,对庆应义University大学医院接受卡巴他赛治疗的41例mCRPC患者进行了回顾性研究。每3或4周施用20-25 mg /m²的卡巴他赛。收集临床病理因素和实验室数据以评估总体生存期(OS)和无进展生存期(PFS)的预后因素。由于一般情况的减轻或年龄的增加,有52.5%的患者需要预先减少剂量。对所有患者均开了预防性G‐CSF处方。 ≥3级中性粒细胞减少和发热性中性粒细胞减少分别发生在21例患者(53.6%)和3例患者(6.8%)中。一般而言,治疗耐受性良好,平均5个周期(范围1-17)。从卡巴他赛治疗开始的中位PFS和OS分别为4.4和15.0个月(95%CI 8.9-21.2)。瀑布图分析显示,在11例接受卡巴他赛的患者中发现前列腺特异性抗原(PSA)下降> 50%(26.8%)。单因素分析显示,不良状态,卡巴他赛治疗前PSA≥100 ng / mL,内脏转移,卡巴他赛治疗期间不存在3/4级嗜中性白血球减少症和中性白细胞-淋巴细胞比值与缩短总生存期密切相关。多因素分析显示,卡巴他赛治疗期间表现不佳,内脏转移以及不存在3/4级中性粒细胞减少是OS的独立预后指标。我们结果的实际含义可能是根据其血液学效应来定制卡巴他赛剂量。

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