Prostate-specific membrane antigen-targeted endoradiotherapy in metastatic prostate cancer

被引:27
|
作者
Lawal, Ismaheel O. [1 ]
Bruchertseifer, Frank [2 ]
Vorster, Mariza [2 ]
Morgenstern, Alfred [1 ,2 ]
Sathekge, Mike M. [1 ]
机构
[1] Univ Pretoria, Dept Nucl Med, ZA-0001 Pretoria, South Africa
[2] European Commiss, Directorate Nucl Safety & Secur, Joint Res Ctr, Karlsruhe, Germany
关键词
Ac-225 prostate-specific membrane antigen; Lu-177 prostate-specific membrane antigen; prostate cancer theranostics; prostate-specific membrane antigen radioligand therapy; targeted alpha therapy; LU-177-PSMA-617 RADIOLIGAND THERAPY; CHEMOTHERAPY; EXPRESSION; ADENOCARCINOMA; THERANOSTICS; EXPERIENCE; CARCINOMA; CYCLES;
D O I
10.1097/MOU.0000000000000685
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
Purpose of review In this review, we present an update on the safety and efficacy of prostate-specific membrane antigen (PSMA) radioligand therapy (PRLT) of metastatic castration-resistant prostate cancer (mCRPC). Recent findings Treatment of mCRPC with approved treatment agents leads to a survival advantage. The disease often progresses despite these treatments. PRLT with Lutetium-177 and Actinium-225 labeled with PSMA (LuPSMA and AcPSMA) have recently been shown to be effective and well tolerated for mCRPC treatment. LuPSMA is currently applied in patients who have exhausted approved treatment options or in whom these approved treatments are contraindicated. In this category of heavily pretreated patients, prostate-specific antigen (PSA) response (>= 50% decline) is achieved in about 46% of patients. Side-effects are tolerable with rare reports of grade III-IV treatment-induced toxicity. AcPSMA is currently applied on a smaller scale in patients who relapsed after LuPSMA or in whom LuPSMA is contraindicated. PSA response occurs in up to 88% of patients treated with AcPSMA. Summary PRLT with LuPSMA and AcPSMA is a well-tolerated and effective treatment modality for mCRPC. Prospective randomized control trials are necessary to facilitate its application as an approved therapy option.
引用
收藏
页码:98 / 105
页数:8
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