Department of Urology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Department of Urology/Renal Transplantation, Yokohama City University Medical Center, 4-57 Urafune, Minami-ku, Yokohama 232-0024, Japan.
Jpn J Clin Oncol. 2019 Aug 1;49(8):766-771. doi: 10.1093/jjco/hyz051.
Cabazitaxel is an efficacious treatment for patients with metastatic castration-resistant prostate cancer who have previously progressed on docetaxel, but febrile neutropenia during the first cycle is a frequent complication. Asian patients are at increased risk of febrile neutropenia. Although primary prophylaxis with granulocyte colony-stimulating factor can reduce the incidence, its efficacy has not been prospectively demonstrated in Japanese patients with cabazitaxel treatment.
PEGAZUS, a prospective, single-arm study conducted at eight clinical sites in Japan, enrolled 21 heavily pretreated patients with metastatic castration-resistant prostate cancer. Patients received cabazitaxel 25 mg/m2 every 3 weeks, up to 10 cycles. Oral prednisolone 10 mg was taken daily. Pegfilgrastim 3.6 mg was administered at least 24 h after the cabazitaxel infusion. The primary endpoint was the incidence of febrile neutropenia in the first cycle.
The median number of treatment cycles was seven. The relative dose intensity of cabazitaxel was 67.4% (range, 53.2-91.3%). Two of 21 patients (9.5%) experienced febrile neutropenia in the first cycle. This rate was lower than the rate (43%) previously observed without prophylactic granulocyte colony-stimulating factor in a similar patient population. Six patients showed a prostate-specific antigen response (28.6%). Three of four patients evaluable for tumor response had stable disease and one had progressive disease. Grade ≥3 diarrhea was not observed. Primary prophylaxis with granulocyte colony-stimulating factor significantly reduced the incidence of febrile neutropenia in this study.
Cabazitaxel plus granulocyte colony-stimulating factor is safe and effective for Japanese patients with metastatic castration-resistant prostate cancer who have previously progressed on docetaxel. Clinical trial registration: ClinicalTrials.gov (NCT02441894).
卡巴他赛对于先前接受多西他赛治疗后进展的转移性去势抵抗性前列腺癌患者是一种有效的治疗方法,但在第一个周期中发热性中性粒细胞减少症是一种常见的并发症。亚洲患者发热性中性粒细胞减少症的风险增加。尽管用粒细胞集落刺激因子进行初级预防可以降低发病率,但在接受卡巴他赛治疗的日本患者中尚未前瞻性地证明其疗效。
PEGAZUS 是一项在日本的 8 个临床中心进行的前瞻性、单臂研究,共纳入 21 例先前接受过多西他赛治疗的转移性去势抵抗性前列腺癌的重度预处理患者。患者接受卡巴他赛 25mg/m2,每 3 周一次,最多 10 个周期。每天口服泼尼松龙 10mg。卡巴他赛输注后至少 24 小时给予培非格司亭 3.6mg。主要终点是第一个周期发热性中性粒细胞减少症的发生率。
中位治疗周期数为 7 个。卡巴他赛的相对剂量强度为 67.4%(范围,53.2-91.3%)。21 例患者中有 2 例(9.5%)在第一个周期发生发热性中性粒细胞减少症。这一发生率低于先前在类似患者人群中未使用预防性粒细胞集落刺激因子观察到的发生率(43%)。6 例患者出现前列腺特异性抗原反应(28.6%)。4 例可评估肿瘤反应的患者中,3 例疾病稳定,1 例疾病进展。未观察到≥3 级腹泻。本研究中,粒细胞集落刺激因子的初级预防显著降低了发热性中性粒细胞减少症的发生率。
卡巴他赛联合粒细胞集落刺激因子对先前接受多西他赛治疗后进展的转移性去势抵抗性前列腺癌的日本患者是安全有效的。临床试验注册:ClinicalTrials.gov(NCT02441894)。