Experience of rescue therapy with [177Lu]Lu-rhPSMA-10.1 in patients with primary or acquired resistance to [177Lu]Lu-PSMA-I&T

被引:0
|
作者
Gaeble, Alexander [1 ,2 ]
Dierks, Alexander [1 ,2 ]
Rinscheid, Andreas [3 ]
Patt, Marianne [1 ,2 ]
Wienand, Georgine [1 ,2 ]
Pfob, Christian H. [1 ,2 ]
Kircher, Malte [1 ,2 ]
Fukushima, Kazuhito [4 ]
Nikolic, Ana Antic [1 ,2 ]
Enke, Johanna S. [1 ,2 ]
Janzen, Tilman [3 ]
Steinestel, Julie [2 ,5 ]
Kempter, Hildegard [2 ,5 ]
Trepel, Martin [2 ,6 ]
Weckermann, Dorothea [2 ,5 ]
Lapa, Constantin [1 ,2 ]
Bundschuh, Ralph A. [1 ,2 ]
机构
[1] Univ Augsburg, Fac Med, Nucl Med, Augsburg, Germany
[2] Bavarian Canc Res Ctr BZKF, Augsburg, Germany
[3] Univ Hosp Augsburg, Med Phys & Radiat Protect, Augsburg, Germany
[4] Kobe Int Collaborat Clin, Radiol, Kobe, Japan
[5] Univ Augsburg, Fac Med, Urol, Augsburg, Germany
[6] Univ Augsburg, Fac Med, Internal Med & Oncol, Augsburg, Germany
关键词
Prostate cancer; Radioligand therapy; Prostate-specific membrane antigen; Therapeutic response; Radiohybrid ligands; PROSTATE-CANCER;
D O I
10.1007/s00259-024-06959-5
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
PurposeRadioligand therapy is an increasingly important option for the treatment of metastatic castrate-resistant prostate cancer (mCRPC). Radiohybrid ligands targeting prostate-specific membrane antigen (PSMA) are a novel group of theranostic radioligand therapy agents for which higher tumour absorbed radiation doses have been demonstrated compared to established PSMA ligands. Here, we report data from ten patients who were treated within a compassionate use program with the radiohybrid PSMA-ligand [177Lu]Lu-rhPSMA-10.1 after experiencing disease progression under treatment with [177Lu]Lu-PSMA-I&T.MethodsTen patients with advanced PSMA-positive prostate cancer who showed progression under treatment with [177Lu]Lu-PSMA-I&T received up to three cycles of rescue therapy with [177Lu]Lu-rhPSMA-10.1 (7.4-8.1 GBq per cycle). Efficacy (PSA response according to PCWG3 and RECIP) and overall survival were evaluated. Adverse events were recorded from first application.ResultsDespite progression with [177Lu]Lu-PSMA-I&T, after the first cycle of [177Lu]Lu-rhPSMA-10.1 rescue therapy, five patients (50%) showed a decrease in serum PSA level. In imaging, three of the ten patients (30%) showed a partial radiologic response. Four of the five patients with a decrease of serum PSA under [177Lu]Lu-rhPSMA-10.1 had initially responded to treatment with [177Lu]Lu-PSMA-I&T but had become resistant. However, the remaining patient had shown continuous disease progression during [177Lu]Lu-PSMA-I&T therapy but showed an immediate response to [177Lu]Lu-rhPSMA-10.1. The additional treatment with [177Lu]Lu-rhPSMA-10.1 was generally well tolerated by all patients.ConclusionsPatients showing tumour progression while receiving [177Lu]Lu-PSMA-I&T radioligand therapy may benefit from rescue therapy with the novel radiohybrid PSMA ligand, [177Lu]Lu-rhPSMA-10.1. Higher tumour absorbed radiation doses with [177Lu]Lu-rhPSMA-10.1 may overcome primary and acquired radiation resistance.
引用
收藏
页码:970 / 978
页数:9
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