Circulating androgen receptor gene amplification and resistance to 177Lu-PSMA-617 in metastatic castration-resistant prostate cancer: results of a Phase 2 trial

前列腺癌 医学 雄激素受体 内科学 优势比 泌尿科 置信区间 肿瘤科 雄激素 前列腺 睾丸切除术 癌症 激素
作者
Ugo De Giorgi,Maddalena Sansovini,Stefano Severi,Silvia Nicolini,Manuela Monti,Giorgia Gurioli,Flavia Foca,Chiara Casadei,Vincenza Conteduca,Monica Celli,Valentina Di Iorio,Daniele Calistri,Federica Matteucci,Finn Edler von Eyben,Gerhardt Attard,Giovanni Paganelli
出处
期刊:British Journal of Cancer [Springer Nature]
卷期号:125 (9): 1226-1232 被引量:21
标识
DOI:10.1038/s41416-021-01508-5
摘要

In a Phase 2 clinical trial, we aimed to determine the lutetium-177 [177Lu]-PSMA-617 activity and the clinical utility of levels of plasma androgen receptor (AR) gene in patients with heavily pretreated metastatic castration-resistant prostate cancer (mCRPC).We determined AR copy number in pretreatment plasma samples. We used logistic regression to estimate the odds ratio (OR) and 95% confidence intervals (95% CIs) in order to evaluate the independent relevance of AR status and to evaluate patients with early progressive disease (PD) defined as treatment interruption occurring within 4 months after the start of 177Lu-PSMA-617.Twelve of the 15 (80%) with AR gene gain and 5 of the 25 (20%) patients with no gain of AR had early PD (p = 0.0002). The OR for patients without PSA response having AR gain was 3.69 (95% CI 0.83-16.36, p = 0.085). The OR for patients with early PD having AR gain was 16.00, (95% CI 3.23-79.27, p = 0.0007). Overall, median PFS and OS were 7.5 and 12.4 months, respectively. AR-gained had a significant shorter OS compared to AR-normal patients (7.4 vs 19.1 months, p = 0.020). No treatment interruptions due to adverse effects were reported.Plasma AR status helped to indicate mCRPC with early resistance to 177Lu-PSMA-617.NCT03454750.
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