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前列腺癌去势抵抗患者的运动处方剂量:I 期处方剂量递增试验。

Exercise prescription dose for castrate-resistant prostate cancer patients: a phase I prescription dose escalation trial.

机构信息

Department of Human Structure and Repair, Ghent University, Corneel Heymanslaan 10, 9000, Ghent, Belgium.

Research Foundation, Flanders (FWO), Brussels, Belgium.

出版信息

World J Urol. 2021 Feb;39(2):357-364. doi: 10.1007/s00345-020-03098-y. Epub 2020 Feb 1.

Abstract

PURPOSE

To determine the start exercise prescription dose in metastatic castrate-resistant prostate cancer (mCRPC) patients receiving second-line hormone treatment and recommended phase II exercise prescription.

METHODS

Patients were enrolled in a 3 + 3 dose escalation phase I trial of aerobic, resistance, and flexibility exercises to evaluate dose-limiting tolerance and safety. Tolerance was defined as Borg score ≤ 16 and safety (pain) as a visual analogue scale score (VAS) ≤ 3 and CTCAE grade < 2. Dose level 1 (escalation start dose) was set at 15 min. Aerobic training (50-80% HRmax warm-up and cooling-down; and 65-80% HRmax. core), 1 set with 8-10 repetitions (reps.) resistance training (50-60% 1-RM, 8 exercises), and 1 set (30s) with 2 reps flexibility training (5 exercises). The prescription dose escalation was designed in four levels (from dose -1 to 3), with a dose escalation in volume and intensity of the exercises.

RESULTS

Nine patients were included in two dosing cohorts and were under active treatment (n = 4 abiraterone acetate and n = 5 enzalutamide). Dose limiting safety concerns were observed in 2 out of 3 patients in dose level 2 and 1 patient out of 6 in dose level 1 due to VAS > 3 during resistance training and/or flexibility training. No tolerance issues were observed in the two dosing cohorts. The optimal start exercise prescription dose was set at dose level 1 due to safety issues at dose level 2.

CONCLUSION

Our findings suggest that exercise is perceived tolerable in mCRPC patients receiving second-line hormone therapy. Caution is indicated on safety during performance of the exercises.

摘要

目的

确定接受二线激素治疗和推荐的 II 期运动处方的转移性去势抵抗性前列腺癌(mCRPC)患者开始运动处方的剂量。

方法

患者参加了一项有氧运动、抗阻运动和柔韧性运动的 3+3 剂量递增 I 期试验,以评估剂量限制的耐受性和安全性。耐受性定义为 Borg 评分≤16,安全性(疼痛)为视觉模拟评分(VAS)≤3 和 CTCAE 分级<2。起始剂量定为 15 分钟。有氧运动训练(热身和冷却期 50-80% HRmax;核心训练期 65-80% HRmax)、1 组 8-10 次重复(重复次数)抗阻运动训练(50-60% 1-RM,8 个动作)和 1 组(30 秒)2 次重复柔韧性训练(5 个动作)。处方剂量递增设计为 4 个级别(从剂量-1 到 3),运动的体积和强度递增。

结果

9 例患者分为 2 个剂量组,接受活性治疗(n=4 例醋酸阿比特龙和 n=5 例恩杂鲁胺)。由于在抗阻训练和/或柔韧性训练期间 VAS>3,2 例患者在剂量水平 2 和 1 例患者在剂量水平 1 中观察到 2 例患者中有 3 例患者出现剂量限制的安全性问题。在两个剂量组中均未观察到耐受性问题。由于剂量水平 2 存在安全性问题,最佳起始运动处方剂量设定为剂量水平 1。

结论

我们的研究结果表明,接受二线激素治疗的 mCRPC 患者认为运动是可耐受的。在进行运动时需要注意安全性。

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