Centre Hospitalier Universitaire de Martinique, Fort-de-France, Martinique, France.
Universitair Ziekenhuis Brussel, Brussels, Belgium.
Clin Genitourin Cancer. 2022 Dec;20(6):e473-e484. doi: 10.1016/j.clgc.2022.05.012. Epub 2022 Jun 6.
Enzalutamide is an important drug in the treatment of prostate cancer. Standard dosing often requires dose reduction because of side effects. There is no information on survival outcomes with lower doses. We investigated the impact of starting enzalutamide at ≤ 50% dose on metastatic prostate cancer outcomes including patients' longevity.
Records of metastatic prostate cancer patients treated with enzalutamide at one center were retrospectively reviewed. Low-dose enzalutamide (≤80 mg/day) was compared with standard-dose (160 mg/day). The primary objective was to compute the restricted mean survival time (RMST - time scale) and restricted mean attained age (RMAA - age scale) using the Irwin method. Secondary objectives included overall survival (OS), progression-free survival (PFS), and PSA progression per PCWG3 criteria (PSA PFS). We used the logrank test and the ∆ difference between RMSTs for comparison.
Of 111 patients treated, 32 received a low-dose and 79 the standard-dose. Low-dose patients had less prior abiraterone or chemotherapy (28.1% vs. 65.8%, P < .001); more testosterone assessment (65.6% vs. 40.5%, P = .016); poorer ECOG performance status (48.3% score ≥2 vs. 26.6%; P = .040), more comorbidities (75.9% vs. 46.3%; P = .010)) including increased cardiovascular disease (51.7% vs. 21.4%, P = .004). Baseline PSA value and doubling time at start of enzalutamide and distribution of metastases were similar between the groups. OS and PFS did not differ between low-dose and standard-dose. Patients on low-dose had a better longevity with significantly longer RMAA, 89.1 years, versus standard-dose RMAA of 83.8 years (∆ = 5.3 years, P = .003, logrank P = .025). In a subgroup analysis by age at start of enzalutamide, <75 versus ≥75 years old, longevity was also better with low-dose in younger patients (∆ = 2.9 years, P = .034, and older, ∆ = 3.3 years, P = .011).
The longevity advantage and reduced adverse events seen in patients with prostate cancer treated with low-dose enzalutamide warrants further investigation.
恩扎鲁胺是治疗前列腺癌的重要药物。由于副作用,标准剂量常常需要减少剂量。对于较低剂量的生存结果尚无信息。我们研究了以≤50%的剂量开始使用恩扎鲁胺对转移性前列腺癌结局(包括患者的寿命)的影响。
回顾性分析了一家中心接受恩扎鲁胺治疗的转移性前列腺癌患者的记录。低剂量恩扎鲁胺(≤80 mg /天)与标准剂量(160 mg /天)进行比较。主要目的是使用 Irwin 方法计算受限平均生存时间(RMST-时间尺度)和受限平均达到年龄(RMAA-年龄尺度)。次要目标包括总生存期(OS),无进展生存期(PFS)和根据 PCWG3 标准的 PSA 进展(PSA PFS)。我们使用对数秩检验和 RMST 之间的∆差异进行比较。
在接受治疗的 111 例患者中,有 32 例接受了低剂量治疗,79 例接受了标准剂量治疗。低剂量患者的既往阿比特龙或化疗较少(28.1%比 65.8%,P <.001);更多的睾丸激素评估(65.6%比 40.5%,P =.016);较差的 ECOG 表现状态(48.3%评分≥2比 26.6%;P =.040),更多合并症(75.9%比 46.3%;P =.010),包括心血管疾病增加(51.7%比 21.4%,P =.004)。两组之间开始使用恩扎鲁胺时的 PSA 值和倍增时间以及转移的分布相似。低剂量和标准剂量之间的 OS 和 PFS 没有差异。低剂量组的患者具有更好的生存时间,RMAA 显著延长,为 89.1 岁,而标准剂量的 RMAA 为 83.8 岁(∆= 5.3 岁,P =.003,logrank P =.025)。在根据开始使用恩扎鲁胺时的年龄进行的亚组分析中,<75 岁与≥75 岁的患者中,低剂量组的生存时间也更长(∆= 2.9 岁,P =.034,而年龄较大的患者,∆= 3.3 岁,P =.011)。
接受低剂量恩扎鲁胺治疗的前列腺癌患者的生存优势和不良反应减少值得进一步研究。