对接受 177Lu 标记 PSMA 靶向放射性配体治疗的 mCRPC 患者进行配对分析,治疗间隔为 4 周和 6 周。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-10-14 DOI:10.1186/s13550-024-01143-0
Amir Karimzadeh, Charlotte-Sophie Hecker, Matthias M Heck, Robert Tauber, Calogero D'Alessandria, Wolfgang A Weber, Matthias Eiber, Isabel Rauscher
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引用次数: 0

摘要

背景:177Lu标记的前列腺特异性膜抗原靶向放射性配体疗法的最佳治疗方案(包括治疗间隔)仍在研究中,有证据表明,缩短治疗间隔可使疾病体积大和病情进展快的患者受益。这项回顾性分析评估了接受177Lu-PSMA-RLT治疗的mCRPC患者的治疗毒性、PSA反应、PSA-无进展生存期(PSA-PFS)和总生存期(OS):治疗间隔为 4 周和 6 周组分别有 47.8% 和 21.7% 的患者达到 PSA 反应(PSA 下降≥ 50%)(p = 0.12)。与 6 周治疗组相比,4 周治疗组的 PSA-PFS 有延长的趋势(PSA-PFS 中位数,26.0 周 vs. 18.0 周;HR 0.6;p = 0.2)。虽然没有统计学意义,但与 6 周组相比,4 周组的 OS 有缩短的趋势(中位 OS,15.1 个月 vs. 18.4 个月;HR 1.3;p = 0.5)。与6周组相比,4周组的白细胞和血小板计数下降幅度明显更大(38.5%对18.2%,26.7%对10.7%;P = 0.047和P = 0.02)。两组的严重不良事件都不多:结论:将治疗间隔从6周缩短至4周,可在一定程度上改善mCRPC患者的PSA反应和PSA-PFS,但对OS无显著影响。此外,强化治疗方案会显著降低骨髓储备。因此,总体疗效仍不确定,需要进一步开展前瞻性研究,对4周和6周的毒性、治疗反应和疗效进行比较。
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Matched-pair analysis of mCRPC patients receiving 177Lu-labeled PSMA-targeted radioligand therapy in a 4-week versus 6-week treatment interval.

Background: The optimal regimen for 177Lu-labeled prostate-specific membrane antigen-targeted radioligand therapy, including treatment intervals, remains under study, with evidence suggesting shorter intervals could benefit patients with high disease volume and rapid progression. This retrospective analysis evaluated treatment toxicity, PSA response, PSA-progression-free survival (PSA-PFS), and overall survival (OS) in matched cohorts of mCRPC patients receiving 177Lu-PSMA-RLT at 4-week versus 6-week intervals.

Results: A PSA response (PSA decline ≥ 50%) was achieved in 47.8% and 21.7% of patients in the 4-week and 6-week treatment interval groups, respectively (p = 0.12). There was a trend towards longer PSA-PFS in the 4-week group compared to the 6-week group (median PSA-PFS, 26.0 weeks vs. 18.0 weeks; HR 0.6; p = 0.2). Although not statistically significant, there was a trend towards shorter OS in the 4-week group compared to the 6-week group (median OS, 15.1 months vs. 18.4 months; HR 1.3; p = 0.5). The 4-week group had a significantly greater decrease in leucocyte and platelet counts compared to the 6-week group (38.5% vs. 18.2% and 26.7% vs. 10.7%; p = 0.047 and p = 0.02). Severe adverse events were modest in both groups.

Conclusions: Intensifying treatment intervals from 6 weeks to 4 weeks showed some improvements in PSA response and PSA-PFS for mCRPC patients, but did not significantly affect OS. Additionally, bone marrow reserve was significantly reduced with the intensified regimen. Therefore, the overall benefit remains uncertain, and further prospective studies are needed to compare 4-week and 6-week intervals regarding toxicity, treatment response, and outcome.

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