Matched-pair analysis of mCRPC patients receiving 177Lu-labeled PSMA-targeted radioligand therapy in a 4-week versus 6-week treatment interval

被引:0
|
作者
Karimzadeh, Amir [1 ,2 ]
Hecker, Charlotte-Sophie [1 ]
Heck, Matthias M. [3 ]
Tauber, Robert [3 ]
D'Alessandria, Calogero [1 ]
Weber, Wolfgang A. [1 ]
Eiber, Matthias [1 ]
Rauscher, Isabel [1 ]
机构
[1] Tech Univ Munich, Sch Med, Dept Nucl Med, Munich, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Dept Diagnost & Intervent Radiol & Nucl Med, Martinistr 52, D-20246 Hamburg, Germany
[3] Tech Univ Munich, Sch Med, Dept Urol, Munich, Germany
来源
EJNMMI RESEARCH | 2024年 / 14卷 / 01期
关键词
Prostate-specific membrane antigen (PSMA); Radioligand therapy (RLT); Metastatic castration-resistant prostate cancer (mCRPC); 4-week treatment interval;
D O I
10.1186/s13550-024-01143-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background The optimal regimen for Lu-177-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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页数:10
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