Current Developments in Combining External-Beam Radiotherapy and 177Lu-Labeled PSMA Ligands for Prostate Cancer Treatment

医学 前列腺癌 外照射放疗 放射治疗 临床试验 谷氨酸羧肽酶Ⅱ 肿瘤科 前列腺 剂量学 核医学 癌症 癌症研究 内科学
作者
Frederik R. Teunissen,Daniela E. Oprea‐Lager,Steffie M. B. Peters,Robert Jan Smeenk,Sandra Heskamp,Johan Bussink
出处
期刊:Journal of nuclear medicine [Society of Nuclear Medicine and Molecular Imaging]
卷期号:66 (12): jnumed.125.270465-jnumed.125.270465
标识
DOI:10.2967/jnumed.125.270465
摘要

The combination of external-beam radiotherapy (EBRT) and 177Lu-labeled prostate-specific membrane antigen (PSMA) ligands may improve the outcome for specific prostate cancer indications. This review aims to introduce the concept of this combined treatment, provide an overview of preclinical and clinical studies (as well as ongoing trials), and address current challenges and future directions to investigate this emerging therapeutic approach. Methods: A comprehensive search was conducted in online research databases (including PubMed) and trial databases (including ClinicalTrials.gov) to gather all relevant preclinical and clinical studies and ongoing trials on the combination of EBRT and 177Lu-labeled PSMA ligands. Results: One completed preclinical study demonstrated increased tumor growth delay and survival with combined EBRT and [177Lu]Lu-PSMA-617, compared with monotherapies, and one an additive effect. Four clinical reports published results on this combination, including series showing tumor regression in metastatic lesions and a pilot study demonstrating an increased biologically effective dose. Ten ongoing prospective clinical trials with varying designs, patient populations (de novo oligometastatic, oligorecurrent, and locally recurrent), treatment schedules ([177Lu]Lu-PSMA ligands neoadjuvant, adjuvant, concurrent with EBRT), and radiation doses and fractionation schemes were identified. Conclusion: The combination of EBRT and [177Lu]Lu-PSMA ligands holds promise to improve tumor control without increasing toxicity across various stages of prostate cancer. However, optimal treatment scheduling, dosing regimens, the role of dosimetry, and specific clinical indications require further investigation through robust preclinical and clinical research to guide future clinical trials.
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