Treatment Outcome, Toxicity, and Predictive Factors for Radioligand Therapy with 177Lu-PSMA-I&T in Metastatic Castration-resistant Prostate Cancer

被引:224
作者
Heck, Matthias M. [1 ]
Tauber, Robert [1 ]
Schwaiger, Sebastian [1 ,2 ]
Retz, Margitta [1 ]
D'Alessandria, Calogero [2 ]
Maurer, Tobias [1 ,4 ]
Gafita, Andrei [2 ]
Wester, Hans-Juergen [3 ]
Gschwend, Juergen E. [1 ]
Weber, Wolfgang A. [2 ]
Schwaiger, Markus [2 ]
Knorr, Karina [2 ]
Eiber, Matthias [2 ]
机构
[1] Tech Univ Munich, Med Ctr Rechts Isar, Dept Urol, Munich, Germany
[2] Tech Univ Munich, Med Ctr Rechts Isar, Dept Nucl Med, Munich, Germany
[3] Tech Univ Munich, Pharmaceut Radiochem, Garching, Germany
[4] Univ Med Ctr Hamburg Eppendorf, Martini Clin, Hamburg, Germany
关键词
Metastatic castration-resistant; prostate cancer; Radioligand therapy; Prostate-specific membrane antigen; Lutetium; MEMBRANE ANTIGEN; RADIATION-DOSIMETRY; PSMA;
D O I
10.1016/j.eururo.2018.11.016
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) is increasingly being used in metastatic castration-resistant prostate cancer (mCRPC). The objective of this study is to report our clinical experience with RLT using 177-lutetium-labeled PSMA-I&T. A total of 100 patients were treated under a compassionate use protocol with a total number of 319 cycles (median two cycles, range 1-6). Eligibility criteria included previous treatment with abiraterone or enzalutamide, previous taxane-based chemotherapy or chemoineligibility, and positive PSMA-ligand uptake at positron-emission tomography scan. The Lu-177-PSMA-I&T was given 6-8 weekly with an activity of 7.4 GBq up to six cycles. The median number of previous mCRPC regimens was 3 (range 1-6), and 35 patients had visceral metastases. Prostate-specific antigen decline of >= 50% was achieved in 38 patients, median clinical progression-free survival (cPFS) was 4.1 mo, and median overall survival (OS) was 12.9 mo. Subgroup analyses identified an association of visceral metastases with a poor prostate-specific antigen (PSA) response and shorter cPFS and OS, and an association of rising lactate dehydrogenase (LDH) with shorter cPFS and OS. Patients achieving PSA decline of >= 50% within 12 wk of treatment showed longer cPFS and OS. Treatment-emergent hematologic grade 3/4 toxicities were anemia (9%), thrombocytopenia (4%), and neutropenia (6%). Grade 3/4 non-hematologic toxicities were not observed. RLT with Lu-177-PSMA-I&T showed good activity in more than one-third of patients with late-stage mCRPC at low toxicity. Presence of visceral metastases and rising LDH were associated with worse treatment outcome. Patient summary: We analyzed the treatment outcome and toxicity of prostate-specific membrane antigen-targeted radioligand therapy in patients with metastatic castration-resistant prostate cancer. We found that a good treatment response could be achieved in a subgroup of patients with few side effects. We also observed that treatment outcome was worse in patients with organ metastases and elevated lactate dehydrogenase in blood tests. (C) 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:920 / 926
页数:7
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